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Study of GS-5718 in Participants With Cutaneous Lupus Erythematosus (CLE) - Trial NCT04809623

Access comprehensive clinical trial information for NCT04809623 through Pure Global AI's free database. This Phase 1 trial is sponsored by Gilead Sciences and is currently Suspended. The study focuses on Cutaneous Lupus Erythematosus. Target enrollment is 12 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.

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NCT04809623
Phase 1
Suspended
drug
Trial Details
ClinicalTrials.gov โ€ข NCT04809623
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Study of GS-5718 in Participants With Cutaneous Lupus Erythematosus (CLE)
A Randomized, Blinded, Placebo-Controlled, Phase 1b Study of GS-5718 in Subjects With Cutaneous Lupus Erythematosus (CLE)

Study Focus

GS-5718

Interventional

drug

Sponsor & Location

Gilead Sciences

Beverly Hills,Clearwater,Indianapolis,Charlotte,Dallas, United States of America

Timeline & Enrollment

Phase 1

Sep 01, 2021

Jan 01, 2023

12 participants

Primary Outcome

Percentage of Participants Experiencing Adverse Events,Percentage of Participants Experiencing Laboratory Abnormalities

Summary

The primary objective of this study is to evaluate the safety and tolerability of GS-5718 in
 participants with Cutaneous Lupus Erythematosus (CLE) with or without Systemic Lupus
 Erythematosus (SLE).

ICD-10 Classifications

Subacute cutaneous lupus erythematosus
Lupus erythematosus
Discoid lupus erythematosus
Systemic lupus erythematosus
Systemic lupus erythematosus, unspecified

Data Source

ClinicalTrials.gov

NCT04809623

Non-Device Trial