Proof-of-Concept Clinical Pharmacology Trial for HIV Antigen Presentation Therapeutic Biologic Mix
NCT07182838 · Status: ACTIVE_NOT_RECRUITING · Phase: EARLY_PHASE1 · Type: INTERVENTIONAL · Enrollment: 20
Last updated 2025-10-07
Summary
Conducting an initial small, controlled clinical pharmacology trial to assess for therapeutic biologics activity (proof-of-concept) that suggests the potential for clinical benefit of HIV (+) patients
1. Treat Infection of Multiple Gene Mutation HIV Virus Strains.
2. Activate Human Antigen Presentation Reaction to HIV Specific Antigen.
3. The human antigen presenting cells (APCs) can take up and process HIV target antigen protein into small peptide fragments, and then HIV virus can be killed by APCs directly.
Conditions
- HIV Infections
Interventions
- BIOLOGICAL
-
HIV Therapeutic Biologic Mix - HIV GP160 plus BCG Vaccine Mix for percutaneous use
* By the percutaneous route with the multiple puncture device * HIV GP160 0.1 mg x 1 mL plus BCG Organism 50 MG Mix
Sponsors & Collaborators
-
UnitedHealthcare
collaborator OTHER -
Han Xu, M.D., Ph.D., FAPCR, Sponsor-Investigator, IRB Chair
lead INDUSTRY
Principal Investigators
-
HAN XU, MD/PhD/FAPCR · Medicine Invention Design Incorporation - IRB00009424
-
HAN XU, MD/PhD/FAPCR · Medicine Invention Design Incorporation - IORG0007849
-
HAN XU, MD/PhD/FAPCR · Medicine Invention Design Incorporation - NPI 1023387701
Study Design
- Allocation
- NA
- Purpose
- HEALTH_SERVICES_RESEARCH
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 24 Years
- Max Age
- 64 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2025-09-12
- Primary Completion
- 2026-08-18
- Completion
- 2026-10-28
- FDA Drug
- Yes
Countries
- United States
Study Locations
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