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Teva’s Cinqair To Join Nucala For Severe Asthma After FDA Approval

 
• By Jessica Merrill

FDA approved the interleukin-5 antagonist reslizumab March 23 for the treatment of severe asthma in patients 18 and older who have an eosinophilic phenotype.

Teva Pharmaceutical Industries Ltd.’s Cinqair (reslizumab) will join GlaxoSmithKline PLC’s Nucala (mepolizumab) as the second biologic on the market for eosinophilic severe asthma following the drug’s FDA approval March 23. The company expects to launch Cinqair in the second quarter.

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