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NCT01800617 · ClinicalTrials.gov registry record · Phase 2

A Study of T3 Therapy in Patients With Hypothyroidism

A Phase 2 study, sponsored by Ipe.

Completed
Registry status
Phase 2
Development phase
18
Enrollment target

NCT01800617: Completed Phase 2 study, sponsored by Ipe.

NCT01800617 is a Phase 2 study that has completed, run by Ipe. The registered enrollment target is 18 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01800617, a Phase 2 study, has completed, sponsored by Ipe.

COMPLETED
Registry status
Phase 2
Development phase
18 participants
Enrollment target

Study Summary

The purpose of this study is to test a new thyroid hormone preparation. The thyroid gland produces two thyroid hormones: mostly T4 and a smaller amount of T3. Thyroid hormone therapy for hypothyroidism or thyroid cancer is generally provided using levothyroxine, which is a synthetic form of T4. T4 is converted into the active hormone T3 in the circulation. Therefore, some researchers believe that T3 levels in T4-treated patients may be slightly lower than in individuals whose own thyroid gland is functioning normally. Symptoms of hypothyroidism have been suggested to occur because of this possible T3 deficiency, although this is controversial. Studies of T3, added to or substituted for T4 in traditional levothyroxine regimens, have generally not shown any benefit of T3. However, it is still possible that no benefit is seen because of the short duration of action or "half-life" of T3. This short-life makes it necessary to dose T3 twice or three times daily. Despite multiple daily doses of T3, T3 levels during its therapy tend to be troubled by peaks and troughs. These peaks can be associated with symptoms of excessive thyroid hormone levels. This study will look at TSH and thyroid hormone levels following a daily dose of a new preparation of T3 that may have longer duration of action than liothyronine. This preparation of T3 is called Thyromax® or BCT303. The investigators believe that steady levels of T3 will be seen after taking Thyromax®. The investigators believe that in patients with hypothyroidism use of Thyromax® in the correct dose will produce normal TSH levels, without producing symptoms of too much thyroid hormone. The goal of future studies is to test whether Thyromax® may be a potential treatment for hypothyroidism, by comparing it with traditional levothyroxine therapy.

Interventions

  • DRUG Liothyronine, Sodium

Trial Details

FieldValue
Enrollment Target 18 participants
Start Date 2013-03
Phase Phase 2

Sponsor

Ipe

2 total trials

What the Registry Record Tells You About NCT01800617

The ClinicalTrials.gov registry entry for NCT01800617 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 18 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Ipe, which has 2 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Liothyronine, Sodium is the first listed.

NCT01800617 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01800617 about?

NCT01800617 is a clinical study titled "A Study of T3 Therapy in Patients With Hypothyroidism". The purpose of this study is to test a new thyroid hormone preparation. The thyroid gland produces two thyroid hormones: mostly T4 and a smaller amount of T3. Thyroid hormone therapy for hypothyroidism or thyroid cancer is generally provided using levothyroxine, which is a synthetic form of T4. T4 i...

What is the current status of trial NCT01800617?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 18 participants. The study started on 2013-03.

What interventions are being tested in trial NCT01800617?

The interventions under investigation include: Liothyronine, Sodium (DRUG).

Who is sponsoring clinical trial NCT01800617?

This trial is sponsored by Ipe, which has 2 total clinical trials registered on ClinicalTrials.gov.

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

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, the data changelog, or report a data error.