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NCT03572140: RAVs

Safety of Sofosbuvir ,Daclatasvir in HCV Patients and RAVS in Resistent and Relapsed Cases

Status unknown Last updated 29 June 2018
What this trial tests

trial testing RAVS In relapsed and resistent cases in HCV in 297 participants. Status unknown.

Timeline
1 July 2018
Primary endpoint
1 July 2020
1 August 2020

Quick facts

Lead sponsorAssiut University
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment297
Start date1 July 2018
Primary completion1 July 2020
Estimated completion1 August 2020

Drugs / interventions tested

Conditions studied

Sponsor

Assiut University

Who can join

Adults 18 to 75, any sex, with HCV. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

To identify side effects of Sofosbuvir/ Daclatasvir treatment regimen of chronic HCV GT-4 infection. * To assess the occurrence and the prevalence of RAVs in patients with treatment failure and relapse after sofosbuvir and daclatasvir with assessment of their types . * To examine the GT4 subtypes by phylogenetic analysis and baseline sequence variability among subtypes and their potential impact on treatment outcome and development of viral resistance in patients who received a regimen of Sofosbuvir/ Daclatasvir for treatment of chronic HCV GT-4. * To assess the differences in patient demographics across GT4 subtypes.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for HCV

Currently open trials in the same condition.

Other Assiut University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03572140.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing