3BNC117 Monoclonal Antibody in HIV-infected Subjects During Treatment Interruption

NCT ID: NCT02446847

Last Updated: 2020-07-23

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 16 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2015-03-11
• Study Completion Date: 2017-03-25

Brief Summary

This study evaluates the effects of two infusions of 3BNC117 in preventing or delaying rebound of viral load during a brief treatment interruption of standard ART and its safety during a brief analytical interruption of antiretroviral therapy.

Detailed Description

The proposed study is a Phase II, open label study to evaluate the safety and antiretroviral activity of two and four infusions of 3BNC117 in HIV-infected subjects on combination ART during a brief analytical treatment interruption.

After meeting enrollment criteria sixteen subjects with 3BNC117 sensitive virus (<2μg/ml IC50) will receive two (Group A) or four (Group B) intravenous infusions of 3BNC117, administered at 30 mg/kg.

In both dosing groups, antiretroviral therapy will be discontinued 2 days after the first 3BNC117 infusion (day 2) until week 12. Combination ART will be resumed at week 12. ART will be resumed sooner if plasma HIV-1 RNA level is ≥ 200 copies/ml or if CD4+ count drops < 350 cells/μl and either result is confirmed upon repeat measurement. Participants will be followed weekly until week 12 for safety assessments and for monitoring plasma HIV-1 RNA levels (viral load). CD4+ T cell counts will be monitored every 2 weeks until week 12.

Participants may remain off antiretroviral therapy after week 12, with weekly viral load monitoring, if viral rebound does not occur by week 12. Participants will be followed for a total of 36 weeks.

Conditions

HIV-1 Infection

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Group A: 3BNC117 IV + ART Interruption

Two intravenous infusions of 3BNC117 (30 mg/kg) at day 0 and day 21, with interruption of antiretroviral treatment (ART) at day 2.

Group Type: EXPERIMENTAL

3BNC117

Intervention Type: DRUG

3BNC117 infusions

ART Interruption

Intervention Type: OTHER

Antiretroviral therapy will be discontinued 2 days after the first 3BNC117 infusion (day 2) and resumed at week 12.

Group B: 3BNC117 IV + ART interruption

Four intravenous infusions of 3BNC117 (30 mg/kg) at day 0, day 14, day 28, and day 42 with interruption of antiretroviral treatment (ART) at day 2.

Group Type: EXPERIMENTAL

3BNC117

Intervention Type: DRUG

3BNC117 infusions

ART Interruption

Intervention Type: OTHER

Antiretroviral therapy will be discontinued 2 days after the first 3BNC117 infusion (day 2) and resumed at week 12.

Interventions

3BNC117

3BNC117 infusions

Intervention Type: DRUG

ART Interruption

Antiretroviral therapy will be discontinued 2 days after the first 3BNC117 infusion (day 2) and resumed at week 12.

Intervention Type: OTHER

Other Intervention Names

3BNC117 antibody; Treatment Interruption

Eligibility Criteria

Inclusion Criteria

• Age 18 to 65
• HIV-1 infection confirmed by ELISA and immunoblot.
• Plasma HIV-1 RNA < 50 copies/ml for at least 12 months while on combination ART and < 20 copies/ml at the screening visit. [Note: One or two viral blips of < 200 copies/mL prior to enrollment are permitted if preceded and followed by test results showing VL less than or equal to 50 copies/mL on the same ARV regimen.]
• 3BNC117 sensitivity (IC50 < 2 μg/ml) of subject derived HIV-1 virus isolates. These are isolated under protocol MCA-823 by co-culture of subject PBMCs with HIV-uninfected donor PBMCs followed by in vitro neutralization assays as previously described
• Current CD4 cell count > 500 cells/μl and no prior CD4 cell count < 200 cells/μl.
• Willing to interrupt antiretroviral treatment for 12 weeks, or until viral rebound occurs.
• If sexually active male or female, and participating in sexual activity that could lead to pregnancy using an effective method of contraception throughout the study period. Subjects should also agree to use a male or female condom during the time of pausing their HIV medication.
• If on an NNRTI-based regimen willing to a switch for 4 weeks to dolutegravir.

Exclusion Criteria

• Have a history of AIDS-defining illness within 1 year prior to enrollment
• History of systemic corticosteroids, immunosuppressive anti-cancer, or other medications considered significant by the trial physician within the last 6 months;
• Chronic hepatitis B or hepatitis C;
• Patient report, or chart history, of significant coronary artery disease, myocardial infarction, percutaneous coronary intervention with placement of cardiac stents;
• Patient report, or chart history, of diabetes type 1 or 2 and/or current use of insulin or oral hypoglycemic medications;
• Uncontrolled hypertension, as defined by a systolic blood pressure > 180 and/or diastolic blood pressure > 120, in the presence or absence of anti-hypertensive medications;
• Any other clinically significant acute or chronic medical condition, such as autoimmune diseases, that in the opinion of the investigator would preclude participation;
• Current cigarette use in excess of 1 pack per day;
• Laboratory abnormalities in the parameters listed below:

• Absolute neutrophil count ≤1,000
• Hemoglobin ≤ 10 gm/dL
• Platelet count ≤125,000
• ALT ≥ 2.0 x ULN
• AST ≥ 2.0 x ULN
• Total bilirubin ≥ 1.5 ULN
• Creatinine ≥ 1.1 x ULN
• Coagulation parameters ≥ 1.5 x ULN;
• Current antiretroviral regimen includes either maraviroc or enfuvirtide;
• Pregnancy or lactation;
• Any vaccination within 14 days prior to 3BNC117 administration;
• Receipt of any monoclonal antibody therapy of any kind in the past;
• Participation in another clinical study of an investigational product currently or within past 12 weeks, or expected participation during this study.
• History of resistance to two or more antiretroviral drug classes

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Rockefeller University

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Marina Caskey, MD

Role: PRINCIPAL_INVESTIGATOR

The Rockefeller University

Locations

The Rockefeller University

New York, New York, United States

Countries

United States

Provided Documents

Document Type: Study Protocol

View Document

Document Type: Statistical Analysis Plan

View Document

Document Type: Informed Consent Form

View Document

Other Identifiers

MCA-0867

Identifier Type: -

Identifier Source: org_study_id