Industry Dynamics

Industry News

03-26

2020

ViiV Healthcare announces first global regulatory approval of CABENUVA; the first complete, long-acting, regimen for the treatment of HIV

March 20, 2020--ViiV Healthcare, the global specialist HIV company majority owned by GSK, with Pfizer Inc. and Shionogi Limited as shareholders, today announced that Health Canada has approved CABENUVA, the first and onl……

03-09

2020

European Commission Grants AbbVie Marketing Authorization Shortening MAVIRET? (glecaprevir/pibrentasvir) Treatment Duration to Eight Weeks for Treatment-Na?ve Chronic HCV Patients with Genotype 3 and Compensated Cirrhosis

March 6, 2020-- AbbVie (NYSE: ABBV), a research-based global biopharmaceutical company, today announced that the European Commission has approved a change to the marketing authorization for MAVIRET? (glecaprevir/pibrenta……

02-26

2020

Sanofi: The world's second largest API company will be created to balance Europe's heavy dependence on Asian APIs!

February 24, 2020/ The French drugmaker said it’s creating the world’s second largest active pharmaceutical ingredients (API) manufacturer by spinning out its six current sites into a standalone company: Brindisi (Italy)……

02-17

2020

Eisai to Voluntarily Withdraw BELVIQ?/BELVIQ XR? in the U.S.

Feb.23, 2020 / Eisai Inc. announced that it will voluntarily withdraw from the market and discontinue sales of BELVIQ? (lorcaserin HCl) CIV and BELVIQ XR (lorcaserin HCl) CIV in the U.S. This action is being taken after ……

01-27

2020

The European Commission Approves Expanded Use of Janssen’s STELARA? (ustekinumab) for the Treatment of Paediatric Patients With Moderate to Severe Plaque Psoriasis

January 23, 2020 / The Janssen Pharmaceutical Companies of Johnson & Johnson today announced that the European Commission (EC) has approved the expanded use of STELARA? (ustekinumab) for the treatment of paediatric patie……

12-27

2019

Bristol-Myers Squibb Receives European Commission Approval for Revlimid? (lenalidomide) in Combination with Rituximab for the Treatment of Adult Patients with Previously Treated Follicular Lymphoma”

PRINCETON, N.J.--(BUSINESS WIRE)--Bristol-Myers Squibb Company (NYSE: BMY) today announced that the European Commission (EC) has approved a new indication for Revlimid (lenalidomide), in combination with rituximab (anti-……

< 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 >

Copyright Nanjing Dorra Pharmaceutical Technology Co.,Ltd. @ 2018 China All Rights Reserved 苏ICP备12056923号-1