Sotorasib

Identification

Summary

Sotorasib is an experimental KRAS inhibitor being investigated for the treatment of KRAS G12C mutant non small cell lung cancer, colorectal cancer, and appendix cancer.

Brand Names

Lumakras

Generic Name

Sotorasib

DrugBank Accession Number

DB15569

Background

Sotorasib, also known as AMG-510, is an acrylamide-derived KRAS inhibitor developed by Amgen.^1,3 It is indicated in the treatment of adult patients with KRAS G12C mutant non-small cell lung cancer.⁶ This mutation makes up >50% of all KRAS mutations.² Mutant KRAS discovered in 1982 but was not considered a druggable target until the mid-2010s.⁵ It is the first experimental KRAS inhibitor.¹ The drug MRTX849 is also currently being developed and has the same target.¹

Sotorasib was granted FDA approval on May 28, 2021,⁶ followed by the European Commission's approval on January 10, 2022.⁷

Type

Small Molecule

Groups

Approved, Investigational

Structure

3D

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MOLSDF3D-SDFPDBSMILESInChI

Similar Structures

Structure for Sotorasib (DB15569)

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Weight

Average: 560.606
Monoisotopic: 560.234745176

Chemical Formula

C₃₀H₃₀F₂N₆O₃

Synonyms

• 6-fluoro-7-(2-fluoro-6-hydroxyphenyl)-(1M)-1-[4-methyl-2-(propan-2-yl)pyridin-3-yl]-4-[(2S)-2- methyl-4-(prop-2-enoyl)piperazin-1-yl]pyrido[2,3-d]pyrimidin-2(1H)-one
• Kras G12C inhibitor 9
• Sotorasib

External IDs

• AMG 510
• AMG-510
• AMG510

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Pharmacology

Indication

Sotorasib is indicated in the treatment of KRAS G12C-mutated locally advanced or metastatic non-small cell lung cancer (NSCLC) in adults who have received at least one prior systemic therapy.⁶

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Associated Conditions

Indication Type	Indication	Combined Product Details	Approval Level	Age Group	Patient Characteristics	Dose Form
Treatment of	Locally advanced non-small cell lung cancer		••••••••••••	•••••	•••••••••• •• ••••••••••• •• ••••• •••••••• •••••••• ••••••• •••• •••••••••• ••••• •••••••••• •••••• •• •••••••••• •••••••••••• • ••••••• •••••••••• •••••••• •••••••• ••••• •••••••	••••••
Treatment of	Locally advanced non-small cell lung cancer		••••••••••••	•••••	••• ••••• •••••••• •••••••	••••••
Treatment of	Metastatic non-small cell lung cancer		••••••••••••	•••••	•••••••• •••••••• ••••• •••••••• •••••••• ••••••• •••• •••••••••• ••••• •••••••••• •••••• •• •••••••••• •••••••••••• • ••••••• •••••••••• •••••••••• •• ••••••••••• •• ••••• •••••••	••••••
Treatment of	Metastatic non-small cell lung cancer		••••••••••••	•••••	••• ••••• •••••••• •••••••	••••••

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Pharmacodynamics

Sotorasib is indicated in the treatment of adults with KRAS G12C mutant non small cell lung cancer.⁶ It has a moderate duration of action as it is given daily.⁶ Patients should be counselled regarding the risks of hepatotoxicity, interstitial lung disease and pneumonitis; and to avoid breastfeeding during treatment and up to 1 week after the last dose.⁶

Mechanism of action

Normally GTP binds to KRAS, activating the protein and promoting effectors to the MAP kinase pathway.³ GTP is hydrolyzed to GDP, and KRAS is inactivated.⁴ KRAS G12C mutations impair hydrolysis of GTP, leaving it in the active form.⁴

Sotorasib binds to the cysteine residue in KRAS G12C mutations, holding the protein in its inactive form.¹ The cysteine residue that sotorasib targets is not present in the wild type KRAS, which prevents off-target effects.⁶ This mutation is present in 13% of non small cell lung cancer, 3% of colorectal and appendix cancer, and 1-3% of solid tumors.¹

Target	Actions	Organism
AGTPase KRas	inhibitor	Humans

Absorption

A 960 mg once daily dose of sotorasib reaches a C_max of 7.50 µg/mL, with a median T_max of 2.0 hours, and an AUC_0-24h of 65.3 h*µg/mL.⁵

Volume of distribution

The volume of distribution of sotorasib is 211 L.⁶

Protein binding

Sotorasib is 89% protein bound in plasma.⁶

Metabolism

Sotorasib is predominantly metabolized through conjugation or by CYP3As.⁶

Route of elimination

Sotorasib is 74% eliminated in the feces and 6% eliminated in the urine.⁶ 53% of the dose recovered in the feces and 1% of the dose recovered in the urine is in the form of the unchanged parent compound.⁶

Half-life

Sotorasib has a terminal elimination half life of 5.5 ± 1.8 hours.^5,6

Clearance

Sotorasib has an apparent clearance at steady state of 26.2 L/h.⁶

Adverse Effects

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Toxicity

Data regarding overdoses of sotorasib are not readily available. However, in clinical trials, signs of dose limiting toxicity were not found.⁵ Patients experiencing an overdose may experience and increased risk and severity of adverse effects such as diarrhea, nausea, vomiting, fatigue, and elevated aminotransferase.⁵

Pathways

Not Available

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Not Available

Interactions

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This information should not be interpreted without the help of a healthcare provider. If you believe you are experiencing an interaction, contact a healthcare provider immediately. The absence of an interaction does not necessarily mean no interactions exist.

• Approved
• Vet approved
• Nutraceutical
• Illicit
• Withdrawn
• Investigational
• Experimental
• All Drugs

Drug	Interaction
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1,2-Benzodiazepine	The serum concentration of 1,2-Benzodiazepine can be decreased when it is combined with Sotorasib.
Abemaciclib	The serum concentration of Abemaciclib can be decreased when it is combined with Sotorasib.
Abiraterone	The serum concentration of Abiraterone can be decreased when it is combined with Sotorasib.
Acalabrutinib	The serum concentration of Acalabrutinib can be decreased when it is combined with Sotorasib.
Acenocoumarol	The serum concentration of Acenocoumarol can be decreased when it is combined with Sotorasib.

Food Interactions

• Avoid antacids. If coadministration cannot be avoided, take sotorasib 4 hours before or 10 hours after antacids.
• Take with or without food. Taking sotorasib with a high fat, high calorie meal increases total exposure to sotorasib by 25%.

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International/Other Brands

Lumakras (Amgen)

Brand Name Prescription Products

Name	Dosage	Strength	Route	Labeller	Marketing Start	Marketing End	Region	Image
Lumakras	Tablet, coated	120 mg/1	Oral	AMGEN INC	2021-05-28	Not applicable
Lumakras	Tablet, coated	320 mg/1	Oral	AMGEN INC	2023-02-02	Not applicable
Lumakras	Tablet	120 mg	Oral	Amgen	2021-10-22	Not applicable
Lumykras	Tablet, film coated	120 mg	Oral	Amgen Europe Bv	2022-05-04	Not applicable
Lumykras	Tablet, film coated	120 mg	Oral	Amgen Europe Bv	2022-05-04	Not applicable

Categories

ATC Codes

L01XX73 — Sotorasib

• L01XX — Other antineoplastic agents
• L01X — OTHER ANTINEOPLASTIC AGENTS
• L01 — ANTINEOPLASTIC AGENTS
• L — ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS

Drug Categories

• Antineoplastic Agents
• Antineoplastic Agents, Immunological
• Antineoplastic and Immunomodulating Agents
• BCRP/ABCG2 Inhibitors
• Cytochrome P-450 CYP2B6 Inducers
• Cytochrome P-450 CYP2B6 Inducers (strength unknown)
• Cytochrome P-450 CYP2C8 Inducers
• Cytochrome P-450 CYP2C8 Inducers (strength unknown)
• Cytochrome P-450 CYP2C9 Inducers
• Cytochrome P-450 CYP2C9 Inducers (strength unknown)
• Cytochrome P-450 CYP3A Substrates
• Cytochrome P-450 Enzyme Inducers
• Cytochrome P-450 Substrates
• Immune Checkpoint Inhibitors
• P-glycoprotein inhibitors
• RAS GTPase Inhibitors

Classification

Not classified

Affected organisms

• Humans

Chemical Identifiers

UNII

2B2VM6UC8G

CAS number

2252403-56-6

InChI Key

NXQKSXLFSAEQCZ-SFHVURJKSA-N

InChI

InChI=1S/C30H30F2N6O3/c1-6-23(40)36-12-13-37(18(5)15-36)28-19-14-21(32)26(24-20(31)8-7-9-22(24)39)34-29(19)38(30(41)35-28)27-17(4)10-11-33-25(27)16(2)3/h6-11,14,16,18,39H,1,12-13,15H2,2-5H3/t18-/m0/s1

IUPAC Name

6-fluoro-7-(2-fluoro-6-hydroxyphenyl)-1-[4-methyl-2-(propan-2-yl)pyridin-3-yl]-4-[(2S)-2-methyl-4-(prop-2-enoyl)piperazin-1-yl]-1H,2H-pyrido[2,3-d]pyrimidin-2-one

SMILES

CC(C)C1=NC=CC(C)=C1N1C(=O)N=C(N2CCN(C[C@@H]2C)C(=O)C=C)C2=CC(F)=C(N=C12)C1=C(O)C=CC=C1F

References

General References

1. Authors unspecified: AMG 510 First to Inhibit "Undruggable" KRAS. Cancer Discov. 2019 Aug;9(8):988-989. doi: 10.1158/2159-8290.CD-NB2019-073. Epub 2019 Jun 12. [Article]
2. Fiala O, Pesek M, Finek J, Benesova L, Belsanova B, Minarik M: The dominant role of G12C over other KRAS mutation types in the negative prediction of efficacy of epidermal growth factor receptor tyrosine kinase inhibitors in non-small cell lung cancer. Cancer Genet. 2013 Jan-Feb;206(1-2):26-31. doi: 10.1016/j.cancergen.2012.12.003. Epub 2013 Jan 10. [Article]
3. Canon J, Rex K, Saiki AY, Mohr C, Cooke K, Bagal D, Gaida K, Holt T, Knutson CG, Koppada N, Lanman BA, Werner J, Rapaport AS, San Miguel T, Ortiz R, Osgood T, Sun JR, Zhu X, McCarter JD, Volak LP, Houk BE, Fakih MG, O'Neil BH, Price TJ, Falchook GS, Desai J, Kuo J, Govindan R, Hong DS, Ouyang W, Henary H, Arvedson T, Cee VJ, Lipford JR: The clinical KRAS(G12C) inhibitor AMG 510 drives anti-tumour immunity. Nature. 2019 Oct 30. pii: 10.1038/s41586-019-1694-1. doi: 10.1038/s41586-019-1694-1. [Article]
4. Christensen JG, Hallin J, Engstrom LD, Hargis L, Calinisan A, Aranda R, Briere DM, Sudhakar N, Bowcut V, Baer BR, Ballard JA, Burkard MR, Fell JB, Fischer JP, Vigers GP, Xue JY, Gatto S, Fernandez-Banet J, Pavlicek A, Velastegui K, Chao RC, Barton J, Pierobon M, Baldelli E, Patricoin EF, Cassidy DP, Marx MA, Rybkin II, Johnson ML, Ou SI, Lito P, Papadopoulos KP, Janne PA, Olson P: The KRASG12C Inhibitor, MRTX849, Provides Insight Toward Therapeutic Susceptibility of KRAS Mutant Cancers in Mouse Models and Patients. Cancer Discov. 2019 Oct 28. pii: 2159-8290.CD-19-1167. doi: 10.1158/2159-8290.CD-19-1167. [Article]
5. Hong DS, Fakih MG, Strickler JH, Desai J, Durm GA, Shapiro GI, Falchook GS, Price TJ, Sacher A, Denlinger CS, Bang YJ, Dy GK, Krauss JC, Kuboki Y, Kuo JC, Coveler AL, Park K, Kim TW, Barlesi F, Munster PN, Ramalingam SS, Burns TF, Meric-Bernstam F, Henary H, Ngang J, Ngarmchamnanrith G, Kim J, Houk BE, Canon J, Lipford JR, Friberg G, Lito P, Govindan R, Li BT: KRAS(G12C) Inhibition with Sotorasib in Advanced Solid Tumors. N Engl J Med. 2020 Sep 24;383(13):1207-1217. doi: 10.1056/NEJMoa1917239. Epub 2020 Sep 20. [Article]
6. FDA Approved Drug Products: Lumakras (Sotorasib) Oral Tablet [Link]
7. BioSpace News: European Commission Approves Lumykras® (Sotorasib) For Patients With KRAS G12C-mutated Advanced Non-Small Cell Lung Cancer [Link]

External Links

Human Metabolome Database

HMDB0304845

KEGG Drug

D12055

ChemSpider

72380148

BindingDB

50514402

RxNav

2550714

ChEBI

178199

ChEMBL

CHEMBL4535757

Wikipedia

Sotorasib

Clinical Trials

Clinical Trials Learn More" title="About Clinical Trials" id="clinical-trials-info" class="drug-info-popup" href="javascript:void(0);">

Phase	Status	Purpose	Conditions	Count
3	Active Not Recruiting	Treatment	Colorectal Cancer	1
3	Active Not Recruiting	Treatment	KRAS p, G12c Mutated /Advanced Metastatic NSCLC	1
3	Not Yet Recruiting	Treatment	Metastatic Colorectal Cancer (CRC)	1
3	Recruiting	Treatment	Non-Small Cell Lung Cancer (NSCLC)	1
2	Active Not Recruiting	Treatment	Efficacy	1

Pharmacoeconomics

Manufacturers

Not Available

Packagers

Not Available

Dosage Forms

Form	Route	Strength
Tablet	Oral	120 mg
Tablet, coated	Oral	120 mg/1
Tablet, coated	Oral	320 mg/1
Tablet, film coated	Oral	120 mg

Prices

Not Available

Patents

Patent Number	Pediatric Extension	Approved	Expires (estimated)	Region
US11236091	No	2020-05-20	2040-05-20
US10519146	No	2019-12-31	2038-05-21
US11426404	No	2020-08-11	2040-08-11
US11827635	No	2020-05-20	2040-05-20

Properties

State

Solid

Experimental Properties

Property	Value	Source
water solubility	1.3 mg/mL at pH 1.2, 0.03 mg/mL at pH 6.8	FDA
pKa	8.06, 4.56	FDA

Predicted Properties

Property	Value	Source
Water Solubility	0.0185 mg/mL	ALOGPS
logP	3.6	ALOGPS
logP	4.74	Chemaxon
logS	-4.5	ALOGPS
pKa (Strongest Acidic)	6.98	Chemaxon
pKa (Strongest Basic)	4.74	Chemaxon
Physiological Charge	-1	Chemaxon
Hydrogen Acceptor Count	7	Chemaxon
Hydrogen Donor Count	1	Chemaxon
Polar Surface Area	102.23 Å2	Chemaxon
Rotatable Bond Count	3	Chemaxon
Refractivity	150.12 m3·mol-1	Chemaxon
Polarizability	57.21 Å3	Chemaxon
Number of Rings	5	Chemaxon
Bioavailability	1	Chemaxon
Rule of Five	No	Chemaxon
Ghose Filter	No	Chemaxon
Veber's Rule	No	Chemaxon
MDDR-like Rule	No	Chemaxon

Predicted ADMET Features

Not Available

Spectra

Mass Spec (NIST)

Not Available

Spectra

Spectrum	Spectrum Type	Splash Key
Predicted MS/MS Spectrum - 10V, Positive (Annotated)	Predicted LC-MS/MS	splash10-08fr-0000090000-512d1faa63b84d4e65c6
Predicted MS/MS Spectrum - 10V, Negative (Annotated)	Predicted LC-MS/MS	splash10-00kr-0000590000-193c2cd436ec9b200f95
Predicted MS/MS Spectrum - 20V, Positive (Annotated)	Predicted LC-MS/MS	splash10-03di-0000390000-7b6d1f2df4a7a5e8fd2b
Predicted MS/MS Spectrum - 20V, Negative (Annotated)	Predicted LC-MS/MS	splash10-00kr-3000490000-95dd578ebbf60c8f5234
Predicted MS/MS Spectrum - 40V, Positive (Annotated)	Predicted LC-MS/MS	splash10-0f7c-0001930000-b951c0e73876d1911d70
Predicted MS/MS Spectrum - 40V, Negative (Annotated)	Predicted LC-MS/MS	splash10-0a4r-3203960000-c268c8cebcaa3a956765

Chromatographic Properties

Collision Cross Sections (CCS)

Not Available

Targets

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Details1. GTPase KRas

Kind

Protein

Organism

Humans

Pharmacological action

Yes

Actions

Inhibitor

General Function

Protein complex binding

Specific Function

Ras proteins bind GDP/GTP and possess intrinsic GTPase activity. Plays an important role in the regulation of cell proliferation (PubMed:23698361, PubMed:22711838).

Gene Name

KRAS

Uniprot ID

P01116

Uniprot Name

GTPase KRas

Molecular Weight

21655.67 Da

References

1. Authors unspecified: AMG 510 First to Inhibit "Undruggable" KRAS. Cancer Discov. 2019 Aug;9(8):988-989. doi: 10.1158/2159-8290.CD-NB2019-073. Epub 2019 Jun 12. [Article]
2. Fiala O, Pesek M, Finek J, Benesova L, Belsanova B, Minarik M: The dominant role of G12C over other KRAS mutation types in the negative prediction of efficacy of epidermal growth factor receptor tyrosine kinase inhibitors in non-small cell lung cancer. Cancer Genet. 2013 Jan-Feb;206(1-2):26-31. doi: 10.1016/j.cancergen.2012.12.003. Epub 2013 Jan 10. [Article]
3. Canon J, Rex K, Saiki AY, Mohr C, Cooke K, Bagal D, Gaida K, Holt T, Knutson CG, Koppada N, Lanman BA, Werner J, Rapaport AS, San Miguel T, Ortiz R, Osgood T, Sun JR, Zhu X, McCarter JD, Volak LP, Houk BE, Fakih MG, O'Neil BH, Price TJ, Falchook GS, Desai J, Kuo J, Govindan R, Hong DS, Ouyang W, Henary H, Arvedson T, Cee VJ, Lipford JR: The clinical KRAS(G12C) inhibitor AMG 510 drives anti-tumour immunity. Nature. 2019 Oct 30. pii: 10.1038/s41586-019-1694-1. doi: 10.1038/s41586-019-1694-1. [Article]
4. Ryan MB, Fece de la Cruz F, Phat S, Myers DT, Wong E, Shahzade HA, Hong CB, Corcoran RB: Vertical Pathway Inhibition Overcomes Adaptive Feedback Resistance to KRAS(G12C) Inhibition. Clin Cancer Res. 2020 Apr 1;26(7):1633-1643. doi: 10.1158/1078-0432.CCR-19-3523. Epub 2019 Nov 27. [Article]
5. Lanman BA, Allen JR, Allen JG, Amegadzie AK, Ashton KS, Booker SK, Chen JJ, Chen N, Frohn MJ, Goodman G, Kopecky DJ, Liu L, Lopez P, Low JD, Ma V, Minatti AE, Nguyen TT, Nishimura N, Pickrell AJ, Reed AB, Shin Y, Siegmund AC, Tamayo NA, Tegley CM, Walton MC, Wang HL, Wurz RP, Xue M, Yang KC, Achanta P, Bartberger MD, Canon J, Hollis LS, McCarter JD, Mohr C, Rex K, Saiki AY, San Miguel T, Volak LP, Wang KH, Whittington DA, Zech SG, Lipford JR, Cee VJ: Discovery of a Covalent Inhibitor of KRAS(G12C) (AMG 510) for the Treatment of Solid Tumors. J Med Chem. 2020 Jan 9;63(1):52-65. doi: 10.1021/acs.jmedchem.9b01180. Epub 2019 Dec 24. [Article]
6. Madhyastha N, Samantha SK, Dittakavi S, Markose M, Mallurwar SR, Zainuddin M, Mullangi R: Validated HPLC-MS/MS method for quantitation of AMG 510, a KRAS G12C inhibitor, in mouse plasma and its application to a pharmacokinetic study in mice. Biomed Chromatogr. 2021 Apr;35(4):e5043. doi: 10.1002/bmc.5043. Epub 2021 Jan 19. [Article]
7. Tanaka N, Lin JJ, Li C, Ryan MB, Zhang J, Kiedrowski LA, Michel AG, Syed MU, Fella KA, Sakhi M, Baiev I, Juric D, Gainor JF, Klempner SJ, Lennerz JK, Siravegna G, Bar-Peled L, Hata AN, Heist RS, Corcoran RB: Clinical acquired resistance to KRASG12C inhibition through a novel KRAS switch-II pocket mutation and polyclonal alterations converging on RAS-MAPK reactivation. Cancer Discov. 2021 Apr 6. pii: 2159-8290.CD-21-0365. doi: 10.1158/2159-8290.CD-21-0365. [Article]

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Drug created at November 01, 2019 18:34 / Updated at February 20, 2024 23:54