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NCT05814016 · ClinicalTrials.gov registry record · Phase 2

A Study of Danavorexton in People With Obstructive Sleep Apnea After General Anesthesia for Abdominal Surgery

A Phase 2 study, sponsored by Takeda.

Terminated
Registry status
Phase 2
Development phase
41
Enrollment target

NCT05814016: Clinical Trial Phase 2 study, sponsored by Takeda.

NCT05814016 is a Phase 2 study that was terminated before completion, run by Takeda. The registered enrollment target is 41 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (69% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05814016, a Phase 2 study, was terminated before completion, sponsored by Takeda.

TERMINATED
Registry status
Phase 2
Development phase
41 participants
Enrollment target

Study Summary

The main aim is to see if danavorexton can help improve people's breathing in the recovery room after abdominal surgery.

Primary Outcome

Respiratory stability in the PACU will be considered as having been achieved if the participant can breathe without problems for 120 minutes in the PACU.

Interventions

  • DRUG Placebo
  • DRUG Danavorexton

Trial Details

FieldValue
Enrollment Target 41 participants
Start Date 2023-05-11
Est. Completion 2024-09-25
Phase Phase 2
Takeda

408 total trials

Why NCT05814016 stopped before completion

NCT05814016 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 41 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (69% lower).

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT05814016 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05814016 about?

NCT05814016 is a clinical study titled "A Study of Danavorexton in People With Obstructive Sleep Apnea After General Anesthesia for Abdominal Surgery". The main aim is to see if danavorexton can help improve people's breathing in the recovery room after abdominal surgery.

What is the current status of trial NCT05814016?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 41 participants. The study started on 2023-05-11. Estimated completion is 2024-09-25.

What interventions are being tested in trial NCT05814016?

The interventions under investigation include: Placebo (DRUG), Danavorexton (DRUG).

Who is sponsoring clinical trial NCT05814016?

This trial is sponsored by Takeda, which has 408 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05814016's enrollment target sits among peer trials

41 1352nd of 2000 higher than 639 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 NCT05814016, the US trial registry maintained by the National Library of Medicine. NCT05814016 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.