XL092 (Not yet branded)

Other Medications

US Experimental EU Experimental ES Not available Oral 2 Clinical Trials
VEGFR PDGFR multiple tyrosine kinases

Description

XL092 is a multi-kinase inhibitor being developed for the treatment of metastatic colorectal cancer, particularly in patients with microsatellite stable (MSS) tumors. This oral targeted therapy is designed to block multiple signaling pathways involved in tumor growth and angiogenesis. In colorectal cancer, XL092 has been evaluated as both monotherapy and in combination with the immunotherapy agent atezolizumab, positioning it as a potential alternative to regorafenib for advanced disease.

Mechanism of Action

XL092 functions as a multi-targeted tyrosine kinase inhibitor that blocks several key pathways involved in tumor progression and blood vessel formation. The drug targets multiple kinases including VEGFR, PDGFR, and other growth factor receptors that promote cancer cell proliferation and angiogenesis. By simultaneously inhibiting these pathways, XL092 aims to reduce tumor growth while cutting off the blood supply that feeds cancer cells.

Molecular Targets

Side Effects

Fatigue Diarrhea Decreased appetite Nausea Hand-foot skin reaction Hypertension Weight loss Abdominal pain

Not all side effects are listed. Side effects vary by individual. Always consult your oncologist.

Clinical Trials

NCT05425940 Phase 3
Active, not recruiting
Study of XL092 + Atezolizumab vs Regorafenib in Participants With Metastatic Colorectal Cancer
United States, Australia, Belgium, France, Germany, Hong Kong, Hungary, New Zeal
NCT03845166 Phase 1
Active, not recruiting
A Study of XL092 as Single-Agent and Combination Therapy in Subjects With Solid Tumors
United States, Australia, Belgium, Czechia, France, Germany, Italy, Netherlands,