Combination Trial of Pimasertib (MSC1936369B) With Temsirolimus

PHASE1TerminatedINTERVENTIONAL
Enrollment

33

Participants

Timeline

Start Date

May 27, 2011

Primary Completion Date

February 23, 2012

Study Completion Date

February 23, 2012

Conditions
Advanced Solid Tumor
Interventions
DRUG

Pimasertib

Pimasertib will be administered in fasted state at a dose of 45 mg once daily orally on Days 1 to 15. Treatment will be continued until disease progression, intolerable toxicity, investigator's decision to discontinue treatment, or withdrawal of consent.

DRUG

Pimasertib

Pimasertib will be administered in fasted state at a dose of 75 mg once daily orally on Days 1 to 15. Treatment will be continued until disease progression, intolerable toxicity, investigator's decision to discontinue treatment, or withdrawal of consent.

DRUG

Temsirolimus

Temsirolimus will be administered at a dose of 12.5 mg as intravenous infusion over a 30-60 minute period once a week within 10 minutes after administration of pimasertib on Days 1, 8 and 15 in successive 21-day cycles. Treatment will be continued until disease progression, intolerable toxicity, investigator's decision to discontinue treatment, or withdrawal of consent.

DRUG

Temsirolimus

Temsirolimus will be administered at a dose of 25 mg as intravenous infusion over a 30-60 minute period once a week within 10 minutes after administration of pimasertib on Days 1, 8 and 15 in successive 21-day cycles. Treatment will be continued until disease progression, intolerable toxicity, investigator's decision to discontinue treatment, or withdrawal of consent.

Trial Locations (3)

Unknown

Cedars-Sinai Medical Center, Los Angeles

For Recruiting Locations in the US contact US Medical Information in, Rockland

The University of Texas MD Anderson Cancer Center, Houston

Sponsors

Lead Sponsor

All Listed Sponsors
lead

EMD Serono

INDUSTRY

NCT01378377 - Combination Trial of Pimasertib (MSC1936369B) With Temsirolimus | Biotech Hunter | Biotech Hunter