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NCT02323906 · ClinicalTrials.gov registry record · Phase 1

Safety and Efficacy Study of CC-122 Combined With Sorafenib for Primary Liver Cancer

A Phase 1 study, sponsored by Celgene.

Terminated
Registry status
Phase 1
Development phase
12
Enrollment target

NCT02323906: Clinical Trial Phase 1 study, sponsored by Celgene.

NCT02323906 is a Phase 1 study that was terminated before completion, run by Celgene. The registered enrollment target is 12 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (80% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02323906, a Phase 1 study, was terminated before completion, sponsored by Celgene.

TERMINATED
Registry status
Phase 1
Development phase
12 participants
Enrollment target

Study Summary

CC-122-HCC-001 is a Phase 1b dose escalation and expansion clinical study of CC-122 in combination with sorafenib for subjects with unresectable HCC who have received no prior systemic therapy for HCC. The dose escalation phase of the study will explore several dose levels of CC-122 in combination with sorafenib, followed by an expansion part of the study using the optimal combination dose regimen.

Primary Outcome

Number of Participants with Adverse Events

Interventions

  • DRUG Sorafenib
  • DRUG CC-122

Trial Details

FieldValue
Enrollment Target 12 participants
Start Date 2015-01-16
Est. Completion 2016-12-21
Phase Phase 1
Celgene

308 total trials

Why NCT02323906 stopped before completion

NCT02323906 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 12 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (80% lower).

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

NCT02323906 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02323906 about?

NCT02323906 is a clinical study titled "Safety and Efficacy Study of CC-122 Combined With Sorafenib for Primary Liver Cancer". CC-122-HCC-001 is a Phase 1b dose escalation and expansion clinical study of CC-122 in combination with sorafenib for subjects with unresectable HCC who have received no prior systemic therapy for HCC. The dose escalation phase of the study will explore several dose levels of CC-122 in combination w...

What is the current status of trial NCT02323906?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 12 participants. The study started on 2015-01-16. Estimated completion is 2016-12-21.

What interventions are being tested in trial NCT02323906?

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

Who is sponsoring clinical trial NCT02323906?

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

How this trial's enrollment target compares

Where NCT02323906's enrollment target sits among peer trials

12 1852nd of 2000 higher than 90 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 NCT02323906, the US trial registry maintained by the National Library of Medicine. NCT02323906 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.