Clinical Trials

MainTitle

3BNC117 and 10-1074 in HIV Uninfected Adults

This study is ongoing, but not recruiting participants.
Sponsor
Rockefeller University


Information provided by (Responsible Party)
Rockefeller University
ClinicalTrials.gov Identifier
NCT02824536

First received: June 28, 2016
Last updated: April 4, 2017
Last Verified: December 2016
History of Changes
Purpose

Purpose

This is a phase 1 clinical trial to evaluate the safety and pharmacokinetics of the highly neutralizing anti-human immunodeficiency virus-1 monoclonal antibodies 3BNC117 and 10-1074, when given in combination, in human immunodeficiency virus (HIV)-uninfected individuals. This study is intended to support the development of the combination of 3BNC117 and 10-1074 mAbs for use as prophylaxis against HIV infection in healthy HIV-uninfected individuals at risk for HIV infection.

Condition Intervention Phase
Human Immunodeficiency Virus

Drug : 3BNC117
Drug : 10-1074
Drug : Placebo
Phase 1

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Triple (Participant, Care Provider, Investigator)
Primary Purpose: Prevention
Official Title: A Phase 1 Study of the Safety and Pharmacokinetics of the Combination of 3BNC117 and 10-1074 in HIV-uninfected Adults

Further study details as provided by Rockefeller University:

Primary Outcome Measures

  • The number of participants who experience adverse events within 1 week after the combination of 3BNC117 and 10-1074 infusion in all study groups. [ Time Frame: 1 week following each combination of 3BNC117 and 10-1074 infusion ]
    Adverse events include signs, symptoms and laboratory abnormalities, in addition to local and systemic reactogenicity adverse events.
Secondary Outcome Measures:
  • Number of participants with induced anti-3BNC117 and anti-10-1074 antibodies [ Time Frame: 8 weeks following each combination of 3BNC117 and 10-1074 infusion ]
  • Level of induced anti-3BNC117 and anti-10-1074 antibodies [ Time Frame: 8 weeks following each combination of 3BNC117 and 10-1074 infusion ]
  • The number of participants who experience adverse events that occur during study follow up after 3BNC117 and 10-1074 infusions in all study groups. [ Time Frame: 24-40 weeks ]
    Adverse events include signs, symptoms and laboratory abnormalities.
Other Outcome Measures:
  • Neutralization activity of serum from study participants against a panel of viruses as measured by the TZM.bl neutralization assay. [ Time Frame: 24-40 weeks ]
  • Elimination half-life (t1/2) of 3BNC117 and 10-1074 [ Time Frame: 24-40 weeks ]
  • Clearance (CL/F) of 3BNC117 and 10-1074 [ Time Frame: 24-40 weeks ]
  • Volume of distribution (Vz/F) of 3BNC117 and 10-1074 [ Time Frame: 24-40 weeks ]
  • Area under the plasma concentration versus time curve (AUC) of 3BNC117 and 10-1074 [ Time Frame: 24-40 weeks ]
  • Decay Curve of of 3BNC117 and 10-1074 [ Time Frame: 24-40 weeks ]

Enrollment: 24
Study Start Date: June 2016
Estimated Study Completion Date: December 2018
Estimated Primary Completion Date: June 2018 (Final data collection date for primary outcome measure)

Arms Assigned Interventions
Experimental: Group 1
Participants will be randomized in a 3:1 ratio to receive one intravenous infusion of 3BNC117 and one intravenous infusion of 10-1074, each dosed at 10 mg/kg OR placebo (sterile saline), on day 0.
Drug: 3BNC117

Intravenous Infusion of 3BNC117

Other Name: Monoclonal Antibody 3BNC117
Drug: 10-1074

Intravenous Infusion of 10-1074

Other Name: Monoclonal Antibody 10-1074
Drug: Placebo

Intravenous Infusion of Sterile Saline (NaCl 0.9%)

Other Name: Sterile Saline (NaCl 0.9%)
Experimental: Group 2
Participants will be randomized in a 3:1 ratio to receive three intravenous infusions of 3BNC117 and three intravenous infusions of 10-1074, each dosed at 3 mg/kg OR placebo (sterile saline), on day 0, week 8, and week 16.
Drug: 3BNC117

Intravenous Infusion of 3BNC117

Other Name: Monoclonal Antibody 3BNC117
Drug: 10-1074

Intravenous Infusion of 10-1074

Other Name: Monoclonal Antibody 10-1074
Drug: Placebo

Intravenous Infusion of Sterile Saline (NaCl 0.9%)

Other Name: Sterile Saline (NaCl 0.9%)
Experimental: Group 3
Participants will be randomized in a 3:1 ratio to receive three intravenous infusions of 3BNC117 and three intravenous infusions of 10-1074, each dosed at 10 mg/kg OR placebo (sterile saline), on day 0, week 8, and week 16.
Drug: 3BNC117

Intravenous Infusion of 3BNC117

Other Name: Monoclonal Antibody 3BNC117
Drug: 10-1074

Intravenous Infusion of 10-1074

Other Name: Monoclonal Antibody 10-1074
Drug: Placebo

Intravenous Infusion of Sterile Saline (NaCl 0.9%)

Other Name: Sterile Saline (NaCl 0.9%)

Detailed Description:

The study will be conducted under a placebo-controlled, double blind, randomized allocation of the study products. Study participants in each study group will be randomized to receive intravenous infusions of 3BNC117 and 10-1074 or placebo. 3BNC117 and 10-1074 will be administered at 2 dose levels (3 mg/kg and 10 mg/kg). These doses were selected based on the planned development of subcutaneous formulations for the prophylactic use of these products. The study will consist of 3 groups. Enrollment in Group 1 will begin first and participants will be enrolled at least one day apart. Eight participants will be enrolled in each group; 6 will be randomized receive the study drugs and 2 will be randomized to receive placebo. Participants in Group 1 will receive a single infusion of each antibody at 10mg/kg at Week 0. Enrollment in Group 2 will begin only after Day 28 safety data from all participants in Group 1, including ophthalmologic exams, are available. Enrollment in Group 3 will begin only after the Day 28 safety data from all participants in Group 2 is available. If > 1 grade 3 or higher adverse events deemed probably or definitely related to the study drugs occurs in a single group, the next group will not be enrolled pending safety monitoring committee (SMC) review. Participants in Groups 2 and 3 will receive 3 infusions of each antibody at Weeks 0, 8, and 16, at a dose of either 3mg/kg or 10mg/kg. The antibodies will be administered sequentially via intravenous infusion. Each antibody will be administered over 60 minutes.
Following product infusions, study participants will return for safety assessments at multiple time points. Blood samples will be collected for safety testing at weeks 1, 2, and 4 following each infusion, then at multiple time points until the end of study follow up.
Baseline pharmacokinetic (PK) assessments will be performed before the start of the first infusion. Peak PK sampling for 3BNC117 will occur following the completion of the 3BNC117 infusion prior to the start of the 10-1074 infusion. Peak PK sampling for 10-1074 will occur following the completion of the 10-1074 infusion. Additional PK assessments will occur at multiple time points during study follow up. Study participants will be followed for a total of 24 weeks following the final antibody infusion.

Eligibility

Eligibility

Ages Eligible for Study: 18 Years to 65 Years  
Sexes Eligible for Study: All  
Accepts Healthy Volunteers: Yes  

Criteria

Inclusion Criteria:

  • Males and females, age 18 to 65.
  • Amenable to HIV risk reduction counseling and agrees to maintain behavior consistent with low risk of HIV exposure.
  • If sexually active male or female, and participating in sexual activity that could lead to pregnancy, agrees to use two effective methods of contraception (i.e. condom with spermicide, diaphragm with spermicide, hormone-eluting IUD, hormone-based contraceptive with condom) for the duration of the study.


Exclusion Criteria:
  • Confirmed HIV-1 or HIV-2 infection.
  • History of immunodeficiency or autoimmune disease; use of systemic corticosteroids, immunosuppressive anti-cancer, or other medications considered significant by the trial physician within the last 6 months.
  • Any clinically significant acute or chronic medical condition (such as autoimmune diseases) that in the opinion of the investigator would preclude participation.
  • Within the 12 months prior to enrollment, the participant has a history of sexually transmitted infection.
  • Chronic Hepatitis B or Hepatitis C infection.
  • Laboratory abnormalities in the parameters listed:
  • Absolute neutrophil count ≤ 2,000;
  • Hemoglobin ≤ 12 gm/dL if female; ≤ 13.5 gm/dL if male;
  • Platelet count ≤ 125,000;
  • Alanine Aminotransferase (ALT) ≥ 1.25 x ULN; Aspartate Aminotransferase (AST) ≥ 1.25 x ULN;
  • Alkaline phosphatase ≥ 1.5 x ULN
  • Total bilirubin > 1.0 x ULN;
  • Creatinine ≥1.1 x ULN;
  • Pregnancy or lactation.
  • Any vaccination within 14 days prior to infusion
  • Receipt of any experimental HIV vaccine in the past.
  • History of severe reaction to a vaccine or drug infusion or history of severe allergic reactions.
  • Participation in another clinical study of an investigational product currently or
within past 12 weeks, or expected participation during this study.

contacts and locations

Contacts and Locations

Choosing to participate in a study is an important personal decision.Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below.For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT02824536

Locations

United States, New York
The Rockefeller University
New York, New York, United States, 10065

Sponsors and Collaborators

Rockefeller University

Investigators

Principal Investigator: Yehuda Cohen, MD Rockefeller University
More Information

More Information


Responsible Party: Rockefeller University  
ClinicalTrials.gov Identifier: NCT02824536   History of Changes  
Other Study ID Numbers: YCO-0899  
Study First Received: June 28, 2016  
Last Updated: April 4, 2017  
Individual Participant Data    
Plan to Share IPD: No  

Keywords provided by Rockefeller University:

3BNC117
10-1074
Broadly neutralizing antibody
HIV Prevention

Additional relevant MeSH terms:
Immunologic Deficiency Syndromes
Acquired Immunodeficiency Syndrome
HIV Infections
Antibodies
Immunoglobulins
Antibodies, Monoclonal

ClinicalTrials.gov processed this data on December 08, 2017
This information is provided by ClinicalTrials.gov.