Pure Global

Study of CDI-31244 in Combination With Sofosbuvir (SOF) and Velpatasvir (VEL) - Trial NCT03501550

Access comprehensive clinical trial information for NCT03501550 through Pure Global AI's free database. This Phase 2 trial is sponsored by Cocrystal Pharma, Inc. and is currently Completed. The study focuses on Chronic Hepatitis C. 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.

Free Database
Powered by Pure Global AI
840K+ Trials
NCT03501550
Phase 2
Completed
drug
Trial Details
ClinicalTrials.gov โ€ข NCT03501550
View on ClinicalTrials.gov
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Study of CDI-31244 in Combination With Sofosbuvir (SOF) and Velpatasvir (VEL)
An Open-Label Phase 2a Study Evaluating the Safety and Efficacy of Combination Treatment With 2 Weeks of the Non-Nucleoside Inhibitor CDI 31244 Plus 6 Weeks of Sofosbuvir/Velpatasvir in Subjects With Chronic Hepatitis C Genotype 1 Infection

Study Focus

Chronic Hepatitis C

CDI-31244

Interventional

drug

Sponsor & Location

Cocrystal Pharma, Inc.

Baltimore, United States of America

Timeline & Enrollment

Phase 2

Jun 26, 2018

Jun 07, 2019

12 participants

Primary Outcome

Number of Subjects With Treatment Emergent Adverse Events,Number of Participants With Sustained Virologic Response (SVR) 12 Weeks After Treatment

Summary

Open label phase 2a study of two week treatment with CDI-31244 and sofosbuvir and veltapasvir
 followed by four week treatment of sofosbuvir and velpatasvir in individuals with chronic
 hepatitis C (HCV) genotype 1 (GT1) infection

ICD-10 Classifications

Chronic viral hepatitis C
Acute hepatitis C
Chronic viral hepatitis
Other chronic viral hepatitis
Chronic hepatitis, unspecified

Data Source

ClinicalTrials.gov

NCT03501550

Non-Device Trial