Phase 1/2 Study of UI-102 in Selected Advanced Cancers
NCT07605962 · Status: NOT_YET_RECRUITING · Phase: PHASE1/PHASE2 · Type: INTERVENTIONAL · Enrollment: 140
Last updated 2026-05-26
Summary
This phase 1/2 first-in-human study is designed to assess the safety and efficacy of UI-102, a TLR7/8 agonist encapsulated in a Cholesteryl Pullulan Nanoparticle.
Conditions
Interventions
- DRUG
-
UI-102
Specified dose on specified days
Sponsors & Collaborators
-
United Immunity, co., Ltd.
lead INDUSTRY
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2026-05-25
- Primary Completion
- 2030-03-31
- Completion
- 2031-03-31
- FDA Drug
- Yes
Countries
- United States
Study Locations
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