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NCT05091723 · ClinicalTrials.gov registry record · Phase 1

TD-0903 Pharmacokinetics Study in Healthy Participants With Supplemental Oxygenation

A Phase 1 study, sponsored by Theravance Biopharma.

Completed
Registry status
Phase 1
Development phase
14
Enrollment target

NCT05091723: Completed Phase 1 study, sponsored by Theravance Biopharma.

NCT05091723 is a Phase 1 study that has completed, run by Theravance Biopharma. The registered enrollment target is 14 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (77% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05091723, a Phase 1 study, has completed, sponsored by Theravance Biopharma.

COMPLETED
Registry status
Phase 1
Development phase
14 participants
Enrollment target

Study Summary

This is a Phase 1 pharmacokinetic (PK) study in healthy participants to assess the plasma pharmacokinetics, safety, and tolerability of a single inhaled dose of nezulcitinib (TD-0903) with supplemental oxygenation.

Primary Outcome

The area under the concentration time curve from time 0 extrapolated to infinity (AUC0-inf) of TD-0903

Interventions

  • DRUG Nezulcitinib (TD-0903) Dose A
  • DRUG Nezulcitinib (TD-0903) Dose B

Trial Details

FieldValue
Enrollment Target 14 participants
Start Date 2021-10-13
Est. Completion 2021-11-24
Phase Phase 1
Theravance Biopharma

38 total trials

What the finished NCT05091723 record still lists

NCT05091723 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 14 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (77% lower).

The record links to 0 conditions, and to 2 interventions - of which Nezulcitinib (TD-0903) Dose A is the first listed.

NCT05091723 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05091723 about?

NCT05091723 is a clinical study titled "TD-0903 Pharmacokinetics Study in Healthy Participants With Supplemental Oxygenation". This is a Phase 1 pharmacokinetic (PK) study in healthy participants to assess the plasma pharmacokinetics, safety, and tolerability of a single inhaled dose of nezulcitinib (TD-0903) with supplemental oxygenation.

What is the current status of trial NCT05091723?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 14 participants. The study started on 2021-10-13. Estimated completion is 2021-11-24.

What interventions are being tested in trial NCT05091723?

The interventions under investigation include: Nezulcitinib (TD-0903) Dose A (DRUG), Nezulcitinib (TD-0903) Dose B (DRUG).

Who is sponsoring clinical trial NCT05091723?

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 NCT05091723's enrollment target sits among peer trials

14 1844th of 2000 higher than 154 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 NCT05091723, the US trial registry maintained by the National Library of Medicine. NCT05091723 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.