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  1. pharmadog
  2. ›drugs
  3. ›Retevmo
drug · small molecule
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selpercatinib

Marketedupdated 3mo ago
by Eli Lilly and Co🔗 ChEMBL
Approved
community read0 votes

🐶 often sniffed alongside

top 4
  • tagApproval76 co-mentions · 19 sources
  • drugRETEVMO76 co-mentions · 19 sources
  • companyEli Lilly and Co38 co-mentions · 19 sources
  • tagSmall Molecule38 co-mentions · 19 sources

Small molecule drug with a maximum clinical stage of Approval (across all indications), with 11 approved and 2 investigational indications.

indications

investigational
NSCLCBreast CancerColorectal Cancer

targets

Coiled-coil domain-containing protein 6/Tyrosine-protein kinase receptor RETProto-oncogene tyrosine-protein kinase receptor RetKinesin-1 heavy chain/ Tyrosine-protein kinase receptor RET

all catalysts(19)

approval · 19
May 8, 2020
approval
$LLY1180.16-2.25%
6y ago
RETEVMO (SELPERCATINIB) — FDA approval
selpercatinib
→
Jan 28, 2021
approval
$LLY1180.16-2.25%
6y ago
RETEVMO (SELPERCATINIB) — FDA approval
selpercatinib
→
Sep 21, 2022
approval
$LLY1180.16-2.25%
4y ago
RETEVMO (SELPERCATINIB) — FDA approval
selpercatinib
→
Sep 21, 2022
approval
$LLY1180.16-2.25%
4y ago
RETEVMO (SELPERCATINIB) — FDA approval
selpercatinib
→
Apr 10, 2024
approval
$LLY1180.16-2.25%
2y ago
RETEVMO (SELPERCATINIB) — FDA approval
selpercatinib
→
Apr 10, 2024
approval
$LLY1180.16-2.25%
2y ago
RETEVMO (SELPERCATINIB) — FDA approval
selpercatinib
→
May 29, 2024
approval
$LLY1180.16-2.25%
2y ago
RETEVMO (SELPERCATINIB) — FDA approval
selpercatinib
→
Jun 12, 2024
approval
$LLY1180.16-2.25%
2y ago
RETEVMO (SELPERCATINIB) — FDA approval
selpercatinib
→
Jun 12, 2024
approval
$LLY1180.16-2.25%
2y ago
RETEVMO (SELPERCATINIB) — FDA approval
selpercatinib
→
Sep 27, 2024
approval
$LLY1180.16-2.25%
2y ago
RETEVMO (SELPERCATINIB) — FDA approval
selpercatinib
→
Sep 27, 2024
approval
$LLY1180.16-2.25%
2y ago
RETEVMO (SELPERCATINIB) — FDA approval
selpercatinib
→
Sep 27, 2024
approval
$LLY1180.16-2.25%
2y ago
RETEVMO (SELPERCATINIB) — FDA approval
selpercatinib
→
Sep 27, 2024
approval
$LLY1180.16-2.25%
2y ago
RETEVMO (SELPERCATINIB) — FDA approval
selpercatinib
→
Dec 18, 2024
approval
$LLY1180.16-2.25%
2y ago
RETEVMO (SELPERCATINIB) — FDA approval
selpercatinib
→
Dec 18, 2024
approval
$LLY1180.16-2.25%
2y ago
RETEVMO (SELPERCATINIB) — FDA approval
selpercatinib
→
Nov 20, 2025
approval
$LLY1180.16-2.25%
9mo ago
RETEVMO (SELPERCATINIB) — FDA approval
selpercatinib
→
Nov 20, 2025
approval
$LLY1180.16-2.25%
9mo ago
RETEVMO (SELPERCATINIB) — FDA approval
selpercatinib
→
Nov 20, 2025
approval
$LLY1180.16-2.25%
9mo ago
RETEVMO (SELPERCATINIB) — FDA approval
selpercatinib
→
Nov 20, 2025
approval
$LLY1180.16-2.25%
9mo ago
RETEVMO (SELPERCATINIB) — FDA approval
selpercatinib
→
view all 19 catalysts →

Trials studying selpercatinib

  • phase2A Study of Selpercatinib (LY3527723) in Participants With Advanced Solid Tumors Including RET Fusion-positive Solid Tumors, Medullary Thyroid Cancer and Other Tumors With RET Activationactive not recruitingn=77
  • phase2Selpercatinib Pre-RAI in Patients With RET Fusion Thyroid Cancer (RAISE)recruitingn=13
  • phase3A Study of Selpercatinib (LY3527723) in Participants With RET-Mutant Medullary Thyroid Canceractive not recruitingn=291
  • phase3A Study of Selpercatinib After Surgery or Radiation in Participants With Non-Small Cell Lung Cancer (NSCLC)active not recruitingn=152
  • phase2A Study of Oral LOXO-292 (Selpercatinib) in Pediatric Participants With Advanced Solid or Primary Central Nervous System (CNS) Tumorsactive not recruitingn=36
  • phase1A Study of Effects of Selpercatinib (LY3527723) on Repaglinide in Healthy Participantscompletedn=16
  • phase3A Study of Selpercatinib (LY3527723) in Participants With Advanced or Metastatic RET Fusion-Positive Non-Small Cell Lung Canceractive not recruitingn=261
  • phase1A Study of Effects of Selpercatinib (LY3527723) on Midazolam in Healthy Participantscompletedn=16
more trials →

Patent cliff

source: FDA Orange Book
first barrier falls
May 8, 2027
266 days

Earliest of all listed patents + FDA exclusivities. Generic / biosimilar entry typically only becomes possible AFTER both patent and exclusivity barriers expire.

patents (56)

  • Apr 10, 2039patentUS 10584124*PED
  • Apr 10, 2039patentUS 10584124*PED
  • Apr 10, 2039patentUS 10786489*PED
  • Apr 10, 2039patentUS 10786489*PED
  • Apr 10, 2039patentUS 12138250*PED
  • Apr 10, 2039patentUS 12138250*PED
  • Apr 10, 2039patentUS 12138250*PED
  • Apr 10, 2039patentUS 12138250*PED
  • Apr 10, 2039patentUS 12138250*PED
  • Apr 10, 2039patentUS 12138250*PED
  • Oct 10, 2038compositionUS 10584124
  • Oct 10, 2038compositionUS 10584124
  • Oct 10, 2038formulationUS 10786489
  • Oct 10, 2038formulationUS 10786489
  • Oct 10, 2038method-of-use (U-3950)US 12138250
  • Oct 10, 2038method-of-use (U-3949)US 12138250
  • Oct 10, 2038method-of-use (U-3949)US 12138250
  • Oct 10, 2038method-of-use (U-3450)US 12138250
  • Oct 10, 2038method-of-use (U-3450)US 12138250
  • Oct 10, 2038method-of-use (U-3949)US 12138250
  • Apr 10, 2038patentUS 10112942*PED
  • Apr 10, 2038patentUS 10112942*PED
  • Apr 10, 2038patentUS 10112942*PED
  • Apr 10, 2038patentUS 10112942*PED
  • Apr 10, 2038patentUS 10112942*PED
  • Apr 10, 2038patentUS 10112942*PED
  • Apr 10, 2038patentUS 10137124*PED
  • Apr 10, 2038patentUS 10137124*PED
  • Apr 10, 2038patentUS 10137124*PED
  • Apr 10, 2038patentUS 10137124*PED
  • Apr 10, 2038patentUS 10137124*PED
  • Apr 10, 2038patentUS 10137124*PED
  • Apr 10, 2038patentUS 10172851*PED
  • Apr 10, 2038patentUS 10172851*PED
  • Apr 10, 2038patentUS 10172851*PED
  • Apr 10, 2038patentUS 10172851*PED
  • Apr 10, 2038patentUS 10172851*PED
  • Apr 10, 2038patentUS 10172851*PED
  • Oct 10, 2037compositionUS 10112942
  • Oct 10, 2037compositionUS 10112942
  • Oct 10, 2037compositionUS 10112942
  • Oct 10, 2037compositionUS 10112942
  • Oct 10, 2037compositionUS 10112942
  • Oct 10, 2037compositionUS 10112942
  • Oct 10, 2037method-of-use (U-3951)US 10137124
  • Oct 10, 2037method-of-use (U-3951)US 10137124
  • Oct 10, 2037method-of-use (U-3950)US 10137124
  • Oct 10, 2037method-of-use (U-3951)US 10137124
  • Oct 10, 2037method-of-use (U-3951)US 10137124
  • Oct 10, 2037method-of-use (U-3951)US 10137124
  • Oct 10, 2037method-of-use (U-3951)US 10172851
  • Oct 10, 2037method-of-use (U-3951)US 10172851
  • Oct 10, 2037method-of-use (U-3951)US 10172851
  • Oct 10, 2037method-of-use (U-3450)US 10172851
  • Oct 10, 2037method-of-use (U-3950)US 10172851
  • Oct 10, 2037method-of-use (U-3951)US 10172851

FDA exclusivities (68)

  • Nov 29, 2031PEDPediatric (6mo bonus)
  • Nov 29, 2031PEDPediatric (6mo bonus)
  • Nov 29, 2031PEDPediatric (6mo bonus)
  • Nov 29, 2031PEDPediatric (6mo bonus)
  • Nov 29, 2031PEDPediatric (6mo bonus)
  • Nov 29, 2031PEDPediatric (6mo bonus)
  • May 29, 2031ODE*ODE*4.8y
  • May 29, 2031ODE-484Orphan Drug (7y)4.8y
  • May 29, 2031ODE-485Orphan Drug (7y)4.8y
  • May 29, 2031ODE-487Orphan Drug (7y)4.8y
  • May 29, 2031ODE-484Orphan Drug (7y)4.8y
  • May 29, 2031ODE-485Orphan Drug (7y)4.8y
  • May 29, 2031ODE-487Orphan Drug (7y)4.8y
  • May 29, 2031ODE*ODE*4.8y
  • May 29, 2031ODE*ODE*4.8y
  • May 29, 2031ODE*ODE*4.8y
  • Mar 21, 2030PEDPediatric (6mo bonus)3.6y
  • Mar 21, 2030PEDPediatric (6mo bonus)3.6y
  • Mar 21, 2030PEDPediatric (6mo bonus)3.6y
  • Mar 21, 2030PEDPediatric (6mo bonus)3.6y
  • Mar 21, 2030PEDPediatric (6mo bonus)3.6y
  • Mar 21, 2030PEDPediatric (6mo bonus)3.6y
  • Sep 21, 2029ODE-412Orphan Drug (7y)3.1y
  • Sep 21, 2029ODE*ODE*3.1y
  • Sep 21, 2029ODE-412Orphan Drug (7y)3.1y
  • Sep 21, 2029ODE*ODE*3.1y
  • Sep 21, 2029ODE*ODE*3.1y
  • Sep 21, 2029ODE-409Orphan Drug (7y)3.1y
  • Sep 21, 2029ODE*ODE*3.1y
  • Sep 21, 2029ODE-409Orphan Drug (7y)3.1y
  • Mar 27, 2028PEDPediatric (6mo bonus)1.6y
  • Mar 27, 2028PEDPediatric (6mo bonus)1.6y
  • Mar 27, 2028PEDPediatric (6mo bonus)1.6y
  • Mar 27, 2028PEDPediatric (6mo bonus)1.6y
  • Mar 27, 2028PEDPediatric (6mo bonus)1.6y
  • Mar 27, 2028PEDPediatric (6mo bonus)1.6y
  • Nov 29, 2027PEDPediatric (6mo bonus)1.3y
  • Nov 29, 2027PEDPediatric (6mo bonus)1.3y
  • Nov 8, 2027PEDPediatric (6mo bonus)1.2y
  • Nov 8, 2027PEDPediatric (6mo bonus)1.2y
  • Nov 8, 2027PEDPediatric (6mo bonus)1.2y
  • Nov 8, 2027PEDPediatric (6mo bonus)1.2y
  • Nov 8, 2027PEDPediatric (6mo bonus)1.2y
  • Nov 8, 2027PEDPediatric (6mo bonus)1.2y
  • Sep 27, 2027M-312Method (3y)1.1y
  • Sep 27, 2027M-312Method (3y)1.1y
  • Sep 27, 2027M-311Method (3y)1.1y
  • Sep 27, 2027M-312Method (3y)1.1y
  • Sep 27, 2027M-312Method (3y)1.1y
  • Sep 27, 2027M-311Method (3y)1.1y
  • Sep 27, 2027M-311Method (3y)1.1y
  • Sep 27, 2027M-312Method (3y)1.1y
  • Sep 27, 2027M-311Method (3y)1.1y
  • Sep 27, 2027M-311Method (3y)1.1y
  • Sep 27, 2027M-312Method (3y)1.1y
  • Sep 27, 2027M-311Method (3y)1.1y
  • May 29, 2027NPPNew Product (3y)287d
  • May 29, 2027NPPNew Product (3y)287d
  • May 8, 2027ODE-301Orphan Drug (7y)266d
  • May 8, 2027ODE-303Orphan Drug (7y)266d
  • May 8, 2027ODE-302Orphan Drug (7y)266d
  • May 8, 2027ODE-301Orphan Drug (7y)266d
  • May 8, 2027ODE*ODE*266d
  • May 8, 2027ODE-302Orphan Drug (7y)266d
  • May 8, 2027ODE-303Orphan Drug (7y)266d
  • May 8, 2027ODE*ODE*266d
  • May 8, 2027ODE*ODE*266d
  • May 8, 2027ODE*ODE*266d

News(2)

  • OncLive Polls Reveal Picks for Top Lung Cancer Abstracts at ASCO 2026
    Lung cancer experts rank key abstracts of interest from the upcoming ASCO Annual Meeting on OncLive’s social media.
    onclive · 3mo ago
  • Track the Lung Cancer Abstracts That are Gaining Attention at ASCO 2026
    Read on to see what data are poised to shape clinical discussions and decision-making in lung cancer at 2026 ASCO Annual Meeting in Chicago, Illinois.
    onclive · 3mo ago
brand
Retevmo
trade names
Retevmo, Retsevmo
generic
selpercatinib
MOA
Coiled-coil domain-containing protein 6/Tyrosine-protein kinase receptor RET inhibitor; Tyrosine-protein kinase receptor RET inhibitor; Kinesin-1 heavy chain/ Tyrosine-protein kinase receptor RET inhibitor
indication
Anaplastic Thyroid Cancer
phase
marketed
Data sources
openFDA · ClinicalTrials.gov · OpenTargets
last refreshed 18m ago
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