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NCT05571163 · ClinicalTrials.gov registry record · Phase 1
A Study to Evaluate the Relative Bioavailability of AMG 510 Administered as Tablets and as a Water Dispersion in Healthy Participants
A Phase 1 study of Healthy Participants, sponsored by Amgen.
- Completed
- Registry status
- Phase 1
- Development phase
- 13
- Enrollment target
- 1
- Study location
NCT05571163: Completed Phase 1 study of Healthy Participants, sponsored by Amgen.
NCT05571163 is a Phase 1 study of Healthy Participants that has completed, run by Amgen. The registered enrollment target is 13 participants, below the 66-participant average among 119 other Healthy Participants trials with a reported enrollment target (80% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT05571163, a Phase 1 study of Healthy Participants, has completed, sponsored by Amgen.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 13 participants
- Enrollment target
- 1
- Study location
Study Summary
The primary objective of the study is to evaluate the pharmacokinetics (PK) of AMG 510 administered as 8 x 120-mg tablets and as water dispersion in healthy participants.
Conditions Studied
Interventions
- DRUG AMG 510
Study Locations (1)
Texas
- Covance Clinical Research Unit, Inc 1341 W Mockingbird Ln, Ste 200E - Dallas
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 13 participants |
| Start Date | 2020-03-06 |
| Est. Completion | 2020-06-14 |
| Phase | Phase 1 |
What the finished NCT05571163 record still lists
NCT05571163 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 13 participants, a relatively small participant target, below the 66-participant average among 119 other Healthy Participants trials with a reported enrollment target (80% lower).
The record links to 1 condition, with Healthy Participants appearing as the primary indexed condition, and to 1 intervention - of which AMG 510 is the first listed.
NCT05571163 reports a single indexed study location in Texas.
Frequently Asked Questions
What is clinical trial NCT05571163 about?
NCT05571163 is a clinical study titled "A Study to Evaluate the Relative Bioavailability of AMG 510 Administered as Tablets and as a Water Dispersion in Healthy Participants". The primary objective of the study is to evaluate the pharmacokinetics (PK) of AMG 510 administered as 8 x 120-mg tablets and as water dispersion in healthy participants.
What is the current status of trial NCT05571163?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 13 participants. The study started on 2020-03-06. Estimated completion is 2020-06-14.
What conditions does trial NCT05571163 study?
This clinical trial studies the following conditions: Healthy Participants.
What interventions are being tested in trial NCT05571163?
The interventions under investigation include: AMG 510 (DRUG).
Who is sponsoring clinical trial NCT05571163?
This trial is sponsored by Amgen, which has 558 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05571163 being conducted?
This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
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Where NCT05571163's enrollment target sits among peer trials
13 110th of 119 higher than 9 of 119 other Healthy Participants trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Healthy Participants trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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