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NCT06167265 · ClinicalTrials.gov registry record · Phase 1

BE Study of Once Daily PMR Compared to Twice Daily Cilostazol Tablets in Healthy Volunteers

A Phase 1 study, sponsored by Genovate Biotechnology Co., Ltd.,.

Completed
Registry status
Phase 1
Development phase
40
Enrollment target

NCT06167265: Completed Phase 1 study, sponsored by Genovate Biotechnology Co., Ltd.,.

NCT06167265 is a Phase 1 study that has completed, run by Genovate Biotechnology Co., Ltd.,. The registered enrollment target is 40 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (33% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06167265, a Phase 1 study, has completed, sponsored by Genovate Biotechnology Co., Ltd.,.

COMPLETED
Registry status
Phase 1
Development phase
40 participants
Enrollment target

Study Summary

The study is designed to evaluate the bioequivalence and the within-subject variability between the test formulation of extended-release tablet of cilostazol (PMR) administered once daily and the reference formulation of immediate- release tablet of cilostazol (Cilostazol) administered twice-daily in normal healthy male and female subjects under fasting conditions.

Interventions

  • DRUG Cilostazol Tablet 100 mg
  • DRUG PMR Tablet 145 mg

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2023-11-28
Est. Completion 2024-01-18
Phase Phase 1

What the finished NCT06167265 record still lists

NCT06167265 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 40 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (33% lower).

The record links to 0 conditions, and to 2 interventions - of which Cilostazol Tablet 100 mg is the first listed.

NCT06167265 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06167265 about?

NCT06167265 is a clinical study titled "BE Study of Once Daily PMR Compared to Twice Daily Cilostazol Tablets in Healthy Volunteers". The study is designed to evaluate the bioequivalence and the within-subject variability between the test formulation of extended-release tablet of cilostazol (PMR) administered once daily and the reference formulation of immediate- release tablet of cilostazol (Cilostazol) administered twice-daily i...

What is the current status of trial NCT06167265?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 40 participants. The study started on 2023-11-28. Estimated completion is 2024-01-18.

What interventions are being tested in trial NCT06167265?

The interventions under investigation include: Cilostazol Tablet 100 mg (DRUG), PMR Tablet 145 mg (DRUG).

Who is sponsoring clinical trial NCT06167265?

This trial is sponsored by Genovate Biotechnology Co., Ltd.,, which has 5 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT06167265's enrollment target sits among peer trials

40 1130th of 2000 higher than 810 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 NCT06167265, the US trial registry maintained by the National Library of Medicine. NCT06167265 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.