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Tuesday, September 3, 2019

Cidara, Mundipharma in Partnership to Develop and Commercialize Rezafungin

Collaboration combines strengths to develop and commercialize life-saving antifungal treatment and prophylaxis, an area of high unmet medical need
Mundipharma acquires exclusive rights to develop and commercialize rezafungin in all markets outside of the United States and Japan, which will be retained by Cidara
Cidara to receive upfront payment of $30 million and equity investment of $9 million, co-development funding, development milestones and tiered royalty stream
Total transaction value could exceed $568 million
Cidara to host conference call today at 8:00 a.m. ET/5:00 a.m. PT

Novartis: Sandoz to Commercialize Polpharma Planned Biosim Natalizumab

Novartis AG’s (NOVN.EB) biosimilars division Sandoz has signed a global agreement with Polpharma SA for the commercialization of a proposed natalizumab biosimilar, the company said Tuesday.
The medicine is in phase 3 clinical development for the treatment of relapsing-remitting multiple sclerosis, Novartis said.
Under the deal, Polpharma will maintain responsibilities for development, manufacturing and supply of proposed biosimilar natalizumab. Sandoz will commercialize and distribute the medicine in all markets upon approval, through an exclusive global license, the company said.
Other terms of the agreement are confidential, it said.

Novartis, Lonza deepen biosimilars push with MS, arthritis drug deals

Swiss drugmakers Novartisand Lonza separately deepened their push into so-called biosimilars, betting cheaper copies of name-brand drugs will make headway among cost-conscious insurers and governments.

Novartis’s Sandoz generics unit, among the biggest biosimilars makers, on Tuesday agreed to license from Poland’s Polpharma Biologics a version of Biogen’s decade-old Tysabri for multiple sclerosis. This is the fifth proposed biosimilar licensed by Sandoz in nine months.
Meanwhile, Lonza announced it had contracted drug substance production for South Korean drugmaker Celltrion’s Remsima, a copy of Johnson & Johnson’s Remicade against autoimmune diseases like rheumatoid arthritis.
Biosimilar versions of patent-expired blockbusters such as Remicade and Tysabri have advanced in Europe, although U.S. adoption has lagged as drugmakers fiercely defend original versions. Novartis has lost its share of fights, including a recent court setback over Amgen’s Enbrel.
Rebates offered to U.S. insurers by drugmakers have also erected barriers, although with markets like MS and immunology each in the tens of billions of dollars the allure remains great. This year, Canada’s British Columbia province began switching patients to biosimilars in a bid to save tens of millions of dollars.
Lonza Chief Executive Marc Funk said his Basel-based company, which helps other drug firms outsource their production, would give Celltrion “the flexible capacity and agile teams it needs to respond to evolving market demand”.
With their deal, Novartis and Sandoz add to a growing stable of MS drugs, including older Gilenya and newly approved Mayzent, as well as a late-stage biological hopeful, ofatumumab, in its pipeline.
“Biosimilars create competition and cost savings, which are proven to make room in healthcare systems to treat more patients,” said Pierre Bourdage, Sandoz’s interim biopharmaceuticals head, without giving financial details of the deal for the Polpharma molecule now in late-stage trials.
Novartis could have decent luck with MS biosimilars, analysts said, given the high costs of the debilitating disease for health systems. “The acceptance for cheaper MS medicines will be great, because around half of all patients cannot afford them,” ZKB analyst Michael Nawrath wrote in a note.
Copies of biological drugs are called biosimilars because, unlike small-molecule chemicals, they cannot be exactly replicated in the factory. Still, studies show they carry the same potential benefits for patients.

Bayer Approaches Glyphosate Critics

Bayer respects that politicians in some European countries want to reduce the use of glyphosate, said the company’s crop-science division president Liam Condon in an interview with German newspaper Tagesspiegel. Mr. Condon said the company will work with institutions and interest groups to develop alternative solutions.
–However, Mr. Condon said glyphosate-based products continue to play an important role in weed-killing worldwide and Bayer remains convinced of the “safety and effectiveness of these products,” reports Tagesspiegel.
Full story (in German): https://bit.ly/2kcyvrj

Another extension for Roche-Spark takeover offer

Roche (OTCQX:RHHBY) and Spark Therapeutics (NASDAQ:ONCE) have announced yet another extension of the Swiss drugmaker’s $4.3B takeover offer for the U.S. gene therapy specialist as regulatory reviews in the U.S. and Britain continue.
The offer for Spark shares now runs to Oct. 1, Roche said, adding that around 24.1% of Spark’s outstanding shares had been tendered as of the end of August.

Monday, September 2, 2019

Community Health Workers Slinging Free Heart Drugs Cut Cardiovascular Risks

A tailored community-based intervention that leaned on the various skills of non-physician health workers (NPHWs) cut the risk of cardiovascular disease in patients with high blood pressure, results of the HOPE 4 trial showed.
Patients exposed to the intervention had an 11.17% reduction (-12.88 to -9.47) in Framingham Risk Score at 12 months versus a 6.40% reduction (95% CI -8.00 to -4.80) in the usual care group, reported Jon-David Schwalm, MD, MSc, of McMaster University and Hamilton Health Sciences in Hamilton, Ontario.
“A comprehensive model of care led by non-physician heath workers, involving primary care physicians and family, along with the provision of free antihypertensive medications and a statin, resulted in a greater than 40% reduction in cardiovascular risk and a doubling in the change in blood pressure control,” he said during a press briefing here at the 2019 European Society of Cardiology congress.
HOPE 4 was a cluster randomized trial in Colombia and Malaysia that used NPHWs to screen and treat participants. The NPHWs used tablets with guideline-recommended treatment algorithms to determine appropriate therapy (after training they attained 93% concordance with physicians) — patients received free antihypertensives and a statin. Family and community members served to support the study participants in terms of lifestyle changes and drug adherence.
In all, 69% of patients in the intervention group were able to get their blood pressure under control (systolic blood pressure [SBP] <140 mm Hg) compared with 30% in the usual care group (P<0.0001).
The intervention group’s 4.78% absolute reduction (95% CI -7.11 to -2.44) in ten-year predicted cardiovascular disease risk — the study’s primary outcome — was underpinned by greater reductions in SBP and LDL cholesterol (P<0.0001 for all):
  • SBP: 11.45 mm Hg (95% CI -14.94 to -7.97)
  • LDL: 0.41 mmol/L (95% CI -0.60 to -0.23)
No significant differences were seen for glucose concentrations or HDL. Results of the study were presented during a late-breaking trials session and published simultaneously in The Lancet.
The tailored aspect of the trial involved an initial systematic analysis of each country to identify patient-, provider-, and healthcare-system barriers to hypertension care. In Colombia for example, while blood pressure drugs may be subsidized for low-income individuals, long wait times often dissuade patients from bothering. In HOPE 4, locally available generic medications were made available free of charge for starters, and the NPHWs delivered them to patients’ homes in some cases.
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Jon-David Schwalm, MD, MSc, discussing the HOPE 4 results at ESC
These workers were already working in the communities and were “repurposed” for cardiovascular disease prevention. “It’s a matter of shifting direction,” Schwalm told MedPage Today.
Asked what lessons could be applied to North America, he said his group piloted the program in Canada, using firefighters as the NPHWs.
“In Canada, medication was not so much an issue,” he said. “Finding what are the barriers in individual countries, I think that’s where we are going to see the biggest benefit.”
Researchers are ever seeking innovative ways to get antihypertensive treatments to patients. At last year’s American College of Cardiology meeting, for example, a group from the University of California Los Angeles made a splash showing a 27 mm Hg drop in blood pressure when pharmacists at barbershops doled out antihypertensives (patients’ primary care physicians had signed off).
In a linked comment in The Lancet, Tazeen H. Jafar, MD, MPH, of Duke-NUS Medical School in Singapore, and colleagues noted that the large effect size observed in the trial, compared with other pragmatic studies, can likely be explained by several key factors.
For starters, patients in HOPE 4 were high risk at baseline (mean Framingham Risk Score >30%). Second, the study relied on NPHWs who possess a “higher mix of skills and competencies,” which is not always the case in such trials. Third, the trial opted for a free statin plus single-pill blood-pressure medication. Lastly, the use of patient support led to excellent adherence to the protocol (64% vs 40% in the usual care group).
“However, these same study design attributes might also limit sustainability and scalability. Of paramount importance is the concept of integration within the existing health-care system,” Jafar’s group wrote. “NPHWs in HOPE 4 were private contractors and hired exclusively for the trial. If staff were employees in existing health systems, rather than private contractors, competing tasks might compromise the acceptability, fidelity, effectiveness, and sustainability of the HOPE 4 intervention strategies when scaled up in the real world.”
They called for a comprehensive analysis to determine the cost-effectiveness of such an approach; Schwalm said his group is in the process of working on such an analysis.
“HOPE 4 and similar highly important studies should prompt the scientific and legislative communities to rethink the scale-up of large, evidence-based approaches to dramatically reduce the burden of uncontrolled hypertension and lower cardiovascular risk,” Jafar and coauthors wrote. “Such bold strategies cannot be ignored.”
From 2014 to 2017, the study enrolled 1,371 hypertensive patients age 50 and older who were screened from 30 communities in Colombia and Malaysia. Door-to-door hypertension screening was performed in Colombia while individuals in Malaysia were screened mostly at community gatherings. In all, 14 of these communities were randomized to the intervention while 16 received usual care.
HOPE 4 was funded by the Canadian Institutes of Health Research, Grand Challenges Canada, the Ontario SPOR Support Unit, the Ontario Ministry of Health and Long-Term Care, Boehringer Ingelheim, the World Health Organization, and the Population Health Research Institute.
Schwalm and co-authors disclosed institutional relationships with the study backers.
Jafar and co-authors declared no conflicts of interests.

Ardelyx Call Sept 3 to Review Results from Pivotal Phase 3 AMPLIFY Study

Ardelyx, Inc. (NASDAQ: ARDX), a specialized biopharmaceutical company focused on developing first-in-class medicines to improve treatment for people with cardiorenal diseases, announced that it will hold a conference call tomorrow, September 3, at 8:30 am Eastern Time to review the results from the pivotal Phase 3 AMPLIFY study of tenapanor in combination with phosphate binders in patients with chronic kidney disease on dialysis whose hyperphosphatemia was not controlled with binders. Tenapanor is Ardelyx’s investigational, first-in-class, small molecule, non-binder, phosphate absorption inhibitor.
To participate in the conference call, please dial (855) 296-9612 (domestic) or (920) 663-6277 (international) and refer to conference ID 9789472. Live audio of the conference call will be simultaneously webcast and will be available under the Investors section of the company’s website at www.ardelyx.com. The webcast will be archived and available for replay for 60 days following the call.