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Prof. George Church on Cellular Reprogramming and Longevity – Lifespan.io News

Professor of Genetics at Harvard Medical School, a veteran geroscientist, and a serial entrepreneur, George Church hardly needs an introduction. While we are always happy to discuss the present and future of geroscience with him, this interview focuses on the two gene therapy papers that he recently co-authored, which drew a lot of attention due to their spectacular and surprising results. In this interview, Prof. Church interprets these results and gives his opinions on a range of longevity-related topics, such as cellular reprogramming and supplements.

Thats a good question, especially given that we were using this huge vector. The whole point of cytomegalovirus is that it can package a lot more. I think its just that these experiments are not cheap, including the mice. What is distinctive about both papers is that they have a Kaplan-Meier plot, and those are more expensive than just showing some reversal of physiological decay or of an age-related disease. Both groups are thinking about combinations, they just havent done all of them yet.

Those are fairly independent pathways. There are arguably ten major pathways of aging, and I think you need to get all ten pathways if you want to impact longevity beyond a certain point. Its been estimated that doing just one of those ten pathways might get you two years of life extension in humans and maybe a few months in mice. But, if you develop something that impacts multiple pathways, some combination drug, that will be very interesting to see when we get to that.

I think the original explanation is that cachexia is muscle wasting that accompanies a lot of aging. You could argue thats just a late-stage thing, and to do real aging reversal youd want to get to the earlier stages, or you could argue that this is one of the ten pathways, and you want to have that part of a combination, but the answer is that its still not clear why it works in itself.

Its one of the mechanisms that cancer can cause death by, but there are others. Cancer can cause death by making it hard to breathe. It can screw up almost any physiological process, depending on where it starts and where it metastasizes, but muscle wasting can be a product of fairly normal aging without cancer as well. Seems like its a nice tool to have in your toolbelt, but I admit it is a little surprising that it works by itself.

First, there are effects that we do know about. If you give a long steady dose, it will increase the probability of tumorigenesis. It also sets you up for additional genetic and epigenetic changes that can make an even more serious cancer. But, if you give intermittent doses, its like with Yamanaka factors in the second study: if you give too much, cells could go back too far in time. So, I think its all about moderation.

The other thing that was done in germline experiments, or earlier animal models, is to use specific safeguards against cancer so that when you then introduce the telomerase, you can express it at higher levels and for longer periods of time. For instance, messing around with the p16 and p53 pathways, i.e., having extra copies of tumor suppressors, can protect you against certain forms of cancer and allow you to use things that would otherwise put you at risk.

Its all about resources. Both those companies are scrappy, young, underfunded, but they make up for it in creativity and delivery. Those are the only two gene therapy papers that I know of that show significant Kaplan-Meier plots. And I really like the gene therapy approach that they share, because you can target alleles, splice isoforms, and gene family members (paralogs). This is something thats very hard to do with small molecules, but very easy to do with either protein or gene therapies.

The slight advantage of gene therapies over protein therapies is that you have a few ways of rigging the specificity. You can have specificity of the vector, specificity of the nucleic acid, and finally, specificity of the protein. With proteins, you only have the latter.

The only thing I dont like about gene therapies is the cost, but one positive side of the COVID dilemma was that we tested five different vaccines that were formulated in the form of a gene therapy on billions of people and got the price down to as low as 2 dollars for one of those five. Its a whole new ballgame now if you have a large market, and I think pandemics and aging are the largest.

We had already done three genes at once at my lab and Rejuvenate Bio. Those were different from the OSK Yamanaka factors. The latter are transcription factors that need to be delivered to the nucleus, while the other set that we had, TGF beta receptor 2 in soluble form, Klotho, and FGF21, could be soluble, secreted, hence they could go into the interstitial, intercellular matrix, or they could go out into the blood. In a certain sense, it requires less delivery, or less ubiquitous delivery of the nucleic acid, because then the proteins do some of the delivery.

Thats the fundamental difference between those two. The significance of using the OSK is that this was the best example that we had of rejuvenation, as opposed to just fighting the symptoms of some age-related disease, making your muscles hurt less or something. This was truly rejuvenating ancient cells all the way back to embryo.

So, if you can control that, dial it up and down, it has some promise. This encouraged several groups, including Altos Labs, which I worked with briefly (many of my alumni are core members of Altos Labs). It is also one of the things that encouraged our collaboration with David Sinclair.

But, except for Rejuvenate Bio, so far, all of those are fairly distantly related to longevity. They might cure something like a crushed optic nerve, but damage to the eye is not aging, certainly not longevity. Now, this wasnt merely the Kaplan-Meier plot where you could see extended life. The injection occurred at the age of 124 weeks. For a mouse, its very late in life. Half of the mice in the cohort are already dead at that point.

The logic behind this was that if you do it as late as possible and show that it still has an effect, thats very encouraging. It broadens the market, thats one way of thinking about it, but it also tells you that you are really getting a reversal as opposed to delay, and thats a fundamental difference. Many drugs that are considered cures are reversing something, but people somehow put reversing aging in a special category, like breaking the sound barrier. However, just like breaking the sound barrier was easy enough to do once we figured it out, reversal of fundamental epigenetic programs that are a natural part of development and aging starts looking easier than it originally did.

There have been two major camps in aging since long ago. One says that aging happens due to damage, to proteins, lipids, RNA, and DNA, and that you have to go in there with your repair kit and fix it as a therapist. The other camp says that its all epigenetic, and that if you convince the cell that its young, it will get its own toolkit out and start repairing as much as it can. Some things are beyond repair. If you delete all copies of a tumor suppressor, thats not something a young cell can repair. But most things are fixable with epigenetics at least, thats how the second hypothesis goes.

I believe in a hybrid model. I think most of the work can be done epigenetically. A surprising amount of it can be done via the bloodstream, but probably not all of it. Then, theres a residual amount that you can fix with the Yamanaka factors and another residual amount that you can fix by restoring genes.

Since we do the epigenetic reprogramming by adding in genes, its not that fundamental a difference between adding in genes that will go into the blood, adding genes that will reprogram the nucleus, and adding genes that are missing, like tumor suppressors. In a certain sense, they are all addressable by multiplex gene therapy. Thats why being able to either use multiple rounds of dosing or to have bigger vectors will become increasingly important.

I think there are subtle but important differences between anti-aging drugs and drugs that improve biomarkers in the way that statins improve cholesterol. That doesnt mean such drugs increase longevity, just that they improve this one biochemical. It could actually hurt you; for instance, it could improve cardiovascular chances for some subset of the population, but for another subset, it could hasten muscle pain.

So, affecting biomarkers is one thing. Reversing diseases of aging is different. You could do it just by addressing that particular disease, or you could do it more broadly, affecting multiple diseases. You might get FDA approval for one of them, but its actually affecting multiple ones, and maybe acting preventatively. Say, there might be a cure for muscle wasting that helps prevent a variety of diseases.

Finally, youre really at the core of aging when you reprogram shared elements with good feedback systems that already exist in the body or with feedback systems that you introduce as part of the therapy.

The thing about clinical trials is that you ideally minimize talking about them before theyre done. This is a second animal trial. We did it in mice already, and it looked good. With the dogs, its not just an animal trial, its also a product, a veterinary product. I understand that some of the pet owners involved have said good things, but, of course, you have to be very cautious with anecdotal evidence. There could be wishful thinking, placebo effect involved. These are randomized clinical trials, so you really wont know until you break blinding at the end.

But the nice thing about veterinary clinical trials is that theyre typically much faster than human clinical trials. COVID-19 trials were an exception, 12 months, but most human clinical trials last about 10 years, and most veterinary trials are more like 18 months. So, well know soon.

We could have gone straight from mice to humans, but we decided to create a veterinary product. People spend a fair amount of money on end of life in dogs, they even clone dogs, but of course, a clone is not what you want. So, its valuable to have two or more animal preclinical trials before you go into clinical trials. Even though were looking into specific diseases, for instance, the mitral valve disease in spaniels, its not limited to that. We hope that it will hit many different diseases. Weve tested it in about five or six different diseases already, in mice and dogs.

To move this into humans, you use the same genes. You might use a human version of them, just like you might switch from mouse to dog genes, but other than that, mode of delivery. You might also change the vector. We use AAV vectors, which is the oldest approved vector and one of the most popular ones. However, dogs have natural immunity to most of the popular AAV vectors.

Thats clearly solvable. Its even solvable for redosing. One of the advantages of certain gene therapies is that you dont have to redose. You might have a once-and-done, lifetime expression, but a couple of my companies are working on improving the AAV delivery. Shape Therapeutics and Dyno Therapeutics are both making quite a progress on this. So, you can make radically different capsids that have radically different tissue tropisms and immune evasion. You basically make viruses that dont exist in the wild or in previous pharmaceuticals, and you can probably keep generating those things for quite a while.

First, with dogs, you can get a lot of feedback on how to maximize your chances of success. Second, its a product, so you can make a profit on the first product to pay for the development of the second product. Human clinical trials are expensive. You could do it by investment, but that would result in dilution of the original founders stake in it.

Also, dogs are just a particularly good intermediate between mice and humans, because they live in a human environment, they have some compatible behavioral traits and eating habits. You can identify personality changes, subtle behavioral changes that you dont identify in mice, because you dont cohabit with them like you do with dogs.

None of this means that we couldnt go directly to humans, its just that failures in human trials can put a damper on the whole field. I hope that all people in the field do their homework and dont rush trials, because they can screw it up for us. Were trying not to screw it up for them, and, hopefully, that will be reciprocated.

I co-founded 46 companies. Im on the scientific advisory board of a few more. Seven of them are related to aging reversal and longevity. They all involve pre-clinical and clinical trials. Some are on nutritional supplements, which you can sell without FDA approval, but nevertheless, theyre doing trials, and thats a strong preference for my involvement in a company: they have to be willing and planning to do, and also have the resources to do, clinical trials, even if not legally required.

I think the whole field is very healthy economically and scientifically. We have passed through multiple valleys of death. Were now in the solid science phase, and this field is going to be very impactful, maybe more impactful than any other pharmaceuticals in history, including even antibiotics, because our very ability to fight off diseases is age-related. Almost every single form of human morbidity and mortality has an age-related component to it. If you want to have a pleiotropic effect on many different diseases, this is the way to go.

So, it seems like a good choice. It also has a good chance of being cost-effective enough. Im not promising this on behalf of any of my companies, but since manufacturers of COVID vaccines can get gene therapy to be as cheap as two dollars a dose, others can do that as well, and thats important to me from the standpoint of equitable distribution of technology. Its not about can we develop a billion-dollar drug? Rather, its can we distribute it to everyone who needs it? And the same way that we got the price of DNA sequencing down seven orders of magnitude, 20-million-fold, I think we need to at least consider that for every new medical technology.

Yes, and I was referring to them when I said theyre willing to do clinical trials even though they are not required to do so.

I think we need to be very cautious about supplements that do not go through clinical trials and also about what trials they went through. If you do a clinical trial on ALS or some other degenerative disease, then thats all youre addressing. Youre not addressing the broader population. And, you have to be cautious, because some supplements have been shown to be detrimental if taken for prolonged periods in particular individuals that may have a pharmacological predisposition.

For example, some encourage cancer. And thats true for all things you put in your body. Just because your grandparents got away with it doesnt mean that its going to work, especially as we now have a more complex environment with a lot of other toxins.

Also, because were staying employed later and later in life, we need to reevaluate the things that were generally recognized as safe. So, Im very enthusiastic about testing and retesting things that have been accepted without formal clinical trials. Theres a lot of placebo effects, long-term effects, and wishful thinking that we need to put to the test. I hope those two companies continue along that pathway.

Im a scientific advisor. We shouldnt ignore companies that need advice, otherwise, they will be operating without advice. As long as theyre doing clinical trials, theyve got my attention.

I think we really need to hit all ten pathways and think about their interactions. In my opinion, the easiest way to go from a hypothesis or a pile of molecular data to a therapy is via gene therapy. In a couple of weeks, you can essentially go from a new research article to a therapy and get that therapy into mice.

So, Im particularly excited about those directions. We dont know yet whether it should be cell-autonomous or something that spreads through the blood, probably both. Im excited about the possibility that this could be low-cost for equitable distribution.All those things are clustered around this multi-drug therapy, which I think is fairly well-validated in other cases: multi-drug antibiotics, multivalent antivirals, cancer, some other diseases as well.

Yes, except you have to test them all in vitro and in animal models, in the exact formulation that you want to use, even if the ingredients were already tested individually. Sometimes with gene therapy, you cant test the very exact molecular form, because theres a difference between the animal form and the human form. But, other than that, everything should be as close as possible.

Its not either or. Cells can deliver genes and proteins. The advantage of cell therapy in principle is that you can debug the gene therapy ex vivo and then deliver it. For example, if you apply gene therapy in vivo to a billion cells, youve got a billion chances for genetic mischief, but with cell therapies, especially clonal cell therapies, you can debug it and make sure this is genetically and epigenetically what you want, that all cells are basically identical.

The downside of it is that many cells just dont deliver very well. For example, neurons are highly connected. Maybe you can deliver a few neuronal stem cells, including into parts of the brain that normally dont have neuronal stem cells, but you also want to keep most of your connections intact and not replace them with some generic neuronal progenitor. The bottom line is that theres room for a lot of different strategies and innovations.

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Prof. George Church on Cellular Reprogramming and Longevity - Lifespan.io News

Integrated analysis of next generation sequencing minimal residual … – Nature.com

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Integrated analysis of next generation sequencing minimal residual ... - Nature.com

Wang Details Caveats to Standards of Care for Treating Patients … – OncLive

When treating patients with mantle cell lymphoma (MCL), early identification and appropriate frontline therapy remains critical, and therapies may vary for those 65 years and older compared with patients under the age of 65, with several additional factomd andersonrs also having a role in approaching treatment options for a new patient in the clinic, according to Michael L. Wang, MD.

Wang, a professor in the Department of Lymphoma/Myeloma at The University of Texas MD Anderson Cancer Center in Houston, explained the factors he considers when determining the optimal therapeutic strategy for patients with MCL during the 27th AnnualInternational Congress on Hematologic Malignancies: Focus on Leukemias, Lymphomas, and Myeloma.1

Although age under 65 years and 65 years and older are used to stratify patients, Wang noted that translating these criteria to the clinic, a range of plus or minus 5 years can be used to adjust for care. Factors to consider include performance score. For example, Wang cited a very healthy 70-year-old patient or a patient who is 60 years with comorbidities and a low performance score.In addition to determining urgency of care, examining the patients cardiac history is crucial with renal and bone marrow function also being key factors. Treatment history with response from last therapy, duration of prior treatments, and history ofBruton tyrosine kinase(BTK) inhibitors should also be considered along with further parameters such as toxicities and transplant history.

Clinically you absolutely want to know the patients cardiac history and you want to know their kidney history, Wang said. Cardiac history is very important; I will not feel comfortable starting the patient with a BTK inhibitor without getting [a] cardiology consultation, electrocardiogram, stress tests, [and] echocardiogram.

Attention should be given to the organ system as a spleen over 20 cm may rupture and gastrointestinal (GI) bleeding can be severe. Central nervous system involvement when it is high-risk should be monitored as well.

Gastric MCL is quite commonly seen and sometimes you do an endoscopy but find that [the patient] had a volcano sitting theretheres a crater and near the crater theres a big artery ready to burst.

Examining pathology is key to determine if the MCL is pleomorphic or blastoid, and as MCL has 2 presentations, one of them being chronic lymphocytic leukemia, and this needs to be specified. Wang also noted he will run laboratory analyses such as creatine and lymphocytosis tests, and staging for MCL is more up in the air than staging is for other types of lymphoma, at MD Anderson Cancer Center, he will confirm complete response with PET/CT scans, bone marrow, and GI biopsies.

As knowledge on the role of genetic abnormalities continues to grow in MCL, there are limited data in many areas and it is unknown whether certain mutations, such as CARD11, will prove to be reliable targets. Other driver mutations, such as NOTCH1, NOTCH2, and c-myc have been shown to be associated with poorer outcomes. Wang highlighted that data may be gleande through programs such as the MCL Program of Excellence at MD Anderson in which patients with relapsed or refractory MCL undergo a front-door genetic panel and minimal residual disease and RNA-sequencing.

Frontline therapy for MCL is the most important therapy [as] many patients have only one opportunity [for treatment], Wang said. Each time you give a therapy the efficacy goes down [and] the interval of remission shortens until about 5 to 10 cycles, [then] the resistance becomes 100 [and] the efficacy becomes 0.

The natural history of MCL has shown that patients tend to be in remission and then relapse, with this occurring multiple times. Giving the best treatment in frontline when the patients immune resources, bone marrow, and organs are still in good condition is important. Wang noted he uses doublet therapies for those with high-risk disease because single-agent rituximab (Rituxan) is not adequate. Maintenance therapy is critical as well and other factors to keep in mind during treatment are toxicities, COVID-19 infection, and the personal history of patients including insurance, family support, and home location.

There is art in maintenance after frontline therapy. Rituximab is useful [to] prolong overall survival after almost any therapies, he said.

Although rituximab plus ibrutinib (Imbruvica) has demonstrated high response rates and can be used effectively, atrial fibrillation remains a prominent cardiac toxicity occurring in approximately 24% of patients.2 The R2 regimen of lenalidomide (Revlimid) and rituximab is an effective therapy that can be dose adjusted for renal failure. Wang noted he would also use the combination in patients with certain disease characteristics, such as tonsillar MCL or lymphoma that moves in the renal gland.

For patients with high-risk diseasea Ki67 index greater than 50%, a TP53 mutation, and/or pleomorphic/blastoid diseasetreatments include the SHINE regimen (ibrutinib, bendamustine[Bendeka]/rituximab and rituximab maintenance)3, rituximab plus ibrutinib maintenance for 2 years, acalabrutinib (Calquence)/venetoclax (Venclexta)/rituximab, or acalabrutinib plus R2. Wang said that rarely are bendamustine/rituximab and rituximab maintenance used or RCHOP plus rituximab.

MD Anderson is also evaluating rituximab plus acalabrutinib, rituximab plus pirtobrutinib, rituximab/pirtobrutinib/venetoclax, and ibrutinib monotherapy for smoldering MCL.

Younger patients with high-risk disease can receive the Window 2 study (NCT03710772) therapy of ibrutinib, venetoclax, and rituximab followed by a risk-stratified observation or short-course R-hyper-CVAD, according to Wang. Additional therapies include rituximab plus ibutinib with or without venetoclax maintenance for 2 years, acalabrutinib/venetoclax/rituximab, or acalabrutinib plus R2.

The Window-3 trial (NCT05495464) is ongoing at MD Anderson evaluating more treatment combinations for patients in this subgroup.

Approved agents for the treatment of MCL are bortezomib, lenalidomide, ibrutinib, acalabrutinib, zanubrutinib, the CAR T-cell therapy brexucabtagene autoleucel (Tecartus), and, most recently, pirtobrutinib (Jaypirca). Targeted agents and combinations such as BTK inhibitors, brexucabtagene autoleucel, chemotherapies, and stem cell transplants are under additional investigation as well.

Additionally, low-dose radiation for patients with an ATM mutation has shown efficacy and Wang noted that only 1 to 2 cycles of radiation are needed. Forty percent of patients have a frontline ATM mutation, he said. When you have ATM mutation the tumor is exquisitely sensitive to radiationso radiation therapy is a great therapy for MCL, sometimes you dont have to use high doses.

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Wang Details Caveats to Standards of Care for Treating Patients ... - OncLive

Enrollment Begins for Phase 2 Trial of IMNN-001 Plus Bevacizumab … – OncLive

Enrollment has commenced for a phase 2 trial (NCT05739981) investigating the DNA-based interleukin-12 (IL-12) immunotherapy IMNN-001 (formerly GEN-1) in combination with bevacizumab (Avastin) and chemotherapy in patients with advanced ovarian cancer.1

The study is expected to enroll 50 patients with stage III/IV advanced ovarian cancer, and it is being led by principal investigator Amir Jazaeri, MD, the vice chair for Clinical Research and director of the Gynecologic Cancer Immunotherapy Program in the Department of Gynecologic Oncology and Reproductive Medicine at The University of Texas MD Anderson Cancer Center.

The medical need for new innovative therapeutic approaches in ovarian cancer is major. The majority of patients with ovarian cancer are diagnosed with stage III/IV disease and face low cure rates of 15% or less, Corinne Le Goff, PharmD, MBA, president and chief executive officer of IMUNON, stated in a news release. The amount of data this study will generate will be a huge contribution to the treatment of ovarian cancer, and we believe the combination of IMNN-001 and bevacizumab has important potential.

In our animal studies, the combination clearly showed strong synergies. We are hoping that with this study we can potentially transform the current treatment landscape and provide new hope to women suffering from this deadly cancer.

IMNN-001 is an IL-12 DNA plasmid vector encased in a nanoparticle delivery system that enables cell transfection followed by persistent, local secretion of the IL-12 protein.

Previously reported data from the phase 1 OVATION 1 trial (NCT02480374) showed that the combination of IMNN-001 plus chemotherapy demonstrated activity and safety in patients with advanced epithelial ovarian cancer. Among 14 enrolled patients, 12 (85.7%) experienced a radiological response, including 2 complete responses and 10 partial responses.2

The most common treatment-emergent adverse effects that were at least possibly related to treatment included nausea, fatigue, abdominal pain/cramping, anorexia, diarrhea, and vomiting. Grade 4 neutropenia occurred in 8 patients, and this was attributed to neoadjuvant chemotherapy. No dose-limiting toxicities were reported.

The phase 2 trial is enrolling patients with a suspected diagnosis of high grade epithelial ovarian, fallopian tube, or primary peritoneal carcinoma with histologic confirmation per pre-treatment biopsies.3 Patients are also required to have an International Federation of Gynecology and Obstetrics stage of III or IV that has been determined to benefit from neoadjuvant therapy.

Other key inclusion criteria include the discontinuation of any hormonal therapy directed at the tumor within at least a week prior to first study treatment, an ECOG performance status of 0 or 1, and adequate bone marrow, renal, hepatic, and neurologic function.

The trial is excluding patients who have received prior treatment with IMNN-001; have had treatment with corticosteroids within 2 weeks of study entry or have a clinical requirement for ongoing systemic immunosuppressive therapy; have autoimmune disease requiring immunosuppressive therapy within the past 2 years; or have received prior radiotherapy or chemotherapy to any portion of the abdominal cavity or pelvis.

Enrolled patients are being randomly assigned 1:1 to receive chemotherapy plus bevacizumab with or without IMNN-001. Chemotherapy will consist of 175 mg/m2 of paclitaxel followed by area under the curve 5/6 of carboplatin on day 1 of each 21-day cycle. Neoadjuvant chemotherapy will consist of 4 to 6 cycles per investigators discretion, and adjuvant chemotherapy will last for another 3 cycles.

Bevacizumab will be administered at 15 mg/kg on day 1 of cycles 2, 3, 6, and 7, and bevacizumab will also be given as a single agent every 3 weeks during the maintenance phase for up to 18 cycles, or until disease progression or unacceptable toxicity. In total, bevacizumab will be given in up to 22 cycles.

Patients in the experimental arm will be given 80 mg/m2 of IMNN-001 once per week on day 15 of cycle 1 and continued through the end of adjuvant therapy. Following the conclusion of chemotherapy, IMNN-001 will be administered every 21 days with bevacizumab in patients who are BRCA negative and homologous recombination proficient.

The primary end point of the study is reducing the minimal residual diseasepositivity rate at second look laparoscopy from an expected 70% in the control group to 35% in the experimental group. Secondary end points include progression-free survival and overall survival.

Break Through Cancer is excited to support this important study, Tyler Jacks, PhD, president of Break Through Cancer, founding director of MITs Koch Institute for Integrative Cancer Research, and the David H. Koch Professor of Biology, stated in a news release.1 Our foundation has brought together some of the nations top cancer research centers to collaborate, accelerate research and clinical trials, and ultimately intercept and find cures for the deadliest cancers.

The phase 1/2 OVATION 2 trial (NCT03393884) is also evaluating IMNN-001 plus paclitaxel/carboplatin vs chemotherapy alone.4

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Enrollment Begins for Phase 2 Trial of IMNN-001 Plus Bevacizumab ... - OncLive

Dr. Van Cutsem on Primary Findings from the SPOTLIGHT and … – OncLive

EricVan Cutsem,MD, PhD, professor of medicine, division head, Department of Digestive Oncology, University of Leuven (KUL), University Hospitals Gasthuisberg, Leuven Belgium, discusses primary efficacy and safety findings from the phase 3 SPOTLIGHT (NCT03504397) and GLOW (NCT03653507) trials investigating the monoclonal antibody zolbetuximab (IMAB362) in metastatic gastric cancer.

The international, randomized, placebo-controlled SPOTLIGHT trial compared the use of zolbetuximab plus mFOLFOX6 vs mFOLXOX6 and placebo in patients with Claudin 18.2 (CLDN18.2)positive, HER2-negative, locally advanced, unresectable or metastatic gastric or gastroesophageal junction (GEJ) adenocarcinoma, Van Cutsem begins. A significant proportion of patients with advanced gastric cancer are CLDN18.2-positive, he notes.

Primary results from the study presented at the 2023 ASCO Gastrointestinal Cancers Symposium showed that zolbetuximab plus mFOLXOX6 elicited statistically and clinically significant improvements in both progression-free survival (PFS) and overall survival (OS), Van Cutsem states.

Positive topline results from the GLOW trial of zolbetuximab in combination with capecitabine and oxaliplatin (CAPOX) were also recently reported, Van Cutsem adds. This trial evaluated this regimen vs CAPOX plus placebo as first-line treatment in the same population as SPOTLIGHT, and zolbetuximab plus data demonstrated a statistically significant PFS and OS for patients treated with zolbetuximab plus CAPOX.

These randomized studies support use of zolbetuximab in combination with current chemotherapy regimens as a novel and effective treatment strategy for CLDN18.2-positive advanced gastric cancer, Van Cutsem states.

Additionally, HER2, microsatellite instability status and PD-1 biomarker testing is now standard in the frontline setting for advanced gastric cancer. If zolbetuximab receives approval in this setting, CLDN18.2 should be assessed as an additional prognostic marker in this disease space, Van Cutsem concludes.

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Dr. Van Cutsem on Primary Findings from the SPOTLIGHT and ... - OncLive

Tech Inventions That Changed The Health Industry Forever – SlashGear

Medical imaging is not, of course, a single technology, but an umbrella term for a bunch of different methods of getting a handle on what's going on within our bodies. One example might be a combination of these methods, like the Explorer total-body scanner, which performs both PET and CT scans. Without these advancements, we'd be devoting a lot more resources to palliative care. The tech in question includes x-rays, CT scans, MRIs, and ultrasounds, and each has changed the diagnostic landscape in its own way.

But x-rays themselves aren't just a diagnostic tool. They are used to guide surgeons, monitor the progress of therapies, and inform treatment strategies for the use of medical devices, cancer treatments, and blockages of various sorts. In 1896, the then-hyphenated New-York Times mocked Wilhelm Conrad Rntgen's medical application of X-ray imaging as an "alleged discovery of how to photograph the invisible." Five years later, Rntgen won the Nobel Prize in Physics. A century later, X-rays have replaced invasive surgeries and guesswork as a core diagnostic tool for doctors at every level.

Less a new imaging technology than a brilliant implementation of existing methods, computed tomography (CT) uses cross-sectional X-ray images acquired from various angles and computer algorithms to rapidly create a navigable, three-dimensional image of small or large parts of the body. Because it's based on X-rays, CT scans are better at imaging bones than soft tissues. CT scans provide many of the same benefits as other medical imaging methods, enhanced for many purposes by their speed and superior imaging of bones.

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Tech Inventions That Changed The Health Industry Forever - SlashGear

KND Labs & ReaGenics Announce Partnership to Expand Food … – Pet Business Magazine

KND Labs, a manufacturer of nutraceutical ingredients with an initial focus on hemp plant-derived cannabinoids, has announced apartnership with Israel-based plant molecular harvesting companyReaGenics. As a new commercial platform for KND Labs, the partnership will enable the company to expand its product offerings in the global nutraceutical and ingredients marketplace.

As a producer of many ingredient forms including powdered isolates, distillate oil, and liquid or powder water-soluble solutions, KND Labs currently serves many industries and is an ingredient partner to many of the worlds largest product brands.

As a proven partner across many industries from food and beverage to nutraceuticals, pet, and cosmetics, KND Labs is thrilled to expand our supply chain and product offerings through this partnership with ReaGenics, said Nich Wilson, KND Labs president. This capability directly supports the companys growth goals and allows us to target, extract and commercialize revolutionary ingredients within the KND Labs platform we are known for.

ReaGenics is a Nes Tziona, Israel-based plant molecular harvesting company that provides technology to support the growth of living plant stem cells economically and at scale, without having to depend upon natures elements. Through its proven technology and process, the company is able to access molecular materials that are of interest in various industries including food and beverage, herbal medicine, and other applications.

With processing plants in the Denver area, KND Labs will utilize the ReaGenics partnership to move into new areas of expertise in the coming years, while offering ReaGenics access to its established production facilities and customer distribution network.

Our world urgently needs a way to keep up with the growing demands of medicines, food supply chains, and the problem of so many of the worlds plant species on their way to extinction, said ReaGenics CEO Dr. Michael Kagan. We believe ReaGenics will be part of the solution to ensure these global needs and challenges are met. This partnership with KND is an important first step.

The partnership will benefit both companies growth efforts in the nutraceutical, food, and pet industries, with KND Labs focusing on making new products available.

Many customers are looking to KND Labs for our industry expertise and scaling capabilities as they aim to diversify their ingredient supply chains, said Dave Swany Swanwick, KND Labs director of sales. "This partnership with ReaGenics enables us to offer a greater variety of ingredients, at scale, to our direct partners as well as for network marketing sellers of hemp plant-derived products, and it will allow us to further grow our footprint as the premier provider of high-demand nutraceutical ingredients. We are very excited to be improving supply chain access and commercializing rare ingredients worldwide.

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KND Labs & ReaGenics Announce Partnership to Expand Food ... - Pet Business Magazine

‘We’re All Exposed’: How Microplastic Is Affecting Our Health and … – The Epoch Times

Expert says mounting microplastic pollution is turning Earth into a giant chemistry experiment

Our world is getting polluted with plastics on a planetary scale. We cant see much of it, but were starting to feel it. And its getting worse.

The plastic bottle tossed by the roadside and the endless trash heaps in third-world countries are just the beginning. As the trash ages, it breaks down into smaller and smaller pieces, until it cant be seen with the naked eye anymore. At that point, however, the problems have barely begun.

These tiny pieces of plastic, called microplastics, have permeated everything, scientists have found in recent years. They can be as large as 5 millimeters and as small as 100 micronsabout as thin as a human hairor even smaller, at which point theyre sometimes referred to as nanoplastics.

Microplastics have been found in the most remote corners of the world.

It doesnt matter where we look. We find microplastics. In the environment, it could be the bottom of the Marianna Trench, it could be the top of Mount Everest and everywhere in between, said Sherri Sam Mason, associate professor at Penn State Behrend and expert on microplastic pollution.

As a consequence of it being everywhere in the environment, its everywhere within living organisms.

Microplastics have been found in the animals we eat, in the water we drink, and in the air we breathe. Its in our blood and in our organ tissues, even the deepest tissue of our lungs.

We have a tendency to have this illusion that our skin separates us from the environment, but it is an illusion, Mason said.

Children, nowadays, are being born with microplastic already in their bodies.

Plastic particles have been found on both sides of the placental boundary, meaning its seeping from the mothers body into the unborn child.

The repercussions of such pollution are largely unknown. Getting definitive answers has proven immensely difficult. What research has been done, however, indicates the effects are negative.

With regard to the human health impacts of it, perhaps unsurprisingly, none of them are good, Mason said.

There are many ways to address the issue, but its not clear whether a definitive solution is practically achievable. The pollution can be greatly reduced by ditching single-use plastic packaging and reforming the fashion industry. That still leaves a massive amount of plastic entering the environment, not to mention the substantial pollution there already is.

So far, research has largely focused on gauging the scale of the issue. It wasnt until 2018, for example, that a paper was published at least somewhat accurately estimating how much plastic is floating in the Great Pacific Garbage Patchthe largest of several massive accumulations of plastic trash in the oceans. Even then, the estimate ranged from 45,000 to 129,000 tonnes.

Worldwide, some 7 billion tonnes of plastic trash are estimated to be in the environment, in landfills, oceans, dumps as well as just strewn around. That amount is expected to grow to 12 billion by 2050.

Research has already found that small pieces of plastic are a problem for fish and birds who mistake them for food. The plastic sits in their stomachs, making them feel full even though they may be malnourished. That in turn affects their growth and ability to procreate.

What the more microscopic plastic particles may do to the bodies of animalsor humans for that matteris mostly unknown and may to a large degree remain so.

One of the problems is isolating the effect of plastics from all the other factors messing with human health.

Some of the impacts are not acute. If you have a liver pack-full of nanoplastics or its in your placenta, how do you correlate that to harm? said Marcus Eriksen, co-founder and researcher at 5 Gyres, an environmental group that aims to reduce plastic pollution.

He cautioned that in many cases, were not going to get clear-cut evidence because of the complexity of trying to establish a cause-effect relationship.

One of the most established ways to discover the health effects of a substance is through placebo-controlled clinical trialspreferably long-term. But thats particularly difficult in this case. Microplastics are so pervasive there may be nobody left to form a control group.

Were all exposed. Whos not? Eriksen commented.

Heath impacts can be studied to some extent through animal experiments. Its also possible to use artificial human tissue grown from stem cells.

Its expensive and time-consuming, he said.

Its easier to look at the effects of chemicals added to the plastics, such as flame retardants in solid plastics or water repellents in fabrics.

We know more about the chemicals than we do the plastics, the material itself, Mason acknowledged, adding that there are more than 10,000 chemicals that are used in the manufacturing of plastics, and many of these we already know have human health impacts.

Moreover, microplastic can act as a temporary sponge, absorbing chemicals from the environment and releasing them later inside an organism, said Lisa Erdle, director of Science & Innovation at 5 Gyres.

Some of the chemicals added to plastics can cause cancer or harm fertility, according to Mason.

As for the plastics themselves, some studies suggest they may worsen Alzheimers disease and disrupt cell function, according to Mason and Erdle.

Theres starting to be a connection being made between this material and certain neurological diseases, Mason said.

Another factor complicating the research is the immense variability of plastics.

At their core, plastics are made of large hydrocarbon molecules that can be assembled into a virtually infinite number of shapes and variations, giving them different physical and chemical properties. The complexity of discerning their health effects one by one and in various combinations is then also nearly infinite.

Moreover, new kinds of plastics are developed all the time. Current science has no way to determine in advance all the long-term health effects of each type of plastic after it breaks down into microplastics and spreads throughout the environment.

We have turned our planet into a giant chemistry experiment, Mason said.

Were doing an experiment on ourselves and our children and our childrens children.

She pointed to hubris as the cause of our throwing caution in the wind as we think that were smarter than we are.

Maybe it will take 10 years, maybe it will take 50 years, but its going to come back to bite us, she said.

Eriksen acknowledged that the jury is still out on the long-term effects of plastic pollution. But he argued its time to pause and rethink how we do things.

The abundance of novel chemicals in society, in our environment, and the lack of understanding of how they affect these living systems and their interaction effects, it makes me want to employ the precautionary principle, he said, though he acknowledged data on the issue is still lacking.

Does the research show that the impacts should cause public fear? Not quite there yet. Because the research, it takes a long time, he said.

But my gut says, Do no harm. Im always for prevention of a problem if you see it happening. Why wait until the problem is much bigger than it already is to then say, Oh, its a big problem?

Even though the plastic pollution problem may be impossible to solve completely, there are ways to mitigate it. About half of all plastic pollution is estimated to come from single-use packaging. Much of it has non-plastic alternatives.

There are also companies working on alternative materials that naturally break down.

Were seeing a lot of investment, [venture capital] money, going to some of the new biomaterial companies. Its pretty inspiring, Eriksen said.

A material called PHA, for example, is made of a chemical that microbes use in their cellular wall to store energy.

We can extract that and make what looks and feels like plastic. It has a long shelf life, it can be translucent, it can be made in different colors, it can be made into rigid plastics or flexible plastics. And in the environment, it begins to break down very quickly, he said.

Theres also a company thats developing a material that works as plastic cling wrap, but is made of seaweed and breaks down after discarding.

Those materials are still more expensive than plastics though.

They have the challenges that any startup might have, Eriksen said, hoping that as the production scales up, the price will drop.

Industries that use plastics for single-use packaging may be willing to pay a bit more in exchange for the positive PR a more nature-friendly material could bring, he suggested, referring to his conversations with corporate executives in the industry.

Theyll shift if the science is good, the packaging works for them, and gives them a good story to tell.

Recycling could work in theory, but in practice remains inefficientnew plastic ends up being cheaper.

You have to get it back from the consumer, then you have to repolymerize it, repelletize it, and distribute that to your costumers, Eriksen said. Those are real expenses and thats not as efficient as the system of extracting raw materials and making virgin resin.

Producers that are willing to use alternative or recycled materials are those in the high-end market able to absorb the costs, he said.

The only way to give recycling an economic chance, he opined, would be to force producers to buy recycled material by government fiat.

Another problem is that a lot of plastics cant be recycled, such as the thin plastic film used for packaging, which is expected to greatly increase in production in the coming years.

Even materials that can be recycled may end up in the landfill if the manufacturer combines them with unrecyclable substances in the same product.

If you take plastics and you line it with metal or paper or use adhesives or have different kinds of polymers in one product, it makes recycling mechanically very difficult, in some cases economically impossiblenot worth it, Eriksen said.

Youve got to set up for success. And thats been an endless fight for decades.

One of the supposed success stories of recycling is turning plastic PET bottles into synthetic fleece fabric.

In Eriksens view, however, thats a marketing scheme rather than a long-term solution.

Synthetic textile, and fleece in particular, stands as the No. 2 plastic pollutant behind single-use packaging. Synthetic threads are the most pervasive microplastic pollutant in human lungs, according to Erdle, who specializes in research in this area.

The fibers shed directly from synthetic fabrics like clothing, carpets, and upholstery. They also shed into wastewater when the fabric is washed.

A single load of laundry can release up to eight million fibers, Erdle said.

Wastewater treatment plants are able to filter out the threads, but some end up in the sludge called biosolids, which is then used as a fertilizer. The fibers are thus dumped into soil from which they are then picked up by wind or surface water and travel large distances in air currents. Just like other plastics, they break down into smaller and smaller pieces over time.

We dont really know how long theyll last in the environment just because all the studies to date that have tested them show little to no degradation, she said.

A partial solution is installing filters in washing machines that can capture most of the escaping lint.

It would also help to use less synthetic fabric, or at least switch to ones that shed less.

There are lots of brands that are working on developing textiles that shed fewer microfibers, or if they do shed fibers, they are less toxic, less persistent, and are ultimately causing less harm, Erdle said.

A major help would be to step back from the current fast fashion culture that produces a never-ending stream of fleeting trends followed by an avalanche of low-quality garments destined to be discarded.

One movie star wears a hat and suddenly there are a gazillion low-quality hats on the market and people buy them. And in a few months, theyre not in fashion anymore, Eriksen commented, noting that trashed clothing has become a major source of pollution.

Many plastics can be easily burned, but that comes with its own suite of problems, Mason said.

Its very dirty.

Burning plastics, particularly those that contain PVC, releases large amounts of toxic chemicals, many of which are highly poisonous and carcinogenic. The fumes can be filtered, but some amount of the chemicals still get through.

You cant engineer these things to perfection. And many of these chemicals are known to have human health impacts at parts-per-trillion levels, she said. Thats like a single drop in an Olympic-size swimming pool.

Mason sees only one true solution: use less plasticsubstantially less.

Both Mason and Eriksen support new government regulations that would ban single-use plastic packaging, for example.

The trouble is, much of the plastic packaging and much of the synthetic fabric is made overseas, in countries like Indonesia, Philippines, Thailand, Vietnam, and China. Even if they were forced to stop exporting such products to the United States, they still produce massive amounts of plastic pollution themselves.

The United States mismanages less than 3 percent of its plastic waste, according to estimates made in a 2020 paper, while China mismanages 25 percent, Thailand and Indonesia over 60 percent, and the Philippines and India over 70 percent.

And that doesnt even begin to address the billions of tons of plastic trash already in the environment that is steadily breaking down into microplastic trash.

Mason and Eriksen place some hope in the United Nations treaty on plastic pollution currently in the works. It was endorsed by 175 countries in a resolution last year (pdf).

But the resolution still emphasizes things like recycling and ocean cleanups, neither of which amount to a solution, Eriksen said.

The solution isnt going to be more cleanups. Were not going to recycle our way out of this problem. Its going to take smart policy that applies to everyone and levels the playing field.

The resolution, however, suggests that it wont apply to everyone equally.

It acknowledges that the effective implementation of some legal obligations under the instrument is dependent on the availability of capacity building and technical and adequate financial assistance and provides for flexibility that some provisions could allow countries discretion in implementation of their commitments taking into account the national circumstances.

Beyond the treaty, Mason and Eriksen suggested the West should still do what it can on its own, but if that doesnt make enough of a dent, there doesnt appear to be a definitive solution, save a miracle.

I do agree that currently it looks dark, that currently, at best, our present efforts are only working to slow the pace and not reverse the tide, which is what we need, Mason said via email.

I do certainly have my times of feeling like it is all hopeless, but cannot stay in that space because well I have a daughter and someday I may have grandchildren, and so I have to keep fighting. History does tell us that all is hopeless until it is not. At some point, and hopefully at a point in which it is not too late, we will have no choice but to change.

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'We're All Exposed': How Microplastic Is Affecting Our Health and ... - The Epoch Times

Best Pet Insurance That Covers Hip Dysplasia – MarketWatch

In this article: About Hip Dysplasia | Top Pet Insurance Companies | Is Pet Insurance Worth It? | Waiting Periods | Is Hip Dysplasia a Preexisting Condition? | FAQs | Methodology

Hip dysplasia is a painful malformation of the hip joint that can affect your pets mobility and quality of life. It can happen to cats and dogs at any age, but older, large-breed dogs such as German shepherds and golden retrievers are most susceptible.

Because hip dysplasia is an expensive chronic condition, many pet insurance companies place exclusions and waiting periods on related expenses. These are the best pet insurance providers for hip dysplasia to ensure your pet receives coverage.

Most pet insurance companies cover hip dysplasia, but only under certain conditions. Most importantly, there must not be any signs or symptoms before your policys effective date or during the waiting period.

Many providers have a special waiting period for orthopedic conditions, including hip dysplasia, typically six to 12 months. Additionally, theres often a bilateral condition exclusion, which means that if your pet shows symptoms in one hip before or during the waiting period, dysplasia in the other hip isnt covered either.

Based on our rigorous research, these are the top pet insurance companies for hip dysplasia.

Spot earns our top spot because it has one of the shortest waiting periods for hip dysplasia: only 14 days, the same as any other illness. The company also has more customizable coverage than competitors, including annual limit options between $2,500 and unlimited.

+ Short hip dysplasia waiting period

+ Option for unlimited annual coverage

+ No upper age limits

Relatively long accident waiting period

Doesnt pay the vet directly

Spot covers hip dysplasia under its accident-and-illness plan. You can add one of its wellness plans for preventive care.

To learn more: Spot Pet Insurance review

Get your quote: Fill out Spots online quote form

Trupanions waiting period for hip dysplasia is also relatively low at 30 days. Theres no upper age limit or bilateral exclusions, which is rare. Trupanion further stands out for its flexible deductible, allowing pet owners to choose a rate between $0 and $1,000. Its deductibles are per condition, not annual, and are paid for the lifetime of your pet once reached.

+ 30-day waiting period for hip dysplasia

+ Pays directly for vet visits, rather than reimbursing you later

+ Unlimited coverage cap

30-day waiting period for illness coverage

No add-on for preventive care

Trupanion covers hip dysplasia under its standard accident-and-illness plan. You can add its Recovery and Complementary Care package to get coverage for healing treatments such as acupuncture, chiropractic adjustments, hydrotherapy and rehabilitative therapy.

To learn more: Trupanion review

Embrace covers hereditary conditions such as hip dysplasia with no per-incident coverage caps. Although theres a six-month waiting period for orthopedic conditions, this can be reduced to as little as 14 days if you fill out a form and take your pet for an orthopedic exam. Embrace also offers multiple discounts and a Healthy Pet Deductible benefit that credits pet owners $50 toward their co-payment each year they dont file a claim.

+ Orthopedic Exam and Waiver reduces the waiting period for hip dysplasia

+ Diminishing deductible for each year without a claim

+ Two-day waiting period for accident coverage

Low coverage limit for preventive care

$25 enrollment fee

Embrace covers hip dysplasia in its standard accident-and-illness plan. You can get wellness coverage by opting for its wellness add-on.

To learn more: Embrace Pet Insurance review

Get your quote: Fill out Embraces online quote form

Formerly PetPlan, Fetch by Dodo covers hip dysplasia after a six-month waiting period. It doesnt limit payouts by condition or lifetime, which will prove valuable for something like total hip replacement surgery. It also offers robust holistic care such as acupuncture, homeotherapy and stem-cell therapy.

+ No per-condition coverage cap

+ Covers alternative therapies

+ Healthy Pet Credit offers discounts for years without filing claims

No routine care coverage

Long average claim processing period

Fetch covers hip dysplasia under its standard accident-and-illness plan. It doesnt offer add-ons for preventive care.

To learn more: Fetch Pet Insurance review

Get your quote: Fill out Fetchs online quote form

Youll need to enroll your pet by age 6 to qualify for hip dysplasia coverage from Healthy Paws. The companys selling point is its unlimited annual and lifetime coverage caps. These ensure you wont have to worry about going over your maximum limit when treating a condition like hip dysplasia, which sometimes requires costly surgery.

+ Most claims processed within two days

+ No coverage caps

+ Covers some alternative treatments

12-month waiting period for hip dysplasia

Other age-based exclusions

Healthy Paws covers hip dysplasia in its standard accident-and-illness plan. It doesnt offer add-ons for preventive care.

To learn more: Healthy Paws Pet Insurance review

Get your quote: Fill out Healthy Paws online quote form

ASPCA pet insurance is a seasoned provider with more than 15 years of experience. Though the company is a little unclear about its coverage policy for hip dysplasia, the condition doesnt appear to be subject to any exclusions apart from a 14-day waiting period.

+ Short waiting period for hip dysplasia

+ Covers alternative therapy, end-of-life expenses and some prescription food

+ Option to add wellness care

Unlimited coverage not available by online quote

Coverage may vary by state

ASPCA covers hip dysplasia in its accident-and-illness plan. It also offers two wellness add-ons with different coverage levels and annual limits.

To learn more: ASPCA Pet Insurance review

Pets Best insures pets of all ages, but it stands out for its coverage of older pets. Unlike competitors, it has no age limit and allows you to enroll your pet anytime. It offers excellent hip dysplasia coverage starting after 14 days and covers wheelchairs prescribed by a vet, which some pets will need when suffering from the condition.

+ Hip dysplasia waiting period is only 14 days

+ Coverage for wheelchairs and prosthetics

+ Vet Direct Pay available in some areas

Illness coverage not available to some pets with severe chronic conditions

Exclusions for parasites and alternative therapies

Pets Best covers hip dysplasia in its accident-and-illness plan. It also offers two wellness add-ons for preventive care.

Pet insurance for hip dysplasia is only worth it if you enroll your pet before it shows signs of the condition. Otherwise, hip dysplasia will be considered a preexisting condition, and you wont be reimbursed for related costs. Enrolling your pet while its still healthy could save you thousands of dollars since hip dysplasia treatments are generally expensive. Most treatments require surgical procedures such as triple pelvic osteotomy and femoral head osteotomy, which can cost $6,000 or more.

Theres always a waiting period for hip dysplasia, as there is for all illnesses and conditions. Many pet insurance policies have much longer waiting periods for hip dysplasia and cruciate ligament problems than other illnesses and conditions.

Preexisting conditions are never covered by pet insurance. If the condition shows up during the waiting period on your policy, its considered preexisting.

If your pet is already showing signs of hip dysplasia, you wont receive coverage for the condition. However, pet insurance will still cover expenses for accidents or unrelated illnesses. So if your pet is still young and healthy but prone to hip dysplasia, its worth buying pet insurance now to know it will be covered later. You could save thousands of dollars.

Frequently Asked Questions About Hip Dysplasia

Our review of pet insurance companies is based on in-depth industry research that includes reading hundreds of customer reviews, simulating the quote and purchasing process, speaking to representatives on the phone to assess the customer service experience and surveying 1,000 dog and cat owners nationwide to determine the most important elements of pet insurance coverage. We have scored each provider on a 100-point scale based on those elements.

Here are more details about each factor and how theyre weighted:

We use our rating system to compare and contrast each company against key factors to help us determine the best pet insurance companies in the industry. Additionally, we keep our research up to date and revisit our reviews on a regular basis.

Dana Getz is a seasoned editor with nearly a decade of experience writing and editing content. She has a background in journalism and worked as a fact-checker for prestigious magazines such as New York and Chicago. She holds a journalism and marketing degree from Northwestern University and has worked across numerous categories within the home services space.

See more here:
Best Pet Insurance That Covers Hip Dysplasia - MarketWatch

Derelict Leigh-on-Sea Post Office to be transformed into new gym – Essex Live

A derelict post office building in a seaside town in Essex is being transformed into a new gym. The former Post Office on Rectory Grove in Leigh-on-Sea closed down around six years ago and is now being turned into an Anytime Fitness gym.

The new gym will be run by Zoe Georgiou and her husband Tony. Speaking to EssexLive, Zoe said she was brought up in Leigh and feels passionately about bringing wellbeing and a healthy lifestyle to the area.

She said: "I know the area well and I know the building well and I remember the post office and so we thought it was perfect for us." She added: "We definitely want to restore the building. We definitely feel that it is vert much a hub of Leigh on Sea and we want to bring that back to life again, for the community.

Read more: The upmarket seaside town that's full of family-run, independent businesses

"And I think the community could benefit massively from a gym where people can come and meet, improve their health and their lifestyle." The building is also located right in the heart of the town, making it accessible for everyone.

Zoe said: "The key thing is that we want to operate our gym on the basis of bringing the community together. And that includes partnering with local businesses in the community to bring our members membership benefits and other benefits."

Due to the size of the building, instead of focusing on classes for members, the new gym will be offering group training with personal trainer-qualified team members as part of memberships. It'll deliver a more personalised experience, Zoe said, being able to see and engage with the instructors more easily and to get more personal training in that time as well.

The Anytime Fitness gym on Rectory Grove in Leigh-on-Sea will be opening in the second half of this year.

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See the article here:
Derelict Leigh-on-Sea Post Office to be transformed into new gym - Essex Live

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