Abstract
Background: Cobicistat (COBI) is a pharmacoenhancer with no antiretroviral activity. Methods: International, randomized double-blind active-controlled trial to evaluate the efficacy and safety of COBI vs ritonavir (RTV) as a pharmacoenhancer of atazanavir in combination with emtricitabine/tenofovir disoproxil fumarate in HIV treatment-naive patients followed through week 144. Results: At Week 144, virologic suppression was achieved in 72% (COBI) and 74% (RTV) of patients. Adverse events leading to study drug discontinuation occurred in 11% of patients in each group. Median changes in serum creatinine (mg/dL) were +0.13 (COBI) and +0.07 (RTV) and were unchanged from week 48. Conclusions: Once-daily COBI is a safe and effective pharmacoenhancer of the protease inhibitor atazanavir.
Original language | English (US) |
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Pages (from-to) | 338-340 |
Number of pages | 3 |
Journal | Journal of Acquired Immune Deficiency Syndromes |
Volume | 69 |
Issue number | 3 |
DOIs | |
State | Published - Jul 1 2015 |
Externally published | Yes |
Keywords
- Antiretroviral
- clinical trial
- Cobicistat
- HIV
- pharmacoenhancer
ASJC Scopus subject areas
- Infectious Diseases
- Pharmacology (medical)
- General Medicine