NCT06402136

Evaluation Safety, Tolerability, and Pharmacokinetics of Single and Multiple Ascending Doses of 83-0060 in Healthy Volunteers

A Randomised, Double-Blind, Placebo-Controlled, First-in-Human Study of Orally Administered 83-0060 to Evaluate the Safety, Tolerability, and Pharmacokinetics of Single and Multiple Ascending Doses of 83-0060 in Healthy Volunteers
Traws Pharma, Inc.·Phase 1·ClinicalTrials.gov·drugRecruiting
View on ClinicalTrials.gov
Study focus
Disease/Condition
Healthy Volunteers Only
Drug/Device/Intervention
83-0060
Study type
Interventional
Intervention type
drug
Sponsor & location
Primary sponsor
Traws Pharma, Inc.
Location
Sydney, Australia
Timeline & enrollment
Phase
Phase 1
Start date
Apr 15, 2024
End date
Sep 01, 2024
Enrollment
64 participants
Primary outcome

Plasma concentration

Summary

This is a clinical study aiming to assess pharmacokinetics, pharmacodynamics and preliminary
 efficacy of 83-0060 in Healthy Volunteers

ICD-10 classifications
Healthy person accompanying sick personRoutine general health check-up of armed forcesRoutine general health check-up of sports teams
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT06402136
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT06402136 through Pure Global AI's free database. This Phase 1 trial is sponsored by Traws Pharma, Inc. and is currently Recruiting. The study focuses on Healthy Volunteers Only. Target enrollment is 64 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.