Carotuximab

drug
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Also known as DE-122TRC-105Trc105c-SN6j

Summary

Carotuximab (CHEMBL2109321) is a phase-3 clinical-stage antibody targeting ENG; indicated across 23 conditions including angiosarcoma and glioblastoma.

At a glance

  • Status: Max clinical phase 3 (not approved)
  • Modality: Antibody
  • Targets: 1 (ENG)
  • Indications: 23 conditions
  • Clinical trials: 23

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL2109321
NameCarotuximab
TypeAntibody
Max phase3

Also known as: Carotuximab, DE-122, TRC-105, Trc105, c-SN6j, CAROTUXIMAB

Targets

Targets

Primary targets (GtoPdb curated mechanism): the Cancer dependency column is the DepMap CRISPR fitness signal (% of screened cell lines dependent on the target).

GeneTargetActionpAffinityCancer dependencyUniProt
ENGendoglin (CD105)Binding90.2%P17813

Bioactivity

No ChEMBL bioactivity rows at pChembl ≥ 5 (expected for biologics / antibodies).

Target pathways

Aggregated over 1 target gene(s): ENG.

Dominant GO biological processes

GO termTargets
negative regulation of transcription by RNA polymerase II1
branching involved in blood vessel morphogenesis1
vasculogenesis1
response to hypoxia1
negative regulation of endothelial cell proliferation1
heart looping1
positive regulation of systemic arterial blood pressure1
outflow tract septum morphogenesis1
epithelial to mesenchymal transition involved in endocardial cushion formation1
endocardial cushion morphogenesis1
cardiac ventricle morphogenesis1
cardiac atrium morphogenesis1
ventricular trabecula myocardium morphogenesis1
cell migration involved in endocardial cushion formation1
regulation of DNA-templated transcription1

Indications & clinical

Indications

18 diseases in clinical trials (phase 1–3, investigational — not approved indications). Highest ChEMBL trial phase per disease; a non-cancer approved use is occasionally logged at phase 3 here.

Disease (in trials)PhaseMONDOEFO
angiosarcoma3MONDO:0016982EFO:0003968
glioblastoma2MONDO:0018177EFO:0000519
hepatocellular carcinoma2MONDO:0007256EFO:0000182
clear cell renal carcinoma2MONDO:0005005EFO:0000349
papillary renal cell carcinoma2MONDO:0017884EFO:0000640
renal cell carcinoma2MONDO:0005086EFO:0000681
choriocarcinoma2MONDO:0005207EFO:0002893
age-related macular degeneration2MONDO:0005150EFO:0001365
placental site trophoblastic tumor2MONDO:0020552EFO:1001111
neoplasm1MONDO:0005070EFO:0000616
anaplastic astrocytoma1MONDO:0016684EFO:0002499
anaplastic oligodendroglioma1MONDO:0016696EFO:0002501
non-small cell lung carcinoma1MONDO:0005233EFO:0003060
gliosarcoma1MONDO:0016681EFO:1001465
soft tissue sarcoma1MONDO:0018078EFO:1001968
glioma1MONDO:0021042MONDO:0003268
breast neoplasm1MONDO:0021100MONDO:0007254
lung neoplasm1MONDO:0021117MONDO:0008903

5 further indication records had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.

Clinical trials

Total trials: 23.

Phase distribution

PhaseTrials
PHASE29
PHASE1/PHASE27
PHASE15
PHASE31
Not specified1

Top trials by phase / activity

NCTPhaseStatusTitle
NCT02979899PHASE3COMPLETEDTrial of TRC105 and Pazopanib Versus Pazopanib Alone in Patients With Advanced Angiosarcoma
NCT05534646PHASE2RECRUITINGStudy of Apalutamide With Carotuximab in Metastatic, Castration-Resistant Prostate Cancer
NCT01090765PHASE1/PHASE2COMPLETEDA Phase I/II Study of TRC105 in Metastatic Castrate Resistant Prostate Cancer (CRPC)
NCT01326481PHASE1/PHASE2COMPLETEDOpen Label Dose-Finding Study of TRC105 Plus Capecitabine for Metastatic Breast Cancer
NCT01328574PHASE2COMPLETEDTRC105 in Adults With Advanced/Metastatic Urothelial Carcinoma
NCT01375569PHASE2COMPLETEDTRC105 for Liver Cancer That Has Not Responded to Sorafenib
NCT01381861PHASE2COMPLETEDEvaluation of TRC105 in the Treatment of Recurrent Ovarian, Fallopian Tube, or Primary Peritoneal Carcinoma
NCT01564914PHASE2COMPLETEDA Phase 2 Evaluation of TRC105 In Combination With Bevacizumab in Patients With Glioblastoma
NCT01778530PHASE2TERMINATEDTRC105 for Recurrent Glioblastoma
NCT01806064PHASE1/PHASE2TERMINATEDRandomized Phase 2 Trial of Axitinib and TRC105 Versus Axitinib Alone in Patients Renal Cell Carcinoma
NCT01975519PHASE1/PHASE2COMPLETEDA Phase 1B Dose-escalation and Phase 2a Study of Carotuximab (TRC105) in Combination With Pazopanib in Patients With Advanced Soft Tissue Sarcoma
NCT02396511PHASE2COMPLETEDTRC105 Combined With Standard-dose Bevacizumab for Two Patients With Metastatic And Refractory Choriocarcinoma
NCT02520063PHASE1/PHASE2COMPLETEDCombination of Letrozole, Everolimus and TRC105 in Postmenopausal Women With Hormone-Receptor Positive and Her2 Negative Breast Cancer
NCT02555306PHASE1/PHASE2COMPLETEDA Phase I/II Safety, Tolerability, Immunogenicity, and Bioactivity Study of DE-122 Injectable Solution for Refractory Exudative Age-related Macular Degeneration
NCT02560779PHASE1/PHASE2COMPLETEDTrial of TRC105 and Sorafenib in Patients With HCC
NCT02664961PHASE2TERMINATEDStudy of TRC105 and Bevacizumab in Patients With Refractory Gestational Trophoblastic Neoplasia (GTN)
NCT03418324PHASE2COMPLETEDStudy of TRC105 With Abiraterone and With Enzalutamide in Prostate Cancer Patients Progressing on Therapy
NCT05401110PHASE1RECRUITINGStudy of Osimertinib With Carotuximab in Advanced, EGFR-mutated Non-Small Cell Lung Cancer
NCT01332721PHASE1COMPLETEDStudy of TRC105 Combined With Standard-Dose Bevacizumab for Advanced Solid Tumors for Which Bevacizumab is Indicated
NCT02429843PHASE1COMPLETEDA Study of TRC105 in Combination With Paclitaxel/Carboplatin and Bevacizumab in Non-Squamous Cell Lung Cancer
NCT03181308PHASE1COMPLETEDStudy of Carotuximab (TRC105) Plus Nivolumab in Patients With Metastatic NSCLC
NCT03780010PHASE1COMPLETEDStudy of TRC105 + Paclitaxel/Carboplatin and Bevacizumab in Patients With NSCLC
NCT02354612Not specifiedNO_LONGER_AVAILABLEOpen Label Continuation Study of TRC105 for Patients Who Have Completed a Prior TRC105 Trial

Clinical evidence (CIViC)

No CIViC predictive evidence (expected for non-precision-medicine drugs).

Pharmacology

Pharmacogenomics

No PharmGKB pharmacogenomic data curated for this drug.

No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).