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A Study to Assess the Effect of Food on the Drug Levels of Admilparant

NCT ID: NCT07225647

Last Updated: 2025-11-10

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

PHASE1

Total Enrollment

56 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-11-07

Study Completion Date

2025-12-28

Brief Summary

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The purpose of this study is to assess the effect of food on the drug levels of Admilparant

Detailed Description

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Conditions

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Healthy Participants

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Part 1: Treatment A

Group Type EXPERIMENTAL

Admilparant

Intervention Type DRUG

Specified dose on specified days

Part 1: Treatment B

Group Type EXPERIMENTAL

Admilparant

Intervention Type DRUG

Specified dose on specified days

Part 2: Treatment C

Group Type EXPERIMENTAL

Admilparant

Intervention Type DRUG

Specified dose on specified days

Part 2: Treatment D

Group Type EXPERIMENTAL

Admilparant

Intervention Type DRUG

Specified dose on specified days

Interventions

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Admilparant

Specified dose on specified days

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Participants must have a body mass index (BMI) of 18.0 kg/m2 to 32.0 kg/m2, inclusive, at screening.
* Participants must have a body weight of ≥ 50 kg for males and ≥ 45 kg for females at screening.

Exclusion Criteria

* Participants must not have any significant medical condition, laboratory abnormality, or psychiatric illness that would prevent the participant from participating in the study.
* Participants must not have had any previous exposure to Admilparant.
* Participants must not have a history of any severe drug allergy or drug reaction (such as anaphylaxis or hepatotoxicity).
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Bristol-Myers Squibb

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Bristol-Myers Squibb

Role: STUDY_DIRECTOR

Bristol-Myers Squibb

Locations

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Local Institution - 0002

Lenexa, Kansas, United States

Site Status

Local Institution - 0001

Salt Lake City, Utah, United States

Site Status

Countries

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United States

Central Contacts

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BMS Clinical Trials Contact Center www.BMSClinicalTrials.com

Role: CONTACT

Phone: 8559073286

Email: [email protected]

First line of the email MUST contain the NCT# and Site#

Role: CONTACT

Facility Contacts

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Site 0002

Role: primary

Site 0001

Role: primary

Related Links

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https://www.bms.com/researchers-and-partners/clinical-trials-and-research.html

BMS Clinical Trial Information

https://www.BMSClinicalTrials.com

BMS Clinical Trial Patient Recruiting

Other Identifiers

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IM027-1052

Identifier Type: -

Identifier Source: org_study_id