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Gilead and Merck Report Results from the P-II Clinical Evaluation of Islatravir + Lenacapavir for HIV

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Gilead and Merck Report Results from the P-II Clinical Evaluation of Islatravir + Lenacapavir for HIV

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  • The P-II trial assessed the safety & efficacy of islatravir (2mg, oral) + lenacapavir (300mg, QW) in virologically suppressed HIV patients (n=104, mean age: 40yrs.) on Biktarvy (bictegravir 50 mg/emtricitabine 200 mg/tenofovir alafenamide 25 mg tablets, B/F/TAF) at wk. 24
  • The study showed a viral load of >50 c/mL in 1 patient, later suppressed at wk. 30, a 94.2% rate of viral suppression that was comparable with those continuing Biktarvy (94.2%) & none in the Biktarvy arm had a viral load of >50 c/mL
  • The P-II trial will extend as an open-label study till wk. 48 with its longer-term results anticipated in the future scientific conferences

Ref: Gilead | Image: Gilead

Related News:- Merck Pauses Enrollment in P-III (IMPOWER 22) and (IMPOWER 24) Clinical Trial of Islatravir for Pre-Exposure Prophylaxis of HIV-1 infection

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Disha Nankani

Disha is a content writer at PharmaShots. She is passionate and curious about recent updates and developments in MedTech and Pharma industry. She covers news related to clinical trial results and updates. She can be contacted at connect@pharmashots.com.

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