Developing Oral LT3 Therapy for Heart Failure - HFpEF

PHASE1/PHASE2CompletedINTERVENTIONAL
Enrollment

28

Participants

Timeline

Start Date

March 8, 2020

Primary Completion Date

October 31, 2023

Study Completion Date

October 31, 2023

Conditions
Heart Failure With Preserved Ejection FractionLow Triiodothyronine Syndrome
Interventions
DRUG

liothyronine

Each treatment period of liothyronine was approximately 8 weeks in duration, with weekly titration of study drug for four weeks, followed by a maintenance dose for 4 weeks, then 2-week washout before crossing over to receive the alternate therapy - placebo.

OTHER

Placebo

Each treatment period of placebo was approximately 8 weeks in duration, with weekly titration of study drug for four weeks, followed by a maintenance dose for 4 weeks, then 2-week washout before crossing over to receive the alternate therapy - LT3.

Trial Locations (1)

19104

Penn Medicine, Philadelphia

All Listed Sponsors
collaborator

National Heart, Lung, and Blood Institute (NHLBI)

NIH

lead

University of Pennsylvania

OTHER

NCT04111536 - Developing Oral LT3 Therapy for Heart Failure - HFpEF | Biotech Hunter | Biotech Hunter