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Two-drug antiretroviral therapy with doravirine/dolutegravir - a prospective cohort study

Two-drug antiretroviral therapy with doravirine/dolutegravir - a prospective cohort study - DoDo

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00030471
Enrollment
200
Registered
2022-12-13
Start date
2021-02-24
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

B24

Interventions

Group 1: People living with HIV infection whose therapy was switched to a combination of doravirine/dolutegravir only (DoDo). Documentation of the treatment course from approx. 1 year before switching

Sponsors

Med. Klinik und Poliklinik IV, Sektion Klinische Infektiologie, LMU Klinikum Innenstadt, Ludwig-Maximilians-Universität München
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: • Persons being cared for in clinics and private practices in German-speaking areas • Age >18 years • documented HIV-1-infection • documented previous treatment with antiretroviral therapy (ART) • switch of ART to exclusively DOR/DTG • written informed consent after discussion of patient information

Exclusion criteria

Exclusion criteria: • Inability to consent • switch of ART to DOR/DTG in a clinic/practice not participating in the study • antiretroviral therapy including other substances except DOR/DTG

Design outcomes

Primary

MeasureTime frame
1) Description of the clinical situation resulting in the prescriptrion of DOR/DTG as a 2-DR. 2) Documentation of the clinicaL and virological efficacy of the 2-DR DOR/DTG

Secondary

MeasureTime frame
1) Frequency and causes for off-label prescription of the 2-DR DOR/DTG. 2) Durability of the 2-DR DOR/DTG: *Time to switch to another combination *Reason for switching to another combination

Countries

Austria, Germany

Contacts

Public ContactUlrich Seybold

Med. Klinik und Poliklinik IV, Sektion Klinische Infektiologie, LMU Klinikum Innenstadt, Ludwig-Maximilians-Universität München

useybold@med.lmu.de+49-89-4400-53550

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026