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Search / Trial NCT01585987

An Efficacy Study in Gastric and Gastroesophageal Junction Cancer Comparing Ipilimumab Versus Standard of Care Immediately Following First Line Chemotherapy

Launched by BRISTOL-MYERS SQUIBB · Apr 25, 2012

Trial Information

Current as of June 09, 2025

Completed

Keywords

ClinConnect Summary

No description provided

Gender

ALL

Eligibility criteria

  • For more information regarding BMS clinical trial participation, please visit www.BMSStudyConnect.com.
  • Key Inclusion Criteria:
  • Histologically confirmed, unresectable locally advanced or metastatic adenocarcinoma of the gastric and gastro-esophageal junction
  • Received first-line chemotherapy using fluoropyrimidine and platinum combination without disease progression
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
  • Measurable disease by modified WHO criteria (unless complete response from previous chemotherapy)
  • Key Exclusion Criteria:
  • Known Human Epidermal growth factor Receptor2 (HER2) positive status
  • Radiological evidence of brain metastases
  • History of severe autoimmune or immune mediated disease requiring prolonged immunosuppressive treatment
  • Inadequate hematologic, renal and hepatic function

About Bristol Myers Squibb

Bristol-Myers Squibb (BMS) is a global biopharmaceutical company dedicated to discovering, developing, and delivering innovative medicines that help patients prevail over serious diseases. With a robust portfolio of products across multiple therapeutic areas, including oncology, immunology, cardiovascular, and fibrotic diseases, BMS emphasizes cutting-edge research and a commitment to advancing medical science through clinical trials. The company is driven by a mission to provide transformative therapies, leveraging collaboration and scientific expertise to address unmet medical needs and improve patient outcomes worldwide.

Locations

New York, New York, United States

New York, New York, United States

Miami Beach, Florida, United States

Taipei, , Taiwan

Hong Kong, , Hong Kong

Houston, Texas, United States

Padova, , Italy

New York, New York, United States

Nice Cedex 03, , France

Mainz, , Germany

Roma, , Italy

Rennes, , France

Krakow, , Poland

Toulouse Cedex 09, , France

Singapore, , Singapore

Madrid, , Spain

Montpellier Cedex, , France

Olsztyn, , Poland

Firenze, , Italy

Pisa, , Italy

Milano, , Italy

Osaka Sayama Shi, Osaka, Japan

Nagoya, Aichi, Japan

Moscow, , Russian Federation

Lodz, , Poland

Gyeonggi Do, , Korea, Republic Of

Seoul, , Korea, Republic Of

Barcelona, , Spain

Saku Shi, Nagano, Japan

Kitaadachi Gun, Saitama, Japan

Katowice, Ochojec, Poland

Patients applied

0 patients applied

Trial Officials

Bristol-Myers Squibb

Study Director

Bristol-Myers Squibb

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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