Nivolumab Monotherapy for Various Tumor Types

Pan Tumor Rollover Study

Recruiting Phase 2 Interventional Study
Cancer
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 2
Study type
Interventional
Purpose
Treatment
Participants needed
1,500 (estimated)
Sponsor
Bristol-Myers Squibb · Industry
Who this trial is looking for

This trial is looking for patients with cancer who have had a good response to previous treatments. Participants will continue receiving nivolumab alone or in combination with other cancer therapies to study long-term safety.

Are You a Good Fit for This Trial?

You may be able to join if

  • I have signed a consent form.
  • I am eligible for continued treatment based on my previous study results.
  • I am on hold for treatment after a long-lasting response.
  • I agree to use contraception if I am a sexually active woman or man.

You may not be able to join if

  • I do not meet the eligibility criteria from my previous study.
  • I am not benefiting from the current treatment as assessed by my doctor.
  • I have an adverse event or illness that makes participation unsafe.
  • Other criteria in the study rules out my participation.

Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.

Think this trial could be right for you?

Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.

Check Your Eligibility
About This Trial

Main Objective of this study is to examine long-term safety of nivolumab monotherapy including combinations and other cancer therapies in various tumor types.

Trial Locations
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Eligibility Criteria
Inclusion Criteria * Signed Written Informed Consent. * Eligible to receive continued study treatment per the Parent Study, including treatment beyond progression per investigator assessment in the Parent Study. * On treatment hold in the Parent Study following long-lasting response or are eligible…
Contacts

BMS Clinical Trials Contact Center www.BMSClinicalTrials.com

855-907-3286

Clinical.Trials@bms.com

CONTACT

First line of the email MUST contain NCT # and Site #.

CONTACT