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Spots Global Cancer Trial Database for A Safety and Efficacy Study of ZW25 (Zanidatamab) Plus Combination Chemotherapy in HER2-expressing Gastrointestinal Cancers, Including Gastroesophageal Adenocarcinoma, Biliary Tract Cancer, and Colorectal Cancer

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Trial Identification

Brief Title: A Safety and Efficacy Study of ZW25 (Zanidatamab) Plus Combination Chemotherapy in HER2-expressing Gastrointestinal Cancers, Including Gastroesophageal Adenocarcinoma, Biliary Tract Cancer, and Colorectal Cancer

Official Title: Phase 2 Study of ZW25 Plus First-line Combination Chemotherapy in HER2-Expressing Gastrointestinal (GI) Cancers, Including Gastroesophageal Adenocarcinoma (GEA), Biliary Tract Cancer (BTC), and Colorectal Cancer (CRC)

Study ID: NCT03929666

Study Description

Brief Summary: This is a multicenter, global, Phase 2, open-label, 2-part, first-line study to investigate the safety, tolerability, and anti-tumor activity of ZW25 (zanidatamab) plus standard first-line combination chemotherapy regimens for selected gastrointestinal (GI) cancers. Eligible patients include those with unresectable, locally advanced, recurrent or metastatic HER2-expressing gastroesophageal adenocarcinoma (GEA), biliary tract cancer (BTC), or colorectal cancer (CRC).

Detailed Description: Part 1 of the study will first evaluate the safety and tolerability of ZW25 plus standard first-line combination chemotherapy (XELOX, FP, or mFOLFOX6 for GEA; mFOLFOX6 with or without bevacizumab for CRC; and CisGem for BTC) and will confirm the recommended dosage (RD) of ZW25 when administered in combination with each of these multi-agent chemotherapy regimens. Then, Part 2 of the study will evaluate the anti-tumor activity of ZW25 plus combination chemotherapy in HER2-expressing GEA, BTC, and CRC.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

USC/Norris Comprehensive Cancer Center, Los Angeles, California, United States

H. Lee Moffitt Cancer Center, Tampa, Florida, United States

University of Chicago, Chicago, Illinois, United States

Cancer and Hematology Centers of Western Michigan, Kalamazoo, Michigan, United States

Nebraska Methodist Hospital, Omaha, Nebraska, United States

Memorial Sloan Kettering Cancer Center, New York, New York, United States

Fox Chase Cancer Center, Philadelphia, Pennsylvania, United States

Sarah Cannon Research Institute, Nashville, Tennessee, United States

MD Anderson Cancer Center, Houston, Texas, United States

Virginia Mason Medical Center, Seattle, Washington, United States

Princess Margaret Cancer Center, Toronto, Ontario, Canada

Centro de Estudios Clinicos SAGA SpA, Santiago, , Chile

Icegclinic Research & Care, Santiago, , Chile

Meditek Ltda, Santiago, , Chile

CECIM Biocinetic, Santiago, , Chile

Seoul National University Bundang Hospital, Seongnam-si, Gyeonggi-do, Korea, Republic of

Pusan National University, Busan, , Korea, Republic of

Korea University Anam Hospital, Seoul, , Korea, Republic of

Seoul National University Hospital, Seoul, , Korea, Republic of

Severance Hospital, Seoul, , Korea, Republic of

Asan Medical Center, Seoul, , Korea, Republic of

Contact Details

Name: Phillip Garfin, MD, PhD

Affiliation: Jazz Pharmaceuticals

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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