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Spots Global Cancer Trial Database for A Study of Nivolumab by Itself or Nivolumab Combined With Ipilimumab in Patients With Advanced or Metastatic Solid Tumors

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Trial Identification

Brief Title: A Study of Nivolumab by Itself or Nivolumab Combined With Ipilimumab in Patients With Advanced or Metastatic Solid Tumors

Official Title: A Phase 1/2, Open-label Study of Nivolumab Monotherapy or Nivolumab Combined With Ipilimumab in Subjects With Advanced or Metastatic Solid Tumors

Study ID: NCT01928394

Study Description

Brief Summary: To investigate the safety and efficacy of nivolumab as a single agent or in combination with ipilimumab in 6 tumor types - triple-negative breast cancer (TNBC), gastric cancer (GC), pancreatic adenocarcinoma (PC), small cell lung cancer (SCLC), bladder cancer (BC), and ovarian cancer (OC). A combination of nivolumab with ipilimumab and cobimetinib is also investigated in PC.

Detailed Description: All tumor types are now closed for enrollment: Triple Negative Breast Cancer Gastric Cancer Pancreatic Cancer Small Cell Lung Cancer Bladder Cancer Ovarian Cancer

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Local Institution - 0047, Muscle Shoals, Alabama, United States

Local Institution - 0044, Aurora, Colorado, United States

Local Institution - 0015, New Haven, Connecticut, United States

Local Institution - 0046, Gainesville, Florida, United States

Local Institution - 0021, Tampa, Florida, United States

Local Institution - 0001, Atlanta, Georgia, United States

Local Institution - 0004, Baltimore, Maryland, United States

Local Institution - 0005, Boston, Massachusetts, United States

Local Institution - 0043, Boston, Massachusetts, United States

Local Institution - 0049, Omaha, Nebraska, United States

Local Institution - 0045, Mineola, New York, United States

Local Institution - 0006, New York, New York, United States

Local Institution - 0003, Charlotte, North Carolina, United States

Local Institution - 0008, Durham, North Carolina, United States

Local Institution - 0007, Portland, Oregon, United States

Local Institution - 0011, Franklin, Tennessee, United States

Local Institution - 0002, Nashville, Tennessee, United States

Local Institution - 0009, Houston, Texas, United States

Local Institution - 0042, Seattle, Washington, United States

Local Institution - 0038, Toronto, Ontario, Canada

Local Institution - 0039, Copenhagen, , Denmark

Local Institution - 0014, Helsinki, Uusimaa, Finland

Local Institution - 0036, Tampere, , Finland

Local Institution - 0048, Bonn, , Germany

Local Institution - 0026, Frankfurt, , Germany

Local Institution - 0016, Heidelberg, , Germany

Local Institution - 0050, Kassel, , Germany

Local Institution - 0024, Bologna, , Italy

Local Institution - 0019, Milano, , Italy

Local Institution - 0020, Napoli, , Italy

Local Institution - 0032, Padova, , Italy

Local Institution - 0037, Barcelona, , Spain

Local Institution - 0023, Madrid, , Spain

Local Institution - 0017, Madrid, , Spain

Local Institution - 0010, Madrid, , Spain

Local Institution - 0018, London, Greater London, United Kingdom

Local Institution - 0012, Glasgow, Lanarkshire, United Kingdom

Local Institution - 0013, Sutton, Surrey, United Kingdom

Contact Details

Name: Bristol-Myers Squibb

Affiliation: Bristol-Myers Squibb

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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