Last updated 16 days ago
Doravirine (DOR) in Human Immunodeficiency Virus (HIV)-Infected Children Ages 4 Weeks to <12 Years and <45 kg (MK-1439-066)
84 patients around the world
Available in Mexico, United States
Participants who complete the Week 96 visit will be eligible to enroll in an Extension
Study in which they may continue to receive DOR until it is commercially available, or
for up to an additional 224 weeks (whichever comes first).
Merck Sharp & Dohme Corp.
3Research sites
84Patients around the world
This study is for people with
Hiv
Requirements for the patient
To 11 Years
All Gender
Medical requirements
- Has HIV-1 infection confirmed at screening.Has treatment history defined as either TN or with documented viral suppression (HIV-1 RNA <50 copies/mL) for ≥3 months on combination antiretroviral therapy (cART).Body weight is >3 kg to <45 kg.If female, is not pregnant or breastfeeding, and one of the following applies.Is not a woman of childbearing potential (WOCBP).Is a WOCBP using an acceptable form of contraception, or is abstinent.If a WOCBP must have a negative pregnancy test (urine or serum) within 24 hours of the first dose of study intervention.Study Extension Inclusion Criteria:Has completed the Week 96 visit.Is considered, in the opinion of the investigator, to have derived benefit from treatment with DOR plus the 2 NRTIs selected by the investigator, or DOR/3TC/TDF, by Week 96 of the study.Is considered, in the opinion of the investigator, to be a clinically appropriate candidate for additional treatment with DOR plus 2 NRTIs selected by the investigator.Understands the procedures in the study extension and has provided (or have the participant's legally acceptable representative, if applicable, provide) documented informed consent/assent to enter the study extension and continue treatment with DOR plus 2 NRTIs selected by the investigator until DOR is available commercially in countries participating in the study or for up to an additional 224 weeks (whichever comes first).
- Has evidence of renal disease.Demonstrates evidence of liver disease.Has clinical or laboratory evidence of pancreatitis.Has any history of malignancy.Has presence of any active acquired immunodeficiency syndrome (AIDS)-defining Opportunistic Infection.Has an active diagnosis of hepatitis, including hepatitis B co-infection.Has current active tuberculosis and/or is being treated with a rifampicin-containing regimen.Has a medical condition that precludes absorption or intake of oral pellets/granules.Has a history or current evidence of any condition, therapy, laboratory abnormality, or other circumstance that might confound results of the study or interfere with participating for the entire duration of the study.Is taking or is anticipated to require systemic immunosuppressive therapy, immune modulators, or other prohibited therapy.Is currently participating in or has participated in an interventional clinical study with an investigational compound or device from 45 days prior to Day 1 through the treatment period.Has a documented or known virologic resistance to DOR.Has any history of viremia (HIV RNA >1000 copies/mL) after at least 3 months on a non-nucleoside reverse transcriptase inhibitor (NNRTI)-based regimen.
Sites
Hospital Infantil de México Federico Gómez
Recruiting
Unidad de Atención Médica e Investigación en Salud - UNAMIS
Recruiting
Instituto Nacional de Pediatría - México
Recruiting
SponsorMerck Sharp & Dohme Corp.
Study typeInterventional
Conditions
Hiv
Requirements
To 11 YearsAll Gender
Unique study IDclinicaltrials.gov
NCT04375800
