Doravirine Dose Optimisation in Pregnancy

Recruiting Phase 4 Interventional Study
HIV
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 and older
Sex
Female
Trial phase
Phase 4
Study type
Interventional
Purpose
Treatment
Participants needed
76 (estimated)
Sponsor
University of Liverpool · Other
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About This Trial

A randomised, open label, controlled PK standard of care vs doravirine plus 2 nucleoside reverse transcriptase inhibitors backbone in pregnant women initiating combination antiretroviral therapy in the second trimester of pregnancy.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Women ≥ 18 years old * Ability to give informed consent prior to participation * Willing and able to comply with all study requirements * HIV positive * Pregnant (initiating cART ≥ 12 weeks and \< 26 weeks gestation) * Intention to breastfeed postpartum Exclusion Criteria: *…
Contacts

Helen Reynolds

+ 44 151 794 5553

dorado@liverpool.ac.uk

CONTACT