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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 weeks
Treatment ~ Varies
Follow Up ~evaluated at each planned visit through study completion, an average of 2 years
This trial's timeline: 3 weeks for screening, Varies for treatment, and evaluated at each planned visit through study completion, an average of 2 years for reporting.

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

~7 spots leftby Apr 2025