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NOT YET RECRUITING
NCT07557615
EARLY_PHASE1

hCG Treatment for Rehabilitation From a TBI

Sponsor: VA Office of Research and Development

View on ClinicalTrials.gov

Summary

The COGNI-REHAB Trial is a single-site, phase O/I, randomized, double-blind, placebo-controlled study of human chorionic gonadotropin (hCG; choriogonadotropin alfa, Ovidrel®) in men with post-acute, moderate to severe traumatic brain injury (msTBI). Its objective is to assess the safety and efficacy of a 24-week regimen of Ovidrel (125 micrograms twice weekly) compared to placebo on treatment-emergent adverse events (TEAEs), cognitive and functional recovery, and circulating sex hormones.

Official title: Chorionic Gonadotropin to Improve Rehabilitation After Brain Injury - The COGNI-REHAB Study

Key Details

Gender

MALE

Age Range

18 Years - 65 Years

Study Type

INTERVENTIONAL

Enrollment

50

Start Date

2027-01-01

Completion Date

2029-12-31

Last Updated

2026-10-13

Healthy Volunteers

No

Interventions

DRUG

Ovidrel

Ovidrel, recombinant human chorionic gonadotropin, comes in a prefilled syringe for subcutaneous injection, is the investigational agent that will be used in this trial. Ovidrel® PreFilled Syringe is a sterile, liquid intended for subcutaneous (s.c.) injection. Each Ovidrel® PreFilled Syringe is filled with 0.515 milliliters (mL) containing 257.5 micrograms of choriogonadotropin alfa, 28.1 milligrams (mg) mannitol, 505 grams (g) 85% O-phosphoric acid, 103 g L-methionine, 51.5 g Poloxamer 188, Sodium Hydroxide (for pH adjustment), and Water for Injection to deliver 125 micrograms of choriogonadotropin alfa in 0.25 milliliters (mL) twice weekly. The pH of the solution is 6.5 to 7.5.

OTHER

Placebo

Prefilled syringe of 0.250 milliliters (mL) normal saline.

Locations (1)

William S. Middleton Memorial Veterans Hospital, Madison, WI

Madison, Wisconsin, United States