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

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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.


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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mi
from
Marietta, GA
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mi
from
Boston, MA
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mi
from
Detroit, MI
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mi
from
Villejuif,
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