rf-fullcolor.png

 

September 17, 2020
by Michael Mezher

Recon: Moderna releases COVID vaccine trial blueprint; BioNTech buys Novartis’ site to boost EU vaccine production

Welcome to Regulatory Reconnaissance, your daily regulatory news and intelligence briefing.
 
In Focus: US
  • Moderna would seek limited emergency use of COVID-19 vaccine based on early data (Reuters) (Boston Globe)
  • Moderna Shares the Blueprint for Its Coronavirus Vaccine Trial (NYTimes)
  • Moderna to develop seasonal flu vaccine (Reuters)
  • Biden-aligned group outlines potential Day 1 drug pricing actions (STAT)
  • US plans for hundreds of millions of cheap, fast COVID-19 tests (Reuters)
  • Lilly, Amgen partner to manufacture potential COVID-19 drugs (Reuters)
  • NIH launches trial of Rigel drug for severe COVID-19 (Reuters)
  • Trump contradicts CDC director on vaccine, masks: 'He was confused' (Reuters)
  • New York charges Johnson & Johnson with insurance fraud over opioid claims (Reuters)
  • Independent review clears Kodak chiefs of insider trading (FT)
In Focus: International
  • AstraZeneca's trial illnesses may not be due to COVID-19 shot, Oxford University says (Reuters)
  • WHO says safety comes first as over 170 nations join COVID-19 vaccine plan (Reuters)
  • BioNTech CEO expects vaccine can be fridge-stored for two weeks (Reuters)
  • BioNTech buys German site from Novartis to boost vaccine output (Reuters) (FT)
  • China's Sinovac to test coronavirus vaccine candidate in teenagers, children (Reuters)
  • Takeda-led COVID-19 plasma product to begin trial this month (Reuters)
  • South Korea approves Phase 2/3 trials of Celltrion COVID-19 antibody drug (Reuters)
  • Japan Pharma Groups Stepping Up Lobbying on FY2021 Budget, Tax Reform (PharmaJapan)
  • Opdivo scores NICE recommendation in two non-small cell lung cancer indications (Pharmafile)
  • WHO prequalifies first clofazimine, ivermectin and Sandoz’ rituximab biosimilar (WHO 1, 2, 3)
Coronavirus Pandemic
  • Sorrento Therapeutics soars 27% after FDA green-lights COVID-19 antibody trial (BI)
  • Vaccines Europe Statement on the safety of COVID-19 vaccines (Efpia)
  • CVS Health plans to double COVID-19 drive-thru test sites to over 4,000 (Reuters)
  • Why Can't America Make Enough N95 Masks? 6 Months Into Pandemic, Shortages Persist (NPR)
  • Nixed Philips, Hamilton, Vyaire ventilator contracts subject of expanding House probe (MedtechDive)
  • Trials 'unable to bounce back' after COVID-19 chaos: report (Fierce)
  • Detection of SARS-CoV-2 with SHERLOCK One-Pot Testing (NEJM)
  • New COVID-19 Vaccines May Be Accelerated By Using Existing Manufacturing Platforms, US FDA's Marks Says (Pink Sheet)
Pharma & Biotech
  • The cost of Gilead’s HIV prevention pill thwarted widespread use, study finds (STAT)
  • A longtime CytomX exec re-emerges at Synthekine, an $82M Stanford spinout (Endpoints)
  • Rare Pediatric Disease Designation Requests Skyrocket Ahead Of Voucher Program’s Sunset (Pink Sheet)
  • Arrowhead shares soar on liver disease data from four patients (BioPharmaDive)
  • New Designations Set To Speed Hemlibra, CAR-T In China (Scrip)
  • Amgen Files Erenumab for Migraine Prevention in Japan (PharmaJapan)
  • Moderna lands $100M upfront in deals with Vertex, Chiesi (Fierce)
  • Novo, Sanofi VC units lead Lava's $83M series C to fund gamma delta T-cell trials (Fierce)
  • Past a turning point, Finch scores $90M to complete the final stretch for oral microbiome therapy (Endpoints)
  • Sarepta faces another gene therapy hiccup as Regenxbio sues over Jim Wilson's patent (Endpoints)
  • Sean Bohen's break from biopharma is over. The ex-AstraZeneca CMO has retired his Big Pharma jersey and is now — happily — running a little biotech (Endpoints)
  • 'The biggest inflection point ever': On R&D day, Moderna CEO Stéphane Bancel doubles down on vaccines and lays out a vision for a '40, 50'-drug biotech (Endpoints)
  • One month after $115M megaround, muscle disease-focused Dyne goes public with $233M IPO (Endpoints)
  • After leading Celgene buyout, Matthew Roden leaves Bristol Myers Squibb for venture capital firm (Endpoints)
  • Jim Broderick reels in a $100M Series B to explore a 'new and big' angle of immune regulation (Endpoints)
  • Lava breaks prolonged silence with an $83M Series C and two I/O programs set for the clinic (Endpoints)
  • Two-Year, Randomized, Controlled Trial of Belimumab in Lupus Nephritis (NEJM)
Medtech
  • FDA Approves Liquid Biopsy Next-Generation Sequencing Companion Diagnostic Test (FDA)
  • Medtronic, Stryker among CEOs weighing in on COVID-19 recovery (MedtechDive)
Government, Regulatory & Legal
  • GAO report finds brokers offered false info on coverage for pre-existing conditions (The Hill)
  • Therapeutic goods advertising compliance: 2019-20 Annual Report (TGA)
  • W.Va. Ax Of Biogen MS Drug Patent Binds Del. Litigation (Law360)
  • USPTO Defers Fees On COVID-19 Provisional Applications (Law360)
  • Natera Fights Illumina's Bid To Invalidate DNA Testing Patent (Law360)
  • Bristol Myers Squibb Announces Settlement of U.S. Patent Litigation for REVLIMID® (lenalidomide) With Dr. Reddy’s (Press)
Regulatory Recon is our daily intelligence briefing for the regulatory affairs space, bringing you the top regulatory, biopharma and medtech news stories from around the globe.
 
A story's inclusion in Regulatory Recon does not imply endorsement by Regulatory Focus or RAPS.
×

Welcome to the new RAPS Digital Experience

We have completed our migration to a new platform and are pleased to introduce the updated site.

What to expect: If you have an existing login, please RESET YOUR PASSWORD before signing in. After you log in for the first time, you will be prompted to confirm your profile preferences, which will be used to personalize content.

We encourage you to explore the new website and visit your updated My RAPS page. If you need assistance, please review our FAQ page.

We welcome your feedback. Please let us know how we can continue to improve your experience.