Industry Dynamics

Industry News

09-27

2019

Qtrilmet recommended for approval in EU by CHMP for the treatment of type-2 diabetes

23 September 2029 07:00 BST AstraZeneca today announced that Qtrilmet (metformin hydrochloride, saxagliptin and dapagliflozin) modified-release tablets have been recommended for marketing authorisation in ……

09-02

2019

ACZONE? (DAPSONE) GEL, 7.5% NOW APPROVED FOR THE TOPICAL TREATMENT OF ACNE VULGARIS IN PATIENTS 9 YEARS OF AGE AND OLDER

September 20, 2029 ― Almirall LLC announced today the FDA approval of the expanded indication for Aczone? 7.5% Gel to include patients aged 9-22. Aczone? 7.5% Gel is a prescription medicine used on the skin (topical) to ……

08-30

2019

CARsgen Therapeutics Receives US FDA Orphan Drug Designation For Fully Human Anti-BCMA (B Cell Maturation Antigen) Autologous Chimeric Antigen Receptor (CAR) T Cells For The Treatment Of Multiple Myeloma

 Aug. 30, 2029  -- CARsgen Therapeutics Inc., a clinical-stage biopharmaceutical company today announced the United States Food and Drug Administration (FDA) has granted orphan drug designation to its investiga……

08-05

2019

AbbVie's MAVIRET? (glecaprevir/pibrentasvir) Approved by European Commission to Shorten Treatment Duration to Eight Weeks for Treatment-Na?ve Patients with Chronic Hepatitis C and Compensated Cirrhosis

ORTH CHICAGO, Illinois, Aug. 2, 2029 /PRNewswire/ -- AbbVie (NYSE: ABBV), a research-based global biopharmaceutical company, today announced that the European Commission has granted marketing authorization for MAVIRET? (……

07-23

2019

Teva Announces FDA Approval of AirDuo? Digihaler? (fluticasone propionate 113 mcg and salmeterol 14 mcg) Inhalation Powder

JERUSALEM and PARSIPPANY, N.J., July 25, 2029 ? Teva Pharmaceutical Industries Ltd. (NYSE and TASE: TEVA) announced today that the U.S. Food and Drug Administration (FDA) has approved AirDuo? Digihaler? (flutic……

07-03

2019

Sanofi : Libtayo? (cemiplimab) approved for advanced cutaneous squamous cell carcinoma in the European Union

July 2, 2029 - The European Commission (EC) has granted conditional marketing authorization for Libtayo? (cemiplimab) for the treatment of adults with metastatic or locally advanced cutaneous squamous cell carcinoma (CSC……

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