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A5394

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This is a phase II, randomized, double-blind, placebo-controlled clinical trial to assess the safety, tolerability, and efficacy of 24 weeks of treatment with Selgantolimod (SLGN). Intensive PK sampling will be…
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NC-009

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In this study, the bactericidal activity and safety of 3 doses of TBAJ876 (25 mg, 50 mg, and 100 mg) in combination with Pretomanid 200 mg and linezolid 600 mg…
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UNIVERSAL 1

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HIV-infected children face unique challenges, such as; perinatal transmission of drug resistant HIV virus, limited safety data, impact of ARVs on their grown and development, need for different formulations and…
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RARA

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Standard detection methods for viral RNA in patients include RNA purification, reverse transcription and quantitative PCR (RT-qPCR). These processes are time consuming, require multiple biochemical reagents, lab-grade instruments and trained…
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PLATINUM STUDY

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There is need for anti-malarial combination therapy (ACT) comprising of at least one partner drug with a new mechanism of action to reduce developing resistance. The purpose of this study…
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IFD Rollover

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This study enables continued access to Rilpivirine (RPV), for the evaluation of the long-term safety and tolerability of RPV in combination with other optimized background ARVs, in HIV-infected children aged…
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GS-US-292-106

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Tenofovir disoproxil fumarate (TDF) is a preferred NRTI among recommended regimens for treatment-naive HIV-infected adults and adolescents, but is associated with nephrotoxicity and reduced bone mineral density. Lifelong antiretroviral treatment…
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