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NCT01024231 · ClinicalTrials.gov registry record · Phase 1

Dose-escalation Study of Combination BMS-936558 (MDX-1106) and Ipilimumab in Subjects With Unresectable Stage III or Stage IV Malignant Melanoma

A Phase 1 study, sponsored by Bristol-Myers Squibb.

Completed
Registry status
Phase 1
Development phase
127
Enrollment target

NCT01024231: Completed Phase 1 study, sponsored by Bristol-Myers Squibb.

NCT01024231 is a Phase 1 study that has completed, run by Bristol-Myers Squibb. The registered enrollment target is 127 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (112% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01024231, a Phase 1 study, has completed, sponsored by Bristol-Myers Squibb.

COMPLETED
Registry status
Phase 1
Development phase
127 participants
Enrollment target

Study Summary

The purpose of this study is to determine the safety and tolerability of treatment with BMS-936558 (MDX-1106) in combination with Ipilimumab (BMS-734016) when given at the same time or as a sequenced regimen in subjects with unresectable Stage III or Stage IV malignant melanoma (MEL)

Primary Outcome

incidence of all cause and treatment related adverse events

Interventions

  • DRUG Ipilimumab
  • DRUG BMS-936558 (MDX1106-04)

Trial Details

FieldValue
Enrollment Target 127 participants
Start Date 2009-12-14
Est. Completion 2019-04-01
Phase Phase 1
Bristol-Myers Squibb

1,025 total trials

What the finished NCT01024231 record still lists

NCT01024231 is an interventional study that assigns participants to a tested intervention. The registered 127 participants enrollment target is mid-sized for trials with a published cap, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (112% higher).

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

NCT01024231 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01024231 about?

NCT01024231 is a clinical study titled "Dose-escalation Study of Combination BMS-936558 (MDX-1106) and Ipilimumab in Subjects With Unresectable Stage III or Stage IV Malignant Melanoma". The purpose of this study is to determine the safety and tolerability of treatment with BMS-936558 (MDX-1106) in combination with Ipilimumab (BMS-734016) when given at the same time or as a sequenced regimen in subjects with unresectable Stage III or Stage IV malignant melanoma (MEL)

What is the current status of trial NCT01024231?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 127 participants. The study started on 2009-12-14. Estimated completion is 2019-04-01.

What interventions are being tested in trial NCT01024231?

The interventions under investigation include: Ipilimumab (DRUG), BMS-936558 (MDX1106-04) (DRUG).

Who is sponsoring clinical trial NCT01024231?

This trial is sponsored by Bristol-Myers Squibb, which has 1,025 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01024231's enrollment target sits among peer trials

127 459th of 2000 higher than 1,540 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 NCT01024231, the US trial registry maintained by the National Library of Medicine. NCT01024231 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.