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Mustang Bio’s MB-101 Receives FDA Orphan Drug Designation for Astrocytomas and Glioblastoma

Jul 8, 2025
Mustang Bio, Inc., a clinical-stage biopharmaceutical company focused on cell therapies for hard-to-treat cancers, announced that the U.S. Food and Drug Administration (FDA) has granted…
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BioVersys and Shionogi Partner on Global NTM Drug Development Collaboration

Jul 4, 2025
Swiss biopharmaceutical company BioVersys AG has entered into a global research and exclusive license option agreement with Japanese pharmaceutical firm Shionogi & Co., Ltd. to…
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Brii Biosciences Licenses BRII-693 Rights to Joincare in Greater China

Jul 4, 2025
Brii Biosciences Limited, a biotechnology company focused on addressing high unmet medical needs, has announced a licensing and technology transfer agreement with Joincare…
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Jazz Pharmaceuticals Gets EU Approval for Ziihera to Treat Advanced HER2-Positive Biliary Tract…

Jul 3, 2025
Jazz Pharmaceuticals plc announced that the European Commission (EC) has granted conditional marketing authorization for Ziihera® (zanidatamab), a dual HER2-targeted bispecific…
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FDA Grants Priority Review for WINREVAIR Label Update Following ZENITH Trial Results

Jul 3, 2025
Merck, known as MSD outside the U.S. and Canada, announced that the U.S. Food and Drug Administration (FDA) has accepted and granted priority review to a supplemental Biologics License…
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FDA Grants Accelerated Approval to ZEGFROVY, First Oral EGFR‑Exon‑20 Insertion NSCLC Therapy

Jul 3, 2025
The U.S. Food and Drug Administration (FDA) has granted accelerated approval to ZEGFROVY (sunvozertinib), a novel oral therapy developed by Dizal, for the treatment of adults with…
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Adagene Secures Up to $25M Strategic Investment from Sanofi

Jul 3, 2025
Adagene Inc., a biotechnology company developing innovative antibody-based cancer therapies, announced that Sanofi will invest up to $25 million in the company as part of an expanded…
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Lynozyfic (linvoseltamab-gcpt) Granted FDA Accelerated Approval for Relapsed/Refractory Multiple…

Jul 3, 2025
Regeneron Pharmaceuticals, Inc. announced that the U.S. Food and Drug Administration (FDA) has granted accelerated approval for Lynozyfic (linvoseltamab-gcpt) to treat adult patients…
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Riliprubart Earns Orphan Drug Designation in Japan for CIDP

Jul 2, 2025
The Japanese Ministry of Health, Labour and Welfare (MHLW) has granted orphan drug designation to riliprubart, an investigational monoclonal antibody developed by Sanofi, for the…
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FDA Approves Gamifant as First Treatment for MAS in Still’s Disease

Jul 1, 2025
Sobi announced that the U.S. Food and Drug Administration (FDA) approved Gamifant (emapalumab-lzsg) for the treatment of adult and pediatric (newborn and older) patients with…
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Press Releases

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