Evaluating Safety and Immune Response to the HIV-1 CH505 Transmitted/Founder gp120 Adjuvanted With GLA-SE in Healthy, HIV-exposed Uninfected Infants (HVTN 135)

HIV Vaccine Trials Network

Status and phase: Completed; Phase 1

Conditions: HIV Infections

Treatments: Biological: GLA-SE adjuvant; Biological: Placebo; Biological: CH505TF gp120

Study type: Interventional

Funder types: NETWORK; NIH

Identifiers

NCT04607408

UM1AI068614 (U.S. NIH Grant/Contract)

HVTN 135

Details and patient eligibility

About

This study will evaluate the safety and immune response in healthy HIV-exposed and uninfected infants to the protein vaccine, CH505TF gp120, adjuvanted with GLA-SE.

Full description

This study will evaluate the safety and immune response in healthy HIV-exposed and uninfected infants to the protein vaccine, CH505TF gp120, adjuvanted with GLA-SE.

This study will enroll 38 mother-infant pairs. To quantify the maternal HIV antibody response, mothers will also be enrolled in the study but will not receive study product. Infants will receive the CH505TF gp120 protein adjuvanted with GLA-SE at Weeks 0, 8, 16, 32, and 54. The first dose will be given within the first five days of life.

The study will be conducted in three parts (Parts A, B, and C), and to ensure safety, enrollment will proceed in stages.

Part A (Initial Safety) will enroll first. 5 infants in Part A will receive a low dose of protein with a low dose of adjuvant and 2 infants will receive placebo.

After safety review post first vaccination of infants in Part A, Part B will enroll. In Part B (Safety Ramp-Up), 2 infants will receive a higher dose of protein with a higher dose of adjuvant and 2 infants will receive placebo.

After safety review post first vaccination of infants in Part B, Part C will enroll. In Part C (Immunogenicity), 5 infants will receive low dose protein with higher dose of adjuvant, 16 infants will receive a higher dose of protein with higher dose of adjuvant, and 6 infants will receive placebo.

There are 14 scheduled clinic visits over 24.5 months. For infants, study visits may include physical examinations, medical history, vaccine injections, HIV testing, and blood, cord blood, and stool collection. For mothers, study visits may include medical history, physical examinations, questionnaires, risk reduction counseling, and blood, breastmilk, and stool collection.

Enrollment: 38 patients

Sex: All

Ages: Under 5 days old

Volunteers: Accepts Healthy Volunteers

Inclusion and exclusion criteria

Infant Inclusion Criteria:

• Born via Caesarean section to an HIV-1-infected woman who meets all maternal inclusion/exclusion criteria listed below.
• Estimated gestational age at birth is at least 37 weeks.
• Weight at birth is at least 2.5 kg.
• Has initiated antiretroviral prophylaxis consistent with current site-specific standard of care.
• Hemoglobin >14.0 g/dL.
• White Blood Cell Count ≥ 7000 cells/mm3
• Platelets > 100,000 cells/mm3
• Alanine aminotransferase (ALT) <1.25 times upper limit of age adjusted normal.
• Creatinine < 1.1 times upper limit of age adjusted normal.
• Negative HIV-1 nucleic acid test on specimen drawn within 72 hours of birth.
• Written informed consent provided by mother.
• Age is equal to or less than five days.

Infant Exclusion Criteria:

• Any clinically significant congenital anomaly/birth defect.
• Documented or suspected serious medical illness, infection, clinically significant finding from physical examination or immediate life-threatening condition, including requirement for ongoing supplemental oxygen, as judged by the examining clinician.
• Receipt of or anticipated need for blood products, immunoglobulin, or immunosuppressive therapy. This includes infants who require Hepatitis B Immunoglobulin (HBIG) but does not require exclusion of infants who receive Hepatitis B vaccine in the newborn period.
• Receipt of any other investigational product.

Mother Inclusion Criteria:

• Mother's age is at least 18 years, and willing and able to provide written informed consent for her and her infant's participation in this study.
• Mother is in the second or third trimester of singleton pregnancy, as determined by a clinical exam, or sonography and reported menstrual history.
• Mother agrees to donate umbilical cord blood.
• Mother has a planned Caesarian Section at Chris Hani Baragwanath Academic Hospital, Soweto and plans to remain in the area after delivery.
• Mother is determined by the site investigator to be in good overall health at the time of delivery based on medical history, and physical exam.
• Mother has a documented CD4 count > 350 cells/microliter during her pregnancy.
• Mother has a documented SARS-CoV-2 negative PCR test within 2 days before delivery to 5 days after delivery
• Mother has access to the participating HVTN CRS and willingness to be followed for the planned duration of the study.
• Assessment of understanding: Mother demonstrates understanding of this study; completes a questionnaire prior to delivery with verbal demonstration of understanding of all questionnaire items answered incorrectly.
• Mother agrees not to enroll either herself or her infant in another research study for the duration of the trial without prior approval of the HVTN 135 PSRT.
• Mother has confirmed HIV-1 infection documented by medical records at any time during or prior to screening, and confirmed by the HVTN CRS by serology.
• Mother has been on cART for at least sixteen weeks prior to delivery and intends to continue with cART for the duration of breastfeeding.\
• Mother has a viral load of less than 400 copies/mL between two weeks before and 5 days after delivery.

Mother Exclusion Criteria:

• Any WHO Grade IV illness within one year prior to study enrollment as determined by the history and physical examination and review of the medical record (if available). These include HIV wasting syndrome, PJP Pneumonia, Cerebral Toxoplasmosis, extrapulmonary Cryptococcosis, Progressive Multifocal Leukoencephalopathy, any disseminated endemic mycosis (histoplasmosis), candidiasis of the esophagus, trachea, bronchi or lung, disseminated atypical mycobacteria, non-typhoid Salmonella septicemia, extrapulmonary tuberculosis, lymphoma, Kaposi's sarcoma.
• Prior participation in any HIV-1 vaccine or anti-HIV antibody-mediated prevention trial.
• Receipt of any investigational agent during this pregnancy.
• Receipt of blood products, immunoglobulin, or immunomodulating therapy within 45 days prior to delivery of the placenta.
• Any medical, psychiatric, occupational, or other condition that, in the judgment of the investigator, would interfere with, or serve as a contraindication to, protocol adherence, assessment of safety or reactogenicity, or a volunteer's ability to give informed consent.
• Any condition that places the newborn at higher risk of early-onset sepsis, such as concern for active maternal infection at delivery as determined by local site investigators (eg, fever).
• Detectable Hepatitis B surface antigen.

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Sequential Assignment

Masking: Quadruple Blind

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38 participants in 8 patient groups, including a placebo group

Part A, Group 1: CH505TF gp120 + GLA-SE

Experimental group

Description:

Participants will receive 20 mcg Stable CH505TF gp120 admixed with 2.5 mcg GLA-SE, to be administered as a 0.25 mL intramuscular (IM) injection into either thigh at Weeks 0, 8, 16, 32, and 54.

Treatment:

Biological: CH505TF gp120

Biological: GLA-SE adjuvant

Part A, Group 2: Placebo

Placebo Comparator group

Description:

Participants will receive Placebo to be administered as a 0.25 mL IM injection, into either thigh at Weeks 0, 8, 16, 32, and 54.

Treatment:

Biological: Placebo

Part B, Group 3: CH505TF gp120 + GLA-SE

Experimental group

Description:

Participants will receive 20 mcg Stable CH505TF gp120 admixed with 5 mcg GLA-SE, to be administered as a 0.5 mL IM injection into either thigh at Weeks 0, 8, 16, 32, and 54.

Treatment:

Biological: CH505TF gp120

Biological: GLA-SE adjuvant

Part B, Group 4: Placebo

Placebo Comparator group

Description:

Participants will receive Placebo to be administered as a 0.5 mL IM injection, into either thigh at Weeks 0, 8, 16, 32, and 54.

Treatment:

Biological: Placebo

Part C, Group 5: CH505TF gp120 + GLA-SE

Experimental group

Description:

Participants will receive 20 mcg Stable CH505TF gp120 admixed with 5 mcg GLA-SE, to be administered as a 0.5 mL IM injection into either thigh at Weeks 0, 8, 16, 32, and 54.

Treatment:

Biological: CH505TF gp120

Biological: GLA-SE adjuvant

Part C, Group 6: Placebo

Placebo Comparator group

Description:

Participants will receive Placebo to be administered as a 0.5 mL IM injection, into either thigh at Weeks 0, 8, 16, 32, and 54.

Treatment:

Biological: Placebo

Part C, Group 7: CH505TF gp120 + GLA-SE

Experimental group

Description:

Participants will receive 5 mcg Stable CH505TF gp120 admixed with 5 mcg GLA-SE, to be administered as a 0.5 mL IM injection into either thigh at Weeks 0, 8, 16, 32, and 54.

Treatment:

Biological: CH505TF gp120

Biological: GLA-SE adjuvant

Part C, Group 8: Placebo

Placebo Comparator group

Description:

Participants will receive Placebo to be administered as a 0.5 mL IM injection, into either thigh at Weeks 0, 8, 16, 32, and 54.

Treatment:

Biological: Placebo