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Evaluation of the Effect of Rifampin and Rabeprazole on the Pharmacokinetics of Camlipixant

NCT05899829 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 42

Last updated 2024-12-04

Study results available
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Summary

This is a phase 1, 2-part, open-label, fixed-sequence study evaluating the effect of rifampin (part 1) and rabeprazole (part 2) on the pharmacokinetics of a single dose of camlipixant (BLU-5937) 50 mg tablet in healthy participants under fasting conditions.

Conditions

Interventions

DRUG

Camlipixant

Camlipixant will be administered

DRUG

Rabeprazole

Rabeprazole will be administered

DRUG

Rifampin

Rifampin will be administered.

Sponsors & Collaborators

  • Bellus Health Inc. - a GSK company

    lead INDUSTRY

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
55 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-06-21
Primary Completion
2023-08-08
Completion
2023-08-08
FDA Drug
Yes

Countries

  • Canada

Study Locations

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Entities

Drugs
Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05899829 on ClinicalTrials.gov