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NCT00648765 · ClinicalTrials.gov registry record · Phase 1

Fed Study of Anagrelide Hydrochloride Capsules 1 mg to Agrylin® Capsules 1 mg

A Phase 1 study, sponsored by Mylan Pharmaceuticals.

Completed
Registry status
Phase 1
Development phase
22
Enrollment target

NCT00648765: Completed Phase 1 study, sponsored by Mylan Pharmaceuticals.

NCT00648765 is a Phase 1 study that has completed, run by Mylan Pharmaceuticals. The registered enrollment target is 22 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (63% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00648765, a Phase 1 study, has completed, sponsored by Mylan Pharmaceuticals.

COMPLETED
Registry status
Phase 1
Development phase
22 participants
Enrollment target

Study Summary

The objective of this study was to investigate the bioequivalence of Mylan's anagrelide HCl 1 mg capsules to Shire US's Agrylin® 1 mg capsules following a single, oral 1 mg (1 x 1 mg) dose administration under fed conditions.

Interventions

  • DRUG Anagrelide Hydrochloride Capsules 1 mg
  • DRUG Agrylin® Capsules 1 mg

Trial Details

FieldValue
Enrollment Target 22 participants
Start Date 2003-01
Est. Completion 2003-01
Phase Phase 1
Mylan Pharmaceuticals

146 total trials

What the finished NCT00648765 record still lists

NCT00648765 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 22 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (63% lower).

The record links to 0 conditions, and to 2 interventions - of which Anagrelide Hydrochloride Capsules 1 mg is the first listed.

NCT00648765 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00648765 about?

NCT00648765 is a clinical study titled "Fed Study of Anagrelide Hydrochloride Capsules 1 mg to Agrylin® Capsules 1 mg". The objective of this study was to investigate the bioequivalence of Mylan's anagrelide HCl 1 mg capsules to Shire US's Agrylin® 1 mg capsules following a single, oral 1 mg (1 x 1 mg) dose administration under fed conditions.

What is the current status of trial NCT00648765?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 22 participants. The study started on 2003-01. Estimated completion is 2003-01.

What interventions are being tested in trial NCT00648765?

The interventions under investigation include: Anagrelide Hydrochloride Capsules 1 mg (DRUG), Agrylin® Capsules 1 mg (DRUG).

Who is sponsoring clinical trial NCT00648765?

This trial is sponsored by Mylan Pharmaceuticals, which has 146 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00648765's enrollment target sits among peer trials

22 1601st of 2000 higher than 386 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 NCT00648765, the US trial registry maintained by the National Library of Medicine. NCT00648765 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.