90
Participants
Start Date
September 23, 2022
Primary Completion Date
March 31, 2024
Study Completion Date
March 31, 2024
Hydroxypropyl Beta Cyclodextrin
Minimum active dose of 500 mg/kg (equivalent to 18,500 mg/m2) as an intravenous (IV) infusion once every 28 days
Placebo
0.5N saline as an intravenous (IV) infusion once every 28 days
RECRUITING
Charter Research, Winter Park
RECRUITING
Access Research Institute, Brooksville
RECRUITING
Tandem/Clincloud, LCC, Marrero
RECRUITING
Wasatch Clinical Research, Salt Lake City
RECRUITING
Advanced Clinical Institute Inc, Neptune City
Lead Sponsor
Cyclo Therapeutics, Inc.
INDUSTRY