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NCT06914869

Drug-Drug Interaction Potential of Mavorixafor

Completed Phase 1 Last updated 1 July 2025
What this trial tests

Phase 1 trial testing Mavorixafor in Healthy Participants in 38 participants. Completed in 19 May 2025.

Timeline
18 February 2025
Primary endpoint
19 May 2025
19 May 2025

Quick facts

Lead sponsorX4 Pharmaceuticals
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designcrossover
Maskingnone
Primary purposebasic science
Enrollment38
Start date18 February 2025
Primary completion19 May 2025
Estimated completion19 May 2025
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

X4 Pharmaceuticals — full company profile →

Who can join

Adults 18 to 55, any sex, with Healthy Participants. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The main purpose of this study is to evaluate drug-drug interaction (DDI) of orally administered mavorixafor with cytochrome P3A (CYP3A) inducers carbamazepine (a strong CYP3A inducer) or efavirenz (a moderate CYP3A inducer) in healthy male and female participants.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other trials of Mavorixafor

Trials testing the same drug.

Other recruiting trials for Healthy Participants

Currently open trials in the same condition.

Other X4 Pharmaceuticals trials

Trials by the same sponsor.

Verify against primary sources

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/NCT06914869.

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