Feasibility Study for Repurposing RET Inhibitors

EARLY_PHASE1Not yet recruitingINTERVENTIONAL
Enrollment

7

Participants

Timeline

Start Date

November 30, 2025

Primary Completion Date

April 23, 2027

Study Completion Date

April 23, 2028

Conditions
Cachexia-Anorexia Syndrome
Interventions
DRUG

Selpercatinib

"Patients will be instructed to take selpercatinib orally (PO) twice daily (BID), approximately every 12 hours. While on study, they will undergo weight measurements and regular blood draws every 4 weeks. At the 16-week post-treatment follow-up, patients will return to the clinic for a weight assessment to evaluate potential changes in body weight.~Patients will be administered assessments including, Functional Assessment of Anorexia Cachexia Therapy (FAACT), administered at screening, at 12 weeks post-discontinuation of the study drug, and again at the 16-week follow-up."

OTHER

Strength Assessment

Several strength assessment will be conducted at baseline and at 12 weeks end-of-treatment, which will include measurements such as grip strength, hallux strength, timed chair stands, leg press, and localized ultrasound of the quadriceps.

Trial Locations (1)

73117

OU Health Stephenson Cancer Center, Oklahoma City

All Listed Sponsors
collaborator

Presbyterian Health Foundation

UNKNOWN

lead

University of Oklahoma

OTHER