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FDA Acknowledges Astellas Pharma's Resubmission Of BLA For Zolbetuximab

TOKYO (dpa-AFX) - The U.S. Food and Drug Administration has acknowledged Astellas Pharma's resubmission of the Biologics License Application (BLA) for zolbetuximab, a first-in-class investigational

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U.S. Food and Drug Administration Acknowledges Astellas Pharma Inc.? Resubmission of Biologics License Application for Zolbetuximab and Sets New Action Date

Astellas Pharma Inc. announced that the U.S. Food and Drug Administration has acknowledged the company s resubmission of the Biologics License Application for zolbetuximab, a first-in-class.

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Fezolinetant Safe, Effective for Moderate-to-Severe Menopause Hot Flashes

Fezolinetant Safe, Effective for Moderate-to-Severe Menopause Hot Flashes
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FDA Accepts BLA Resubmission for Zolbetuximab in CLDN18.2+ Advanced Gastric/GEJ Adenocarcinoma

FDA Accepts BLA Resubmission for Zolbetuximab in CLDN18.2+ Advanced Gastric/GEJ Adenocarcinoma
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Nanoform's biologics technology showcased by large pharma at drug delivery conference; Nanoenzalutamide and nanoapalutamide partnering discussions progress as planned

Nanoform's biologics technology showcased by large pharma at drug delivery conference; Nanoenzalutamide and nanoapalutamide partnering discussions progress as planned
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