Drug intelligence / Profile preview

SM08502 + FOLFIRI + panitumumab

Development stage
Unknown
Lead developer
Sumitomo Pharma America
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Classical Binding Small Molecules → Small Molecules, Covalent Small Molecules → Small Molecules, Nucleic Acid-Directed Small Molecules → Small Molecules
Administration
Intravenous
01

Overview

**SM08502 + FOLFIRI + panitumumab** is an investigational combination regimen under clinical evaluation primarily for advanced or metastatic colorectal cancer. \n- **SM08502** is a novel, investigational small molecule inhibitor targeting aberrant Wnt signaling, a pathway commonly implicated in colorectal and other cancers. \n- **FOLFIRI** is a standard chemotherapy regimen, comprising folinic acid (leucovorin), fluorouracil (5-FU), and irinotecan. These agents disrupt DNA synthesis and cell division, primarily through inhibition of thymidylate synthase (by 5-FU), DNA damage incorporation (5-FU), and inhibition of topoisomerase I (irinotecan)[1][2][3][4][5]. \n- **Panitumumab** is a monoclonal antibody targeting the epidermal growth factor receptor (EGFR), blocking the signaling pathways that promote cancer cell proliferation and survival. \nThe regimen combines cytotoxic, targeted therapy, and pathway inhibition to enhance antitumor activity, particularly in patients with metastatic colorectal cancer who may have failed prior therapies. \nClinical trials are ongoing.

Other names
SM08502 + FOLFIRI + panitumumab
02

Targets

CLK1 (CDC-like kinase 1)DYRK1B (Dual specificity tyrosine-phosphorylation-regulated kinase 1B)CLK3 (CDC-like kinase 3)CLK4TS (Thymidylate synthase)TOP1 (DNA Topoisomerase I)CDK1 (Cyclin-dependent kinase 1)EGFR T790M (Epidermal growth factor receptor T790M mutant)CLK2 (CDC-like kinase 2)DYRK1A (Dual-specificity tyrosine-phosphorylation-regulated kinase 1A)

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