The purpose of this study is to evaluate the safety and effectiveness of TGR-1202 in patients with advanced hematologic malignancies.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
90
TGR-1202 Daily Oral Dose
TG Therapeutics Trial Site
Sarasota, Florida, United States
TG Therapeutics Trial Site
Hackensack, New Jersey, United States
TG Therapeutics Trial Site
New York, New York, United States
TG Therapeutics Trial Site
Durham, North Carolina, United States
Maximum Tolerated Dose acceptable for participants
To determine the incidence of adverse events, any potential abnormal laboratory results and any dose-limiting toxicities.
Time frame: 28 days (1 cycle of therapy)
Overall Response Rate
To assess the overall response rate (ORR) in patients with hematologic malignancies treated with TGR-1202
Time frame: Up to 1 year
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TG Therapeutics Trial Site
Cincinnati, Ohio, United States
TG Therapeutics Trial Site
Nashville, Tennessee, United States
TG Therapeutics Investigational Trial Site
Milwaukee, Wisconsin, United States