MLN0264 in Previously Treated Asian Participants With Advanced Gastrointestinal Carcinoma or Metastatic or Recurrent Gastric or Gastroesophageal Junction Adenocarcinoma Expressing Guanylyl Cyclase C

• Status: Terminated
• Trial end date: 2015-10-01
• Target enrollment: 0
• Participant gender: All

Summary

The purpose of this study is to evaluate the effects of MLN0264 in previously treated Asian participants with Advanced Gastrointestinal (GI) Carcinoma (Phase 1) or Metastatic or Recurrent Gastric or Gastroesophageal Junction Adenocarcinoma (Phase 2) Expressing Guanylyl Cyclase C (GCC).

• Phase: Phase 1
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Millennium Pharmaceuticals, Inc.

Criteria

Inclusion Criteria:

• Has Diagnosis of GI carcinoma with Immunohistochemistry/ Immunohistochemical (IHC) evidence of expression of GCC protein (H-score of 10 or greater), for which standard treatment is no longer effective or does not offer curative or life-prolonging potential.

• Has completed prior chemotherapy, immunotherapy or radiation therapy at least 4 weeks prior to enrollment (except for Avastin [bevacizumab] for which at least 8 weeks from its last administration should elapse prior to enrollment).

• Histologically confirmed metastatic or advanced inoperable adenocarcinoma of the stomach or gastroesophageal junction with IHC evidence of expression of GCC indicated by an H-score of 10 or greater.

• Has completed prior chemotherapy, immunotherapy or radiation therapy at least 4 weeks prior to enrollment.

• Has measurable disease as defined by Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1 guidelines.

• Has Eastern Cooperative Oncology Group performance status of 0 or 1 (within 14 days prior to enrollment).

• Females must be 1-year postmenopausal, or even if surgically sterile, agree to use other acceptable forms of birth control.

• Has adequate organ and hematological function.

• Has resolution of all toxic effects of prior treatments except alopecia to Grade 0 or 1 by National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) version 4.03

Exclusion Criteria:

• Has Concurrent treatment or treatment within 4 weeks of study entry with any other investigational agent.

• Female participants who are in the lactation period, even if they discontinue breastfeeding, or have a positive pregnancy test during the Screening period.

• Has uncontrolled, clinically significant, symptomatic cardiovascular disease within 6 months prior to enrollment.

• Has treatment with any medication that has a clinically relevant potential risk of prolonging the QT interval or inducing Torsades de Pointes that cannot be discontinued or switched to a different medication prior to starting study drug.

• Participants with electrocardiogram (ECG) abnormalities considered by the investigator to be clinically -significant, or repeated baseline prolongation of the rate-corrected QT interval millisecond (msec) of electrocardiograph (QTc).

• Ongoing or clinically significant active infection.

• Has signs of peripheral neuropathy.

• Concomitant chemotherapy, hormonal therapy, immunotherapy, or any other form of cancer treatment.

• Use of strong cytochrome P450 (CYP) 3A4 inhibitors within 2 weeks before the first dose of study drug.

• Has any preexisting medical condition of sufficient severity to prevent full compliance with the study.

• Has past or concurrent history of neoplasm other than GI carcinoma (phase 1) or gastric adenocarcinoma (phase 2), except for curatively treated nonmelanoma skin cancer or in situ carcinoma of the cervix uteri.

• Known diagnosis of human immunodeficiency virus (HIV) infection.

• Has asymptomatic brain metastases.

• Has an alcohol or substance abuse disorder.

• Has positive test for hepatitis B surface antigen.

• History of hypersensitivity to any ingredient of MLN0264.