Iclusig(ponatinib)
Iclusig (ponatinib) is a small molecule pharmaceutical. Ponatinib was first approved as Iclusig on 2012-12-14. It is used to treat myeloid leukemia in the USA. It has been approved in Europe to treat lymphoid leukemia and myeloid leukemia. The pharmaceutical is active against tyrosine-protein kinase ABL1. In addition, it is known to target cyclin-dependent kinase 19, cyclin-dependent kinase 8, proto-oncogene tyrosine-protein kinase receptor Ret, receptor-interacting serine/threonine-protein kinase 3, receptor-interacting serine/threonine-protein kinase 2, and receptor-interacting serine/threonine-protein kinase 1.
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Commercial
Trade Name
FDA
EMA
Iclusig
Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
Ponatinib hydrochloride
Tradename | Company | Number | Date | Products |
---|---|---|---|---|
ICLUSIG | Takeda | N-203469 RX | 2012-12-14 | 4 products, RLD, RS |
Labels
FDA
EMA
Brand Name | Status | Last Update |
---|---|---|
iclusig | New Drug Application | 2020-12-23 |
Agency Specific
FDA
EMA
Expiration | Code | ||
---|---|---|---|
PONATINIB HYDROCHLORIDE, ICLUSIG, TAKEDA PHARMS USA | |||
2023-12-18 | I-849 |
Patent Expiration
Patent | Expires | Flag | FDA Information |
---|---|---|---|
Ponatinib Hydrochloride, Iclusig, Takeda Pharms Usa | |||
9493470 | 2033-12-12 | DS, DP | U-1700, U-1948 |
11192895 | 2033-12-12 | U-1700, U-1701, U-1948 | |
11192897 | 2033-12-12 | DP | U-1700, U-1701, U-1948 |
11384086 | 2033-12-12 | DS, DP | U-1700, U-1701, U-1948 |
8114874 | 2027-01-24 | DS, DP | |
9029533 | 2026-12-22 | U-836, U-1283, U-1699, U-1700, U-1701 |
HCPCS
No data
Clinical
Clinical Trials
60 clinical trials
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Indications Phases 4
No data
Indications Phases 2
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Myeloid leukemia acute | D015470 | C92.0 | 5 | 7 | — | — | — | 9 | |
Leukemia | D007938 | C95 | 2 | 4 | — | — | 1 | 5 | |
Philadelphia chromosome | D010677 | 1 | 4 | — | — | 1 | 5 | ||
Neoplasms | D009369 | C80 | 1 | 3 | — | — | — | 3 | |
Myelodysplastic syndromes | D009190 | D46 | 1 | 1 | — | — | — | 2 | |
Breast neoplasms | D001943 | EFO_0003869 | C50 | 1 | 1 | — | — | — | 2 |
Myelomonocytic leukemia chronic | D015477 | C93.1 | 1 | 1 | — | — | — | 2 | |
Gastrointestinal stromal tumors | D046152 | EFO_0000505 | C49.A | — | 2 | — | — | — | 2 |
Gastrointestinal neoplasms | D005770 | C26.9 | — | 1 | — | — | — | 1 | |
Glioblastoma | D005909 | EFO_0000515 | — | 1 | — | — | — | 1 |
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Indications Phases 1
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Hematologic neoplasms | D019337 | 2 | — | — | — | — | 2 | ||
Prostatic neoplasms | D011471 | C61 | 1 | — | — | — | — | 1 | |
Castration-resistant prostatic neoplasms | D064129 | 1 | — | — | — | — | 1 | ||
Pancreatic neoplasms | D010190 | EFO_0003860 | C25 | 1 | — | — | — | — | 1 |
Non-hodgkin lymphoma | D008228 | C85.9 | 1 | — | — | — | — | 1 | |
Primary myelofibrosis | D055728 | D47.4 | 1 | — | — | — | — | 1 | |
Multiple myeloma | D009101 | C90.0 | 1 | — | — | — | — | 1 | |
B-cell chronic lymphocytic leukemia | D015451 | C91.1 | 1 | — | — | — | — | 1 | |
Anemia | D000740 | EFO_0004272 | D64.9 | 1 | — | — | — | — | 1 |
Hodgkin disease | D006689 | C81 | 1 | — | — | — | — | 1 |
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Indications Without Phase
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Endometrial neoplasms | D016889 | EFO_0004230 | — | — | — | — | 1 | 1 |
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common name | PONATINIB |
INN | ponatinib |
Description | Ponatinib is a benzamide obtained by the formal condensation of the carboxy group of 3-(imidazo[1,2-b]pyridazin-3-ylethynyl)-4-methylbenzoic acid with the anilino group of 4-[(4-methylpiperazin-1-yl)methyl]-3-(trifluoromethyl)aniline. It is a multi-target tyrosine kinase inhibitor that targets ABL, SRC, FGFR, and others and was designed to overcome the resistance of BCR-ABL mutation to imatinib, in particular the gatekeeper mutation ABL(T315I). It has a role as an antineoplastic agent and a tyrosine kinase inhibitor. It is a N-methylpiperazine, a member of benzamides, an acetylenic compound, an imidazopyridazine and a member of (trifluoromethyl)benzenes. It is a conjugate base of a ponatinib(1+). |
Classification | Small molecule |
Drug class | tyrosine kinase inhibitors |
Image (chem structure or protein) | |
Structure (InChI/SMILES or Protein Sequence) | Cc1ccc(C(=O)Nc2ccc(CN3CCN(C)CC3)c(C(F)(F)F)c2)cc1C#Cc1cnc2cccnn12 |
Identifiers
PDB | 7WF5 |
CAS-ID | 943319-70-8 |
RxCUI | 1364347 |
ChEMBL ID | CHEMBL1171837 |
ChEBI ID | 78543 |
PubChem CID | 24826799 |
DrugBank | DB08901 |
UNII ID | 4340891KFS (ChemIDplus, GSRS) |
Target
Agency Approved
ABL1
ABL1
Organism
Homo sapiens
Gene name
ABL1
Gene synonyms
ABL, JTK7
NCBI Gene ID
Protein name
tyrosine-protein kinase ABL1
Protein synonyms
Abelson murine leukemia viral oncogene homolog 1, Abelson tyrosine-protein kinase 1, ABL protooncogene 1 nonreceptor tyrosine kinase, BCR-ABL1 p190, BCR/ABL e8a2 fusion, BCR/ABL1 e1a2 fusion protein, bcr/c-abl oncogene protein, c-abl oncogene 1, receptor tyrosine kinase, p150, Proto-oncogene c-Abl, proto-oncogene tyrosine-protein kinase ABL1, v-abl Abelson murine leukemia viral oncogene homolog 1
Uniprot ID
Mouse ortholog
Abl1 (11350)
tyrosine-protein kinase ABL1 (P00520)
Alternate
CDK19
CDK19
CDK8
CDK8
RET
RET
RIPK3
RIPK3
RIPK2
RIPK2
RIPK1
RIPK1
Organism
Homo sapiens
Gene name
CDK19
Gene synonyms
CDC2L6, CDK11, KIAA1028
NCBI Gene ID
Protein name
cyclin-dependent kinase 19
Protein synonyms
CDC2-related protein kinase 6, CDK8-like cyclin-dependent kinase, cell division cycle 2-like 6 (CDK8-like), Cell division cycle 2-like protein kinase 6, Cell division protein kinase 19, cyclin-dependent kinase (CDC2-like) 11, Cyclin-dependent kinase 11, Death-preventing kinase
Uniprot ID
Mouse ortholog
Cdk19 (78334)
cyclin-dependent kinase 19 (Q8BWD8)
Variants
Clinical Variant
No data
Financial
Iclusig - Takeda
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Iclusig - Incyte
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Tabular view
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 4,512 documents
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Safety
Black-box Warning
Black-box warning for: Iclusig
Adverse Events
Top Adverse Reactions
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58,091 adverse events reported
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