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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 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.
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 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05571163
The ClinicalTrials.gov registry entry for NCT05571163 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 13 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 66-participant average among 119 other Healthy Participants trials with a reported enrollment target (80% lower). The listed sponsor is Amgen, which has 558 total studies on file at ClinicalTrials.gov.
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 1 study location spanning 1 distinct geographic area - top geographies include 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.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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