Study of Oral Ceritinib in Patients With ALK and ROS1 Activated Gastrointestinal Malignancies

PHASE2TerminatedINTERVENTIONAL
Enrollment

4

Participants

Timeline

Start Date

December 31, 2015

Primary Completion Date

March 29, 2018

Study Completion Date

March 29, 2018

Conditions
Colorectal AdenocarcinomaCholangiocarcinomaPancreatic AdenocarcinomaHepatocellular AdenocarcinomaGastric AdenocarcinomaEsophageal Adenocarcinoma
Interventions
DRUG

ceritinib

Treatment with ceritinib will continue until patient experiences unacceptable toxicity that precludes further treatment, discontinues treatment at the discretion of the investigator or patient, starts a new anticancer therapy and/or dies.

Trial Locations (6)

10016

Laura & Isaac Permutter Cancer Center at NYU Langone, New York

43210

The Ohio State University, James Cancer Hospital, Columbus

80045

University of Colorado Cancer Center, Aurora

90033

USC/Norris Comprehensive Cancer Center, Los Angeles

98104

Swedish Cancer Institute, Seattle

06520

Yale University, Yale Cancer Center, New Haven

Sponsors

Lead Sponsor

Collaborators (1)

All Listed Sponsors
collaborator

University of Colorado, Denver

OTHER

collaborator

Novartis

INDUSTRY

lead

Criterium, Inc.

INDUSTRY

NCT02638909 - Study of Oral Ceritinib in Patients With ALK and ROS1 Activated Gastrointestinal Malignancies | Biotech Hunter | Biotech Hunter