A Phase 1 Study of MM-141 in Patients With Advanced Solid Tumors
Status: | Completed |
---|---|
Conditions: | Liver Cancer, Cancer |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 8/5/2016 |
Start Date: | November 2012 |
This study is a Phase 1 and pharmacologic open-labeled dose-escalation trial using a "3+3"
design, evaluating MM-141 at varying dose levels and frequencies.
design, evaluating MM-141 at varying dose levels and frequencies.
Inclusion Criteria:
- Advanced malignant solid tumors for which no curative therapy exists that has
recurred or pgrogressed following standard therapy
- Eighteen years of age or above
- Able to understand and sign an informed consent (or have a legal representative who
is able to do so)
- Measurable disease according to RECIST v1.1
- ECOG Performance Score of 0 or 1
- Adequate bone marrow, hepatic, renal and cardiac function
- Willing to abstain from sexual intercourse or to use an effective form of
contraception during the study and for 90 days following the last dose of MM-141
Exclusion Criteria:
- Active infection or fever > 38.5°C during screening visits or on the first scheduled
day of dosing
- Symptomatic CNS disease
- Received other recent antitumor therapy
- Pregnant or breast feeding
We found this trial at
4
sites
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