Last reviewed · How we verify

NCT04612452: DTG-SWITCH

The DTG-SWITCH Study: Longitudinal Analysis of Virologic Failure and Drug Resistance at and After Switching to Dolutegravir-based First-line ART

Completed Last updated 24 March 2023
What this trial tests

trial in Hiv in 2,820 participants. Completed in 22 March 2023.

Timeline
5 November 2019
Primary endpoint
22 March 2023
22 March 2023

Quick facts

Lead sponsorUniversity of Bern
StatusCompleted
Study typeOBSERVATIONAL
Enrollment2,820
Start date5 November 2019
Primary completion22 March 2023
Estimated completion22 March 2023
Sites2 locations across Malawi, Zambia

Conditions studied

Sponsor

University of Bern

Who can join

18 and older, any sex, with Hiv or Drug Resistancy. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a prospective observational cohort study of 2820 patients on first-line ART switching to a DTG-based first-line regimen, according to the standard of care. The study is conducted in Malawi and Zambia, in ART programs that participate in the IeDEA collaboration. Sequencing will be done on blood samples of patients with a viral load above 400 copies/mL to identify mutations.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Virologic Failure and Drug Resistance After Programmatic Switching to Dolutegravir-based First-line Antiretroviral Therapy in Malawi and Zambia.
    Skrivankova VW, Huwa J, Muula G, Chiwaya GD, et al · · 2025 · cited 12× · PMID 38847281 · DOI 10.1093/cid/ciae261

Verify or expand the search:

Other recruiting trials for Hiv

Currently open trials in the same condition.

Other University of Bern 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/NCT04612452.

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