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Completed Phase 1Phase 2 Interventional

Ublituximab + Ibrutinib in Select B-cell Malignancies

ClinicalTrials.gov ID: NCT02013128

Public ClinicalTrials.gov record NCT02013128. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 21, 2026, 4:46 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multi-center Phase II Study With Safety Run-in Evaluating the Efficacy and Safety of Ublituximab in Combination With Ibrutinib in Patients With Select B-Cell Malignancies

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to evaluate the safety and effectiveness of Ublituximab in combination with Ibrutinib in patients with advanced hematologic malignancies.

Study identification

NCT ID
NCT02013128
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
TG Therapeutics, Inc.
Industry
Enrollment
66 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jan 6, 2014 (Actual)
Primary completion
Dec 2015 (Actual)
Completion
Dec 2015 (Actual)
Last update posted
Oct 24, 2022

2014 – 2015

United States locations

U.S. sites
18
U.S. states
13
U.S. cities
18
Facility City State ZIP Site status
TG Therapeutics Investigational Trial Site Huntsville Alabama 35805 —
TG Therapeutics Investigational Trial Site Tucson Arizona 85710 —
TG Therapeutics Investigational Trial Site Santa Barbara California 93105 —
TG Therapeutics Investigational Trial Site Boulder Colorado 80303 —
TG Therapeutics Investigational Trial Site Niles Illinois 60714 —
TG Therapeutics Investigational Trial Site Urbana Illinois 61801 —
TG Therapeutics Investigational Trial Site Bethesda Maryland 20817 —
TG Therapeutics Investigational Trial Site Morristown New Jersey 07962 —
TG Therapeutics Investigational Trial Site Portland Oregon 97213 —
TG Therapeutics Investigational Trial Site Springfield Oregon 97477 —
TG Therapeutics Investigational Trial Site Greenville South Carolina 29615 —
TG Therapeutics Investigational Trial Site Memphis Tennessee 38120 —
TG Therapeutics Investigational Trial Site Austin Texas 78705 —
TG Therapeutics Investigational Trial Site Dallas Texas 75230 —
TG Therapeutics Investigational Trial Site Tyler Texas 75702 —
TG Therapeutics Investigational Trial Site Blacksburg Virginia 24060 —
TG Therapeutics Investigational Trial Site Fairfax Virginia 22031 —
TG Therapeutics Investigational Trial Site Vancouver Washington 98684 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02013128, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 24, 2022 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02013128 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →