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NCT02954263 · ClinicalTrials.gov registry record · Phase 1

Multiple Ascending Dose Study of TD-1439 in Healthy Adult and Elderly Subjects

A Phase 1 study of Healthy Adults, Elderly Subjects, sponsored by Theravance Biopharma.

Completed
Registry status
Phase 1
Development phase
40
Enrollment target
1
Study location

NCT02954263 is a Phase 1 study of Healthy Adults, Elderly Subjects that has completed, run by Theravance Biopharma. The registered enrollment target is 40 participants. The trial reports 1 study location across 1 state.

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The verdict

NCT02954263, a Phase 1 study of Healthy Adults, Elderly Subjects, has completed, sponsored by Theravance Biopharma.

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

Study Summary

Multiple ascending dose study to evaluate the safety, tolerability, pharmacokinetics, and pharmacodynamics of TD-1439 in healthy adult and elderly subjects

Interventions

  • DRUG Placebo
  • DRUG TD-1439

Study Locations (1)

Nebraska

  • Celerion - Lincoln

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2016-11
Est. Completion 2017-04
Phase Phase 1

Sponsor

Theravance Biopharma

38 total trials

What the Registry Record Tells You About NCT02954263

The ClinicalTrials.gov registry entry for NCT02954263 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 40 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Theravance Biopharma, which has 38 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Healthy Adults, Elderly Subjects appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT02954263 reports 1 study location spanning 1 distinct geographic area - top geographies include Nebraska.

Frequently Asked Questions

What is clinical trial NCT02954263 about?

NCT02954263 is a clinical study titled "Multiple Ascending Dose Study of TD-1439 in Healthy Adult and Elderly Subjects". Multiple ascending dose study to evaluate the safety, tolerability, pharmacokinetics, and pharmacodynamics of TD-1439 in healthy adult and elderly subjects

What is the current status of trial NCT02954263?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 40 participants. The study started on 2016-11. Estimated completion is 2017-04.

What conditions does trial NCT02954263 study?

This clinical trial studies the following conditions: Healthy Adults, Elderly Subjects.

What interventions are being tested in trial NCT02954263?

The interventions under investigation include: Placebo (DRUG), TD-1439 (DRUG).

Who is sponsoring clinical trial NCT02954263?

This trial is sponsored by Theravance Biopharma, which has 38 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02954263 being conducted?

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

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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.