A Phase 2, Multicenter, Three-part Study to Establish the Dosage, Safety and Antiviral Activity of Combination Therapy With Albuvirtide and 3BNC117 as Long-Acting Maintenance Therapy in Virologically Suppressed Subjects With HIV-1 Infection
Overview
- Phase
- Phase 2
- Intervention
- Albuvirtide
- Conditions
- HIV-1-infection
- Sponsor
- Frontier Biotechnologies Inc.
- Enrollment
- 80
- Locations
- 1
- Primary Endpoint
- Proportion of participants with HIV-1 RNA < 50 copies/mL at the end of treatment phase in Part 3 of the study.
- Last Updated
- 4 years ago
Overview
Brief Summary
The study is an adaptive, phase 2, multicenter, three-part study to establish the dosage, safety and antiviral activity of combination therapy with albuvirtide (ABT) and 3BNC117 as long-acting maintenance therapy in virologically suppressed subjects with HIV-1 infection.
Detailed Description
This is a three-part, multicenter study that will enroll a total of 80 eligible, HIV-1 subjects who are virologically suppressed and stable on daily oral combination antiretroviral therapy. The study will be conducted in three parts. Part 1 and Part 2 are the dose-ranging portions of the study. In Part 1, 30 eligible subjects will be randomized in a 1:1:1 ratio to receive 16 weeks of combination treatment with albuvirtide and 3BNC117 or continue on the existing ART regimen under one of the three cohorts as follows: * Cohort 1: albuvirtide 0.32 g and 3BNC117 2 g every 2 weeks * Cohort 2: albuvirtide 0.32 g and 3BNC117 2 g every 4 weeks * Control Arm 1: Subjects continuing on baseline ART In Part 2 of the study, 20 eligible subjects will be randomized in a 1:1 ratio to receive 16 weeks of combination treatment with albuvirtide and 3BNC117 under one of the two cohorts as follows: * Cohort 3: albuvirtide 0.32 g and 3BNC117 0.8 g every 4 weeks * Cohort 4: albuvirtide 0.16 g and 3BNC117 0.8 g every 4 weeks Part 3 of this study will enroll an additional 30 subjects in a 2:1 ratio to receive up to 28 weeks of combination treatment with optimal dose of albuvirtide and 3BNC117 or continue on the existing ART regimen as follows: * Optimal Dose: albuvirtide and 3BNC11 every 2 or 4 weeks * Control Arm 2: Subjects continuing on baseline ART All consenting patients, in Cohort 1 and 2 (Part 1) and Cohort 3 and 4 (Part 2) of the study, will be shifted from daily oral combination antiretroviral regimen to an intravenous infusion of ABT and 3BNC117. The total treatmentduration with the ABT and 3BNC117 combination regimen will be up to 16 weeks (for Part 1 and Part 2) or 28 weeks (for Part 3) with a two week overlap of the baseline oral antiretroviral regimen and the ABT-3BNC117 combination regimen at the beginning of the study treatment and at the end of the treatment phase in subjects who do not experience virologic rebound. During the two week overlap of baseline oral antiretrovirals and ABT-3BNC117 combination regimen at the beginning of the study treatment, subject will receive weekly doses of ABT and 3BNC117 as intravenous infusions. Beyond the overlap period, subjects in Cohort 1 will receive study treatments every two weeks and subjects in Cohort 2, 3, and 4 will receive study treatments every four weeks. Study participants will be monitored for viral rebound every two weeks following initiation of ABT-3BNC117 combination and will re-initiate an oral antiretroviral regimen if virologic rebound is confirmed with plasma HIV-1 RNA levels above 200 copies/ml on two consecutive blood draws. Pharmacokinetics of ABT and 3BNC117 will be assessed in this study.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Potential subjects are required to meet all of the following criteria for enrollment into the study.
- •HIV-1 seropositive;
- •Males and females, age ≥18 years;
- •Receiving oral combination antiretroviral therapy for last 24 weeks;
- •No change in antiretroviral regimen within last 4 weeks prior to Screening Visit and in-between Screening Visit and First Treatment Visit with an exception that subjects on NNRTI-containing regimens will be allowed to switch to protease inhibitor- or integrase strand transferase inhibitor-based regimens and such change, if needed, should occur at least 4 weeks prior to cessation of oral antiretroviral therapy;
- •Subject has two or more potential alternative antiretroviral drug options available;
- •Plasma HIV-1 RNA \<50 copies/mL at Screening Visit as determined by Human Immunodeficiency Virus 1 (HIV-1) Quantitative, RNA (Taqman® Real-Time PCR);
- •No documented detectable viral loads (HIV-1 RNA \> 50 copies/mL) within the last 24 weeks prior to Screening Visit. An exception for a recorded HIV-1 RNA "blip" (e.g., transient HIV-1 RNA \<400 copies/mL) can be considered, although the preceding and following HIV-1 RNA measurements should be \<50 copies/mL;
- •CD4 cell count of \>300 cells/mm3 at Screening Visit;
- •Laboratory values at Screening:
Exclusion Criteria
- •Potential subjects meeting any of the following criteria will be excluded from enrollment.
- •Any active infection or malignancy requiring acute therapy;
- •Hepatitis B infection as manifest by the presence of Hepatitis B surface antigen (HBsAg);
- •Hepatitis C infection as manifest by positive anti-HCV antibody and positive HCV RNA assay at the time of screening;
- •Grade 4 DAIDS laboratory abnormality;
- •Females who are pregnant, lactating, or breastfeeding, or who plan to become pregnant during the study;
- •Unexplained fever or clinically significant illness within 1 week prior to the first study dose;
- •Any vaccination within 2 weeks prior to the first study dose;
- •Subjects weighing \<35kg;
- •History of anaphylaxis to any oral or parenteral drugs;
Arms & Interventions
Optimal Dose: albuvirtide & 3BNC117
albuvirtide and 3BNC117 every 2 or 4 weeks
Intervention: Albuvirtide
Optimal Dose: albuvirtide & 3BNC117
albuvirtide and 3BNC117 every 2 or 4 weeks
Intervention: 3BNC117
Control Arm 2: Baseline ART
Subjects continuing on baseline ART
Intervention: Baseline ART
Cohort 1: albuvirtide & 3BNC117
albuvirtide 0.32 g and 3BNC117 2 g every 2 weeks
Intervention: Albuvirtide
Cohort 1: albuvirtide & 3BNC117
albuvirtide 0.32 g and 3BNC117 2 g every 2 weeks
Intervention: 3BNC117
Cohort 2: albuvirtide & 3BNC117
albuvirtide 0.32 g and 3BNC117 2 g every 4 weeks
Intervention: Albuvirtide
Cohort 2: albuvirtide & 3BNC117
albuvirtide 0.32 g and 3BNC117 2 g every 4 weeks
Intervention: 3BNC117
Control Arm 1: Baseline ART
Subjects continuing on baseline ART
Intervention: Baseline ART
Cohort 3: albuvirtide & 3BNC117
albuvirtide 0.32 g and 3BNC117 0.8 g every 4 weeks
Intervention: Albuvirtide
Cohort 3: albuvirtide & 3BNC117
albuvirtide 0.32 g and 3BNC117 0.8 g every 4 weeks
Intervention: 3BNC117
Cohort 4: albuvirtide & 3BNC117
albuvirtide 0.16 g and 3BNC117 0.8 g every 4 weeks
Intervention: Albuvirtide
Cohort 4: albuvirtide & 3BNC117
albuvirtide 0.16 g and 3BNC117 0.8 g every 4 weeks
Intervention: 3BNC117
Outcomes
Primary Outcomes
Proportion of participants with HIV-1 RNA < 50 copies/mL at the end of treatment phase in Part 3 of the study.
Time Frame: 28 weeks in Part 3
Secondary Outcomes
- Proportion of participants with HIV-1 RNA < 50 copies/mL at the end of treatment phase in Part 2 of the study(16 weeks in Part 2)
- Proportion of participants with HIV-1 RNA < 50 copies/mL at the end of treatment phase in Part 1 of the study(16 weeks in Part 1)
- Time to virologic rebound after discontinuation of baseline ART regimen(16 weeks in Part 1 and part 2, 28 weeks in part 3)
- Proportion of participants achieving HIV-1 RNA < 50 copies/mL after experiencing virologic rebound(16 weeks in Part 1 and part 2, 28 weeks in part 3)
- Time to achieving HIV-1 RNA < 50 copies/mL after experiencing virologic rebound(16 weeks in Part 1 and part 2, 28 weeks in part 3)
- Mean change in HIV-1 RNA, at each visit within the treatment phase(16 weeks in Part 1 and part 2, 28 weeks in part 3)
- Mean change in CD4 cell count, at each visit within the treatment phase(16 weeks in Part 1 and part 2, 28 weeks in part 3)
- Mean change in CD4:CD8 ratio, at each visit within the treatment phase(16 weeks in Part 1 and part 2, 28 weeks in part 3)
- Emergence of new resistance mutations to antiretroviral drugs as evaluated by GenoSure Archive or PhenoSense GT Assay(16 weeks in Part 1 and part 2, 28 weeks in part 3)
- Measurement of treatment adherence to the ABT and 3BNC117 combination regimen(16 weeks in Part 1 and part 2, 28 weeks in part 3)