Pharma Focus Asia

U.S. FDA Approves Teva's Biotech Drug for Severe Asthma

Thursday, March 24, 2016

The U.S. Food and Drug Administration said on Wednesday it had approved Teva Pharmaceutical Industries Ltd's drug to treat asthma in adults who have a history of severe attacks despite taking medication.

The drug, Cinqair, part of a new wave of biotech drugs for severe asthma, is administered intravenously every four weeks in combination with other drugs. (1.usa.gov/1LGGELI)

Teva's treatment will compete with GlaxoSmithKline Plc's recently approved Nucala, as well as Xolair, an established drug jointly developed by Novartis AG and Roche Holding AG.

Nucala was approved by the FDA in November and, like Cinqair, is an antibody that reduces levels of eosinophils, a type of white blood cell that contributes to the development of asthma.

Over-production of eosinophils can cause inflammation in the lungs, increasing the frequency of asthma attacks.

More than 22 million Americans suffered from asthma in 2013, according to the Centers for Disease Control and Prevention, which estimates there are more than 400,000 asthma-related hospitalizations each year.

 

Source : reuters.com

magazine-slider-imageMFA + MMA 2024CPHI Chine || PMEC China 2024Asia Healthcare Week 2024Advance DoE WorkshopNitrosamine Advance Workshop 2024CPHI Korea 2024CHEMICAL INDONESIA 2024INALAB 2024 Thermo Scientific - DynaDrive and DynaSpinDigital Health Asia 2024Rehab Expo 2024ISPE Singapore Affiliate Conference & Exhibition 20242024 PDA Pharmaceutical Manufacturing & Quality Conference2024 PDA Cell and Gene Pharmaceutical Products Conference 2024 PDA Aseptic Manufacturing Excellence Conference2024 PDA Aseptic Processing of Biopharmaceuticals ConferencePharma Quality Excellence Awards 20244th Annual Pharma GMP Quality Management 20243rd World ADC Asia 2024LogiPharma Asia 2024