Phase 1 Study of MLN0264 in Adult Patients With Advanced Gastrointestinal Malignancies Expressing Guanylyl Cyclase C

Completed · Phase 1

Conditions studied: Advanced Gastrointestinal Malignancies

In brief

This is an Open-Label, Multicenter, Dose Escalation, First-in-Human Study of MLN0264 in Adult Patients With Advanced Gastrointestinal Malignancies Expressing Guanylyl Cyclase C.

Key facts

Study ID

NCT01577758

Run by

Millennium Pharmaceuticals, Inc.

People needed

41

Starts

2012-06-01

Expected to finish

2014-02-01

Last updated by the study team

2016-09-07

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Voluntary consent form
• Diagnosis of GI malignancy with a GCC protein expressing tumor
• Male or female patients 18 years or older with measurable disease as defined by Response Evaluation Criteria in Solid Tumors (RECIST)
• Female patients who are post menopausal, surgically sterile, or agree to practice 2 effective methods of contraception or agree to abstain from heterosexual intercourse
• Male patients who agree to practice effective barrier contraception or agree to abstain from heterosexual intercourse
• Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
• Adequate bone marrow, hepatic and renal function as specified in the protocol

You may not qualify if…

• Female patients who are lactating or have a positive serum pregnancy test during the screening period
• Any serious medical or psychiatric illness that could interfere with the completion of treatment
• Major surgery or treatment with investigational drug before the first dose
• Serious infection within 14 days before the first dose of study drug
• Known HIV, inflammatory bowel disease, viral hepatitis or cerebral/meningeal brain metastases
• Patients with cardiovascular conditions specified in protocols
• Patients with history of another primary malignancy not in remission for at least 3 years
• Please note that there are additional inclusion and exclusion criteria. The study center will determine if you meet all of the criteria.
• Site personnel will explain the trial in detail and answer any question you may have if you do qualify for the study. You can then decide whether or not you wish to participate. If you do not qualify for the trial, site personnel will explain the reasons.

Where it is running

• Moffitt Cancer Center — Tampa, Florida, United States

Full record on ClinicalTrials.gov

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