Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT05598281 · ClinicalTrials.gov registry record · Phase 1

Study to Evaluate the Effect of AMG 510 on the Pharmacokinetics (PK) of Digoxin in Healthy Participants

A Phase 1 study of Healthy Participants, sponsored by Amgen.

Completed
Registry status
Phase 1
Development phase
14
Enrollment target
1
Study location

NCT05598281: Completed Phase 1 study of Healthy Participants, sponsored by Amgen.

NCT05598281 is a Phase 1 study of Healthy Participants that has completed, run by Amgen. The registered enrollment target is 14 participants, below the 66-participant average among 119 other Healthy Participants trials with a reported enrollment target (79% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT05598281, a Phase 1 study of Healthy Participants, has completed, sponsored by Amgen.

COMPLETED
Registry status
Phase 1
Development phase
14 participants
Enrollment target
1
Study location

Study Summary

The primary objective of the study is to evaluate the PK of digoxin administered alone and in combination with AMG 510 in healthy participants.

Conditions Studied

Interventions

  • DRUG AMG 510
  • DRUG Digoxin

Study Locations (1)

Florida

  • Covance Clinical Research Unit, Inc - Daytona Beach

Trial Details

FieldValue
Enrollment Target 14 participants
Start Date 2019-11-05
Est. Completion 2019-11-19
Phase Phase 1
Amgen

558 total trials

What the finished NCT05598281 record still lists

NCT05598281 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 14 participants, a relatively small participant target, below the 66-participant average among 119 other Healthy Participants trials with a reported enrollment target (79% lower).

The record links to 1 condition, with Healthy Participants appearing as the primary indexed condition, and to 2 interventions - of which AMG 510 is the first listed.

NCT05598281 reports a single indexed study location in Florida.

Frequently Asked Questions

What is clinical trial NCT05598281 about?

NCT05598281 is a clinical study titled "Study to Evaluate the Effect of AMG 510 on the Pharmacokinetics (PK) of Digoxin in Healthy Participants". The primary objective of the study is to evaluate the PK of digoxin administered alone and in combination with AMG 510 in healthy participants.

What is the current status of trial NCT05598281?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 14 participants. The study started on 2019-11-05. Estimated completion is 2019-11-19.

What conditions does trial NCT05598281 study?

This clinical trial studies the following conditions: Healthy Participants.

What interventions are being tested in trial NCT05598281?

The interventions under investigation include: AMG 510 (DRUG), Digoxin (DRUG).

Who is sponsoring clinical trial NCT05598281?

This trial is sponsored by Amgen, which has 558 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05598281 being conducted?

This trial has 1 study location across Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Healthy Participants

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT05598281's enrollment target sits among peer trials

14 107th of 119 higher than 11 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02523092 · 14 participants · Phase 4

    Use of CXCL9 as a Biomarker of Acthar Efficacy

  • NCT04263285 · 14 participants · NA

    Treatment of Depression Post-SCI

  • NCT04743271 · 14 participants · NA

    Food and Circadian Timing

  • NCT05065671 · 14 participants · Phase 1

    Microbiome Derived Metabolism and Pharmacokinetics

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT06358040 · started 2026-10 · NA

    Opioid Dispenser for Microdiscectomy/Laminectomy

Source: ClinicalTrials.gov NCT05598281, the US trial registry maintained by the National Library of Medicine. NCT05598281 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.