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NCT02406742 · ClinicalTrials.gov registry record · Phase 1

A Phase 1/2, Open-label, Dose Finding Study to Evaluate CC-122 in Combination With Ibrutinib and Obinutuzumab in Subjects With Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma

A Phase 1 study, sponsored by Celgene.

Completed
Registry status
Phase 1
Development phase
47
Enrollment target

NCT02406742: Completed Phase 1 study, sponsored by Celgene.

NCT02406742 is a Phase 1 study that has completed, run by Celgene. The registered enrollment target is 47 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (22% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02406742, a Phase 1 study, has completed, sponsored by Celgene.

COMPLETED
Registry status
Phase 1
Development phase
47 participants
Enrollment target

Study Summary

Safety, pharmacokinetics, and preliminary efficacy of CC-122 alone and in combination with ibrutinib and obinuzutumab. CC-122 has multiple activities, including immune modulation of several immune cell subsets and antiproliferative activity in CLL. CC-122 has also been shown to have a tolerable safety profile with some preliminary signs of efficacy with early human experience.

Primary Outcome

Number and severity of adverse events using the NCI CTCAE criteria (version 4.03), including DLTs

Interventions

  • DRUG Obinutuzumab
  • DRUG Ibrutinib
  • DRUG CC-122

Trial Details

FieldValue
Enrollment Target 47 participants
Start Date 2015-07-27
Est. Completion 2020-07-07
Phase Phase 1
Celgene

308 total trials

What the finished NCT02406742 record still lists

NCT02406742 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 47 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (22% lower).

The record links to 0 conditions, and to 3 interventions - of which Obinutuzumab is the first listed.

NCT02406742 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02406742 about?

NCT02406742 is a clinical study titled "A Phase 1/2, Open-label, Dose Finding Study to Evaluate CC-122 in Combination With Ibrutinib and Obinutuzumab in Subjects With Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma". Safety, pharmacokinetics, and preliminary efficacy of CC-122 alone and in combination with ibrutinib and obinuzutumab. CC-122 has multiple activities, including immune modulation of several immune cell subsets and antiproliferative activity in CLL. CC-122 has also been shown to have a tolerable saf...

What is the current status of trial NCT02406742?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 47 participants. The study started on 2015-07-27. Estimated completion is 2020-07-07.

What interventions are being tested in trial NCT02406742?

The interventions under investigation include: Obinutuzumab (DRUG), Ibrutinib (DRUG), CC-122 (DRUG).

Who is sponsoring clinical trial NCT02406742?

This trial is sponsored by Celgene, which has 308 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02406742's enrollment target sits among peer trials

47 1053rd of 2000 higher than 943 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other 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 NCT02406742, the US trial registry maintained by the National Library of Medicine. NCT02406742 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.