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Nasal Spray and Mouth Rinse Demonstrate Efficiency in Preventing COVID-19 and Other Infections
BMG Pharma's clinical trial has demonstrated positive results in the efficacy of BMG0705 Nasal Spray and BMG0703A Mouth Rinse as treatments for asymptomatic COVID-19 patients.
Evonik Expands Biomaterials Portfolio through JeNaCell Acquisition
Evonik has acquired the German biotech company JeNaCell, expanding its biomaterials portfolio.
Nanoform, Boehringer Ingelheim Collaborate on Pre-Clinical Development Projects
Nanoform and Boehringer Ingelheim have executed a master services agreement in relation to pre-clinical development projects.
Imugene and Celularity to Develop Solid Tumor Treatment
A research collaboration will combine Imugene’s oncolytic virus technology with Celularity’s allogeneic CAR T-cell therapy.
EC Confirms Go-Live Date for Clinical Trials Information System
EC has confirmed that the entry into application of the Clinical Trials Regulation and, as such, the go-live date for the Clinical Trials Information System (CTIS) will be Jan. 31, 2022.
WuXi STA Finalizes Acquisition of BMS’ Swiss Manufacturing Facility
WuXi STA has finalized its acquisition of Bristol Myers Squibb’s drug product manufacturing facility based in Couvet, Switzerland.
BMS Gains European Approval for Opdivo
Bristol Myers Squibb has been granted approval by the European Commission for Opdivo (nivolumab) as an adjuvant treatment
CHMP Approves Manufacturing Scale-Up for Spikevax
EMA’s CHMP has approved the increased manufacturing capacity and supply of Moderna’s COVID-19 vaccine active substance in its US manufacturing site.
Bioiberica Obtains CSR Management System Certification Aligned with UN Sustainable Development Goals
Bioiberica has received certification of its CSR management system as aligned with the United Nations Sustainable Development Goals.
University of Sheffield and CGT Catapult Launch Innovative Gene Therapy Program
The University of Sheffield has launched an innovative gene therapy program that could pave the way for novel treatments for neurodegenerative diseases.
Analysis Demonstrates No Increased Incidence of Thrombosis with TTS After Vaxzevria Second Dose
A global safety database analysis has demonstrated no increased incidence of thrombosis with TTS after the second dose of Vaxzevria.
Sanofi Acquires Translate Bio for $3.2 Billion
Sanofi has acquired Translate Bio in a bid to further their mRNA research.
CMA Fines Advanz for Over-Pricing Liothyronine Tablets
CMA fines Advanz and investors for more than £100 million (approximately US$139 million) after the company increased the price of thyroid tablet packs from £20 (US$23.74) in 2009 to £248 (approximately US$295) in 2017.
FDA Approves Expanded Label of Allergan’s Botox to Treat Upper Limb Spasticity
FDA approved an expanded Botox label, which now includes eight new muscles to treat adults with upper limb spasticity.
Nitric Oxide Nasal Spray for COVID-19 to Be Distributed to India and Other Asia Markets
Glenmark Pharmaceuticals has partnered with SaNOtize to manufacture, market, and distribute NONS to India, Singapore, Malaysia, Hong Kong, and more.
Janssen Collaborates with BioMedX in Autoimmunity and Drug Delivery Research
BioMed X Institute and Janssen Research & Development to start two new research programs in the field of autoimmune diseases and drug delivery.
FDA Approves AstraZeneca’s Lupus mAb, Saphnelo
FDA has approved AstraZeneca’s Saphnelo, a type I interferon receptor antibody for treating systemic lupus erythematosus.
FDA Accepts Genentech’s Application for Bispecific Antibody to Treat Eye Diseases
FDA has accepted Genetech’s BLA for faricimab, a bispecific antibody in development for treating wet age-related macular degeneration and diabetic macular edema.
EC Makes Supply Agreement with GSK and Vir Biotechnology for mAb COVID-19 Treatment
The European Commission has entered into a supply agreement with GlaxoSmithKline and Vir Biotechnology for up to 220,000 doses of sotrovimab, an investigational mAb for treating COVID-19.
DisperSol and Catalent Announce Manufacturing Collaboration
DisperSol and Catalent announce manufacturing collaboration to accelerate DisperSol’s pharmaceutical production.
FDA Launches New Crowdsourcing Challenge for Pediatric Research Questions
FDA is launching a new crowdsourcing challenge to solicit ideas for pediatric research.
Regeneron Receives Expanded Authorized Use from FDA for Antibody COVID-19 Treatment
The expanded authorization from FDA enables the use of Regeneron Pharmaceuticals’ REGEN-COV antibody cocktail therapy for post-exposure prophylaxis in certain people exposed to SARS-CoV-2.
FDA Approves Interchangeable Biosimilar Insulin
FDA has approved Mylan Pharmaceuticals’ Semglee, the first interchangeable biosimilar insulin product for treating diabetes.
Regeneron and AstraZeneca Partner to Create Small-Molecule Obesity Drug
Regeneron and AstraZeneca have entered an agreement to create a small-molecule medicine designed to treat obesity.
FDA Approves GSK’s Treatment for Chronic Rhinosinusitis with Nasal Polyps
GSK announced that FDA has approved a new indication for Nucala (mepolizumab), a monoclonal antibody that targets interleukin-5.
FDA’s Pazdur Challenges Attack on Accelerated Approval Program
The agency’s leading cancer expert lashed out at the alarmists and urged continued support for the early access process.
FDA Gives Green Light to Emergent BioSolutions to Resume COVID-19 Vaccine Manufacturing
Emergent BioSolutions is being allowed to restart manufacturing operations for the J&J COVID-19 vaccine at its Bayview, Baltimore, Md., facility.
18th Annual CPhI Pharma Awards to Take Place in Milan, Italy
Entries are now open for the 18th Annual CPhI Pharma Awards in Milan.
FDA Grants Orphan Drug Designation to VICO Therapeutics for Huntington’s Disease Drug
VICO Therapeutics’ drug candidate, VO659, for treating Huntington’s Disease was granted orphan drug designation by FDA.
New Drug Approvals on Track at FDA
In the first half of 2021, the Center for Drug Evaluation and Research and the Center for Biologics Evaluation and Research approved 29 novel therapies.
