Stivarga(regorafenib)
Stivarga (regorafenib) is a small molecule pharmaceutical. Regorafenib was first approved as Stivarga on 2012-09-27. It is used to treat colorectal neoplasms, gastrointestinal stromal tumors, and hepatocellular carcinoma in the USA. It has been approved in Europe to treat colorectal neoplasms. The pharmaceutical is active against serine/threonine-protein kinase B-raf. In addition, it is known to target vascular endothelial growth factor receptor 2.
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Commercial
Trade Name
FDA
EMA
Stivarga
Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
Regorafenib
Tradename | Company | Number | Date | Products |
---|---|---|---|---|
STIVARGA | Bayer | N-203085 RX | 2012-09-27 | 1 products, RLD, RS |
Labels
FDA
EMA
Brand Name | Status | Last Update |
---|---|---|
stivarga | New Drug Application | 2020-12-09 |
Agency Specific
FDA
EMA
Expiration | Code | ||
---|---|---|---|
REGORAFENIB, STIVARGA, BAYER HLTHCARE | |||
2024-04-27 | ODE-139 |
HCPCS
No data
Clinical
Clinical Trials
237 clinical trials
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Indications Phases 4
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Colorectal neoplasms | D015179 | 19 | 52 | 16 | 3 | 15 | 90 | ||
Gastrointestinal stromal tumors | D046152 | EFO_0000505 | C49.A | 2 | 7 | 2 | 1 | 3 | 14 |
Indications Phases 3
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Liver neoplasms | D008113 | EFO_1001513 | C22.0 | 3 | 13 | 2 | — | 5 | 21 |
Hepatocellular carcinoma | D006528 | C22.0 | 1 | 3 | 1 | — | 2 | 7 | |
Glioblastoma | D005909 | EFO_0000515 | — | 3 | 1 | — | 1 | 4 |
Indications Phases 2
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Neoplasms | D009369 | C80 | 18 | 11 | — | — | 2 | 27 | |
Sarcoma | D012509 | 1 | 7 | — | — | — | 7 | ||
Adenocarcinoma | D000230 | 3 | 6 | — | — | — | 7 | ||
Pancreatic neoplasms | D010190 | EFO_0003860 | C25 | 1 | 5 | — | — | — | 6 |
Rectal neoplasms | D012004 | 2 | 4 | — | — | — | 6 | ||
Osteosarcoma | D012516 | 1 | 5 | — | — | 1 | 6 | ||
Ovarian neoplasms | D010051 | EFO_0003893 | C56 | — | 5 | — | — | — | 5 |
Renal cell carcinoma | D002292 | 1 | 4 | — | — | — | 5 | ||
Colonic neoplasms | D003110 | C18 | 2 | 2 | — | — | — | 4 | |
Non-small-cell lung carcinoma | D002289 | 1 | 3 | — | — | — | 3 |
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Indications Phases 1
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Myeloid leukemia acute | D015470 | C92.0 | 2 | — | — | — | — | 2 | |
Pharmacokinetics | D010599 | 2 | — | — | — | — | 2 | ||
Myelodysplastic syndromes | D009190 | D46 | 1 | — | — | — | — | 1 | |
Hematologic neoplasms | D019337 | 1 | — | — | — | — | 1 | ||
Prostatic neoplasms | D011471 | C61 | 1 | — | — | — | — | 1 | |
Primary myelofibrosis | D055728 | D47.4 | 1 | — | — | — | — | 1 | |
Precursor cell lymphoblastic leukemia-lymphoma | D054198 | C91.0 | 1 | — | — | — | — | 1 | |
B-cell chronic lymphocytic leukemia | D015451 | C91.1 | 1 | — | — | — | — | 1 | |
Bcr-abl positive chronic myelogenous leukemia | D015464 | EFO_0000340 | 1 | — | — | — | — | 1 | |
Myelomonocytic leukemia chronic | D015477 | C93.1 | 1 | — | — | — | — | 1 |
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Indications Without Phase
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Covid-19 | D000086382 | U07.1 | — | — | — | — | 1 | 1 |
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common name | REGORAFENIB |
INN | regorafenib |
Description | Regorafenib is a pyridinecarboxamide obtained by condensation of 4-[4-({[4-chloro-3-(trifluoromethyl)phenyl]carbamoyl}amino)-3-fluorophenoxy]pyridine-2-carboxylic acid with methylamine. Used for for the treatment of metastatic colorectal cancer in patients who have previously received chemotherapy, anti-EGFR or anti-VEGF therapy. It has a role as an antineoplastic agent, a tyrosine kinase inhibitor and a hepatotoxic agent. It is an aromatic ether, a pyridinecarboxamide, a member of monochlorobenzenes, a member of (trifluoromethyl)benzenes, a member of monofluorobenzenes and a member of phenylureas. |
Classification | Small molecule |
Drug class | rapidly accelerated fibrosarcoma (RAF) kinase inhibitors |
Image (chem structure or protein) | |
Structure (InChI/SMILES or Protein Sequence) | CNC(=O)c1cc(Oc2ccc(NC(=O)Nc3ccc(Cl)c(C(F)(F)F)c3)c(F)c2)ccn1 |
Identifiers
PDB | — |
CAS-ID | 755037-03-7 |
RxCUI | 1312397 |
ChEMBL ID | CHEMBL1946170 |
ChEBI ID | 68647 |
PubChem CID | 11167602 |
DrugBank | DB08896 |
UNII ID | 24T2A1DOYB (ChemIDplus, GSRS) |
Target
Agency Approved
BRAF
BRAF
Organism
Homo sapiens
Gene name
BRAF
Gene synonyms
BRAF1, RAFB1
NCBI Gene ID
Protein name
serine/threonine-protein kinase B-raf
Protein synonyms
94 kDa B-raf protein, B-Raf proto-oncogene serine/threonine-protein kinase (p94), B-Raf serine/threonine-protein, murine sarcoma viral (v-raf) oncogene homolog B1, p94, Proto-oncogene B-Raf, v-raf murine sarcoma viral oncogene homolog B, v-Raf murine sarcoma viral oncogene homolog B1
Uniprot ID
Mouse ortholog
Braf (109880)
serine/threonine-protein kinase B-raf (P28028)
Alternate
KDR
KDR
Organism
Homo sapiens
Gene name
KDR
Gene synonyms
FLK1, VEGFR2
NCBI Gene ID
Protein name
vascular endothelial growth factor receptor 2
Protein synonyms
CD309, Fetal liver kinase 1, fetal liver kinase-1, FLK-1, KDR, Kinase insert domain receptor, kinase insert domain receptor (a type III receptor tyrosine kinase), Protein-tyrosine kinase receptor flk-1, soluble VEGFR2, tyrosine kinase growth factor receptor
Uniprot ID
Mouse ortholog
Kdr (16542)
vascular endothelial growth factor receptor 2 (Q8VCD0)
Variants
Clinical Variant
No data
Financial
No data
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 9,315 documents
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Safety
Black-box Warning
Black-box warning for: Stivarga
Adverse Events
Top Adverse Reactions
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4,158 adverse events reported
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