For Healthcare Professionals

Pan Tumor Rollover Study

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About the study

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

You may be eligible to participate in the study if you meet the following criteria:

INCLUSION CRITERIA

Inclusion Criteria:

  1. Signed Written Informed Consent.
  2. Eligible to receive continued study treatment per the Parent Study, including treatment beyond progression per investigator assessment in the Parent Study.
  3. On treatment hold in the Parent Study following long-lasting response or are eligible for treatment rechallenge as defined in the Parent Study.
  4. WOCBP and male participants who are sexually active must agree to follow instructions for method(s) of contraception as described below and included in the ICF.

EXCLUSION CRITERIA

Exclusion Criteria:

  1. Participant is not eligible for study treatment per the Parent Study eligibility criteria.
  2. Participants not receiving clinical benefit as assessed by the Investigator.
  3. Any clinical adverse event (AE), laboratory abnormality, or intercurrent illness which, in the opinion of the Investigator, indicates that participation in the study is not in the best interest of the participant.
  4. * Other protocol-defined Inclusion/Exclusion Criteria apply

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Study Locations

Enter your ZIP code/Postal code/PIN code to locate study sites near you:

How to Apply


Contact the study center to learn if this study is a good match for you.
Phone iconCall 855-907-3286Email iconEmail Study Center

Study Details


Contition

Cancer

Age

18+

Phase

PHASE2

Participants Needed

1500

Est. Completion Date

Aug 25, 2029

Treatment Type

INTERVENTIONAL


Sponsor

Bristol-Myers Squibb

ClinicalTrials.gov NCT Identifier

NCT03899155

Study Number

CA209-8TT

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