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  • bristol-myers-squibb

Tag: bristol myers squibb

You Searched For "bristol-myers-squibb"
Bristol Myers Squibb must face USD 6.4 billion lawsuit over delayed cancer drug

Bristol Myers Squibb must face USD 6.4 billion lawsuit over delayed cancer drug

Ruchika Sharma25 Jun 2022 3:30 PM IST
The case arose from the company's agreement to pay Celgene shareholders holding "contingent value rights" an extra $9 per share in cash if it won U.S....
USFDA nod to Alembic Pharma cancer drug Dasatinib

USFDA nod to Alembic Pharma cancer drug Dasatinib

Ruchika Sharma10 Jun 2022 12:58 PM IST
Vadodara: Drugmaker, Alembic Pharmaceuticals Limited, today announced that the company has received tentative approval from the US Food & Drug...
Bristol Myers Squibb withdraws supplemental biologics license application for Reblozyl for Non-transfusion Dependent (NTD) Beta Thalassemia

Bristol Myers Squibb withdraws supplemental biologics license application for Reblozyl for Non-transfusion Dependent (NTD) Beta Thalassemia

Ruchika Sharma5 Jun 2022 5:00 PM IST
Reblozyl, a first-in-class therapeutic option, is currently approved in the United States, European Union and Canada to address transfusion-dependent...
Bristol Myers Squibb to acquire Turning Point Therapeutics for USD 76.00 per share

Bristol Myers Squibb to acquire Turning Point Therapeutics for USD 76.00 per share

Ruchika Sharma5 Jun 2022 9:30 AM IST
New York: Bristol Myers Squibb and Turning Point Therapeutics, Inc. have announced a definitive merger agreement under which Bristol Myers...
Bristol Myers Opdivo fails to meet primary endpoint in CheckMate -901 trial

Bristol Myers Opdivo fails to meet primary endpoint in CheckMate -901 trial

Ruchika Sharma19 May 2022 10:15 AM IST
Urothelial carcinoma, which most frequently begins in the cells that line the inside of the bladder, accounts for approximately 90% of bladder cancer...
Bristol Myers Squibb to sell its East Syracuse facility to LOTTE

Bristol Myers Squibb to sell its East Syracuse facility to LOTTE

Ruchika Sharma15 May 2022 10:15 AM IST
Following the closing of the transaction, LOTTE, under a newly-established CDMO relationship, will manufacture product for Bristol Myers Squibb from...
Bristol Myers Squibb gets USFDA nod for obstructive hypertrophic cardiomyopathy drug Camzyos

Bristol Myers Squibb gets USFDA nod for obstructive hypertrophic cardiomyopathy drug Camzyos

Ruchika Sharma1 May 2022 10:30 AM IST
Princeton: Bristol Myers Squibb has announced that the U.S. Food and Drug Administration (USFDA) has approved Camzyos (mavacamten, 2.5 mg, 5...
Bristol Myers Squibb, Nektar halt Bempegaldesleukin, Opdivo cocktail trials for cancer treatment

Bristol Myers Squibb, Nektar halt Bempegaldesleukin, Opdivo cocktail trials for cancer treatment

Ruchika Sharma16 April 2022 2:57 PM IST
Princeton: Nektar Therapeutics and Bristol Myers Squibb have announced that based on results from pre-planned analyses of two...
Roche, Bristol Myers Squibb ink pact to advance personalised healthcare through digital pathology solutions

Roche, Bristol Myers Squibb ink pact to advance personalised healthcare through digital pathology solutions

Ruchika Sharma28 March 2022 10:00 AM IST
Data from both projects will be used to aid in cancer diagnosis and to advance personalised healthcare treatment options, with the aim of improving...
Bristol Myers  gets USFDA approval  for First LAG-3-Blocking Antibody Combination, Opduala

Bristol Myers gets USFDA approval for First LAG-3-Blocking Antibody Combination, Opduala

MD Bureau20 March 2022 2:30 PM IST
The trial met its primary endpoint, progression-free survival, and Opdualag more than doubled the median PFS when compared to nivolumab monotherapy,...
Bristol Myers Squibb Nivolumab marketing approval to be revoked for hepatocellular carcinoma: CDSCO panel

Bristol Myers Squibb Nivolumab marketing approval to be revoked for hepatocellular carcinoma: CDSCO panel

Dr. Divya Colin14 March 2022 6:30 PM IST
New Delhi: In a major setback for Bristol Myers Squibb, the Subject Expert Committee (SEC) of the Central Drugs Standard Control Organisation (CDSCO)...
USFDA accepts  Bristol Myers Squibbs Application for Opdivo

USFDA accepts Bristol Myers Squibb's Application for Opdivo

MD Bureau2 March 2022 12:10 PM IST
The FDA granted the application Priority Review status and assigned a Prescription Drug User Fee Act (PDUFA) goal date of July 13, 2022.
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