search
Back to results

Active Immunization of HIV-Infected Pregnant Women: A Phase I Study of Safety and Immunogenicity of a rgp120/HIV-1 Vaccine (NOTE: Some Patients Receive Placebo)

Primary Purpose

HIV Infections, Pregnancy, HIV Seronegativity

Status
Withdrawn
Phase
Phase 1
Locations
Study Type
Interventional
Intervention
MF59
rgp120/HIV-1 SF-2
Sponsored by
National Institute of Allergy and Infectious Diseases (NIAID)
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional prevention trial for HIV Infections focused on measuring Vaccines, Synthetic, Pregnancy, Pregnancy Complications, Infectious, AIDS-Related Complex, HIV Envelope Protein gp120, HIV Preventive Vaccine, HIV Therapeutic Vaccine

Eligibility Criteria

16 Years - 40 Years (Child, Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria Concurrent Medication: Allowed during pregnancy: AZT. Methadone maintenance. NOTE: Patients may not initiate antiretroviral therapy for disease progression. NOTE: Patients may change from AZT to another antiretroviral agent or may begin antiretroviral therapy following delivery, if clinically indicated. Patients must have: Documented HIV infection. CD4 count >= 400 cells/mm3 (average of two determinations obtained 1 week apart). No clinical criteria for a diagnosis of AIDS. HIV p24 antigen <= 30 pg/ml. Estimated gestational age between 16 and 24 weeks, confirmed by baseline sonogram that does not demonstrate any congenital abnormalities considered to be incompatible with life. Intention to carry pregnancy to term. Willingness to be followed by an ACTU for the duration of the study. NOTE: Father of the fetus (if available after a reasonable attempt to contact him) must provide informed consent. Prior Medication: Allowed: AZT. Exclusion Criteria Co-existing Condition: Patients with the following symptoms or conditions are excluded: Known hypersensitivity to a component of the vaccine. Hepatitis B antigen positive at study entry. Evidence of life-threatening or other serious pre-existing fetal abnormalities (e.g., anencephaly, renal agenesis, Potter's syndrome). Evidence of syphilis that requires therapy during this pregnancy. Intention to breast-feed. Presence of obstetrical high-risk factors such as: insulin-dependent diabetes hypertension requiring the use of anti-hypertensive therapy repeated intrauterine fetal demise Rh-sensitization or other blood group alloimmunization diseases requiring use of immunosuppressive therapy (e.g., asthma, lupus). Concurrent Medication: Excluded during pregnancy: Antiretrovirals other than AZT. Immunomodulating agents (e.g., HIVIG, IVIG). Other investigational drugs or immunosuppressive agents. NOTE: Patients may change from AZT to another antiretroviral agent or may begin antiretroviral therapy following delivery, if clinically indicated. Prior Medication: Excluded within 90 days prior to study entry: Antiretrovirals other than AZT. Immunomodulating agents (e.g., HIVIG, IVIG). Current use of illicit drugs or chronic alcohol use by patient history.

Sites / Locations

    Outcomes

    Primary Outcome Measures

    Secondary Outcome Measures

    Full Information

    First Posted
    November 2, 1999
    Last Updated
    October 28, 2021
    Sponsor
    National Institute of Allergy and Infectious Diseases (NIAID)
    search

    1. Study Identification

    Unique Protocol Identification Number
    NCT00001046
    Brief Title
    Active Immunization of HIV-Infected Pregnant Women: A Phase I Study of Safety and Immunogenicity of a rgp120/HIV-1 Vaccine (NOTE: Some Patients Receive Placebo)
    Official Title
    Active Immunization of HIV-Infected Pregnant Women: A Phase I Study of Safety and Immunogenicity of a rgp120/HIV-1 Vaccine (NOTE: Some Patients Receive Placebo)
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    October 2021
    Overall Recruitment Status
    Withdrawn
    Study Start Date
    undefined (undefined)
    Primary Completion Date
    undefined (undefined)
    Study Completion Date
    undefined (undefined)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    National Institute of Allergy and Infectious Diseases (NIAID)

    4. Oversight

    5. Study Description

    Brief Summary
    PRIMARY: To evaluate the short-term safety of rgp120/HIV-1SF2 vaccine versus MF59 placebo administered to HIV-infected pregnant women. SECONDARY: To evaluate the immunogenicity and long-term safety of rgp120/HIV-1SF2 in HIV-infected pregnant women who received the vaccine during pregnancy only or during pregnancy and postpartum. To evaluate immunogenicity and safety in the infant through 18 months of age following maternal immunization with the vaccine during pregnancy. Active immunization of HIV-infected women during pregnancy may slow the progression of maternal disease, reduce the titer of virus in maternal plasma, and increase the titer of epitope-specific antibody. Also, active immunization has the potential to induce primary immunity in the fetus and to boost both T-cell and humoral immune responses to HIV in the mothers.
    Detailed Description
    Active immunization of HIV-infected women during pregnancy may slow the progression of maternal disease, reduce the titer of virus in maternal plasma, and increase the titer of epitope-specific antibody. Also, active immunization has the potential to induce primary immunity in the fetus and to boost both T-cell and humoral immune responses to HIV in the mothers. Women are randomized to receive rgp120/HIV-1SF2 vaccine or MF59 placebo. Patients receive the first immunization between 16 and 24 weeks gestation and monthly thereafter until delivery, for a maximum of five immunizations. Patients may continue to receive the immunization regimen to which they were originally assigned at 3, 6, 9, and 12 months postpartum. Maternal follow-up continues until 18 months postpartum; infants are followed until age 18 months.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    HIV Infections, Pregnancy, HIV Seronegativity
    Keywords
    Vaccines, Synthetic, Pregnancy, Pregnancy Complications, Infectious, AIDS-Related Complex, HIV Envelope Protein gp120, HIV Preventive Vaccine, HIV Therapeutic Vaccine

    7. Study Design

    Primary Purpose
    Prevention
    Study Phase
    Phase 1
    Interventional Study Model
    Parallel Assignment
    Enrollment
    0 (Actual)

    8. Arms, Groups, and Interventions

    Intervention Type
    Biological
    Intervention Name(s)
    MF59
    Intervention Type
    Biological
    Intervention Name(s)
    rgp120/HIV-1 SF-2

    10. Eligibility

    Sex
    Female
    Minimum Age & Unit of Time
    16 Years
    Maximum Age & Unit of Time
    40 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria Concurrent Medication: Allowed during pregnancy: AZT. Methadone maintenance. NOTE: Patients may not initiate antiretroviral therapy for disease progression. NOTE: Patients may change from AZT to another antiretroviral agent or may begin antiretroviral therapy following delivery, if clinically indicated. Patients must have: Documented HIV infection. CD4 count >= 400 cells/mm3 (average of two determinations obtained 1 week apart). No clinical criteria for a diagnosis of AIDS. HIV p24 antigen <= 30 pg/ml. Estimated gestational age between 16 and 24 weeks, confirmed by baseline sonogram that does not demonstrate any congenital abnormalities considered to be incompatible with life. Intention to carry pregnancy to term. Willingness to be followed by an ACTU for the duration of the study. NOTE: Father of the fetus (if available after a reasonable attempt to contact him) must provide informed consent. Prior Medication: Allowed: AZT. Exclusion Criteria Co-existing Condition: Patients with the following symptoms or conditions are excluded: Known hypersensitivity to a component of the vaccine. Hepatitis B antigen positive at study entry. Evidence of life-threatening or other serious pre-existing fetal abnormalities (e.g., anencephaly, renal agenesis, Potter's syndrome). Evidence of syphilis that requires therapy during this pregnancy. Intention to breast-feed. Presence of obstetrical high-risk factors such as: insulin-dependent diabetes hypertension requiring the use of anti-hypertensive therapy repeated intrauterine fetal demise Rh-sensitization or other blood group alloimmunization diseases requiring use of immunosuppressive therapy (e.g., asthma, lupus). Concurrent Medication: Excluded during pregnancy: Antiretrovirals other than AZT. Immunomodulating agents (e.g., HIVIG, IVIG). Other investigational drugs or immunosuppressive agents. NOTE: Patients may change from AZT to another antiretroviral agent or may begin antiretroviral therapy following delivery, if clinically indicated. Prior Medication: Excluded within 90 days prior to study entry: Antiretrovirals other than AZT. Immunomodulating agents (e.g., HIVIG, IVIG). Current use of illicit drugs or chronic alcohol use by patient history.
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Starr S
    Official's Role
    Study Chair
    First Name & Middle Initial & Last Name & Degree
    Allen M
    Official's Role
    Study Chair
    First Name & Middle Initial & Last Name & Degree
    Scott GB
    Official's Role
    Study Chair
    First Name & Middle Initial & Last Name & Degree
    Silverman N
    Official's Role
    Study Chair

    12. IPD Sharing Statement

    Learn more about this trial

    Active Immunization of HIV-Infected Pregnant Women: A Phase I Study of Safety and Immunogenicity of a rgp120/HIV-1 Vaccine (NOTE: Some Patients Receive Placebo)

    We'll reach out to this number within 24 hrs