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Eratrectinib

From Wikipedia, the free encyclopedia

Eratrectinib
Clinical data
Other namesVC004
Identifiers
  • (6R)-15-cyclopropyl-9-fluoro-2,11,15,16,20,21,24-heptazapentacyclo[16.5.2.02,6.07,12.021,25]pentacosa-1(24),7(12),8,10,18(25),19,22-heptaen-17-one
CAS Number
PubChem CID
IUPHAR/BPS
UNII
Chemical and physical data
FormulaC21H22FN7O
Molar mass407.453 g·mol−1
3D model (JSmol)
  • C1C[C@@H]2C3=C(CCN(NC(=O)C4=C5N=C(N2C1)C=CN5N=C4)C6CC6)N=CC(=C3)F
  • InChI=InChI=1S/C21H22FN7O/c22-13-10-15-17(23-11-13)5-8-28(14-3-4-14)26-21(30)16-12-24-29-9-6-19(25-20(16)29)27-7-1-2-18(15)27/h6,9-12,14,18H,1-5,7-8H2,(H,26,30)/t18-/m1/s1
  • Key:URXMBXJZRCIDQB-GOSISDBHSA-N

Eratrectinib is an investigational new drug that is being developed by Jiangsu Vcare Pharmatech for the treatment of solid tumors. It is a Trk receptor antagonist targeting specifically TRKA, TRKB and TRKC.[1][2]

It has been approved in June 2026 for use in treating for solid tumors in China.[3]

References

[edit]
  1. "Eratrectinib". AdisInsight. Springer Nature Switzerland AG. Retrieved 3 July 2026.
  2. Zhou S, Zhang C, Wang G, Qian J, Huang G, Wang J, et al. (June 2026). "Safety, efficacy, and pharmacokinetics of eratrectinib (VC004) in solid tumors with NTRK fusions: phase 1 results from a phase 1/2 study". Experimental Hematology & Oncology. doi:10.1186/s40164-026-00799-9. PMID 42351304.
  3. "NMPA Approves Vcare's Eratrectinib for NTRK Tumors". AllSci. 5 June 2026.