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

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, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (33% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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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
Theravance Biopharma

38 total trials

What the finished NCT02954263 record still lists

NCT02954263 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 40 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (33% lower).

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 a single indexed study location in 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.

Similar trials for Healthy Adults, Elderly Subjects

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 NCT02954263's enrollment target sits among peer trials

40 1130th of 2000 higher than 810 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 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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Source: ClinicalTrials.gov NCT02954263, the US trial registry maintained by the National Library of Medicine. NCT02954263 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.