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NCT02481297 · ClinicalTrials.gov registry record · Phase 2

Lirilumab With Rituximab for Relapsed, Refractory or High-risk Untreated Chronic Lymphocytic Leukemia (CLL) Patients

A Phase 2 study, sponsored by M.D. Anderson Cancer Center.

Completed
Registry status
Phase 2
Development phase
7
Enrollment target

NCT02481297: Completed Phase 2 study, sponsored by M.D. Anderson Cancer Center.

NCT02481297 is a Phase 2 study that has completed, run by M.D. Anderson Cancer Center. The registered enrollment target is 7 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (95% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

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The verdict

NCT02481297, a Phase 2 study, has completed, sponsored by M.D. Anderson Cancer Center.

COMPLETED
Registry status
Phase 2
Development phase
7 participants
Enrollment target

Study Summary

The goal of this clinical research study is to learn if lirilumab in combination with rituximab can help to control either CLL or Small lymphocytic lymphoma (SLL). The safety of the drug combination will also be studied.

Primary Outcome

Response is defined as complete remission (CR), complete remission with incomplete marrow recovery (CRi) or partial remission (PR) that occurs during the first 6 months of therapy. CR requires the absence of peripheral blood clonal lymphocytes by immunophenotyping, absence of lymphadenopathy, absence of hepatomegaly or splenomegaly, absence of constitutional symptoms and satisfactory blood counts. CRi is Complete remission with incomplete bone marrow recovery. PR, defined as ≥ 50% fall in lympho

Interventions

  • DRUG Rituximab
  • DRUG Lirilumab

Trial Details

FieldValue
Enrollment Target 7 participants
Start Date 2015-06-23
Est. Completion 2019-08-15
Phase Phase 2
M.D. Anderson Cancer Center

2,692 total trials

What the finished NCT02481297 record still lists

NCT02481297 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 7 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (95% lower).

The record links to 0 conditions, and to 2 interventions - of which Rituximab is the first listed.

NCT02481297 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02481297 about?

NCT02481297 is a clinical study titled "Lirilumab With Rituximab for Relapsed, Refractory or High-risk Untreated Chronic Lymphocytic Leukemia (CLL) Patients". The goal of this clinical research study is to learn if lirilumab in combination with rituximab can help to control either CLL or Small lymphocytic lymphoma (SLL). The safety of the drug combination will also be studied.

What is the current status of trial NCT02481297?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 7 participants. The study started on 2015-06-23. Estimated completion is 2019-08-15.

What interventions are being tested in trial NCT02481297?

The interventions under investigation include: Rituximab (DRUG), Lirilumab (DRUG).

Who is sponsoring clinical trial NCT02481297?

This trial is sponsored by M.D. Anderson Cancer Center, which has 2,692 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02481297's enrollment target sits among peer trials

7 1996th of 2000 higher than 5 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02481297, the US trial registry maintained by the National Library of Medicine. NCT02481297 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.