Safety and Pharmacokinetics of the Combination Broadly Neutralizing Antibodies, 3BNC117-LS-J and 10-1074-LS-J, in Healthy American and African Adults

I

International AIDS Vaccine Initiative

Status and phase

Active, not recruiting
Phase 2
Phase 1

Conditions

HIV-1-infection

Treatments

Biological: Placebo
Biological: Combination 3BNC117-LS-J and 10-1074-LS-J Ratio 3
Biological: Combination 3BNC117-LS-J and 10-1074-LS-J
Biological: Combination 3BNC117-LS-J and 10-1074-LS-J Ratio 2
Biological: 3BNC117-LS-J
Biological: Combination 3BNC117-LS-J and 10-1074-LS-J Ratio 1
Biological: 10-1074-LS-J

Study type

Interventional

Funder types

Other
NETWORK

Identifiers

NCT04173819
IAVI C100

Details and patient eligibility

About

This is a Phase 1/2 study to evaluate the safety, tolerability, and pharmacokinetics of two broadly neutralizing monoclonal human antibodies (bNAbs), 3BNC117-LS-J, which targets the CD4 binding site on HIV-1 envelope protein, and 10-1074-LS-J which targets the V3 loop of HIV-1 envelope protein. The hypothesis is that the two antibodies will be safe for healthy HIV-1 uninfected adults when co-administered subcutaneously or intravenously and, after subcutaneous administration in the optimal ratio, each antibody will maintain serum levels >10 µg/ml for at least 3 months in HIV-uninfected participants.

Enrollment

225 estimated patients

Sex

All

Ages

18 to 45 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Healthy male and female individuals, as assessed by a medical history, physical exam, and laboratory tests
  • At least 18 years of age on the day of screening and have not reached their 46th birthday on the day of the first administration
  • Willing to undergo HIV testing, risk reduction counseling and receive HIV test results; committed to maintaining low-risk behavior for the trial duration
  • Willing to comply with the requirements of the protocol and available for follow-up for the planned duration of the study
  • All male and female participants of reproductive potential who are engaging in sexual activity that could lead to pregnancy must commit to use an effective method of contraception from enrollment until 9 months after the last administration
  • Willing to forgo donations of blood, or any other tissues during the study following confirmation of study eligibility and, for those who test HIV-positive due to antibody-induced seropositivity, until the anti-HIV antibody titers become undetectable on HIV tests used in the community

Exclusion criteria

  • Confirmed HIV infection
  • Reported risk for HIV infection within 6 months prior to investigational product administration, as defined by: Unprotected sexual intercourse with a known HIV-infected person, a partner known to be at high risk for HIV infection and/or a casual partner (i.e. no continuing established relationship), engaged in sex work, frequent excessive daily alcohol use or frequent binge drinking or any other use of illicit drugs, history of newly-acquired syphilis, gonorrhea, non-gonococcal urethritis, HSV-2, chlamydia, pelvic inflammatory disease (PID), trichomonas, mucopurulent cervicitis, epididymitis, proctitis, lymphogranuloma venereum, chancroid, or hepatitis B or hepatitis C, three or more sexual partners
  • Any clinically significant acute or chronic medical condition that is considered progressive or in the opinion of the investigator makes the participant unsuitable for participation in the study
  • Infectious disease diagnosis: Hepatitis B infection as measured by HbsAg and/or PCR, Hepatitis C infection (US: HCV RNA positive, or interferon-alpha treatment for hepatitis C infection in the past year, or interferon-alpha-free treatment for hepatitis C infection completed in the past 6 months; Africa: HCV Ab positive and/or PCR positive), active syphilis (positive RPR confirmed by TPHA)
  • Receipt of blood transfusion or blood-derived products within the previous 3 months
  • Participation in another clinical trial of an investigational product currently, within the previous 3 months or expected participation during this study (Concurrent participation in an observational trial not requiring blood or tissue sample collection is not an exclusion)
  • Psychiatric condition that compromises safety of the participant and precludes compliance with the protocol. Specifically excluded are persons with psychoses within the past 3 years, ongoing risk for suicide, or history of suicide attempt or gesture within the past 3 years
  • Body mass index (BMI) >40
  • Active tuberculosis

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

225 participants in 10 patient groups

Group 1
Experimental group
Description:
Single Agent, abdominal subcutaneous injection, 10:2 ratio for Ab:placebo
Treatment:
Biological: 3BNC117-LS-J
Biological: Placebo
Group 2
Experimental group
Description:
Single agent, abdominal subcutaneous injection 10:2 ratio for Ab:placebo
Treatment:
Biological: 10-1074-LS-J
Biological: Placebo
Group 3
Experimental group
Description:
Single agent intravenous injection 10:2 ratio for Ab:placebo
Treatment:
Biological: 3BNC117-LS-J
Biological: Placebo
Group 4
Experimental group
Description:
Single agent intravenous injection 10:2 ratio for Ab:placebo
Treatment:
Biological: 10-1074-LS-J
Biological: Placebo
Group 5
Experimental group
Description:
Combined agent intravenous injection 10:2 ratio for Ab:placebo
Treatment:
Biological: Combination 3BNC117-LS-J and 10-1074-LS-J
Biological: Placebo
Group 6
Experimental group
Description:
Subcutaneous injection combined ratio 1 with loading dose 30:3 ratio of Ab:Placebo
Treatment:
Biological: Combination 3BNC117-LS-J and 10-1074-LS-J Ratio 1
Biological: Placebo
Group 7
Experimental group
Description:
Subcutaneous injection in abdomen combined ratio 2 with loading dose 30:3 ratio of Ab:Placebo
Treatment:
Biological: Combination 3BNC117-LS-J and 10-1074-LS-J Ratio 2
Biological: Placebo
Group 8
Experimental group
Description:
Subcutaneous injection in abdomen combined ratio 3 with loading dose 30:3 ratio of Ab:Placebo
Treatment:
Biological: Placebo
Biological: Combination 3BNC117-LS-J and 10-1074-LS-J Ratio 3
Group 9
Experimental group
Description:
Subcutaneous injection in abdomen combined ratio 2 without loading dose 30:3 ratio of Ab:Placebo
Treatment:
Biological: Combination 3BNC117-LS-J and 10-1074-LS-J Ratio 2
Biological: Placebo
Group 10
Experimental group
Description:
Subcutaneous injection in arm combined ratio 2 without loading dose 30:3 ratio of Ab:Placebo
Treatment:
Biological: Combination 3BNC117-LS-J and 10-1074-LS-J Ratio 2
Biological: Placebo

Trial contacts and locations

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Data sourced from clinicaltrials.gov

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