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Synonyms: ABL001 | CTX-009 | CTX009
Compound class:
Antibody
Comment: Tovecimig (CTX-009; formerly ABL001) is a bispecific monoclonal antibody that simultaneously blocks the signalling pathways that are activated by the delta-like ligand-4 (DLL4; Notch signaling) and vascular endothelial growth factor A (VEGF-A) [4]. The VEGF-A binding heavy chains of tovecimig are derived from the established anti-VEGF-A biologic bevacizumab. Two single chain variable fragments (scFv) that bind to human DLL4 are linked to the C-termini of the anti-VEGF-A heavy chains [1].
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| No information available. |
Summary of Clinical Use ![]() |
| Tovecimig (CTX-009) was progressed as a clinical candidate for the treatment of advanced/metastatic solid tumours. The FDA granted orphan drug designation in Aprl 2026, for the treatment of biliary tract cancer [3]. |
| Clinical Trials | |||||
| Clinical Trial ID | Title | Type | Source | Comment | References |
| NCT06548412 | CTX-009 With Gemcitabine, Cisplatin, and Durvalumab as First-line Therapy in Patients With Unresectable or Metastatic Biliary Tract Cancers | Phase 1/Phase 2 Interventional | M.D. Anderson Cancer Center | ||
| NCT07392957 | Safety and Efficacy of CTX-009 With or Without CTX-471 for Recurrent Glioblastoma | Phase 1/Phase 2 Interventional | Washington University School of Medicine | ||
| NCT05506943 | A Study of CTX-009 in Combination With Paclitaxel in Adult Patients With Unresectable Advanced, Metastatic or Recurrent Biliary Tract Cancers (COMPANION-002) | Phase 2/Phase 3 Interventional | Compass Therapeutics | The COMPANION-002 study | 1 |
| NCT05513742 | A Study of CTX-009 in Adult Patients With Metastatic Colorectal Cancer | Phase 2 Interventional | Compass Therapeutics | The COMPANION-003 study | 2 |