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An open-label, single-sequence study to investigate the effects of gastric acid suppression by Rabeprazole on the pharmacokinetics of BMS-986165 in healthy participants

Completed
Conditions
Psoriasis
systemic lupus erythematosus and Crohn's disease.
10003816
Registration Number
NL-OMON47975
Lead Sponsor
BritsolMyers Squibb Research and Development
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
20
Inclusion Criteria

- Healthy male and female subjects
- Age of 18 to 50 years (inclusive)
- BMI of 18.0 to 32.0 kg/m2 (inclusive)

Exclusion Criteria

Suffering from hepatitis B, hepatitis C, cancer or HIV/AIDS. Donation of blood
to a blood bank or in a clinical study (except a screening visit) within 4
weeks of study drug administration (within 2 weeks for plasma only). Blood
transfusion within 4 weeks of study drug administration.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>PK parameters in healthy participants administered BMS-986165 alone (reference)<br /><br>versus in combination with rabeprazole (test):<br /><br>- BMS-986165: Cmax, AUC(0-T), AUC(INF)</p><br>
Secondary Outcome Measures
NameTimeMethod
<p>PK of BMS-986165 administered alone (reference) versus in combination with<br /><br>rabeprazole (test)<br /><br>- BMS-986165: Tmax, T-Half<br /><br>- Total active circulating species: Cmax, AUC(0-T), AUC(INF)</p><br>
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