Clinical Trials Directory

Trials / Completed

CompletedNCT02029716

RTA 408 Lotion in Healthy Volunteers

A Phase 1 Study to Evaluate the Safety, Tolerability, Pharmacodynamics, and Pharmacokinetics of RTA 408 Lotion in Healthy Volunteers

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
109 (actual)
Sponsor
Biogen · Industry
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Accepted

Summary

This study is a first-in-human study of a topical dermal lotion formulation of RTA 408, a novel small molecule which suppresses oxidative stress and inflammation. In this study, the safety, local pharmacodynamics (PD), and systemic pharmacokinetics (PK) of RTA 408 will be evaluated following topical application of RTA 408 Lotion to healthy volunteers. This study will be conducted in three parts. In Part A of the study, healthy volunteers will have RTA 408 Lotion Vehicle and RTA 408 Lotion (0.5%, 1%, and 3%) applied to a small skin surface area (four individual 4-cm2 sites; 16 cm2 total area) twice daily for 14 days to assess the local skin tolerability, local PD, and systemic PK of these treatments. Part B will be conducted after completion of Part A and will assess the safety, tolerability, local PD, and systemic PK of RTA 408 Lotion applied topically twice daily for 14 days to a larger skin surface area (\~100 cm2). Part C will be conducted after completion of Part B and will assess the safety, tolerability, local PD, and systemic PK of RTA 408 Lotion applied topically twice daily for 28 days to a larger skin surface area (\~500 cm2). The maximum tolerated drug concentration in Part A will be used in Part B and Part C. Approximately 32 healthy adult volunteers will be enrolled in this study with 12 volunteers in Part A and 10 volunteers each, in Parts B and C.

Conditions

Interventions

TypeNameDescription
DRUGRTA 408 Lotion 0.5%, 1%, 3%
DRUGLotion vehicle/placebo

Timeline

Start date
2013-12-31
Primary completion
2014-04-01
Completion
2014-04-01
First posted
2014-01-08
Last updated
2025-05-28

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02029716. Inclusion in this directory is not an endorsement.