Status:
COMPLETED
Study to Evaluate the Safety and Immunogenicity of an HIV-1 Vaccine Regimen of Adjuvanted UVAX-1107 Followed by Adjuvanted UVAX-1107 or Adjuvanted UVAX-1197 in Healthy Subjects Aged 25-55 Years.
Lead Sponsor:
Uvax Bio LLC
Conditions:
AIDS/HIV - RelatedDisease Associated With AIDS
Vaccine-Preventable Diseases
Eligibility:
All Genders
25-55 years
Phase:
EARLY_PHASE1
Brief Summary
This is a first in human testing of novel HIV-1 protein nanoparticles vaccine candidates, UVAX-1107 and UVAX-1197 mixed with Aluminum Hydroxide (AH) and CpG 1018 adjuvants. After meeting all eligibili...
Detailed Description
This is a first in human testing of a novel HIV-1 vaccine candidate. Both UVAX-1197 and UVAX-1107 are protein nanoparticle vaccines displaying an uncleaved, prefusion-optimized (UFO) envelope (Env) gl...
Eligibility Criteria
Inclusion
- Male or female, 25-55 years of age, inclusive, at screening.
- Stable health status, as established by physical examination and medical history.
- Capable of providing written informed consent.
- Female participants of reproductive potential must be non-pregnant and non lactating, and if of child-bearing potential must agree to be heterosexually inactive from at least 21 days prior to enrolment (Day 1)and through 90 days following last study vaccination or agrees to consistently use highly effective method of birth control and refrain from donating oocytes from at least 21 days prior to enrolment and through 90 days following last study vaccination.
- Male participants must:
- Agree not to donate sperm from the time of signing consent until at least 90 days after the last dose of study drug.
- If engaging in sexual intercourse with a female partner who could become pregnant, must agree to use adequate contraception until at least 90 days after the last dose of study drug.
- If engaging in sexual intercourse with a female partner who is not of childbearing potential or a same-sex partner, must agree to use a condom.
Exclusion
- Chronic illness being treated actively and with evidence of recent adjustments in medications for worsening or fluctuating symptoms in the past 3 months, or hospitalizations / procedural interventions in the past 6 months.
- Body mass index (BMI) of less than 17 and greater than 32 kg/m2 at screening.
- Vital signs grading greater than 1 at screening
- Toxicity grading greater than 1 for screening laboratory test results.
- Any abnormal, clinically significant ECG result at screening.
- High risk of contracting HIV.
- History of cancer (malignancy) in the last 10 years.
- Use of narcotic/illicit drugs or a history of drug/alcohol abuse within the past 2 years.
- Has donated blood or suffered from blood loss of more than 450 mL (1 unit of blood) within 60 days prior to screening, or donated plasma within 14 days prior to screening.
- Receipt of immunoglobulin, blood-derived products, high dose systemic corticosteroids, or other immunosuppressant drugs within 90 days prior to Day 1 or who expect to receive immunoglobulin or another blood product during the study.
- Receipt of a licensed or emergency/provisional approval vaccine within the last 30 days prior to Day 1.
- Known hypersensitivity to any component of the study vaccines, including history of anaphylaxis or other significant allergy in the opinion of the Investigator.
- Any autoimmune or immunodeficiency disease/condition (inherited or iatrogenic) or chronic hematologic disorder (anemia, sickle cell, thalassemia).
- Evidence of HIV, positive hepatitis B surface antigen or core antibody or hepatitis C antibodies by screening test.
- Any chronic or degenerative neurological disease or history of significant neurological disorder.
- Evidence of cardiovascular, pulmonary, renal, hepatobiliary disease or any other baseline condition (history and medication review) that has required active treatment or intervention.
- Evidence of major depression disorder not well controlled in the past 2 years or history of suicidal ideation or attempt in the past 2 years.
Key Trial Info
Start Date :
January 30 2024
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
March 21 2025
Estimated Enrollment :
34 Patients enrolled
Trial Details
Trial ID
NCT06541093
Start Date
January 30 2024
End Date
March 21 2025
Last Update
May 23 2025
Active Locations (1)
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1
Nucleus Network Melbourne
Melbourne, Victoria, Australia, 3004