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NCT00978055 · ClinicalTrials.gov registry record · Phase 1

Fasting Study of Liothyronine Sodium Tablets (50 Mcg) to Cytomel® Tablets (50 Mcg)

A Phase 1 study, sponsored by Mylan Pharmaceuticals.

Completed
Registry status
Phase 1
Development phase
31
Enrollment target

NCT00978055 is a Phase 1 study that has completed, run by Mylan Pharmaceuticals. The registered enrollment target is 31 participants.

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The verdict

NCT00978055, a Phase 1 study, has completed, sponsored by Mylan Pharmaceuticals.

COMPLETED
Registry status
Phase 1
Development phase
31 participants
Enrollment target

Study Summary

The objective of this study was to investigate the bioequivalence of Mylan's liothyronine sodium 50 mcg tablets to King's Cytomel® 50 mcg tablets following a single, oral 100 mcg (2 x 50 mcg) dose administration under fasting conditions.

Interventions

  • DRUG 1: Liothyronine Sodium Tablets
  • DRUG 2: Cytomel® Tablets

Trial Details

FieldValue
Enrollment Target 31 participants
Start Date 2007-10
Est. Completion 2007-12
Phase Phase 1

Sponsor

Mylan Pharmaceuticals

146 total trials

What the Registry Record Tells You About NCT00978055

The ClinicalTrials.gov registry entry for NCT00978055 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 31 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Mylan Pharmaceuticals, which has 146 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which 1: Liothyronine Sodium Tablets is the first listed.

NCT00978055 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00978055 about?

NCT00978055 is a clinical study titled "Fasting Study of Liothyronine Sodium Tablets (50 Mcg) to Cytomel® Tablets (50 Mcg)". The objective of this study was to investigate the bioequivalence of Mylan's liothyronine sodium 50 mcg tablets to King's Cytomel® 50 mcg tablets following a single, oral 100 mcg (2 x 50 mcg) dose administration under fasting conditions.

What is the current status of trial NCT00978055?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 31 participants. The study started on 2007-10. Estimated completion is 2007-12.

What interventions are being tested in trial NCT00978055?

The interventions under investigation include: 1: Liothyronine Sodium Tablets (DRUG), 2: Cytomel® Tablets (DRUG).

Who is sponsoring clinical trial NCT00978055?

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

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.