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NCT07046975 · ClinicalTrials.gov registry record · Phase 3

Bioavailability and Bioequivalence Study of Extended Release Torsemide and Spironolactone

A Phase 3 study, sponsored by Sarfez Pharmaceuticals.

Completed
Registry status
Phase 3
Development phase
24
Enrollment target

NCT07046975: Completed Phase 3 study, sponsored by Sarfez Pharmaceuticals.

NCT07046975 is a Phase 3 study that has completed, run by Sarfez Pharmaceuticals. The registered enrollment target is 24 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (97% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07046975, a Phase 3 study, has completed, sponsored by Sarfez Pharmaceuticals.

COMPLETED
Registry status
Phase 3
Development phase
24 participants
Enrollment target

Study Summary

To study intrasubject variability and steady-state pharmacokinetics of multiple-doses of Extended Release Torsemide and Spironolactone Fixed Dose Combination (FDC) tablets given together in healthy adult subjects.

Primary Outcome

Measurement of torsemide in the blood for Cmax.

Interventions

  • DRUG Torsemide and Spironolactone tablet
  • DRUG Torsemide Tablets and Spironolactone Tablets

Trial Details

FieldValue
Enrollment Target 24 participants
Start Date 2025-06-15
Est. Completion 2026-02-28
Phase Phase 3
Sarfez Pharmaceuticals

6 total trials

What the finished NCT07046975 record still lists

NCT07046975 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 24 participants, a relatively small participant target, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (97% lower).

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

NCT07046975 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT07046975 about?

NCT07046975 is a clinical study titled "Bioavailability and Bioequivalence Study of Extended Release Torsemide and Spironolactone". To study intrasubject variability and steady-state pharmacokinetics of multiple-doses of Extended Release Torsemide and Spironolactone Fixed Dose Combination (FDC) tablets given together in healthy adult subjects.

What is the current status of trial NCT07046975?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 24 participants. The study started on 2025-06-15. Estimated completion is 2026-02-28.

What interventions are being tested in trial NCT07046975?

The interventions under investigation include: Torsemide and Spironolactone tablet (DRUG), Torsemide Tablets and Spironolactone Tablets (DRUG).

Who is sponsoring clinical trial NCT07046975?

This trial is sponsored by Sarfez Pharmaceuticals, which has 6 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT07046975's enrollment target sits among peer trials

24 1943rd of 2000 higher than 49 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 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 NCT07046975, the US trial registry maintained by the National Library of Medicine. NCT07046975 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.