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Orexigen Hopes FDA Sees The LIGHT On Contrave NDA

 
• By Jessica Merrill

Contrave could be approved by FDA in 2014, making it the third obesity therapeutic to reach the market in the last two years. An interim analysis of the CV outcomes study LIGHT demonstrates a favorable risk-benefit profile, management said.

Orexigen Therapeutics Inc. expects its obesity medication Contrave (naltrexone SR/bupropion SR) will be on the market in the U.S. and Europe in 2014 after an interim analysis from the ongoing cardiovascular outcomes trial, LIGHT, showed the drug has a favorable risk-benefit profile, the company reported Nov. 25. Orexigen is partnered on Contrave in North America with Takeda Pharmaceutical Co. Ltd. and is seeking a commercial partner in other regions of the world.

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