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ViiV Healthcare Files NDA for Cabotegravir + Edurant (rilpivirine) to the US FDA to Treat HIV-1 Infection in Adults

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ViiV Healthcare Files NDA for Cabotegravir + Edurant (rilpivirine) to the US FDA to Treat HIV-1 Infection in Adults

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  • The submission is based on P-III ATLAS (Antiretroviral Therapy as Long-Acting Suppression) and FLAIR (First Long-Acting Injectable Regimen) studies results assessing Cabotegravir + Edurant (rilpivirine) (injected monthly) vs SOC (three-drug regimen) in 1-100+ patients infected with HIV + viral suppression across 16 countries for 48wks.
  • The P-III ATLAS & FLAIR studies resulted in maintaining viral suppression period @48wks. and safety & efficacy of two-drug regime- with 85% patients preferring it over prior treatment and if approved will reduce the no. of days of treatment from 365 to 12/year
  • Cabotegravir is an investigational integrase inhibitor (INI) developed by ViiV Healthcare to treat HIV. Edurant (rilpivirine) is a non-nucleoside reverse transcriptase inhibitor (NNRTI). ViiV Healthcare and Janssen plans to submit a regulatory application for the combination to EMA- Health Canada in 2019

Ref: ViiV Healthcare | Image: Twitter

Click here to­ read the full press release 

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This content piece was prepared by our former Senior Editor. She had expertise in life science research and was an avid reader. For any query reach out to us at connect@pharmashots.com

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