CompletedPhase 2NCT03364231
Study to Assess the Efficacy and Safety of Umbralisib in Participants With Non-Follicular Indolent Non-Hodgkin's Lymphoma
Studying Indolent B-cell non-Hodgkin lymphoma
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- TG Therapeutics, Inc.
- Principal Investigator
- Bruce Cheson, MDLombardi Comprehensive Cancer Center
- Intervention
- Umbralisib(drug)
- Enrollment
- 21 target
- Eligibility
- 18 years · All sexes
- Timeline
- 2017 – 2022
Study locations (4)
- TG Therapeutics Investigational Trial Site, Washington D.C., District of Columbia, United States
- TG Therapeutics Investigational Trial Site, Boston, Massachusetts, United States
- TG Therapeutics Investigational Trial Site, Hackensack, New Jersey, United States
- TG Therapeutics Investigational Trial Site, New York, New York, United States
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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