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Clinical Trials/EUCTR2013-002844-10-GB
EUCTR2013-002844-10-GB
Active, not recruiting
Phase 1

A Phase 1/2, Open-label Study of Nivolumab Monotherapy or Nivolumab combined with Ipilimumab in Subjects with Advanced or Metastatic Solid Tumors - CheckMate 032:CHECKpoint pathway and nivoluMAb clinical Trial Evaluation 032

Bristol-Myers Squibb International Corporation0 sites1,620 target enrollmentOctober 2, 2013

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Advanced or metastatic solid tumors: 1) Triple Negative Breast Cancer (TNBC) 2) Gastric Cancer (GC) 3) Pancreatic Cancer (PC) 4) Small Cell Lung Cancer (SCLC). 5) Bladder Cancer (BC) 6) Ovarian Cancer (OC)
Sponsor
Bristol-Myers Squibb International Corporation
Enrollment
1620
Status
Active, not recruiting
Last Updated
6 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
October 2, 2013
End Date
TBD
Last Updated
6 years ago
Study Type
Interventional clinical trial of medicinal product

Investigators

Eligibility Criteria

Inclusion Criteria

  • \- Subjects with histologically confirmed locally advanced or metastatic disease of the following tumor types:
  • \- Triple Negative Breast Cancer
  • \- Gastric Cancer
  • \- Pancreatic Cancer
  • \- Small Cell Lung Cancer
  • \- Ovarian Carcinoma
  • \- Bladder Cancer
  • \- Subjects must have measurable disease
  • \- ECOG of 0 or 1\.
  • Are the trial subjects under 18? no

Exclusion Criteria

  • Active brain metastases or leptomeningeal metastases.
  • Subjects with active, known or suspected autoimmune disease.
  • Subjects with a condition requiring systemic treatment with either corticosteroids (\> 10 mg daily prednisone equivalents) or other immunosuppressive medications within 14 days of treatment.
  • Prior therapy with experimental anti\-tumor vaccines; any T cell co\-stimulation or checkpoint pathways, such as anti\-PD\-1, anti\-PD\-L1, anti\-PD\-L2, anti\-CD137, or anti\-CTLA\-4 antibody, including ipilimumab; or other medicines specifically targeting T cell is also prohibited.

Outcomes

Primary Outcomes

Not specified

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