A Clinical Phase 3 Study of VLA1553 in Adult Participants With Human Immunodeficiency Virus (HIV)

Overview

This is a phase 3 clinical study to evaluate the safety, tolerability, and immunogenicity of VLA1553 in moderately immunocompromised adults with HIV infection.

Description

This is a multicenter, prospective, open-label, uncontrolled, single arm, phase 3 clinical study evaluating the final dose of VLA1553. The safety, tolerability, and immunogenicity of VLA1553 will be assessed in moderately immunocompromised adult participants infected with HIV living in CHIKV endemic areas. Approximately 75 male and female adults (aged 18 years or above) infected with HIV will be enrolled. Participants will be screened by ELISA for evidence of previous CHIKV exposure excluding CHIKV seropositive participants from study participation.

Eligibility

Inclusion Criteria:

Participants who meet ALL of the following criteria are eligible for this study:

1. Adult participant aged 18 years or above infected with HIV of either gender
2. Participant has an understanding of the study and its procedures, agrees to its provisions, and voluntarily gives written informed consent prior to any study-related procedures
3. Stage of disease A1, A2, B1 or B2 according to the revised CDC classification system for HIV infection from 1993 or Stages 1 or 2 in the absence of AIDS defining conditions (CDC update from 1994)
4. Participants are recruited in Cohorts:
   1. For Cohort I:

      Participant has CD4+ T cell counts >350-≤400 cells/μL, is receiving antiretroviral therapy (ART) for at least 6 months and plasma HIV RNA < 400 copies/ mL prior enrollment

   2. For Cohort II:

             Participant has CD4+ T cell counts >200 cells/μL (no upper limit), is receiving ART
             for at least 3 months and plasma HIV RNA < 50 copies/ mL prior enrollment
          5. Participant is seronegative for previous CHIKV exposure (i.e. IgM- and IgG-) as
             screened by CHIKV-specific ELISA
          6. If female participant is of childbearing potential:
               1. Participant has a negative urine pregnancy test at screening (Visit 0) or Day 1
                  (Visit 1), respectively
               2. Participant has practiced an adequate method of contraception during the 30 days
                  before screening (Visit 0)
               3. Participant agrees to employ adequate birth control measures for the first three
                  months post-vaccination (i.e. until Day 85, Visit 6).
          7. Female/male participant agrees to employ adequate birth control measures for the first
             three months post-vaccination (i.e., until Day 85, Visit 7)
        Exclusion Criteria:
        Participants who meet ANY of the following criteria are NOT eligible for this study:
          1. Participant is taking medication or other treatment for unresolved symptoms attributed
             to a previous CHIKV infection; or has participated in a clinical study involving an
             investigational CHIKV vaccine
          2. Participant has an acute or recent infection (and who is not symptom-free in the week
             prior to the Screening Visit (Visit 0) and Visit 1)
          3. Participant tests positive for human immunodeficiency virus (HIV) and fulfills AIDS
             indicator T cell counts or AIDS indicator conditions (disease stages C1, C2 or C3 or
             stage
          4. Participant tests positive for HIV with the actual target disease stages A1, A2, B1 or
             B2 (or stage 1 or 2), but was classified in the past at least once as fulfilling AIDS
             indicator conditions (disease stage C1, C2 or C3) or AIDS indicator T cell counts
             (CD4+ lymphocyte count <200/μL or CD4+ percentage <14%)
          5. Participant tests PCR positive for active hepatitis B or hepatitis C virus (HCV)
          6. Participant has received any vaccine within 28 days prior to vaccination in this study
             or plans to receive any vaccine within 28 days after vaccination
          7. Participant has abnormal findings in any required study investigations (e.g. medical
             history, physical examination, and laboratory findings) considered clinically relevant
             by the Investigator and which pose a risk for participation in the study based on
             his/her judgement
          8. Participant currently has or had a history of significant cardiovascular, respiratory,
             metabolic, neurological, hepatic, rheumatic, autoimmune, hematological,
             gastrointestinal or renal disorder (of note: Mild asthma that requires low dose
             corticosteroid inhalation only, during limited time periods of the year is not an
             exclusion criterion)
          9. Participant has an abnormal, clinically significant 12-lead ECG at screening
         10. Participant has a history of immune-mediated or clinically relevant
             arthritis/arthralgia
         11. Participant has a history of malignancy
         12. Participant has a known or suspected defect of the immune system that can be expected
             to influence the immune response to the vaccine other than asymptomatic or moderately
             symptomatic HIV infection, such as participants with congenital immunodeficiency,
             status post organ transplantation or immuno-suppressive therapy within four weeks
             prior to Visit 1. Immuno-suppressive therapy is defined as administration of chronic
             (longer than 14 days) prednisone or equivalent ≥0.05 mg/kg/day within 4 weeks prior to
             study entry, radiation therapy or immunosuppressive cytotoxic drugs/ monoclonal
             antibodies in the previous three years; topical and inhaled steroids are allowed
         13. Participant has a history of any vaccine related contraindicating event (e.g.,
             anaphylaxis, allergy to components of the candidate vaccine, other known
             contraindications including febrile convulsions)
         14. Participant presents with clinical conditions representing a contraindication to
             intramuscular vaccination and blood draws
         15. Participant is pregnant (positive urine pregnancy test at screening or Visit 1,
             respectively), is lactating at the time of enrollment, has plans to become pregnant or
             subject's female partner plans to become pregnant during the first three months
             post-vaccination or practices unreliable contraception
         16. Participant received blood-derived products (e.g. plasma) within 90 days prior to
             vaccination in this study
         17. Participant has a rash, dermatological condition or tattoos that would, in the opinion
             of the Investigator, interfere with injection site reaction rating
         18. Participant has participated in another clinical study involving an investigational
             medicinal product (IMP) or device within 30 days prior to vaccination or is scheduled
             to participate in another clinical study involving an IMP, or device during the course
             of this study
         19. Participant is a member of the team conducting the study or in a dependent
             relationship with one of the study team members. Dependent relationships include close
             relatives (i.e., children, partner/spouse, siblings, parents) as well as employees of
             the Investigator or site personnel conducting the study.