General Information of Drug (ID: DMWM4D0)

Drug Name
Futibatinib Drug Info
Synonyms TAS-120
Indication
Disease Entry ICD 11 Status REF
Intrahepatic cholangiocarcinoma 2C12.10 Approved [1]
Cholangiocarcinoma 2C12.10 Phase 3 [2]
Multiple myeloma 2A83 Phase 1/2 [3]
Solid tumour/cancer 2A00-2F9Z Phase 1/2 [4]
Cross-matching ID
PubChem CID
71621331
CAS Number
CAS 1448169-71-8
TTD Drug ID
DMWM4D0

Molecule-Related Drug Atlas

Molecule-Related Drug Atlas
Molecule Type:
DTT
Drug Status:
Approved Drug(s)
Clinical Trial Drug(s)
Investigative Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
Erdafitinib DMI782S Bladder cancer 2C94 Approved [6]
Infigratinib DMNKBEC Cholangiocarcinoma 2C12.10 Approved [4]
HIF-1alpha DM4OQRD Lymphoma 2A80-2A86 Phase 4 [7]
ARQ-087 DM02BVQ Intrahepatic cholangiocarcinoma 2C12.10 Phase 3 [4]
AZD4547 DM3827C Solid tumour/cancer 2A00-2F9Z Phase 2/3 [4]
Debio 1347 DMZW50O Solid tumour/cancer 2A00-2F9Z Phase 2 [8]
BAY1163877 DMCSGJ2 Bladder cancer 2C94 Phase 2 [9]
ICP-192 DM524GR Bladder cancer 2C94 Phase 2 [10]
PRN1371 DMR7BAO Solid tumour/cancer 2A00-2F9Z Phase 1 [4]
PD173074 DMP0N4U Nasopharyngeal carcinoma 2B6B Investigative [7]
⏷ Show the Full List of 10 Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
Recombinant acidic fibroblast growth factor DM8HVNR Skin burns ME65.0 Phase 3 [11]
GSK3052230 DMCKNJX Solid tumour/cancer 2A00-2F9Z Phase 1 [12]

Molecular Interaction Atlas of This Drug

Molecular Interaction Atlas

Drug Therapeutic Target (DTT)
DTT Name DTT ID UniProt ID MOA REF
Fibroblast growth factor receptor (FGFR) TT0LF7H NOUNIPROTAC Antagonist [5]
Fibroblast growth factor (FGF) TT5HU6Z NOUNIPROTAC Inhibitor [4]

References

1 FDA Approved Drug Products from FDA Official Website. 2022. Application Number: 214801.
2 ClinicalTrials.gov (NCT04093362) Futibatinib Versus Gemcitabine-Cisplatin Chemotherapy as First-Line Treatment of Patients With Advanced Cholangiocarcinoma Harboring FGFR2 Gene Rearrangements (FOENIX-CCA3). U.S. National Institutes of Health.
3 ClinicalTrials.gov (NCT02052778) A Dose Finding Study Followed by a Safety and Efficacy Study in Patients With Advanced Solid Tumors or Multiple Myeloma With FGF/FGFR-Related Abnormalities. U.S. National Institutes of Health.
4 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
5 TAS-120, a highly potent and selective irreversible FGFR inhibitor, is effective in tumors harboring various FGFR gene abnormalities. Molecular Cancer Therapeutics. 01/2014; 12(11_Supplement):A270-A270.
6 Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health Human Services. 2019
7 Tumor angiogenesis as a therapeutic target. Drug Discov Today. 2001 Oct 1;6(19):1005-1024.
8 The fibroblast growth factor receptor genetic status as a potential predictor of the sensitivity to CH5183284/Debio 1347, a novel selective FGFR inhibitor. Mol Cancer Ther. 2014 Nov;13(11):2547-58.
9 Preclinical profile of BAY 1163877 - a selective pan-FGFR inhibitor in phase 1 clinical trial. Cancer Research. 10/2014; 74(19 Supplement):1739-1739.
10 Clinical pipeline report, company report or official report of InnoCare Pharma.
11 Molecular characterization of recombinant human acidic fibroblast growth factor produced in E. coli: comparative studies with human basic fibroblast growth factor. Mol Endocrinol. 1990 Jun;4(6):869-79.
12 National Cancer Institute Drug Dictionary (drug id 599037).