Study of Dose Adjustment From Levothyroxine to a New Levothyroxine Sodium Test Formulation

NCT01916304 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 101

Last updated 2015-07-20

Study results available
· View outcomes & findings →

Summary

The purpose of this study is to investigate the effect of switching participants taking levothyroxine to a new sodium formulation.

Conditions

Interventions

DRUG

Levothyroxine sodium new formulation

Levothyroxine tablets

Sponsors & Collaborators

Principal Investigators

  • Medical Responsible · Takeda

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-07-31
Primary Completion
2014-06-30
Completion
2014-06-30

Countries

  • Belgium

Study Locations

More Related Trials

Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01916304 on ClinicalTrials.gov