University of Chicago Medicine Comprehensive Cancer Center
Chicago, Illinois, 60637, United States
Location status: Recruiting
NCT Number: NCT06669572
The purpose of this study is to gather information on the safety and effectiveness of lenvatinib combined with pembrolizumab in anal/rectal cancer that has spread to other parts of the body and will not respond to standard care.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Phase 2
Chicago, Illinois, 60637, United States
Location status: Recruiting
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Pembrolizumab 200 mg will be administered as a 30 minute IV infusion every 3 weeks.
Pembrolizumab will be given for a maximum of 2 years (total 35 cycles) with dosing every 3 weeks.
Lenvatinib will be taken once daily, with or without food, at the same time each day.
Time frame: End of treatment up to 2 years
Number of participants who achieve a complete or partial response based on Response Evaluation Criteria In Solid Tumors (RECIST) 1.1.
Time frame: End of treatment up to 2 years
To evaluate the efficacy of combination treatment of lenvatinib plus pembrolizumab, by disease control rate (DCR), in patients with unresectable locally advanced and/or metastatic anorectal squamous cell carcinoma progressed on first-line chemotherapy.
Time frame: 2 years after end of treatment
To evaluate the efficacy of combination treatment of lenvatinib plus pembrolizumab, by progression free survival (PFS), in patients with unresectable locally advanced and/or metastatic anorectal squamous cell carcinoma progressed on first-line chemotherapy.
Time frame: 2 years after end of treatment
To evaluate the efficacy of combination treatment of lenvatinib plus pembrolizumab, overall survival (OS), in patients with unresectable locally advanced and/or metastatic anorectal squamous cell carcinoma progressed on first-line chemotherapy.
Time frame: End of treatment up to 2 years
Percentage of subjects with treatment emergent grade 3-4 toxicities, as defined by the NCI Common Terminology Criteria for Adverse Events (NCI CTCAE) v5.
Contact information is provided by the study sponsor or research team.
University of Chicago
Other
A Phase II, Multi-center, Single Arm Trial of Lenvatinib Plus Pembrolizumab in Patients With Unresectable Locally Advanced and/or Metastatic Anorectal Squamous Cell Carcinoma (ASCC) After Progression on First Line Chemotherapy.
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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