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Drug ReportsPexidartinib
Pexidartinib
Turalio (pexidartinib) is a small molecule pharmaceutical. Pexidartinib was first approved as Turalio on 2019-08-02. It is used to treat giant cell tumor of tendon sheath in the USA. The pharmaceutical is active against mast/stem cell growth factor receptor Kit and macrophage colony-stimulating factor 1 receptor. In addition, it is known to target tyrosine-protein kinase Lck, NT-3 growth factor receptor, vascular endothelial growth factor receptor 2, vascular endothelial growth factor receptor 1, receptor-type tyrosine-protein kinase FLT3, and cyclin-dependent kinase 19.
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FDA Novel Drug Approvals 2019
Events Timeline
Commercial
Clinical
Drug
Target
Variants
Financial
Trends
Safety
Events Timeline
5D
1M
3M
6M
YTD
1Y
2Y
5Y
Max
Events
FDA approval date
EMA approval date
Patent expiration date
Study first post date
Last update post date
Start date
Primary completion date
Completion date
Results first post date
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Commercial
Therapeutic Areas
Therapeutic Area
MeSH
neoplasmsD009369
musculoskeletal diseasesD009140
Trade Name
FDA
EMA
Turalio
Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
Pexidartinib hydrochloride
Tradename
Company
Number
Date
Products
TURALIODaiichi PharmaceuticalN-211810 RX2022-10-14
1 products, RLD
Show 1 discontinued
Labels
FDA
EMA
Brand Name
Status
Last Update
turalioNew Drug Application2023-11-21
Indications
FDA
EMA
Indication
Ontology
MeSH
ICD-10
giant cell tumor of tendon sheath—D000070779—
Agency Specific
FDA
EMA
Expiration
Code
PEXIDARTINIB HYDROCHLORIDE, TURALIO, DAIICHI SANKYO INC
2026-08-02ODE*, ODE-250
2024-08-02NCE
Patent Expiration
Patent
Expires
Flag
FDA Information
Pexidartinib Hydrochloride, Turalio, Daiichi Sankyo Inc
104354042038-07-24DP
109411422038-07-24DP
109612402038-07-24U-2606
98029322036-05-05DP
101898332036-05-05U-2606
107308762036-05-05DP
93582352033-06-08U-2606
78930752033-05-04DP
84611692028-04-19U-2606
84047002027-11-21DP
87227022027-11-21DP
91692502027-11-21DP
ATC Codes
L: Antineoplastic and immunomodulating agents
— L01: Antineoplastic agents
— L01E: Protein kinase inhibitors, antineoplastic and immunomodulating agents
— L01EX: Other protein kinase inhibitors in atc
— L01EX15: Pexidartinib
HCPCS
No data
Clinical
Clinical Trials
30 clinical trials
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Indications Phases 4
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Giant cell tumorsD005870——112116
Giant cell tumor of tendon sheathD000070779——112116
Indications Phases 3
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
NeoplasmsD009369—C804—1——5
SynovitisD013585EFO_0008997M67.5——1——1
Pigmented villonodular synovitisD013586EFO_1001106M12.2——1——1
Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
MelanomaD008545——22——14
Gastrointestinal stromal tumorsD046152EFO_0000505C49.A32———3
Breast neoplasmsD001943EFO_0003869C5012———2
SarcomaD012509——21———2
GlioblastomaD005909EFO_0000515—12———2
Prostatic neoplasmsD011471—C6111———2
LeukemiaD007938—C9521———2
Triple negative breast neoplasmsD064726———1———1
HemangiosarcomaD006394———1———1
Ovarian neoplasmsD010051EFO_0003893C5611———1
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Indications Phases 1
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Healthy volunteers/patients———2————2
Colorectal neoplasmsD015179——1————1
Pancreatic neoplasmsD010190EFO_0003860C251————1
Rheumatoid arthritisD001172EFO_0000685M06.91————1
ArthritisD001168HP_0001369M05-M141————1
AdenocarcinomaD000230——1————1
Drug interactionsD004347——1————1
Liver diseasesD008107HP_0002910K70-K771————1
Hepatic insufficiencyD048550——1————1
Promyelocytic leukemia acuteD015473—C92.41————1
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Indications Without Phase
No data
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common namePexidartinib
INNpexidartinib
Description
Pexidartinib is a pyrrolopyridine that is 5-chloro-1H-pyrrolo[2,3-b]pyridine which is substituted by a [6-({[6-(trifluoromethyl)pyridin-3-yl]methyl}amino)pyridin-3-yl]methyl group at position 3. It is a potent multi-targeted receptor tyrosine kinase inhibitor of CSF-1R, KIT, and FLT3 (IC50 of 20 nM, 10 nM and 160 nM, respectively). Approved by the FDA for the treatment of adult patients with symptomatic tenosynovial giant cell tumor (TGCT). It has a role as an EC 2.7.10.1 (receptor protein-tyrosine kinase) inhibitor and an antineoplastic agent. It is a pyrrolopyridine, an organochlorine compound, an aminopyridine, an organofluorine compound and a secondary amino compound.
Classification
Small molecule
Drug classtyrosine kinase inhibitors
Image (chem structure or protein)Loading
Structure (InChI/SMILES or Protein Sequence)
FC(F)(F)c1ccc(CNc2ccc(Cc3c[nH]c4ncc(Cl)cc34)cn2)cn1
Identifiers
PDB—
CAS-ID1029044-16-3
RxCUI—
ChEMBL IDCHEMBL3813873
ChEBI ID—
PubChem CID25151352
DrugBankDB12978
UNII ID6783M2LV5X (ChemIDplus, GSRS)
Target
Agency Approved
KIT
KIT
CSF1R
CSF1R
Organism
Homo sapiens
Gene name
KIT
Gene synonyms
SCFR
NCBI Gene ID
Protein name
mast/stem cell growth factor receptor Kit
Protein synonyms
c-Kit protooncogene, CD117, p145 c-kit, PBT, Piebald trait protein, Proto-oncogene c-Kit, proto-oncogene tyrosine-protein kinase Kit, Tyrosine-protein kinase Kit, v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog, v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene-like protein
Uniprot ID
Mouse ortholog
Kit (16590)
mast/stem cell growth factor receptor Kit (Q8C8K9)
Alternate
LCK
LCK
NTRK3
NTRK3
KDR
KDR
FLT1
FLT1
FLT3
FLT3
CDK19
CDK19
Organism
Homo sapiens
Gene name
LCK
Gene synonyms
NCBI Gene ID
Protein name
tyrosine-protein kinase Lck
Protein synonyms
Leukocyte C-terminal Src kinase, LSK, Lymphocyte cell-specific protein-tyrosine kinase, p56(LSTRA) protein-tyrosine kinase, p56-LCK, Protein YT16, Proto-oncogene Lck, proto-oncogene tyrosine-protein kinase LCK, T cell-specific protein-tyrosine kinase, T-lymphocyte specific protein tyrosine kinase p56lck
Uniprot ID
Mouse ortholog
Lck (16818)
proto-oncogene tyrosine-protein kinase LCK (Q91X65)
Variants
No data
Financial
No data
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Safety
Black-box Warning
Black-box warning for: Turalio
Adverse Events
Top Adverse Reactions
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787 adverse events reported
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