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FDA approves Roche’s Phesgo for HER2-positive breast cancer

Jul 1, 2020
Roche announced that the US Food and Drug Administration (FDA) has approved Phesgo, a fixed-dose combination of Perjeta (pertuzumab) and Herceptin (trastuzumab) with hyaluronidase,…
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Meissa Vaccines Provides a Pipeline Update on Vaccine Candidates for COVID-19 and RSV

Jul 1, 2020
Meissa Vaccines announced that the company has initiated preclinical studies and manufacturing and completed a pre-IND meeting with the U.S. Food and Drug Administration (FDA) for the…
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Carmine Therapeutics and Takeda Collaborate to Discover and Develop Rare Disease Gene Therapies

Jun 30, 2020
Carmine Therapeutics announced that it has signed a research collaboration agreement with Takeda Pharmaceutical Company Limited to discover, develop and commercialize transformative…
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Sinclair Research Announces Successful Validation of GLP Ototoxicity Testing Services

Jun 30, 2020
Sinclair Research announced completion of successful validation of GLP ototoxicity testing services in partnership with Turner Scientific, an industry leader specializing in nonclinical…
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FDA Approves Merck’s KEYTRUDA for First-Line Treatment of Patients With Unresectable or Metastatic…

Jun 30, 2020
Merck, known as MSD outside the United States and Canada, announced that the U.S. Food and Drug Administration (FDA) has approved KEYTRUDA, Merck’s anti-PD-1 therapy, as monotherapy for…
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VITRAC Therapeutics Initiated Global Clinical Development of VIC-1911, licensed from Taiho…

Jun 30, 2020
VITRAC Therapeutics, LLC (VITRAC) initiated the global clinical development of VIC-1911, an oncology candidate formally known as TAS-119, which was licensed from Taiho Pharmaceutical…
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Biocare Medical and Bethyl Laboratories Announce Strategic Partnership for Antibody Development

Jun 30, 2020
Biocare Medical announces a collaborative partnership with Bethyl Laboratories to develop targeted antibodies for cancer research and oncology diagnostics. Bethyl Laboratories has 45…
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SFA Therapeutics Announces FDA Approval To Begin IND Trial

Jun 30, 2020
SFA Therapeutics, Inc. announced that the US FDA has provided approval to conduct a clinical trial (officially referred to as an IND) for the treatment of "the appearance of the…
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Nordic Nanovector’s Betalutin Receives Fast-track Designation from US FDA for Marginal Zone…

Jun 30, 2020
Nordic Nanovector ASA announces that the US Food and Drug Administration (FDA) has granted Fast Track designation for investigating Betalutin (177Lu lilotomab satetraxetan) for the…
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GSK receives first regulatory approval for Duvroq (daprodustat) in Japan for patients with anaemia…

Jun 30, 2020
GlaxoSmithKline plc announced the approval of a Japanese New Drug Application (JNDA) by the Ministry of Health, Labour and Welfare for Duvroq (daprodustat) tablets, an oral…
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Press Releases

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