Aticaprant: Difference between revisions
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Aticaprant is a [[potency (pharmacology)|potent]], [[binding selectivity|selective]], short-acting (i.e., non-"inactivating") [[receptor antagonist|antagonist]] of the KOR (K<sub>i</sub> = 0.81 nM vs. 24.0 nM and 155 nM for the [[mu-opioid receptor|μ-opioid receptor]] (MOR) and [[delta-opioid receptor|δ-opioid receptor]] (DOR), respectively; approximately 30-fold selectivity for the KOR).<ref name="pmid24071566" /><ref name="pmid24619932" /><ref name="Rorick-Kehn2014" /> The drug has been found to dose-dependently block [[fentanyl]]-induced [[miosis]] at 25 mg and 60 mg in humans (with minimal to no blockade at doses of 4 to 10 mg), suggesting that the drug significantly occupies and antagonizes the MOR at a dose of at least 25 mg but not of 10 mg or less.<ref name="Rorick-Kehn2014" /> However, a more recent study assessing neuroendocrine effects of the drug in normal volunteers and subjects with a history of cocaine dependence reported observations consistent with modest MOR antagonism at the 10 mg dose.<ref>{{cite journal | vauthors = Reed B, Butelman ER, Fry RS, Kimani R, Kreek MJ | title = Repeated Administration of Opra Kappa (LY2456302), a Novel, Short-Acting, Selective KOP-r Antagonist, in Persons with and without Cocaine Dependence | journal = Neuropsychopharmacology | volume = 43 | issue = 4 | pages = 928 | date = March 2018 | pmid = 29422497 | doi = 10.1038/npp.2017.245 | pmc = 5809790 }}</ref> In [[animal model]]s of [[depression (mood)|depression]], aticaprant has been found to have potent synergistic efficacy in combination with other antidepressants such as [[citalopram]] and [[imipramine]].<ref name="pmid24690494" /> |
Aticaprant is a [[potency (pharmacology)|potent]], [[binding selectivity|selective]], short-acting (i.e., non-"inactivating") [[receptor antagonist|antagonist]] of the KOR (K<sub>i</sub> = 0.81 nM vs. 24.0 nM and 155 nM for the [[mu-opioid receptor|μ-opioid receptor]] (MOR) and [[delta-opioid receptor|δ-opioid receptor]] (DOR), respectively; approximately 30-fold selectivity for the KOR).<ref name="pmid24071566" /><ref name="pmid24619932" /><ref name="Rorick-Kehn2014" /> The drug has been found to dose-dependently block [[fentanyl]]-induced [[miosis]] at 25 mg and 60 mg in humans (with minimal to no blockade at doses of 4 to 10 mg), suggesting that the drug significantly occupies and antagonizes the MOR at a dose of at least 25 mg but not of 10 mg or less.<ref name="Rorick-Kehn2014" /> However, a more recent study assessing neuroendocrine effects of the drug in normal volunteers and subjects with a history of cocaine dependence reported observations consistent with modest MOR antagonism at the 10 mg dose.<ref>{{cite journal | vauthors = Reed B, Butelman ER, Fry RS, Kimani R, Kreek MJ | title = Repeated Administration of Opra Kappa (LY2456302), a Novel, Short-Acting, Selective KOP-r Antagonist, in Persons with and without Cocaine Dependence | journal = Neuropsychopharmacology | volume = 43 | issue = 4 | pages = 928 | date = March 2018 | pmid = 29422497 | doi = 10.1038/npp.2017.245 | pmc = 5809790 }}</ref> In [[animal model]]s of [[depression (mood)|depression]], aticaprant has been found to have potent synergistic efficacy in combination with other antidepressants such as [[citalopram]] and [[imipramine]].<ref name="pmid24690494" /> |
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[[Positron emission tomography]] imaging revealed that brain KORs were almost completely saturated by the drug 2.5 hours following a single dose of 10 mg, which supported the 4 mg to 25 mg dosages that aticaprant is being explored in clinical trials.<ref name="BusinessWire2015" /><ref name="NaganawaDickinson2015">{{cite journal | vauthors = Naganawa M, Dickinson GL, Zheng MQ, Henry S, Vandenhende F, Witcher J, Bell R, Nabulsi N, Lin SF, Ropchan J, Neumeister A, Ranganathan M, Tauscher J, Huang Y, Carson RE | display-authors = 6 | title = Receptor Occupancy of the κ-Opioid Antagonist LY2456302 Measured with Positron Emission Tomography and the Novel Radiotracer 11C-LY2795050 | journal = The Journal of Pharmacology and Experimental Therapeutics | volume = 356 | issue = 2 | pages = 260–6 | date = February 2016 | pmid = 26628406 | pmc = 4727157 | doi = 10.1124/jpet.115.229278 }}</ref> Occupancy was 35% for a 0.5 mg dose and 94% for a 10 mg dose.<ref name="NaganawaDickinson2015" /> At 24 hours post-dose, receptor occupancy was 19% for 0.5 mg and 82% for 25 mg.<ref name="NaganawaDickinson2015" /> No serious [[side effect]]s were observed, and all side effects seen were mild to moderate and not |
[[Positron emission tomography]] imaging revealed that brain KORs were almost completely saturated by the drug 2.5 hours following a single dose of 10 mg, which supported the 4 mg to 25 mg dosages that aticaprant is being explored at in clinical trials.<ref name="BusinessWire2015" /><ref name="NaganawaDickinson2015">{{cite journal | vauthors = Naganawa M, Dickinson GL, Zheng MQ, Henry S, Vandenhende F, Witcher J, Bell R, Nabulsi N, Lin SF, Ropchan J, Neumeister A, Ranganathan M, Tauscher J, Huang Y, Carson RE | display-authors = 6 | title = Receptor Occupancy of the κ-Opioid Antagonist LY2456302 Measured with Positron Emission Tomography and the Novel Radiotracer 11C-LY2795050 | journal = The Journal of Pharmacology and Experimental Therapeutics | volume = 356 | issue = 2 | pages = 260–6 | date = February 2016 | pmid = 26628406 | pmc = 4727157 | doi = 10.1124/jpet.115.229278 }}</ref> Occupancy was 35% for a 0.5 mg dose and 94% for a 10 mg dose.<ref name="pmid34363128">{{cite journal | vauthors = Placzek MS | title = Imaging Kappa Opioid Receptors in the Living Brain with Positron Emission Tomography | journal = Handb Exp Pharmacol | volume = | issue = | pages = | date = August 2021 | pmid = 34363128 | doi = 10.1007/164_2021_498 | url = }}</ref><ref name="NaganawaDickinson2015" /> At 24 hours post-dose, receptor occupancy was 19% for 0.5 mg and 82% for 25 mg.<ref name="pmid34363128" /><ref name="NaganawaDickinson2015" /> No serious [[side effect]]s were observed, and all side effects seen were mild to moderate and were not thought to be due to aticaprant.<ref name="NaganawaDickinson2015" /> |
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===Pharmacokinetics=== |
===Pharmacokinetics=== |
Revision as of 00:51, 30 October 2021
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Clinical data | |
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Other names | JNJ-67953964; CERC-501; LY-2456302 |
Routes of administration | By mouth[1] |
Pharmacokinetic data | |
Bioavailability | 25%[1] |
Elimination half-life | 30–40 hours[1] |
Identifiers | |
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CAS Number | |
PubChem CID | |
ChemSpider | |
UNII | |
KEGG | |
ChEMBL | |
CompTox Dashboard (EPA) | |
Chemical and physical data | |
Formula | C26H27FN2O2 |
Molar mass | 418.512 g·mol−1 |
3D model (JSmol) | |
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Aticaprant (developmental codes JNJ-67953964, CERC-501, and LY-2456302) is a selective antagonist of the κ-opioid receptor (KOR) which was originally developed by Eli Lilly and is now under development by Janssen Pharmaceuticals for the treatment of major depressive disorder and smoking withdrawal.[2][3][4][5][6]
Pharmacology
Pharmacodynamics
Aticaprant is a potent, selective, short-acting (i.e., non-"inactivating") antagonist of the KOR (Ki = 0.81 nM vs. 24.0 nM and 155 nM for the μ-opioid receptor (MOR) and δ-opioid receptor (DOR), respectively; approximately 30-fold selectivity for the KOR).[3][4][5] The drug has been found to dose-dependently block fentanyl-induced miosis at 25 mg and 60 mg in humans (with minimal to no blockade at doses of 4 to 10 mg), suggesting that the drug significantly occupies and antagonizes the MOR at a dose of at least 25 mg but not of 10 mg or less.[5] However, a more recent study assessing neuroendocrine effects of the drug in normal volunteers and subjects with a history of cocaine dependence reported observations consistent with modest MOR antagonism at the 10 mg dose.[7] In animal models of depression, aticaprant has been found to have potent synergistic efficacy in combination with other antidepressants such as citalopram and imipramine.[8]
Positron emission tomography imaging revealed that brain KORs were almost completely saturated by the drug 2.5 hours following a single dose of 10 mg, which supported the 4 mg to 25 mg dosages that aticaprant is being explored at in clinical trials.[6][9] Occupancy was 35% for a 0.5 mg dose and 94% for a 10 mg dose.[10][9] At 24 hours post-dose, receptor occupancy was 19% for 0.5 mg and 82% for 25 mg.[10][9] No serious side effects were observed, and all side effects seen were mild to moderate and were not thought to be due to aticaprant.[9]
Pharmacokinetics
The oral bioavailability of aticaprant is 25% and is regarded as good.[1] The drug is rapidly absorbed, with maximal concentrations occurring 1 to 2 hours after administration.[1] It has an elimination half-life of 30 to 40 hours in healthy subjects.[1] The circulating levels of aticaprant increase proportionally with increasing doses.[1] Steady-state concentrations are reached after 6 to 8 days of once-daily dosing.[1] Aticaprant has been shown to reproducibly penetrate the blood–brain barrier.[6][9]
History
Aticaprant was originally developed by Eli Lilly under the code name LY-2456302.[2] It first appeared in the scientific literature in 2010.[11]
In February 2015, Cerecor Inc. announced that they had acquired the rights from Eli Lilly to develop and commercialize LY-2456302 (under the new developmental code CERC-501).[12]
As of 2016, aticaprant has reached phase II clinical trials as an augmentation to antidepressant therapy for treatment-resistant depression.[13][8] A phase II study of aticaprant in heavy smokers was commenced in early 2016 and results of the study were expected before the end of 2016.[9] Aticaprant failed to meet its main endpoint for nicotine withdrawal in the study.[14]
In August 2017, it was announced that Cerecor had sold its rights to aticaprant to Janssen Pharmaceuticals.[15][14] Janssen was also experimenting with esketamine for the treatment of depression as of 2017.[14]
See also
References
- ^ a b c d e f g h Li W, Sun H, Chen H, Yang X, Xiao L, Liu R, Shao L, Qiu Z (2016). "Major Depressive Disorder and Kappa Opioid Receptor Antagonists". Translational Perioperative and Pain Medicine. 1 (2): 4–16. PMC 4871611. PMID 27213169.
- ^ a b "CERC 501". Adis Insight. 30 January 2018.
- ^ a b Rorick-Kehn LM, Witkin JM, Statnick MA, Eberle EL, McKinzie JH, Kahl SD, et al. (February 2014). "LY2456302 is a novel, potent, orally-bioavailable small molecule kappa-selective antagonist with activity in animal models predictive of efficacy in mood and addictive disorders". Neuropharmacology. 77: 131–44. doi:10.1016/j.neuropharm.2013.09.021. PMID 24071566.
- ^ a b Lowe SL, Wong CJ, Witcher J, Gonzales CR, Dickinson GL, Bell RL, et al. (September 2014). "Safety, tolerability, and pharmacokinetic evaluation of single- and multiple-ascending doses of a novel kappa opioid receptor antagonist LY2456302 and drug interaction with ethanol in healthy subjects". Journal of Clinical Pharmacology. 54 (9): 968–78. doi:10.1002/jcph.286. PMID 24619932.
- ^ a b c Rorick-Kehn LM, Witcher JW, Lowe SL, Gonzales CR, Weller MA, Bell RL, et al. (October 2014). "Determining pharmacological selectivity of the kappa opioid receptor antagonist LY2456302 using pupillometry as a translational biomarker in rat and human". The International Journal of Neuropsychopharmacology. 18 (2): pyu036. doi:10.1093/ijnp/pyu036. PMC 4368892. PMID 25637376.
- ^ a b c BusinessWire (11 December 2015). "Publication Reports Human Brain Penetration and Target Engagement of Cerecor's Oral Kappa Opioid Receptor Antagonist, CERC-501".
{{cite news}}
:|author=
has generic name (help) - ^ Reed B, Butelman ER, Fry RS, Kimani R, Kreek MJ (March 2018). "Repeated Administration of Opra Kappa (LY2456302), a Novel, Short-Acting, Selective KOP-r Antagonist, in Persons with and without Cocaine Dependence". Neuropsychopharmacology. 43 (4): 928. doi:10.1038/npp.2017.245. PMC 5809790. PMID 29422497.
- ^ a b Urbano M, Guerrero M, Rosen H, Roberts E (May 2014). "Antagonists of the kappa opioid receptor". Bioorganic & Medicinal Chemistry Letters. 24 (9): 2021–32. doi:10.1016/j.bmcl.2014.03.040. PMID 24690494.
- ^ a b c d e f Naganawa M, Dickinson GL, Zheng MQ, Henry S, Vandenhende F, Witcher J, et al. (February 2016). "Receptor Occupancy of the κ-Opioid Antagonist LY2456302 Measured with Positron Emission Tomography and the Novel Radiotracer 11C-LY2795050". The Journal of Pharmacology and Experimental Therapeutics. 356 (2): 260–6. doi:10.1124/jpet.115.229278. PMC 4727157. PMID 26628406.
- ^ a b Placzek MS (August 2021). "Imaging Kappa Opioid Receptors in the Living Brain with Positron Emission Tomography". Handb Exp Pharmacol. doi:10.1007/164_2021_498. PMID 34363128.
- ^ Zheng MQ, Nabulsi N, Kim SJ, Tomasi G, Lin SF, Mitch C, et al. (March 2013). "Synthesis and evaluation of 11C-LY2795050 as a κ-opioid receptor antagonist radiotracer for PET imaging". Journal of Nuclear Medicine. 54 (3): 455–63. doi:10.2967/jnumed.112.109512. PMC 3775344. PMID 23353688.
- ^ "Cerecor Bolsters Clinical Pipeline with Acquisition of Phase 2-ready Kappa Opioid Receptor Antagonist from Eli Lilly and Company". cerecor.com. February 20, 2015. Archived from the original on 2015-02-23. Retrieved March 18, 2015.
- ^ Rankovic Z, Hargreaves R, Bingham M (2012). Drug Discovery for Psychiatric Disorders. Royal Society of Chemistry. pp. 314–317. ISBN 978-1-84973-365-6.
- ^ a b c Bushey R (August 2017). "J&J Adds New Depression Drug to Portfolio". Drug Discovery and Development Magazine.
- ^ "Cerecor Announces Divestiture of CERC-501 to Janssen Pharmaceuticals, Inc". Marketwired. August 2017.
Further reading
- Carlezon WA, Krystal AD (October 2016). "Kappa-Opioid Antagonists for Psychiatric Disorders: From Bench to Clinical Trials". Depress Anxiety. 33 (10): 895–906. doi:10.1002/da.22500. PMC 5288841. PMID 27699938.
- Li W, Sun H, Chen H, Yang X, Xiao L, Liu R, Shao L, Qiu Z (2016). "Major Depressive Disorder and Kappa Opioid Receptor Antagonists". Transl Perioper Pain Med. 1 (2): 4–16. PMC 4871611. PMID 27213169.
- Dhir A (January 2017). "Investigational drugs for treating major depressive disorder". Expert Opin Investig Drugs. 26 (1): 9–24. doi:10.1080/13543784.2017.1267727. PMID 27960559.
- Reed, Brian; Butelman, Eduardo R; Kreek, Mary Jeanne (2017). "Endogenous opioid system in addiction and addiction-related behaviors". Current Opinion in Behavioral Sciences. 13: 196–202. doi:10.1016/j.cobeha.2016.12.002. ISSN 2352-1546.
- Rakesh G, Pae CU, Masand PS (August 2017). "Beyond serotonin: newer antidepressants in the future". Expert Rev Neurother. 17 (8): 777–790. doi:10.1080/14737175.2017.1341310. PMID 28598698.
- Helal MA, Habib ES, Chittiboyina AG (December 2017). "Selective kappa opioid antagonists for treatment of addiction, are we there yet?". Eur J Med Chem. 141: 632–647. doi:10.1016/j.ejmech.2017.10.012. PMID 29107424.
- McHugh KL, Kelly JP (2018). "Modulation of the central opioid system as an antidepressant target in rodent models". Prog. Brain Res. 239: 49–87. doi:10.1016/bs.pbr.2018.07.003. PMID 30314569.
- Bailey, Sarah J.; Husbands, Stephen M. (2018). "Targeting opioid receptor signaling in depression: do we need selective κ opioid receptor antagonists?". Neuronal Signaling. 2 (2). doi:10.1042/NS20170145. ISSN 2059-6553.
- Chavkin C (August 2018). "Kappa-opioid antagonists as stress resilience medications for the treatment of alcohol use disorders". Neuropsychopharmacology. 43 (9): 1803–1804. doi:10.1038/s41386-018-0046-4. PMC 6046055. PMID 29752444.
- Krystal AD, Pizzagalli DA, Mathew SJ, Sanacora G, Keefe R, Song A, Calabrese J, Goddard A, Goodman W, Lisanby SH, Smoski M, Weiner R, Iosifescu D, Nurnberger J, Szabo S, Murrough J, Shekhar A, Potter W (December 2018). "The first implementation of the NIMH FAST-FAIL approach to psychiatric drug development". Nat Rev Drug Discov. 18 (1): 82–84. doi:10.1038/nrd.2018.222. PMC 6816017. PMID 30591715.
- Lazar, Max A.; McIntyre, Roger S. (2019). "Novel Therapeutic Targets for Major Depressive Disorder": 383–400. doi:10.1016/B978-0-12-813333-0.00034-2.
{{cite journal}}
: Cite journal requires|journal=
(help) - Browne CA, Lucki I (September 2019). "Targeting opioid dysregulation in depression for the development of novel therapeutics". Pharmacol. Ther. 201: 51–76. doi:10.1016/j.pharmthera.2019.04.009. PMC 6859062. PMID 31051197.
- Banks ML (2020). "The Rise and Fall of Kappa-Opioid Receptors in Drug Abuse Research". Handb Exp Pharmacol. 258: 147–165. doi:10.1007/164_2019_268. PMC 7756963. PMID 31463605.
- Browne CA, Jacobson ML, Lucki I (2020). "Novel Targets to Treat Depression: Opioid-Based Therapeutics". Harv Rev Psychiatry. 28 (1): 40–59. doi:10.1097/HRP.0000000000000242. PMID 31913981.
- Jacobson ML, Browne CA, Lucki I (January 2020). "Kappa Opioid Receptor Antagonists as Potential Therapeutics for Stress-Related Disorders". Annu. Rev. Pharmacol. Toxicol. 60: 615–636. doi:10.1146/annurev-pharmtox-010919-023317. PMID 31914893.
- Mercadante S, Romualdi P (2020). "The Therapeutic Potential of Novel Kappa Opioid Receptor-based Treatments". Curr. Med. Chem. 27 (12): 2012–2020. doi:10.2174/0929867326666190121142459. PMID 30666905.