A Study to Evaluate the Drug-drug Interaction Effect of Rifampin on the Pharmacokinetics of AMG 510 in Healthy Participants
NCT ID: NCT05577624
Last Updated: 2025-03-18
Study Results
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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COMPLETED
PHASE1
14 participants
INTERVENTIONAL
2019-11-05
2019-12-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
BASIC_SCIENCE
NONE
Study Groups
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AMG 510 + Rifampin
AMG 510
Oral tablet
Rifampin
Oral capsule
Interventions
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AMG 510
Oral tablet
Rifampin
Oral capsule
Eligibility Criteria
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Inclusion Criteria
* Body mass index, between 18 and 30 kg/m2 (inclusive), at the time of Screening.
* Females of nonchildbearing potential
Exclusion Criteria
* History of hypersensitivity, intolerance, or allergy to any drug compound, food, or other substance, unless approved by the Investigator (or designee) and in consultation with the Sponsor.
* Poor peripheral venous access.
* History or evidence, at Screening or Check in, of clinically significant disorder, condition, or disease not otherwise excluded that, in the opinion of the Investigator (or designee), would pose a risk to subject safety or interfere with the study evaluation, procedures, or completion.
18 Years
60 Years
ALL
Yes
Sponsors
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Amgen
INDUSTRY
Responsible Party
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Principal Investigators
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MD
Role: STUDY_DIRECTOR
Amgen
Locations
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Covance Clinical Research Unit, Inc 3402 Kinsman Boulevard
Madison, Wisconsin, United States
Countries
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Related Links
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AmgenTrials clinical trials website
Other Identifiers
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20190319
Identifier Type: -
Identifier Source: org_study_id
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