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NCT02657122 · ClinicalTrials.gov registry record · Phase 1

SAD and MAD Study to Evaluate Safety, Tolerability, and Pharmacokinetics (PK) of TD-1473 in Healthy Subjects

A Phase 1 study, sponsored by Theravance Biopharma.

Completed
Registry status
Phase 1
Development phase
72
Enrollment target

NCT02657122: Completed Phase 1 study, sponsored by Theravance Biopharma.

NCT02657122 is a Phase 1 study that has completed, run by Theravance Biopharma. The registered enrollment target is 72 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (20% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02657122, a Phase 1 study, has completed, sponsored by Theravance Biopharma.

COMPLETED
Registry status
Phase 1
Development phase
72 participants
Enrollment target

Study Summary

The purpose of this study is to evaluate the safety, tolerability, and pharmacokinetics of single ascending doses and multiple ascending doses of the investigational drug TD-1473 compared to placebo in healthy subjects.

Interventions

  • DRUG TD-1473 for SAD
  • DRUG Placebo for SAD
  • DRUG TD-1473 for MAD
  • DRUG Placebo for MAD

Trial Details

FieldValue
Enrollment Target 72 participants
Start Date 2015-12
Est. Completion 2016-04
Phase Phase 1
Theravance Biopharma

38 total trials

What the finished NCT02657122 record still lists

NCT02657122 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 72 participants, a relatively small participant target, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (20% higher).

The record links to 0 conditions, and to 4 interventions - of which TD-1473 for SAD is the first listed.

NCT02657122 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02657122 about?

NCT02657122 is a clinical study titled "SAD and MAD Study to Evaluate Safety, Tolerability, and Pharmacokinetics (PK) of TD-1473 in Healthy Subjects". The purpose of this study is to evaluate the safety, tolerability, and pharmacokinetics of single ascending doses and multiple ascending doses of the investigational drug TD-1473 compared to placebo in healthy subjects.

What is the current status of trial NCT02657122?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 72 participants. The study started on 2015-12. Estimated completion is 2016-04.

What interventions are being tested in trial NCT02657122?

The interventions under investigation include: TD-1473 for SAD (DRUG), Placebo for SAD (DRUG), TD-1473 for MAD (DRUG), Placebo for MAD (DRUG).

Who is sponsoring clinical trial NCT02657122?

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

How this trial's enrollment target compares

Where NCT02657122's enrollment target sits among peer trials

72 736th of 2000 higher than 1,254 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 NCT02657122, the US trial registry maintained by the National Library of Medicine. NCT02657122 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.