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NCT02869789 · ClinicalTrials.gov registry record · Phase 4

An Investigational Immuno-therapy Study for Safety of Nivolumab in Combination With Ipilimumab to Treat Advanced Cancers

A Phase 4 study, sponsored by Bristol-Myers Squibb.

Completed
Registry status
Phase 4
Development phase
1,041
Enrollment target

NCT02869789: Completed Phase 4 study, sponsored by Bristol-Myers Squibb.

NCT02869789 is a Phase 4 study that has completed, run by Bristol-Myers Squibb. The registered enrollment target is 1,041 participants, above the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (101% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02869789, a Phase 4 study, has completed, sponsored by Bristol-Myers Squibb.

COMPLETED
Registry status
Phase 4
Development phase
1,041 participants
Enrollment target

Study Summary

A study to evaluate the safety of Nivolumab given in combination with Ipilimumab in patients with advanced cancers. The initial group will enroll patients with newly diagnosed Stage 4 or non-small cell lung cancer that has come back.

Primary Outcome

Drug related AEs are those events with relationship to study drug. If the relationship to study drug is missing, the AE will be considered as drug-related. The select AEs of interest are the following: Pulmonary, Renal, Gastrointestinal, Hepatic, Skin, Endocrine, and hypersensitivity/infusion reaction events. AEs are reported using the National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) version 4. Grade 3= Prolonged severe reaction Grade 4= Life threatening Gr

Interventions

  • DRUG Nivolumab in combination with Ipilimumab

Trial Details

FieldValue
Enrollment Target 1,041 participants
Start Date 2016-10-05
Est. Completion 2022-05-13
Phase Phase 4
Bristol-Myers Squibb

1,025 total trials

What the finished NCT02869789 record still lists

NCT02869789 is an interventional study that assigns participants to a tested intervention. Its 1,041 participants enrollment target places it among the larger protocols in the corpus, above the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (101% higher).

The record links to 0 conditions, and to 1 intervention - of which Nivolumab in combination with Ipilimumab is the first listed.

NCT02869789 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02869789 about?

NCT02869789 is a clinical study titled "An Investigational Immuno-therapy Study for Safety of Nivolumab in Combination With Ipilimumab to Treat Advanced Cancers". A study to evaluate the safety of Nivolumab given in combination with Ipilimumab in patients with advanced cancers. The initial group will enroll patients with newly diagnosed Stage 4 or non-small cell lung cancer that has come back.

What is the current status of trial NCT02869789?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 1,041 participants. The study started on 2016-10-05. Estimated completion is 2022-05-13.

What interventions are being tested in trial NCT02869789?

The interventions under investigation include: Nivolumab in combination with Ipilimumab (DRUG).

Who is sponsoring clinical trial NCT02869789?

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 NCT02869789's enrollment target sits among peer trials

1,041 66th of 2000 higher than 1,935 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 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 NCT02869789, the US trial registry maintained by the National Library of Medicine. NCT02869789 (large enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.