EICHORCondition: Non-Hodgkin's Lymphoma · Chronic Lymphocytic Leukemia · Peripheral T-Cell Lymphoma · Sponsor: TG Therapeutics, Inc.
The purpose of this study is to evaluate the safety and effectiveness of TGR-1202 in patients with advanced hematologic malignancies.
This description comes directly from the study's public registry record.
No contact information is available for this study as per the public registry record.
Always discuss trial participation with your own doctor first.
Inclusion Criteria: * Refractory to or relapsed after at least 1 prior treatment regimen; * Eastern Cooperative Oncology Group (ECOG) score of 0 to 2; * At least 18 years of age. Exclusion Criteria: * Any major surgery, chemotherapy or immunotherapy within the last 21 days (limited palliative radiation is allowed ≥ 2 weeks); * Autologous hematologic stem cell transplant within 3 months of study entry or Allogeneic hematologic stem cell transplant within 12 months; * Known hepatitis B virus, hepatitis C virus or HIV infection; * Previous therapy with GS-1101 (CAL-101), IPI-145 or any drug that specifically inhibits the PI3K or mTOR pathway;
Reproduced word-for-word from the public registry record — the study team can answer questions about it.
| 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 | — |
| 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 | — |
This study lists sites in the areas below. Each link shows other recruiting studies near that city, from the public registry record.
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Source record: clinicaltrials.gov/study/NCT01767766