Safety of and Immune Response to an HIV-1 Vaccine (ALVAC-HIV vCP1521) in Infants Born to HIV Infected Mothers

HIV Infections Clinical Trial

Official title:

A Phase I Study to Evaluate the Safety and Immunogenicity of ALVAC-HIV vCP1521 in Infants Born to HIV-1 Infected Women in Uganda

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00098163
• Other study ID #: HPTN 027
• Secondary ID: 10141
• Status: Completed
• Phase: Phase 1
• Est. completion date: May 2009

Study information

• Verified date: October 2021
• Source: National Institute of Allergy and Infectious Diseases (NIAID)
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to test the safety of and immune response to an HIV-1 vaccine, ALVAC-HIV vCP1521, given to infants born to HIV-1 infected mothers in Uganda.

Description:

Mother-to-child transmission (MTCT) of HIV can be caused either by perinatal transmission of HIV or by breastfeeding, a common practice in poorer regions of the world. HIV preventive vaccines are currently under investigation as potential solutions to worldwide MTCT of HIV. This study will evaluate the safety and immunogenicity of an HIV-1 vaccine, ALVAC-HIV vCP1521, in infants born to HIV-1 infected mothers in Uganda. The vaccine is a preparation of a live attenuated recombinant canarypox virus, encoding HIV clades B and E envelope proteins. This study will be conducted at Mulago Hospital in Uganda.

Mothers will enroll in this study during their third trimesters of pregnancy. During screening, mothers will undergo medical history assessment, a physical exam, and blood collection. After delivery and prior to infant enrollment, mothers will have another physical exam; mothers and their infants will be accompanied home by a home visitor who will document contact information.

Infants will be followed for 24 months after birth. Infants will be randomly assigned to receive 4 injections of vaccine or placebo. Study injections will be given at the start of the study and at Weeks 4, 8, and 12. Infants will be observed for 1 hour after each vaccine administration to check for body temperature and local and systemic reactions. They will also be evaluated in the clinic the day after each immunization for any local or systemic reactions. Infants will be visited at home 2 days after vaccine administration by a trained study nurse who will assess reactogenicity. Blood will be collected at 9 selected times: study entry, Weeks 2, 6, 10, and 14, and Months 6, 12, 18, and 24. Sixteen study visits occurring over 2 years will include medical history assessment and physical exams. Childhood immunizations will be given to infants at study entry and at Weeks 6, 10, and 14 and Months 6 and 12.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 60
• Est. completion date: May 2009
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria for HIV Infected Women:

• HIV infected

• In third trimester of pregnancy

• CD4 count of more than 500 cells/mm3 at screening

• Intends to give birth at Mulago Hospital, Uganda

• Willing to be taken home by a home visitor after delivery to document locator information and willing to be visited at home later

Inclusion Criteria for Infants Born to HIV Infected Women:

• 3 or fewer days of age

• Born to an HIV infected woman eligible for the study

• Weight at birth at least 2000 g (4.4 lbs)

Exclusion Criteria for HIV Infected Women:

• Prior participation in an HIV-1 vaccine trial

• Investigational agents, blood products, immunoglobulin, or immunotherapy any time during this pregnancy

• Documented or suspected serious medical illness or life-threatening condition that may interfere with the study

• Multiple birth predicted in current pregnancy

Exclusion Criteria for Infants Born to HIV Infected Women:

• Mother left study prior to infant enrollment and randomization

• Mother or infant received any active or passive HIV immunotherapy or investigational product other than the study vaccine. Mothers and infants who have taken nevirapine prior to study entry are not excluded.

• Blood products, immunoglobulin, or immunosuppressive therapy during labor and delivery or prior to study enrollment

• Abnormal vital signs prior to vaccination or clinical symptoms that may interfere with vaccine reaction assessment

• Part of a multiple birth

Related Conditions & MeSH terms

• HIV Infections

Intervention

Biological:
• ALVAC-HIV vCP1521
One 1-ml dose of HIV-1 vaccine administered after birth on or before Day 3 and at weeks 4, 8, and 12.
• ALVAC HIV-1 vCP1521
One 1-ml dose of HIV-1 vaccine placebo administered after birth on or before Day 3 and at Weeks 4, 8, and 12.

Locations

Country	Name	City	State
Uganda	Makerere University- JHU Research Collaboration {MUJHU CARE LTD} CRS	Kampala

Sponsors (4)

Lead Sponsor	Collaborator
National Institute of Allergy and Infectious Diseases (NIAID)	Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), National Institute of Mental Health (NIMH), National Institute on Drug Abuse (NIDA)

Country where clinical trial is conducted

Uganda, 

References & Publications (4)

Cao H, Mani I, Vincent R, Mugerwa R, Mugyenyi P, Kanki P, Ellner J, Walker BD. Cellular immunity to human immunodeficiency virus type 1 (HIV-1) clades: relevance to HIV-1 vaccine trials in Uganda. J Infect Dis. 2000 Nov;182(5):1350-6. Epub 2000 Oct 9. — View Citation

de Bruyn G, Rossini AJ, Chiu YL, Holman D, Elizaga ML, Frey SE, Burke D, Evans TG, Corey L, Keefer MC. Safety profile of recombinant canarypox HIV vaccines. Vaccine. 2004 Jan 26;22(5-6):704-13. — View Citation

Franchini G, Gurunathan S, Baglyos L, Plotkin S, Tartaglia J. Poxvirus-based vaccine candidates for HIV: two decades of experience with special emphasis on canarypox vectors. Expert Rev Vaccines. 2004 Aug;3(4 Suppl):S75-88. Review. — View Citation

Safrit JT, Ruprecht R, Ferrantelli F, Xu W, Kitabwalla M, Van Rompay K, Marthas M, Haigwood N, Mascola JR, Luzuriaga K, Jones SA, Mathieson BJ, Newell ML; Ghent IAS Working Group on HIV in Women Children. Immunoprophylaxis to prevent mother-to-child transmission of HIV-1. J Acquir Immune Defic Syndr. 2004 Feb 1;35(2):169-77. Review. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Grade 3 or higher adverse events attributable to the vaccine. Mild and moderate adverse event rates will also be tabulated		At Day 0 and throughout study
Primary	Cell-mediated immunologic response as measured by HIV-specific cytotoxic T-lymphocyte activity against viral antigens		At Day 0 and throughout study
Primary	Humoral immunologic response as measured by detection of binding antibody to vaccine antigens and by neutralizing antibody assay		At Day 0 and throughout study
Secondary	Immune status as measured by CD4 cell counts in all immunized infants		Over the 24-month follow-up period
Secondary	Development of immunity to routine vaccination as measured by antibody levels and Bacillus Calmette-Guéerin (BCG) scar formation		At the end of study

External Links

•   Click here for more information on HIV and pregnancy
•   Click here for more information on preventive HIV vaccines
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