It was the best of all possible worlds in the worst of all times for biotech in 2020. What comes now? (Endpoints)
2020’s NDA list is packed with commercial firsts — from historic to haphazard. Have we reached a tipping point? (Endpoints)
The biotech 2021 preview, from M&A to gene therapy and more (STAT)
The Biotech Paradox of 2020: A Year In Review (LifeSciVC)
US FDA 2020 Novel Approval Count Rises To 53 At CDER, Plus 5 New CBER Biologics (Pink Sheet)
Pharma Breathes Sigh Of Relief Over Post-Brexit Trade Deal (Pink Sheet)
EU-UK Trade Deal Allows For Mutual Recognition Of GMP Inspections (Pink Sheet)
UK Regulator Vaunts A 'New Era' In Drug Approvals (Pink Sheet)
FDA lifts clinical hold on Audentes' gene therapy program after three patient deaths triggered alarms (Endpoints)
Pfizer, Opko's growth hormone med en route to October FDA decision (Fierce)
Slammed with PhII flop for lead drug, Calithera lays off a third of its staffers (Endpoints)
Alkermes sees swift turnaround for rejected schizophrenia med as FDA accepts resubmission (Fierce)
USFDA informs Biocon Biologics, Mylan of deferred action on Avastin biosimilar license application (Economic Times)
With pipeline setbacks mounting, United snares priority voucher for inhaled formulation of PAH med Tyvaso (Endpoints)
Bristol Myers Squibb walks on Opdivo's FDA nod for small-cell lung cancer after middling OS data couldn't back approval (Endpoints)
Pfizer’s Lorbrena scores US priority review (PharmaTimes)
CRUK scientists develop drug that targets KRAS pathways (PharmaTimes)
Janssen files EGFR-targeting antibody amivantamab with EMA (PharmaTimes)
Pharma heavyweight Pfizer stepping into the prostate cancer ring with AbbVie after inking a $4.2B alliance with Myovant (Endpoints)
Lynn Seely hits the exit as Myovant graduates to commercial space — handing the reins to Amgen vet (Endpoints)
Oncorus plots early-stage plant in Boston area as it walks I-O candidate through the clinic (Endpoints)
Charles River bags antibody discovery-focused Distribution Bio for $104M, signaling return to pre-pandemic buyout spree (Endpoints)
After a ‘breakthrough’ beginning to 2020, little Aprea gets crushed by a PhIII failure (Endpoints)
Fast-expanding Shanghai Pharma breaks ground on $1.8B biotech park focused on next-gen R&D, antibody production (Endpoints)
In quick start to new year's M&A, Arvelle Therapeutics hands reins to Angelini as it nears EU approval for cenobamate (Endpoints)
FDA Approves First Generic of Drug Used to Treat Severe Hypoglycemia (FDA)
FDA Announces OTC Monograph Drug User Fees for Manufacturers for FY2021 (FDA Law Blog) (FDA)
Medtech
The top medtech deals of 2020 (and one that got away) (MedtechDive)
Brexit deal creates regulatory barriers to UK-EU medical device trade (MedtechDive) (MedtechInsight)
Senseonics' 180-day Eversense glucose monitor delayed at FDA by COVID-19 pandemic (Fierce)
Ra Medical settles DOJ false claims investigations (Fierce)
Hologic starts spending its COVID-19 testing windfall, with $64M Somatex breast cancer biopsy acquisition (Fierce)
Product Labeling for Laparoscopic Power Morcellators; Guidance for Industry and Food and Drug Administration Staff; Availability (FDA)
Government, Regulatory & Legal
Seniors Face Crushing Drug Costs as Congress Stalls on Capping Medicare Out-Of-Pockets (KHN)
Federal Courts in Maryland and California Block Trump Administration’s Most Favored Nation Drug Pricing Rule on Procedural Grounds (FDA Law Blog)
New ASP Reporting Requirement for Manufacturers without a Medicaid Drug Rebate Agreement (FDA Law Blog)
Eli Lilly & Co. v. Apotex, Inc. (Fed. Cir. 2020) (Patent Docs)
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.
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