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Small Molecule
TGR-1202 for Chronic Lymphocytic Leukemia
Phase 2
Waitlist Available
Research Sponsored by TG Therapeutics, Inc.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Timeline
Screening 3 weeks
Treatment Varies
Follow Up evaluated at each planned visit through study completion, an average of 2 years
Awards & highlights
Study Summary
This trial is for people with B-cell Non-Hodgkin's Lymphoma or Chronic Lymphocytic Leukemia who are already receiving treatment with Ublituximab and/or TGR-1202.
Eligible Conditions
- Chronic Lymphocytic Leukemia
- Non-Hodgkin's Lymphoma
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ evaluated at each planned visit through study completion, an average of 2 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~evaluated at each planned visit through study completion, an average of 2 years
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Adverse Events of TGR-1202 and/or TGR-1202 + ublituximab treatment, including delayed toxicities
Secondary outcome measures
Progression-free survival of TGR-1202 and/or TGR-1202 + ublituximab treatment
Trial Design
2Treatment groups
Experimental Treatment
Group I: TGR-1202 + UblituximabExperimental Treatment1 Intervention
Oral TGR-1202 in combination with Ublituximab intravenous administration
Group II: TGR-1202Experimental Treatment1 Intervention
Oral TGR-1202 Daily
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
TGR-1202
2015
Completed Phase 3
~810
Find a Location
Who is running the clinical trial?
TG Therapeutics, Inc.Lead Sponsor
36 Previous Clinical Trials
5,580 Total Patients Enrolled
Frequently Asked Questions
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