Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Pralsetinib
Drug ID BADD_D02585
Description Pralsetinib, similar to the previously approved [selpercatinib], is a kinase inhibitor with enhanced specificity for RET tyrosine kinase receptors (RTKs) over other RTK classes.[A202055, A219751, L15986] Enhanced RET (Rearranged during transfection) oncogene expression is a hallmark of many cancers, including non-small cell lung cancer. Although multikinase inhibitors, including [cabozantinib], [ponatinib], [sorafenib], [sunitinib], and [vandetanib], have shown efficacy in RET-driven cancers, their lack of specificity is generally associated with substantial toxicity.[A202055] Pralsetinib (BLU-667) and [selpercatinib] (LOXO-292) represent the first generation of specific RET RTK inhibitors for the treatment of RET-driven cancers.[A202049, A202055, L15986] Although a phase 1/2 trial of pralsetinib termed ARROW (NCT03037385) is still ongoing, pralsetinib was granted accelerated FDA approval on September 4, 2020, for the treatment of metastatic RET-fusion positive non-small cell lung cancer. It is currently marketed under the brand name GAVRETO™ by Blueprint Medicines.[L15986]
Indications and Usage Pralsetinib is indicated for the treatment of metastatic non-small cell lung cancer (NSCLC) in adult patients who are confirmed to possess a rearranged during transfection (RET) gene fusion, as determined by an FDA approved test.[L15986] It is also indicated in adult and pediatric patients 12 years of age and older for the treatment of advanced or metastatic _RET_-mutant medullary thyroid cancer, and in this same population for the treatment of advanced or metastatic _RET_ fusion-positive thyroid cancer who require systemic therapy and for whom radioactive iodine is not appropriate.[L15986] Pralsetinib is currently approved for this indication under an accelerated approval scheme and continued approval may be contingent on future confirmatory trials.[L15986]
Marketing Status approved; investigational
ATC Code L01EX23
DrugBank ID DB15822
KEGG ID D11712
MeSH ID C000655704
PubChem ID Not Available
TTD Drug ID D0OD2I
NDC Product Code 50242-210; 11014-0438
UNII 1WPE73O1WV
Synonyms pralsetinib | BLU-667 | gavreto | trans-N-((1S)-1-(6-(4-Fluoro-1H-pyrazol-1-yl)-3-pyridinyl)ethyl)-1-methoxy-4-(4-methyl-6-((5-methyl-1H-pyrazol-3-yl)amino)-2-pyrimidinyl)cyclohexanecarboxamide | Cyclohexanecarboxamide, N-((1S)-1-(6-(4-fluoro-1H-pyrazol-1-yl)-3-pyridinyl)ethyl)-1-methoxy-4-(4-methyl-6-((5-methyl-1H-pyrazol-3-yl)amino)-2-pyrimidinyl)-, trans-
Chemical Information
Molecular Formula Not Available
CAS Registry Number 2097132-94-8
SMILES Not Available
Chemical Structure
ADRs Induced by Drug
*The priority for ADR severity classification is based on FAERS assessment, followed by the most severe level in CTCAE rating. If neither is available, it will be displayed as 'Not available'.
**The 'Not Available' level is hidden by default and can be restored by clicking on the legend twice..
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Oedema14.05.06.010; 08.01.07.0060.000224%Not Available
Petechiae01.01.03.002; 24.07.06.004; 23.06.01.0030.000381%Not Available
Pleural effusion22.05.02.0020.000112%
Pneumonitis22.01.01.0060.000392%
Productive cough22.02.03.0050.000112%
Pyrexia08.05.02.0030.000280%
Sudden death02.03.04.013; 08.04.01.0030.000112%
Thrombocytopenia01.08.01.0020.000168%Not Available
General physical health deterioration08.01.03.0180.000246%Not Available
Chylothorax22.05.02.0060.000112%
Hypoaesthesia oral17.02.06.021; 07.05.05.0030.000112%Not Available
Disease progression08.01.03.0380.001108%
Drug intolerance08.06.01.0130.000381%Not Available
Renal impairment20.01.03.0100.000280%Not Available
Myelosuppression01.03.03.0150.000638%Not Available
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