A Study to Evaluate Solriktug in Adult Participants With Asthma
NCT06496607 · Status: ACTIVE_NOT_RECRUITING · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 145
Last updated 2026-05-01
Summary
Phase 2 study to evaluate the safety, tolerability, PK, immunogenicity, and pharmacodynamics of solriktug with adult participants with asthma.
Conditions
Interventions
- BIOLOGICAL
-
NSI-8226
Solrikitug
- BIOLOGICAL
-
NSI-8226
Solrikitug
- BIOLOGICAL
-
NSI-8226
Solrikitug
- BIOLOGICAL
-
Placebo
Sponsors & Collaborators
-
DevPro Biopharma
collaborator INDUSTRY -
Uniquity One (UNI)
lead INDUSTRY
Principal Investigators
-
Andrew W Lee, MD · Vice President, Clinical Research
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- QUADRUPLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 75 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2024-07-26
- Primary Completion
- 2026-06-30
- Completion
- 2026-09-30
- FDA Drug
- Yes
Countries
- United States
Study Locations
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