EICHORCondition: Human Immunodeficiency Virus · Human Immunodeficiency Virus I Infection · Sponsor: Immuno Cure Holding (HK) Limited
The goal of this randomized clinical trial is to evaluate the safety and immunogenicity of the HIV Therapeutic DNA Vaccine (ICVAX) in participants with HIV-1 infection under antiretroviral therapy (ART). The study compares three delivery methods - Teresa -EPT I, PharmaJet Tropis, and PapiVax TriGrid EP - to induce antigen-specific T cell responses in the participants. The primary objectives are to evaluate the safety of ICVAX delivered using three different devices in the participants within the period Day 0-Day 336, and to evaluate the antigen-specific T cell responses induced by ICVAX in the participants within the period Day 0-Day 168. The participants will receive four injections of ICVAX administered at 4-week intervals. Following the final dose, participants will be monitored for 36 weeks.
This description comes directly from the study's public registry record.
Grace Chung Yan Lui, Dr. · (852) 5569 9539 · gracelui@cuhk.edu.hk
Always discuss trial participation with your own doctor first.
| The Chinese University of Hong Kong Phase 1 Clinical Trial Centre at Prince of Wales Hospital | Shatin, New Territories, Hong Kong | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07530198