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A Study of T3 Therapy in Patients With Hypothyroidism

Information source: Ipe, LLC
ClinicalTrials.gov processed this data on August 23, 2015
Link to the current ClinicalTrials.gov record.

Condition(s) targeted: Hypothyroidism

Intervention: Liothyronine, Sodium (Drug)

Phase: Phase 2

Status: Completed

Sponsored by: Ipe, LLC


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.

Clinical Details

Official title: Phase II Single Daily-Dose Response Study of a New Liothyronine Sodium (T3) Preparation With Sustained Effects in Hypothyroid Patients

Study design: Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Primary outcome: Measurement of Blood Levels of Thyroid Hormone Sensitive Parameters

Secondary outcome: Measurement of Oxygen Consumption


Minimum age: 18 Years. Maximum age: 65 Years. Gender(s): Both.


Inclusion Criteria:

- Hypothyroid patients taking levothyroxine

- Age 18-65

- Able to make weekly in-person visits to Washington, D. C.

Exclusion Criteria:

- Pregnancy or lactation

- Chronic medical conditions such as heart disease or any other chronic medical

conditions such as lung disease (e. g. asthma), kidney disease (e. g. kidney failure), liver disease (e. g. hepatitis), diabetes, or cancer.

- Steroid medications such as estrogen, progesterone, estrogen or progesterone related

medications, testosterone, or glucocorticoids

- Already taking T3

Locations and Contacts

Georgetown University Hospital, Washington, District of Columbia 20007, United States
Additional Information

Starting date: March 2013
Last updated: July 1, 2014

Page last updated: August 23, 2015

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