Sitravatinib and Nivolumab in Urothelial Carcinoma Study
Status: | Recruiting |
---|---|
Conditions: | Prostate Cancer |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 3/23/2019 |
Start Date: | September 11, 2018 |
End Date: | September 30, 2020 |
Contact: | Mirati Therapeutics Study Locator Services |
Email: | Mirati516003@mirati.com |
Phone: | 1-844-893-5530 (toll free) |
A Phase 2 Study of Sitravatinib in Combination With Nivolumab in Patients With Advanced or Metastatic Urothelial Carcinoma
The study will evaluate the clinical activity of nivolumab in combination with the
investigational agent sitravatinib in patients with advanced or metastatic urothelial
carcinoma.
investigational agent sitravatinib in patients with advanced or metastatic urothelial
carcinoma.
Sitravatinib is an orally-available, potent small molecule inhibitor of a closely related
spectrum of receptor tyrosine kinases (RTKs) including MET, Axl, MERTK, VEGFR family, PDGFR
family, KIT, FLT3, Trk family, RET, DDR2 and selected Eph family members. Nivolumab is a
human IgG monoclonal antibody that binds to the programmed cell death-1(PD-1) receptor and
blocks its interaction with programmed cell death ligand-1 (PD-L1) and PD-L2, releasing PD-1
pathway-mediated inhibition of the immune response including anti-tumor immune response.
Combining an immunotherapeutic PD-L1 checkpoint inhibitor with an agent that has both immune
modulatory and antitumor properties could enhance the antitumor efficacy observed with either
agent alone. Sitravatinib selectively inhibits key molecular and cellular pathways strongly
implicated in checkpoint inhibitor resistance and therefore represents a rational strategy to
enhance or restore anti-tumor immunity when combined with nivolumab, a checkpoint inhibitor
therapy.
spectrum of receptor tyrosine kinases (RTKs) including MET, Axl, MERTK, VEGFR family, PDGFR
family, KIT, FLT3, Trk family, RET, DDR2 and selected Eph family members. Nivolumab is a
human IgG monoclonal antibody that binds to the programmed cell death-1(PD-1) receptor and
blocks its interaction with programmed cell death ligand-1 (PD-L1) and PD-L2, releasing PD-1
pathway-mediated inhibition of the immune response including anti-tumor immune response.
Combining an immunotherapeutic PD-L1 checkpoint inhibitor with an agent that has both immune
modulatory and antitumor properties could enhance the antitumor efficacy observed with either
agent alone. Sitravatinib selectively inhibits key molecular and cellular pathways strongly
implicated in checkpoint inhibitor resistance and therefore represents a rational strategy to
enhance or restore anti-tumor immunity when combined with nivolumab, a checkpoint inhibitor
therapy.
Inclusion Criteria:
- Diagnosis of urothelial carcinoma
- Most recent treatment must have included a checkpoint inhibitor
- Adequate bone marrow and organ function
Exclusion Criteria:
- Uncontrolled tumor in the brain
- Unacceptable toxicity with prior checkpoint inhibitor
- Impaired heart function
We found this trial at
17
sites
Ohio State University The Ohio State University’s main Columbus campus is one of America’s largest...
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University of Chicago One of the world's premier academic and research institutions, the University of...
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9280 W. Sunset Road
Suite 100
Las Vegas, Nevada 89148
Las Vegas, Nevada 89148
702.952.1251
Comprehensive Cancer Centers of Nevada Comprehensive Cancer Centers of Nevada (CCCN) is the award-winning multidisciplinary...
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