Adults living with untreated HIV-1 were randomized (1:1) to a DOR-containing regimen or comparator (darunavir/ritonavir- or efavirenz-containing), each with 2 nucleos(t)ide reverse transcriptase inhibitors, for 96 weeks (double-blind base), followed by 96 weeks of a DOR-containing regimen (open-label extension). Clinical Trials Registration. ClinicalTrials.gov NCT02275780, NCT02403674.
P=N/A, N=250, Recruiting, Pomeranian Medical University Szczecin | Not yet recruiting --> Recruiting | Trial completion date: Feb 2026 --> Mar 2027 | Initiation date: Feb 2026 --> May 2026 | Trial primary completion date: Feb 2026 --> Feb 2027
7 days ago
Enrollment open • Trial completion date • Trial initiation date • Trial primary completion date • Real-world evidence
These results suggest that concomitant use of quizartinib and moderate CYP3A inducers should be avoided. Concomitant use of weak CYP3A inducers does not warrant dose adjustment, since the impact on quizartinib exposure is clinically nonrelevant.