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NCT04664894

Direct Acting Anti-Viral's In Chronic HCV Patients

Completed Last updated 11 December 2020
What this trial tests

trial testing Sofosbuvir in Safety Issues in 511 participants. Completed in 30 May 2019.

Timeline
15 May 2018
Primary endpoint
30 May 2019
30 May 2019

Quick facts

Lead sponsorGetz Pharma
StatusCompleted
Study typeOBSERVATIONAL
Enrollment511
Start date15 May 2018
Primary completion30 May 2019
Estimated completion30 May 2019
Sites1 location across Pakistan

Drugs / interventions tested

Conditions studied

Sponsor

Getz Pharma — full company profile →

Who can join

18 and older, any sex, with Safety Issues. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The objective of the study is to determine the safety of DAA's among chronic HCV patients. The outcomes of the study are; To determine the frequency of adverse events while receiving DAAs with or without RBV and/or Pegylated Interferon To calculate the percentage of patients with severity of medical event as per Karch and Lasagna classification To determine the percentage of patient having serious adverse event as per ICH Classification

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of Sofosbuvir

Trials testing the same drug.

Other recruiting trials for Safety Issues

Currently open trials in the same condition.

Other Getz Pharma 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/NCT04664894.

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