A First in Human Study to Evaluate the Safety and Immunogenicity of RBM-001 in Healthy Adult Volunteers
NCT06878170 · Status: ACTIVE_NOT_RECRUITING · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 60
Last updated 2025-08-08
Summary
A First in Human Study to Evaluate the Safety and Immunogenicity of RBM-001 in Healthy Adult Volunteers
Conditions
Interventions
- BIOLOGICAL
-
RBM-001
To evaluate the safety and tolerability of the RBM-001 vaccination in healthy adults.
Sponsors & Collaborators
-
Rock BioMedical, Inc.
lead INDUSTRY
Study Design
- Allocation
- RANDOMIZED
- Purpose
- PREVENTION
- Masking
- DOUBLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 55 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2024-09-30
- Primary Completion
- 2025-05-30
- Completion
- 2026-01-30
- FDA Drug
- Yes
Countries
- United States
Study Locations
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