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Tuesday, October 2, 2018
Centene price target raised to $158 from $146 at Oppenheimer
Oppenheimer analyst Michael Wiederhorn raised his price target for Centene to $158 from $146 given the company’s continued bullish prospects. The analyst believes the company remains well-positioned due to stable cost-trend and the potential for growth in the coming years, particularly in the Medicare and Exchange businesses. Furthermore, the recent integration of the Fidelis deal remains on track, and the additional accretion/synergies should drive incremental earnings growth in 2019 and beyond, he contends. Wiederhorn reiterates an Outperform rating on the shares.
https://thefly.com/landingPageNews.php?id=2798361
Cellectar Biosciences updates interim overall survival data from myeloma trial
Cellectar Biosciences updates interim overall survival, or OS data from the company’s ongoing Phase 1b clinical trial evaluating CLR 131 for the treatment of relapsed/refractory multiple myeloma, or MM. The results to date show that OS is currently at 19.4 months. Cellectar continues to monitor these patients and intends to update OS results as data become available. All 15 patients from the Phase 1b, single-dose cohorts were heavily pretreated, receiving an average of 5 previous lines of multidrug therapy including anti CD38, immunomodulating drugs and proteasome inhibitors. All patients were relapsed or refractory to at least one proteasome inhibitor and IMiD. Most patients presented with advanced stage 2 or 3 disease and 67% had previously received at least 1 stem cell transplant.
https://thefly.com/landingPageNews.php?id=2798367
Seattle Genetics price target raised to $98 from $90 at RBC Capital
RBC Capital analyst Kennen MacKay raised his price target on Seattle Genetics to $98 and kept his Outperform rating, saying its ECHELON-2 trial “exceeded best case scenario” with a “surprise” overall survival benefit. The analyst notes that the results were a “clean win with E-2’s magnitude of PFS benefit”, raising his probability of success for the program to 100% from 75%.
https://thefly.com/landingPageNews.php?id=2798375
LeMaitre downgraded to Neutral from Buy at Roth Capital
Roth Capital analyst David Solomon downgraded LeMaitre to Neutral from Buy, while raising the shares’ price target to $39 from $38, citing valuation after assuming coverage of the stock. The analyst notes that the company announced that it acquired Applied Medical’s vascular clot management business for $14.2M. Among the key takeaways, the analyst highlights that the acquired products bolster its line of embolectomy catheters, and points out that LeMaitre’s appetite for another acquisition remains.
https://thefly.com/landingPageNews.php?id=2798381
Baxter, Mayo Clinic Collaborate to Establish Renal Care Center of Excellence
- Collaboration combines the clinical expertise of Mayo Clinic and Baxter Renal Care Services
- Outpatient clinic to provide chronic kidney disease management, home dialysis and in-center dialysis services
- Project stems from five-year collaboration to advance care across different therapeutic areas
“The collaboration between Mayo Clinic and Baxter combines the best of our clinical, research and innovation expertise, and is rooted in the shared goal to improve the way we care for patients with serious and complex illnesses,” says Gianrico Farrugia, M.D., CEO of Mayo Clinic in Florida and president-elect of Mayo Clinic. “We are excited to establish this new renal care center of excellence with Baxter.”
For people with kidney disease or kidney failure requiring kidney dialysis, the Mayo Clinic Dialysis Center offers:
- Chronic Kidney Disease Clinic, where a dedicated team of providers work together to provide comprehensive care to people with kidney disorders
- Home dialysis training and support for both home hemodialysis and peritoneal dialysis
- In-center hemodialysis
- Outpatient dialysis services
- Nephrology Nutrition Clinic, where registered dieticians with expertise in kidney disorders provide ongoing guidance for nutritional needs
- Temporary dialysis if patients need treatment while traveling
Baxter Renal Care Services cares for more than 25,000 patients through its clinics across Asia, Europe and Latin America. Baxter Renal Care Services has historically worked closely with local experts to establish clinics where there is a need for centers of excellence that provide comprehensive care to help patients sequence through their therapy journey. These clinics often feature a successful CKD program focused on slowing the progression of kidney disease, as well as Baxter’s latest technologies to support patients’ clinical and lifestyle needs.
The dialysis clinic collaboration is the first launched initiative from the Baxter and Mayo Clinic five-year agreement announced in 2017, allowing the two healthcare leaders to bring together their respective clinical and development expertise. The primary emphasis of the broader agreement focuses on new research and development projects to advance innovation across different therapeutic areas where there are high unmet patient needs, such as renal disease. The initial agreement is for a five-year period, with a five-year renewal option.
New IPO filings include NGM, Arog, Gamida
Three more biotechs filed late Friday to go public on NASDAQ, adding new companies to a 2018 class of IPOs that could surpass 2015’s record for funds raised. The group includes NGM Biopharmaceuticals Inc. (South San Francisco, Calif.), Arog Pharmaceuticals Inc. (Dallas, Tex.) and Gamida Cell Ltd. (Jerusalem, Israel).
NGM, a liver disease and metabolic company, filed to raise up to $75 million in a listing. Among the company’s five clinical candidates, the most advanced, NGM282, is due to begin a Phase IIb trial in 1Q19 to treat non-alcoholic steatohepatitis (NASH). The listing’s underwriters are Goldman Sachs, Citigroup and Cowen.
NGM282, an engineered form of fibroblast growth factor 19 (FGF19), is wholly owned by the company. The company said preliminary results of Phase II studies have shown that the molecule significantly reduced liver fat and improved liver histology and fibrosis.
In 2015, NGM entered a broad collaboration with Merck & Co. Inc. (NYSE:MRK) giving the pharma exclusive, worldwide rights to its program targeting growth differentiation factor 15 (GDF15) and options to other programs, not including those targeting FGF19.
Next year, Merck plans to start two of NGM’s engineered variants of GDF15 to treat obesity, including a Phase IIa trial of NGM386 and a Phase I trial of NGM395.
By year end, Merck may opt to license NGM313, the biotech’s mAb activating the klotho ? (KLB)-FGF receptor 1c isoform (FGFR1c) complex. Preliminary data from a Phase Ib trial showed that NGM313 led to a significant reduction in liver fat in patients with non-alcoholic fatty liver disease (NAFLD).
The biotech’s NGM120, an agonist of GDNF family receptor ? like (GFRAL) designed to inhibit the effects of GDF15 elevations, is due to start a Phase Ib trial next half in cancer patients with anorexia/cachexia syndrome. Merck may opt to license that program after proof of concept (see “Appetite for GFRAL”).
Since beginning operations in 2008, NGM has raised $294.9 million in equity funding. Under its deal with Merck, the pharma has paid NGM $94 million up front, purchased $106 million in equity, and has reimbursed $189 million to NGM for R&D through June 30.
The Column Group is NGM’s largest shareholder with 25%. Merck owns 16%, while Prospect Ventures and Topspin Fund each hold about 9% and Rho Ventures has 7%.
Last month, NGM shuffled its management team. William Rieflin, who had been CEO since 2010, became executive chairman, while CFO David Woodhouse became CEO.
Arog filed to raise up to $74.8 million in its offering. Underwriters are Citigroup, RBC Capital Markets and Nomura. The company’s crenolanib is in two Phase III trials to treat FMS-like tyrosine kinase 3 (FLT3; CD135)-mutant acute myelogenous leukemia (AML). It is also in a Phase III trial to treat patients with gastrointestinal stromal tumors (GIST) with a specific mutation in the platelet derived growth factor receptor ? (PDGFR?) gene. The therapy has Orphan Drug designation in the U.S. and EU and Fast Track designation in the U.S. for both indications.
Gamida hopes to raise $69 million through its listing. BMO Capital Markets, RBC Capital Markets, Needham and Oppenheimer are underwriters. Its lead program is NiCord, which consists of umbilical cord blood-derived ex vivo nicotinamide-expanded hematopoietic stem and progenitor cells. Top-line data are due in 1H20 from a Phase III trial of the product as a universal stem cell graft in blood cancer patients who require a hematopoietic stem cell transplant (HSCT).
EpiPen shortage shows company, regulator failure, FT says
The worldwide shortage of EpiPens shows a failure by Mylan (MYL), the company that owns the rights to the auto-injectors, and the regulators to monitor them, the Financial Times says, in an opinion piece by Michael Skapinker. Mylan did not pay enough to sub-contractor Pfizer’s (PFE) performance and unnecessarily early expiration dates on the EpiPens increased sales but contributed to the shortage, according to Skapinker.
https://thefly.com/landingPageNews.php?id=2798217
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