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NCT03920254 · ClinicalTrials.gov registry record · Phase 2

TD-1473 Long-Term Safety (LTS) Ulcerative Colitis (UC) Study

A Phase 2 study, sponsored by Theravance Biopharma.

Terminated
Registry status
Phase 2
Development phase
46
Enrollment target

NCT03920254: Clinical Trial Phase 2 study, sponsored by Theravance Biopharma.

NCT03920254 is a Phase 2 study that was terminated before completion, run by Theravance Biopharma. The registered enrollment target is 46 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (65% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03920254, a Phase 2 study, was terminated before completion, sponsored by Theravance Biopharma.

TERMINATED
Registry status
Phase 2
Development phase
46 participants
Enrollment target

Study Summary

A 3-Year Multi-Center, Long-Term Safety (LTS) Study to Evaluate the Safety and Tolerability of TD-1473 in Subjects with Ulcerative Colitis who have participated in the Maintenance Study of Protocol 0157

Primary Outcome

A TEAE was defined as any AE with a recorded start date on or after the date of the first dose of study drug up through 4 weeks after the last dose of study drug. Any clinically significant changes in laboratory safety tests, electrocardiograms (ECGs) and vital signs, were also recorded as TEAEs.

Interventions

  • DRUG TD-1473 Dose A
  • DRUG TD-1473 Dose B
  • DRUG TD-1473 Dose C

Trial Details

FieldValue
Enrollment Target 46 participants
Start Date 2020-07-23
Est. Completion 2021-10-27
Phase Phase 2
Theravance Biopharma

38 total trials

Why NCT03920254 stopped before completion

NCT03920254 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 46 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (65% lower).

The record links to 0 conditions, and to 3 interventions - of which TD-1473 Dose A is the first listed.

NCT03920254 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03920254 about?

NCT03920254 is a clinical study titled "TD-1473 Long-Term Safety (LTS) Ulcerative Colitis (UC) Study". A 3-Year Multi-Center, Long-Term Safety (LTS) Study to Evaluate the Safety and Tolerability of TD-1473 in Subjects with Ulcerative Colitis who have participated in the Maintenance Study of Protocol 0157

What is the current status of trial NCT03920254?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 46 participants. The study started on 2020-07-23. Estimated completion is 2021-10-27.

What interventions are being tested in trial NCT03920254?

The interventions under investigation include: TD-1473 Dose A (DRUG), TD-1473 Dose B (DRUG), TD-1473 Dose C (DRUG).

Who is sponsoring clinical trial NCT03920254?

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 NCT03920254's enrollment target sits among peer trials

46 1286th of 2000 higher than 705 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT03920254, the US trial registry maintained by the National Library of Medicine. NCT03920254 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.