SKL35501 + SKL35502 for Colorectal Cancer
What You Need to Know Before You Apply
What is the purpose of this trial?
This Phase 1, open-label study will evaluate two investigational radiopharmaceuticals in adults with selected advanced or metastatic solid tumors. SKL35502 is an imaging agent used with SPECT scans to identify tumors with neurotensin receptor 1 (NTSR1), a protein found on some cancer cells, and to assess where the agent travels in the body and the radiation dose delivered to tissues. Participants with sufficient SKL35502 tumor uptake may receive SKL35501, a treatment designed to deliver targeted alpha radiation to NTSR1-expressing tumor cells.
Part A will evaluate the safety and imaging performance of SKL35502 and the safety, tolerability, pharmacokinetics, biodistribution, dosimetry, and biologically active dose range of SKL35501, as well as preliminary antitumor activity. Part B will further evaluate selected SKL35501 dose levels, including randomized low- and high-dose groups in participants with colorectal cancer, and will expand evaluation in selected tumor types. The study will also examine relationships among SKL35502 imaging, NTSR1 expression, SKL35501 tumor uptake, and treatment outcomes.
Are You a Good Fit for This Trial?
This trial is for adults with advanced or metastatic solid tumors (like bile duct, pancreas, stomach, colon, esophagus, head and neck, or gallbladder cancers) whose tumors have the NTSR1 protein. Participants must be able to undergo imaging scans and meet general health requirements.Inclusion Criteria
Exclusion Criteria
What Are the Treatments Tested in This Trial?
Interventions
- SKL35501
- SKL35502
Trial Overview
The study tests two new drugs: SKL35502 (an imaging agent used in SPECT scans to find NTSR1-positive tumors) and SKL35501 (a targeted radiation treatment given only if enough tumor uptake is seen on imaging). Different doses of SKL35501 will be studied.
How Is the Trial Designed?
2
Treatment groups
Experimental Treatment
Description: For dose optimization, one cohort with 2 groups (Low Dose SKL35501 group and High Dose SKL35501 group) will be initiated in part B of the study
Description: For dose optimization, one cohort with 2 groups (Low Dose SKL35501 group and High Dose SKL35501 group) will be initiated in part B of the study
Find a Clinic Near You
Who Is Running the Clinical Trial?
SK Life Science, Inc.
Lead Sponsor
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