drugset / Trial / NCT05477095

A Phase 1 Study to Evaluate the Safety, Tolerability, and Immunogenicity of UB-313 in Healthy Participants

NCT05477095 ↗

Phase 1 Completed 40 enrolled Vaxxinity, Inc.
RandomizedParallel-groupQuadruple-blindPrevention

Summary

This first in-human (FIH) study of UB-313, an anti-calcitonin gene-related peptide based immunotherapeutic candidate, is designed to assess the safety, tolerability, and immunogenicity of 4 selected UB-313 dose regimens in healthy adults.

Timeline

Start
2022-07-06
Primary completion
2023-10-06
Completion
2023-10-06

Drugs

EvaluationDrugModalityDoseRoute
Subject UB-313 Peptide 100 ug Intramuscular
Subject UB-313 Peptide 300 ug Intramuscular

Indications