MacroGenics Announces Positive Results from Pivotal Phase 3 SOPHIA Study of...
Source: globenewswire.com
MacroGenics Inc. has announced positive results from SOPHIA, a Phase 3 clinical study of margetuximab in HER2-positive metastatic breast cancer patients. Margetuximab is...
FDA Approves BAVENCIO® (avelumab) Plus INLYTA® (axitinib) Combination for Patients with...
ROCKLAND, Mass. and NEW YORK, May 14, 2019 /PRNewswire/ -- BAVENCIO is the first anti-PD-L1 in combination with INLYTA approved by FDA for first-line treatmen
Osiris Therapeutics, Inc. Appoints Samson Tom, PhD, MBA to Serve as...
Source: globenewswire.com
Columbia based, Osiris Therapeutics (NASDAQ: OSIR), is engaged in the research, development, and manufacturing of regenerative medicine products intended to improve the health...
European Commission approves Roche’s MabThera (rituximab) for a rare autoimmune disease
Source: globenewswire.com
The European Commission has given approval to Roche’s drug MabThera (rituximab). This drug helps treat adults with moderate to severe pemphigus vulgaris (PV),...
Novartis investigational therapy crizanlizumab (SEG101) receives FDA Breakthrough Therapy designation for...
Source: www.novartis.com
The US Food and Drug Administration (FDA) has granted Novartis Breakthrough Therapy designation for its investigational therapy crizanlizumab (SEG101). This revolutionary treatment is...
Done Deal: Bristol-Myers Squibb Shareholders Vote to Buy Celgene
Although it was probably not in serious jeopardy, Bristol-Myers Squibb’s shareholders voted today to approve the acquisition of Celgene Corporation for about $74 billion.
Phase 3 ARCHES Trial Shows XTANDI® (enzalutamide) Significantly Improved Radiographic Progression-Free...
Pfizer Inc. (NYSE: PFE) and Astellas Pharma Inc. (TSE: 4503, President and CEO: Kenji Yasukawa, Ph.D., “Astellas”) announced today results from the Ph
Thermo Fisher Scientific to Acquire Manufacturing Site in Cork, Ireland, from...
WALTHAM, Mass., May 16, 2019 /PRNewswire/ -- Thermo Fisher Scientific Inc. (NYSE: TMO), the world leader in serving science, announced today that i
FDA Approves VAXELIS™, Sanofi and Merck’s Pediatric Hexavalent Combination Vaccine
Source: www.news.sanofi.us
The U.S. Food and Drug Administrator (FDA) has given its approval for Sanofi and Merck’s drug VAXELIS. This drug can be used as...
Perrigo Announces Tentative FDA Approval For The Generic Version Of Finacea®...
DUBLIN, March 18, 2019 /PRNewswire/ -- Perrigo Company plc (NYSE; TASE: PRGO) a leading global provider of "Quality, Affordable, Self-Care Products™