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NCT02132429 · ClinicalTrials.gov registry record · Phase 1

Phase I, Double-Blind,Placebo, MAD Study to Evaluate the Safety, Tolerability, PK, and PD of AMG 333 in Healthy Subjects and Migraine Subjects

A Phase 1 study, sponsored by Amgen.

Terminated
Registry status
Phase 1
Development phase
16
Enrollment target

NCT02132429 is a Phase 1 study that was terminated before completion, run by Amgen. The registered enrollment target is 16 participants.

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The verdict

NCT02132429, a Phase 1 study, was terminated before completion, sponsored by Amgen.

TERMINATED
Registry status
Phase 1
Development phase
16 participants
Enrollment target

Study Summary

The primary purpose of this study is to evaluate the safety and tolerability of multiple oral doses of AMG 333 for 14 days in healthy subjects and migraine subjects. As part of the secondary objectives, the study will characterize the pharmacokinetic (PK) profile of AMG 333 after multiple oral doses in healthy subjects and migraine subjects, as well as characterize the effect of multiple doses of AMG 333 on increases in blood pressure (BP) induced by the cold pressor test (CPT) in healthy subjects.

Interventions

  • DRUG Placebo
  • DRUG AMG 333

Trial Details

FieldValue
Enrollment Target 16 participants
Start Date 2014-05
Est. Completion 2014-12
Phase Phase 1

Sponsor

Amgen

558 total trials

What the Registry Record Tells You About NCT02132429

The ClinicalTrials.gov registry entry for NCT02132429 describes a study currently listed as terminated, categorized as Phase 1. The registered enrollment target is 16 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Amgen, which has 558 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT02132429 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT02132429 about?

NCT02132429 is a clinical study titled "Phase I, Double-Blind,Placebo, MAD Study to Evaluate the Safety, Tolerability, PK, and PD of AMG 333 in Healthy Subjects and Migraine Subjects". The primary purpose of this study is to evaluate the safety and tolerability of multiple oral doses of AMG 333 for 14 days in healthy subjects and migraine subjects. As part of the secondary objectives, the study will characterize the pharmacokinetic (PK) profile of AMG 333 after multiple oral doses...

What is the current status of trial NCT02132429?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 16 participants. The study started on 2014-05. Estimated completion is 2014-12.

What interventions are being tested in trial NCT02132429?

The interventions under investigation include: Placebo (DRUG), AMG 333 (DRUG).

Who is sponsoring clinical trial NCT02132429?

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

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.