Drug intelligence / Profile preview

SI-B001 + FOLFIRI

Development stage
Unknown
Lead developer
Simcere Zaiming
Modality
Small Molecules
Administration
Intravenous (folfiri), Unknown (SI-B001; Likely Intravenous As Per Trial Norm, But Not Confirmed)
01

Overview

SI-B001 + FOLFIRI is an investigational **combination therapy** under clinical development for advanced or metastatic solid tumors, primarily metastatic colorectal cancer. SI-B001 is a novel agent whose precise molecular characterization is not fully disclosed in public sources yet, but is known to be combined with the FOLFIRI regimen in clinical trials. FOLFIRI is a well-established chemotherapy regimen consisting of folinic acid (leucovorin), fluorouracil (5-FU), and irinotecan, each of which disrupts cancer cell growth through complementary mechanisms. This regimen is administered in cycles and works by: - enhancing 5-FU's binding to its target protein (leucovorin), - blocking DNA synthesis and repair (5-FU), - inhibiting topoisomerase I to prevent cancer cell division (irinotecan)[1][3][7]. The addition of SI-B001 aims to further improve efficacy, though public documentation of SI-B001’s exact mechanism and target is limited. The combination is being studied for efficacy, safety, and tolerability in patients who have failed standard treatments.

02

Targets

DNAEGFR (Epidermal growth factor receptor)ERBB3 (Erb-b2 receptor tyrosine kinase 3)TS (Thymidylate synthase)TOP1 (DNA Topoisomerase I)

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