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Pfizer's Beqvez taking on Hemgenix with FDA nod in hemophilia B

Pfizer Inc.’s Beqvez (fidanacogene elaparvovec) won FDA approval for use in adults with hemophilia B, making it the second adeno-associated viral (AAV) vector-based gene therapy available for patients in the U.S., following the late 2022 approval of CSL Behring’s Hemgenix (etranacogene dezaparvovec).

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Pfizer's first gene therapy gets approval for clotting disorder

Pfizer Inc. won U.S. approval for its first gene therapy, expanding into a promising field of medicine that has proved to be a challenging business.
The treatment, called Beqvez, gained clearance for ...

Australia , Australian , Ellis-neufeld , Biomarin-roctavian , Pfizer-inc , Pfizer , Jude-children-research-hospital-in-memphis , Marin-pharmaceutical , Jude-children , Research-hospital , Wall-street ,

Salix Pharmaceuticals, Ltd. v. Norwich Pharmaceuticals Inc. (Fed. Cir. 2024) | McDonnell Boehnen Hulbert & Berghoff LLP

The Federal Circuit handed down an opinion last week that invalidated several asserted claims and found infringement under 35 U.S.C. § 271(e)(2) of the claims, while refusing to modify...

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BioRestorative Therapies (BRTX) vs. Its Competitors Head to Head Analysis

BioRestorative Therapies (BRTX) vs. Its Competitors Head to Head Analysis
themarketsdaily.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from themarketsdaily.com Daily Mail and Mail on Sunday newspapers.

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Puma Biotechnology (NASDAQ:PBYI) & Shattuck Labs (NASDAQ:STTK) Critical Review

Puma Biotechnology (NASDAQ:PBYI – Get Free Report) and Shattuck Labs (NASDAQ:STTK – Get Free Report) are both small-cap medical companies, but which is the superior investment? We will contrast the two companies based on the strength of their earnings, profitability, dividends, institutional ownership, valuation, analyst recommendations and risk. Earnings & Valuation This table compares Puma […]

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Why this money manager is venturing back into emerging markets and adding more U.S. tech

Andrew Pyle, portfolio manager and senior investment advisor at CIBC Wood Gundy, is increasing his exposure to China, India, Japan and the U.S.

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U.S. FDA Approves Pfizer's BEQVEZ™ (fidanacogene elaparvovec-dzkt), a One-Time Gene Therapy for Adults with Hemophilia B

A one-time dose of BEQVEZ has reduced bleeds post-treatment compared to standard of care with a median of zero bleeds after up to three years of follow-up, providing sustained bleed protection and...

United-states , Canada , Adam-cuker , Thromb-haemost , Kim-phelan , Aamir-malik , Drug-administration , Linkedin , Pfizer-inc , Hemophilia-thrombosis-program , Facebook , Pfizer

Global Penicillin Analysis Report 2024: Market to Grow by

Dublin, April 26, 2024 (GLOBE NEWSWIRE) -- The

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FDA approves Pfizer gene therapy Beqvez for treatment of hemophilia B

The agency greenlighted the drug, which will be marketed as Beqvez, for adults with moderate to severe hemophilia B.

Australia , Behring-hemgenix , Adam-cuker , Hemophilia-thrombosis-program , Drug-administration-on , Pfizer , Drug-administration , Spark-therapeutics , Breaking-news , Health-care-industry , Pharmaceuticals , Biotech-and-pharmaceuticals

Pfizer's Beqvez Receives FDA Approval For Treatment Of Adults With Hemophilia B

Pfizer's Beqvez Receives FDA Approval For Treatment Of Adults With Hemophilia B
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