Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Selpercatinib
Drug ID BADD_D02593
Description Selpercatinib is a kinase inhibitor with enhanced specificity for RET tyrosine kinase receptors (RTKs) over other RTK classes.[A202055, A202052, L13604] Enhanced RET (Rearranged during transfection) oncogene expression is a hallmark of many cancers. 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. Selpercatinib (LOXO-292) and pralsetinib (BLU-667) represent the first generation of specific RET RTK inhibitors for the treatment of RET-driven cancers.[A202049, A202055, A202052, L13604] Although selpercatinib is currently still under investigation in clinical trial NCT04211337, it was granted accelerated FDA approval on May 8, 2020, for specific RET-driven cancer indications. It is currently marketed under the brand name RETEVMO™ by Loxo Oncology Inc.[L13604]
Indications and Usage Selpercatinib is indicated for the treatment of _RET_ fusion-positive non-small cell lung cancer in adult patients. Selpercatinib is also indicated for the systemic treatment of advanced or metastatic _RET_-mutant medullary thyroid cancer and for the systemic treatment of _RET_ fusion-positive radioactive iodine-refractory thyroid cancer in both adult and pediatric patients aged 12 and over.[L13604] Selpercatinib is currently approved for these indications under an accelerated approval scheme and continued approval may be contingent on future confirmatory trials.[L13604]
Marketing Status approved; investigational
ATC Code L01EX22
DrugBank ID DB15685
KEGG ID D11713
MeSH ID C000656166
PubChem ID 134436906
TTD Drug ID D01KOA
NDC Product Code 71794-397; 0002-2980; 63419-0597; 71794-298; 0002-3977; 0110-2980; 0110-3977; 63419-0681
UNII CEGM9YBNGD
Synonyms selpercatinib | serpercatinib | LOXO-292 | 6-(2-hydroxy-2-methylpropoxy)-4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo(3.1.1)heptan-3-yl)pyridin-3-yl)pyrazolo(1,5-a)pyridine-3-carbonitrile
Chemical Information
Molecular Formula C29H31N7O3
CAS Registry Number 2152628-33-4
SMILES CC(C)(COC1=CN2C(=C(C=N2)C#N)C(=C1)C3=CN=C(C=C3)N4CC5CC(C4)N5CC6=CN=C(C=C6)OC)O
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)
Abdominal distension07.01.04.0010.000381%
Abdominal pain07.01.05.0020.000571%
Anaemia01.03.02.0010.000112%
Anxiety19.06.02.0020.000246%
Ascites07.07.01.001; 02.05.04.002; 09.01.05.0030.000392%
Asthenia08.01.01.0010.000302%Not Available
Cerebrovascular accident24.03.05.001; 17.08.01.0070.000112%
Chest pain22.12.02.003; 08.01.08.002; 02.02.02.0110.000381%Not Available
Cough22.02.03.0010.000246%
Death08.04.01.0010.000783%
Diarrhoea07.02.01.0010.000873%
Dry mouth07.06.01.0020.000683%
Dysphagia07.01.06.0030.000873%
Fatigue08.01.01.0020.001421%
Headache17.14.01.0010.000739%
Hepatotoxicity12.03.01.008; 09.01.07.0090.000302%Not Available
Hypersensitivity10.01.03.0030.000627%
Hypertension24.08.02.0010.000739%
Hypocalcaemia14.04.01.0040.000112%
Myalgia15.05.02.0010.000437%
Neutropenia01.02.03.0040.000437%Not Available
Oedema14.05.06.010; 08.01.07.0060.000492%Not Available
Oedema peripheral08.01.07.007; 02.05.04.007; 14.05.06.0110.001063%
Oesophagitis07.08.05.0010.000246%
Paraesthesia23.03.03.094; 17.02.06.0050.000761%
Pleural effusion22.05.02.0020.000112%
Pneumonitis22.01.01.0060.000112%
Pulmonary embolism24.01.06.001; 22.06.02.0010.000112%Not Available
Pulmonary oedema22.01.03.003; 02.05.02.0030.000302%
Pyrexia08.05.02.0030.001142%
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