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Sunday, December 8, 2019

US eyes faster launch for biosimilars in North American trade pact

Biosimilars could be brought to market much quicker in North America if a Trump administration proposal makes it into a new US-Canada-Mexico (USMCA) trade pact, according to press reports.
Citing people familiar with the matter, the Wall Street Journal says the US government is considering a reduction in the protections from competition for biologic drugs detailed in the USMCA from 10 years to five, to try to win support for the deal from Democrats in Congress.
Biologics have 12 years’ market exclusivity in the US, but the current wording of the trade agreement would reduce that to 10.
For comparison, Canada currently has eights years’ protection and Mexico five, so under the current wording patients would have to wait longer for biosimilars in the latter two countries.
Democrats and other groups have argued for the duration of the additional protection to be reduced to to allow cheaper copies of reference biologic drugs to get to market more quickly, as that would help cut spending on medicines by healthcare systems in all three countries.
Some have also argued for the provision to be dropped altogether, with the three countries retaining the status quo on biologics protection.
Companies that produce biosimilars in the US are also pushing for the reduction of course. The Association of Accessible Medicines – which represents generic and biosimilar manufacturers – argues that passing the USMCA with a five-year provision would prevent a biopharma monopoly from being expanded beyond the US and lower prescription drug prices for America’s patients.
Trump is keen to get the USMCA passed, as he has pledged a series of trade deals to boost the US economy in the build-up to the Presidential election next year. USMCA was agreed in principle by the US, Canada and Mexico a year ago, but still needs to be ratified by Congress.
The governments of Mexico and Canada would clearly need to agree any changes to the biologics’ exclusivity provisions in the trade deal if they do make it into the document.
Trump signed the USMCA in November 2018, shortly before the Democrats took control of the House of Representatives in the midterms. The shift in power has held up the treaty, which is the successor the North American Free Trade Agreement (NAFTA).
Last week, top Democrat Nancy Pelosi said that discussions with US Trade Representative (USTR) Robert Lighthizer were getting closer to an accord that could allow the USMCA to be tabled for a vote, with a few ‘wrinkles’ – such as enforcement of the provisions – still to be worked out.

Saturday, December 7, 2019

Takeda to develop home hemophilia bleeding risk test with Enzyre

Takeda is teaming up with the Dutch testing firm Enzyre to develop an at-home diagnostic device that will help people with hemophilia determine their own coagulation status.
Enzyre will receive funding from the Japanese drugmaker to refine its existing technology, with the goal of building a platform that will allow patients to share test results with their care teams over a smartphone.
“Diabetics have long been able to individually manage their disease through home glucose measurement, and we are determined to make this the case for those living with hemophilia,” Enzyre CEO Dirk Pollet said in a statement.
Patients with the rare genetic disorder lack sufficient levels of blood-clotting proteins, such as the factor VIII protein. With about 400,000 hemophilia patients worldwide, many receive treatment at home and only meet with their physicians annually.

“We are delighted to have Takeda on board as our development partner,” added Waander van Heerde, Enzyre’s chief scientific officer. “Next to their financial support, they also bring a wealth of knowledge on the treatment of hemophilia.”
Regular measures of coagulation status and the blood’s ability to clot can help caregivers manage a patient’s risk of excessive and dangerous bleeding or conversely developing clots within blood vessels.
“I hope in the near future we will be able to offer patients and their caregivers an easier, more innovative solution to manage hemophilia at home, while helping the healthcare team provide more holistic, personalized care to their patients,” said Alvaro Herreros, head of Takeda’s rare hematology and neuroscience franchises.

Earlier this year, Takeda was saddled with a $155 million bill over patent infringement, payable to its hemophilia rival Bayer—stemming from a December 2016 lawsuit initially filed by the German pharma against Shire’s Baxalta unit.
Following its $59 billion takeover of Shire—which included Baxalta’s Adynovate recombinant hemophilia treatment, the focus of Bayer’s patent suit—the first half of Takeda’s current fiscal year saw its rare disease business decline, with revenues dropping 11% year over year.
In October, Takeda CEO Christophe Weber cited competitive pressure in hemophilia as one of the causes. Formerly Shire’s flagship hemophilia A treatment, and now Takeda’s third best-selling product, Advate sales alone dropped 16% following the fast growth of Roche’s Hemlibra.

Xenon Updates on Partnered Neurology Pipeline Programs at Epilepsy Society

Overview of Clinical Stage XEN901 and Related Patient Survey to be Presented in the “Genetic Epilepsies – Updates in the Science and Diagnosis” Exhibit in Room 318-319 on Sunday, December 8th
Pre-Clinical Work Suggests Selective Sodium Channel Inhibitors that Reduce Action Potential Firing in Excitatory Neurons, While Sparing Inhibitory Interneurons, May Provide Promising Drug Profile

Fate Phase 1 Data on 1st Universal Off-the-shelf NK Cell Cancer Immunotherapy

No Morphologic Evidence of Leukemia and Complete Neutrophil Recovery Observed in First Patient Treated with FT516 Monotherapy for AML following First Dosing Cycle
No Dose-limiting Toxicities or FT500-related SAEs Reported in First 12 Patients Treated with FT500 for Advanced Solid Tumors
Favorable FT500 Phase 1 Safety, Tolerability and Immunogenicity Profile Validates Novel Multi-dose Treatment Paradigm for Off-the-shelf, iPSC-derived NK Cell Products
Fate Therapeutics, Inc. (NASDAQ: FATE), a clinical-stage biopharmaceutical company dedicated to the development of programmed cellular immunotherapies for cancer and immune disorders, announced initial clinical data for its FT516 and FT500 off-the-shelf, iPSC-derived natural killer (NK) cell product candidates.
“The safety, tolerability, and immunogenicity data from the Phase 1 dose-escalation stage of FT500, the first-ever cell therapy derived from a clonal master induced pluripotent stem cell line to undergo clinical investigation in the U.S., provide compelling evidence that multiple doses of iPSC-derived NK cells can be delivered off-the-shelf and administered without patient matching,” said Wayne Chu, M.D., Vice President of Clinical Development of Fate Therapeutics. “Additionally, initial clinical observations with FT516 are very encouraging, as an assessment of the first AML patient’s bone marrow at Day 42 following three once-weekly doses of FT516 demonstrated anti-leukemia activity and hematopoietic recovery.”

Corvus Preclinical, Initial Phase 1/1b Lymphoma Data at Hematology Meet

Corvus Pharmaceuticals, Inc. (Nasdaq: CRVS), a clinical-stage biopharmaceutical company focused on the development and commercialization of precisely targeted oncology therapies with biomarker patient enrichment selection, announced initial results from its Phase 1/1b trial of CPI-818, the Company’s ITK-inhibitor. The early clinical data from the study demonstrated specific target engagement by CPI-818. The results were presented in a poster at the American Society of Hematology (ASH) 61st Annual Meeting 2019 in Orlando, Florida, taking place December 7-10, 2019.
“We are excited to report the first clinical experience with CPI-818, our selective covalent ITK inhibitor designed to address T-cell lymphomas, a category of hematologic cancers with great need for novel therapeutic options,” said Richard A. Miller, M.D., co-founder, president and chief executive officer of Corvus. “The results show that CPI-818 achieved specific and sustained target occupancy and we look forward to continuing the dose escalation portion of the study to identify an optimum dose. In addition to T-cell lymphomas, we believe CPI-818 may have applications in other immune mediated diseases.  Overall, our team is now advancing three candidates in clinical trials for a wide range of cancers, and each of our programs remains on track with enrollment and progress towards next data milestones.”

GW Unit New Epidiolex (cannabidiol) Data at American Epilepsy Society

GW Pharmaceuticals plc (Nasdaq: GWPH), the world leader in the science, development, and commercialization of cannabinoid prescription medicines, along with U.S. subsidiary Greenwich Biosciences, today presented new data from a Phase 3 clinical trial of EPIDIOLEX® (cannabidiol or CBD) oral solution, CV in tuberous sclerosis complex (TSC) at the American Epilepsy Society (AES) Annual Meeting. The study found that patients treated with EPIDIOLEX 25 mg/kg/day or 50 mg/kg/day experienced a significantly greater reduction in TSC-associated seizures (49% for 25 mg/kg/day and 48% for 50 mg/kg/day) compared to placebo (27%; p=0.0009 and p=0.0018, respectively).

Seattle Genetics Updates Data on Hodgkin treatment combo at ASH19

– Additional Analysis in Phase 2 Trial of ADCETRIS plus OPDIVO in Patients with Frontline Hodgkin Lymphoma Aged 60 Years and Older –
– Two-Year Follow-up Results from Phase 1/2 Trial in Relapsed Hodgkin Lymphoma –