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hCG Treatment for Rehabilitation From a TBI
Sponsor: VA Office of Research and Development
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
Conditions
Interventions
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.
Placebo
Prefilled syringe of 0.250 milliliters (mL) normal saline.
Locations (1)
William S. Middleton Memorial Veterans Hospital, Madison, WI
Madison, Wisconsin, United States