Synonyms: example 163 [WO2018071447A1] | LOXO-292 | LOXO292 | LY3527723 | Retevmo®
selpercatinib is an approved drug (FDA (2020), EMA (2021))
Compound class:
Synthetic organic
Comment: Selpercatinib (LOXO-292) is a potent, selective and orally bioavailable ATP-competitive RET kinase inhibitor that was developed by Loxo Oncology. It inhibits wild-type RET, RET fusions,and RET carrying activating mutations and acquired resistance mutations [5]. This reference by Subbiah et al. contains preclinical and proof-of-concept data for LOXO-292. This compound was rationally designed to offer a novel therapeutic option for heavily pretreated, multikinase inhibitor-experienced patients whose tumours carry diverse RET alterations.
![]() Ligand Activity Visualisation ChartsThese are box plot that provide a unique visualisation, summarising all the activity data for a ligand taken from ChEMBL and GtoPdb across multiple targets and species. Click on a plot to see the median, interquartile range, low and high data points. A value of zero indicates that no data are available. A separate chart is created for each target, and where possible the algorithm tries to merge ChEMBL and GtoPdb targets by matching them on name and UniProt accession, for each available species. However, please note that inconsistency in naming of targets may lead to data for the same target being reported across multiple charts. ✖ |
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No information available. |
Summary of Clinical Use ![]() |
LOXO-292 was advanced to clinical evaluation in patients with RET fusion-positive solid tumours. Click here to link to ClinicalTrials.gov's full list of LOXO-292/selpercatinib studies. Eli Lilly's New Drug Application for selpercatinib (for use in certain RET-fusion positive tumours) received FDA priority review, based on positive outcome data from the LIBRETTO-001 Phase 1/2 trial NCT03157128 [11]. In May 2020, this led to accelerated approval as a treatment for RET-fusion positive NSCLC or advanced/metastatic RET-mutant medullary thyroid cancer (MTC) [2]. More extensive trials are ongoing. FDA accelerated approval for treatment of applicable RET-altered MTC/thyroid cancers/other solid tumours in pediatric patients ≥2 years old was issued in May 2024, and this converted to regular approval in September that year. |
Clinical Trials | |||||
Clinical Trial ID | Title | Type | Source | Comment | References |
NCT04194944 | A Study of Selpercatinib (LY3527723) in Participants With Advanced or Metastatic RET Fusion-Positive Non-Small Cell Lung Cancer | Phase 3 Interventional | Eli Lilly and Company | LIBRETTO-431 study. | 4,10 |
NCT04211337 | A Study of Selpercatinib (LY3527723) in Participants With RET-Mutant Medullary Thyroid Cancer | Phase 3 Interventional | Eli Lilly and Company | LIBRETTO-531 study. | 8 |
NCT03157128 | Phase 1/2 Study of LOXO-292 in Patients With Advanced Solid Tumors, RET Fusion-Positive Solid Tumors, and Medullary Thyroid Cancer | Phase 1/Phase 2 Interventional | Loxo Oncology, Inc. | LIBRETTO-001 study. | 3,6 |
NCT04280081 | A Study of Selpercatinib (LY3527723) in Participants With Advanced Solid Tumors Including RET Fusion-positive Solid Tumors, Medullary Thyroid Cancer and Other Tumors With RET Activation | Phase 2 Interventional | Eli Lilly and Company | LIBRETTO-321 study. | 9 |
NCT04819100 | A Study of Selpercatinib After Surgery or Radiation in Participants With Non-Small Cell Lung Cancer (NSCLC) | Phase 3 Interventional | Eli Lilly and Company | LIBRETTO-432 study. | 7 |