NCT01854775 Study to Evaluate the Pharmacokinetics, Safety, and Antiviral Activity of the Elvitegravir/Cobicistat/Emtricitabine/Tenofovir Alafenamide (E/C/F/TAF) Single Tablet Regimen (STR) in HIV-1 Infected Antiretroviral Treatment-Naive Adolescents and Virologically Suppressed Children Status COMPLETED Phase PHASE2/PHASE3
NCT01851330 Safety and Efficacy of Ledipasvir/Sofosbuvir Fixed-Dose Combination ± Ribavirin for the Treatment of HCV (ION-3) Status COMPLETED Phase PHASE3
NCT01850212 A Phase 4 Cross-Sectional Study of Bone Mineral Density in HIV-1 Infected Subjects Status COMPLETED Phase N/A
NCT01847391 A Phase 1 Study to Assess the Safety,Tolerability, and Pharmacokinetics of GS-6615 in Healthy Subjects Status COMPLETED Phase PHASE1
NCT01843127 A Study to Evaluate the Effect of Ranolazine on Postprandial Glucagon in Subjects With Type 2 Diabetes. Status COMPLETED Phase PHASE1
NCT01841489 A Phase 1 Study of Novel GS-9973 Tablet Formulations to Evaluate the Effect of Acid Reducing Agents, Relative Bioavailability, and Food Effect on GS-9973 Pharmacokinetics Status COMPLETED Phase PHASE1
NCT01840735 Phase 1b Safety, Tolerability, and PK Study to Assess GS-5737 in Subjects With CF Status COMPLETED Phase PHASE1
NCT01838590 Sofosbuvir Plus Ribavirin Administered for Either 12 or 24 Weeks in Treatment-Naive and Treatment-Experienced Egyptian Adults With Chronic Genotype 4 Hepatitis C Virus (HCV) Infection Status COMPLETED Phase PHASE3
NCT01838434 Lenalidomide With or Without Idelalisib in Treating Patients With Relapsed or Refractory Mantle Cell Lymphoma Status COMPLETED Phase PHASE1
NCT01831427 Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Efficacy of GS-5745 (Andecaliximab) in Adults With Moderate to Severe Active Ulcerative Colitis Status COMPLETED Phase PHASE1
NCT01826981 Efficacy and Safety of Sofosbuvir Containing Regimens for the Treatment of Chronic HCV Infection in Participants With Chronic Genotype 1, 2, 3, or 6 HCV Infection Status COMPLETED Phase PHASE2
NCT01818596 Open-label Safety Study of E/C/F/TAF (Genvoya®) in HIV-1 Positive Patients With Mild to Moderate Renal Impairment Status COMPLETED Phase PHASE3
NCT01817985 A Phase 1 Study to Evaluate the Pharmacokinetics of GS-5816 in Subjects With Normal Hepatic Function and Moderate or Severe Hepatic Impairment Status COMPLETED Phase PHASE1
NCT01815736 Study to Evaluate Switching From a TDF-Containing Combination Regimen to a TAF-Containing Fixed Dose Combination (FDC) in Virologically-Suppressed, HIV-1 Positive Participants Status COMPLETED Phase PHASE3