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NCT02966730 · ClinicalTrials.gov registry record · Early Phase 1

Ibrutinib for Patients With Follicular Lymphoma Without Complete Response to Initial Chemoimmunotherapy

A Early Phase 1 study, sponsored by Memorial Sloan Kettering Cancer Center.

Terminated
Registry status
Early Phase 1
Development phase
2
Enrollment target

NCT02966730: Clinical Trial Early Phase 1 study, sponsored by Memorial Sloan Kettering Cancer Center.

NCT02966730 is a Early Phase 1 study that was terminated before completion, run by Memorial Sloan Kettering Cancer Center. The registered enrollment target is 2 participants, below the 53-participant average among 2,764 other Early Phase 1 trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02966730, a Early Phase 1 study, was terminated before completion, sponsored by Memorial Sloan Kettering Cancer Center.

TERMINATED
Registry status
Early Phase 1
Development phase
2 participants
Enrollment target

Study Summary

The purpose of this study is to find out how successful ibrutinib is at putting follicular lymphoma into full remission. In this study, remission will be determined by achieving a normal PET scan after treatment. A PET scan is an imaging test that looks for active lymphoma. People who don't have a complete remission on PET after their first treatment are at high risk for having their lymphoma return. This study will investigate if ibrutinib will help participants achieve a complete remission without giving additional chemotherapy. The study will also investigate any possible side effects of the study drug ibrutinib.

Primary Outcome

The primary objective is to determine the rate of conversion from FDG-PET positive to negative at 12 months from the start of ibrutinib in patients receiving at least 6 months of Ibrutinib consolidation therapy for follicular lymphoma achieving at least a PR but remaining FDG-PET positive after first line chemoimmunotherapy.

Interventions

  • DRUG Ibrutinib

Trial Details

FieldValue
Enrollment Target 2 participants
Start Date 2016-11
Est. Completion 2019-06-20
Phase Early Phase 1
Memorial Sloan Kettering Cancer Center

1,884 total trials

Why NCT02966730 stopped before completion

NCT02966730 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 2 participants, a relatively small participant target, below the 53-participant average among 2,764 other Early Phase 1 trials with a reported enrollment target (96% lower).

The record links to 0 conditions, and to 1 intervention - of which Ibrutinib is the first listed.

NCT02966730 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02966730 about?

NCT02966730 is a clinical study titled "Ibrutinib for Patients With Follicular Lymphoma Without Complete Response to Initial Chemoimmunotherapy". The purpose of this study is to find out how successful ibrutinib is at putting follicular lymphoma into full remission. In this study, remission will be determined by achieving a normal PET scan after treatment. A PET scan is an imaging test that looks for active lymphoma. People who don't have a c...

What is the current status of trial NCT02966730?

This trial is currently terminated. It is a Early Phase 1 study. The enrollment target is 2 participants. The study started on 2016-11. Estimated completion is 2019-06-20.

What interventions are being tested in trial NCT02966730?

The interventions under investigation include: Ibrutinib (DRUG).

Who is sponsoring clinical trial NCT02966730?

This trial is sponsored by Memorial Sloan Kettering Cancer Center, which has 1,884 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02966730's enrollment target sits among peer trials

2 1973rd of 2000 higher than 16 of 2,000 other Early Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Early Phase 1 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 NCT02966730, the US trial registry maintained by the National Library of Medicine. NCT02966730 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.