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NCT04194021: NewHorizon

Characteristics and Outcomes of Patients Who Received Etravirine and/or Darunavir

Status unknown Last updated 18 April 2023
What this trial tests

trial in HIV/AIDS in 871 participants. Status unknown.

Timeline
1 January 2019
Primary endpoint
31 December 2022
31 December 2023

Quick facts

Lead sponsorElizabeth Glaser Pediatric AIDS Foundation
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment871
Start date1 January 2019
Primary completion31 December 2022
Estimated completion31 December 2023
Sites5 locations across Cameroon, Lesotho, Kenya, Eswatini, Uganda

Conditions studied

Sponsor

Elizabeth Glaser Pediatric AIDS Foundation

Who can join

Under 25, any sex, with HIV/AIDS. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The objectives of this data collection activity are to: 1. Describe the baseline demographics, clinical and laboratory profile of patients who ever received darunavir (DRV) and/or etravirine (ETR), at the time of initiation on DRV and/or ETR; 2. Describe the clinical and laboratory profile of patients who ever received DRV and/or ETR every 6 months from the first data collection point through 2021; 3. Describe dynamics in HIV drug resistance mutations among patients who fail treatment on new regimens including DRV and/or ETR; 4. Describe demographics, clinical and laboratory profile of young adults who transition out of the donation program after the age of 25 years at 12 months after their transition.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for HIV/AIDS

Currently open trials in the same condition.

Other Elizabeth Glaser Pediatric AIDS Foundation trials

Trials by the same sponsor.

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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/NCT04194021.

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