词条 | Naldemedine |
释义 |
| IUPAC_name = 17-(cyclopropylmethyl)-6,7-didehydro-4,5α-epoxy-3,6,14-trihydroxy-N-[2-(3-phenyl-1,2,4-oxadiazol-5-yl)propan-2-yl]morphinan-7-carboxamide | image = Naldemedine.svg | tradename = Symproic | Drugs.com = {{Drugs.com|parent|symproic}} | CAS_number = 916072-89-4 | CAS_supplemental = {{CAS|1345728-04-2}} (tosylate) | ATC_prefix = A06 | ATC_suffix = AH05 | PubChem = 135626906 | DrugBank = DB11691 | UNII = 03KSI6WLXH | KEGG = D10188 | C=32 | H=34 | N=4 | O=6 | molecular_weight = 570.63556 g/mol | ChemSpiderID = 28530803 | smiles = CC(C)(c1nc(no1)c2ccccc2)NC(=O)C3=C([C@H]4[C@@]56CCN([C@@H]([C@@]5(C3)O)Cc7c6c(c(cc7)O)O4)CC8CC8)O | StdInChI = 1S/C32H34N4O6/c1-30(2,29-33-27(35-42-29)18-6-4-3-5-7-18)34-28(39)20-15-32(40)22-14-19-10-11-21(37)25-23(19)31(32,26(41-25)24(20)38)12-13-36(22)16-17-8-9-17/h3-7,10-11,17,22,26,37-38,40H,8-9,12-16H2,1-2H3,(H,34,39)/t22-,26+,31+,32-/m1/s1 | StdInChIKey = AXQACEQYCPKDMV-RZAWKFBISA-N | bioavailability = | protein_bound = | metabolism = | elimination_half-life = | excretion = | pregnancy_AU = | pregnancy_category = | legal_US = Investigational New Drug | legal_status = | routes_of_administration = Oral }}Naldemedine (INN, USAN; S-297,995, Symproic) is a peripherally-selective μ-opioid receptor antagonist developed by Shionogi which is approved for the treatment of opioid-induced constipation in adult patients with chronic non-cancer pain.[1] Clinical studies have thus far found it to possess statistically significant effectiveness for these indications and to be generally well-tolerated with predominantly mild to moderate gastrointestinal side effects.[2][3] No effects indicative of central opioid withdrawal or impact on the analgesic or miotic effects of co-administered opioids have been observed.[2] CommercializationNaldemedine is manufactured by Shionogi Inc., a U.S.-based subsidiary of Shionogi & Co., Ltd. Shionogi & Co., Ltd. (SGIOF) is a Japanese pharmaceutical company founded in 1878 based in Osaka, Japan. Shionogi Inc. is fully funded by its parent company, Shionogi & Co., Ltd. The parent company specializes in pharmaceuticals, diagnostic reagents and medical devices in Japan and internationally. Naldemedine is their only gastroenterology product in the United States. In the US market, Shionogi Inc. has partnered with Purdue Pharma in a joint venture for US commercialization of Symproic.[4] Purdue Pharma LP is a privately held pharmaceutical company based in the United States that specializes in chronic pain disorders.[5] Purdue Pharma appealed to remove the Class II scheduling of Symproic as accordant to the Controlled Substances Act. The appeal was posted to the Federal Register on July 12, 2017.[6] The Drug Enforcement Administration officially removed the Class II scheduling in September 2017.[7] Manufacturer financesSince 2015, Shionogi & Co., Ltd. has produced increasing net income. At the end of fiscal year 2016, Shionogi & Co., Ltd. had a net income of $66,687,000. At the end of fiscal year 2017, they increased their net income to $83,879,000.[8] How much of this is attributed to sales of Symproic is unknown. Shionogi & Co., Ltd. ends their fiscal year on March 31 of each year. Considering the drug was only FDA approved on March 23 of 2017, the true valuation of the drug is yet to be seen. Purdue Pharma has begun advertising for the medication to be available by October 2017.[9] Intellectual propertyThere are currently three patents issued for naldemedine tosylate by the United States Patent and Trademark Office. All patents are owned by Shionogi Inc. and will expire from 2026-2031.[10] Naldemedine tosylate has 46 other patents in 18 different countries.[11] Preclinical trials12 Phase I clinical trials were reported for the use of naldemedine in healthy volunteers.[12] In a single ascending dose study, subjects received one dose of naldemedine (0.1–100 mg) or one dose of a placebo. In a multiple ascending dose study, subjects received once daily naldemedine (3–30 mg) or placebo for 10 days. Maximum plasma concentrations were reached within 0.5-0.75 hours. There were no reported major safety concerns, even at doses 150-500 times the available dose of 0.2 mg. In both studies, gastrointestinal events occurred more frequently with naldemedine, but researchers concluded these to be treatment related.[13] Clinical trialsThe approval of naldemedine came from the results of the COMPOSE program, a phase three clinical studies program conducted in adults 18–80 years of age with chronic non-cancer pain opioid induced constipation. COMPOSE-I and COMPOSE-II were 12-week double blind randomized controlled trials comparing the use of naldemedine to placebo in the patient population. COMPOSE-I began in August 2013 until January 2015 in 68 outpatient clinic in seven countries. COMPOSE-II began in November 2013 until June 2015 taking place in 69 outpatient clinics in six countries. In both trials, patients were randomly assigned to receive either naldemedine 0.2 mg or placebo once daily for 12 weeks. A responder had at least three spontaneous bowel movements per week with an increase of one spontaneous bowel movement for nine of the 12 weeks, including three of the final four weeks of the study. In COMPOSE-I and COMPOSE-II, the proportion of responders were significantly higher in the naldemedine group than the placebo group. Adverse events were similar in both trials, however, patients in the naldemedine group had slightly higher rates of adverse events.[14] COMPOSE-III was a 52-week clinical trial examining the long term safety with naldemedine in patients with non cancer chronic pain. Results from this trial showed statistical significance for increased weekly bowel movements and no opioid withdrawal symptoms. The study also concluded adverse effects were more similar between two groups.[12] All trials were conducted following Good Clinical Practice guidelines.[12] See also
References1. ^{{Cite news|url=http://www.chemdiv.com/da-approves-symproic-naldemedine-treatment-opioid-induced-constipation/|title=FDA Approves Symproic (naldemedine) for the Treatment of Opioid-Induced Constipation - Chemdiv|date=2017-03-27|work=Chemdiv|access-date=2017-04-05|language=en-US}} {{Antiemetics}}{{Laxatives}}{{Opioidergics}}2. ^1 {{cite book|title=Constipation - Causes, Diagnosis and Treatment|date=2012-03-07|publisher=|isbn=978-953-51-0237-3|page=7|chapter=Drugs in Development for Opioid-Induced Constipation|doi=10.5772/30377|last1=De Sarro|first1=Giovambattista|author2=Kelly S. Sprawls|author3=Egilius L.H. Spierings|author4=Dustin Tran|editor1-first=Anthony|editor1-last=Catto-Smith G.|chapterurl=http://cdn.intechopen.com/pdfs/31222/InTech-Drugs_in_development_for_opioid_induced_constipation.pdf|accessdate=12 May 2012}} 3. ^{{cite web|url=http://www.shionogi.co.jp/ir_en/explanatory/pdf/e_p090327.pdf|title=Research and Development at Shionogi (as of March 2009)|date=2009-03-27|format=PDF|author=Shionogi|accessdate=2012-05-12|deadurl=yes|archiveurl=https://web.archive.org/web/20130522233917/http://www.shionogi.co.jp/ir_en/explanatory/pdf/e_p090327.pdf|archivedate=2013-05-22|df=}} 4. ^{{cite web|title=SHIONOGI AND PURDUE PHARMA ESTABLISH ALLIANCE FOR JOINT U.S. COMMERCIALIZATION OF NALDEMEDINE|url=http://www.purduepharma.com/news-media/2016/12/shionogi-and-purdue-pharma-establish-alliance-for-joint-u-s-commercialization-of-naldemedine/|website=Purdue Pharma|publisher=Purdue Pharma|accessdate=31 October 2017}} 5. ^{{cite web|title=FDA Approves Symproic® (naldemedine) Once-Daily Tablets C-II for the Treatment of Opioid-Induced Constipation in Adults with Chronic Non-Cancer Pain|url=http://www.purduepharma.com/news-media/2017/03/fda-approves-symproic-naldemedine-once-daily-tablets-c-ii-for-the-treatment-of-opioid-induced-constipation-in-adults-with-chronic-non-cancer-pain/|website=Purdue Pharma|publisher=Purdue Pharma|accessdate=31 October 2017}} 6. ^{{cite web|title=Schedules of controlled substances: removal of naldemedine from control|url=http://www.gpo.gov/fdsys/pkg/FR-2017-07-12/pdf/2017-14482.pdf|website=Federal Register|publisher=Federal Register|accessdate=1 November 2017}} 7. ^{{Cite news|url=http://www.empr.com/news/naldemedine-symproic-opioid-constipation-pain/article/699733/|title=Symproic Now Available for Opioid-Induced Constipation|date=2017-10-12|work=MPR|access-date=2017-11-08|language=en}} 8. ^{{cite web|title=Shionogi & Co., Ltd.|url=https://finance.yahoo.com/quote/SGIOF/financials?p=SGIOF|website=Yahoo Finance|publisher=Yahoo Finance|accessdate=31 October 2017}} 9. ^{{cite web|title=Opioid Induced Constipation|url=http://www.purduepharma.com/healthcare-professionals/products/|website=Opioid Induced Constipation|publisher=Purdue Pharma|accessdate=31 October 2017}} 10. ^{{cite web|title=Generic Symproic Availability|url=https://www.drugs.com/availability/generic-symproic.html|website=Drugs.com|publisher=Drugs.com|accessdate=31 October 2017}} 11. ^{{cite web|title=Naldemedine tosylate - generic drug details|url=https://www.drugpatentwatch.com/p/generic-api/naldemedine+tosylate#patent_family|website=Drug Patent Watch|publisher=Drug Patent Watch|accessdate=31 October 2017}} 12. ^1 2 {{cite web|title=Center for Drug Evaluaiton and Research Medication Review|url=https://www.accessdata.fda.gov/drugsatfda_docs/nda/2017/208854Orig1s000MedR.pdf|website=FDA|publisher=FDA|accessdate=31 October 2017}} 13. ^{{cite journal|last1=Fukumura|first1=K|last2=Yokota|first2=T|last3=Baba|first3=Y|last4=Arjona Ferreira|first4=JC|title=Phase 1, Randomized, Double-Blind, Placebo-Controlled Studies on the Safety, Tolerability, and Pharmacokinetics of Naldemedine in Healthy Volunteers.|journal=Clinical pharmacology in drug development|date=27 September 2017|doi=10.1002/cpdd.387|pmid=28960888}} 14. ^{{cite journal|last1=Hale|first1=M|last2=Wild|first2=J|last3=Reddy|first3=J|last4=Yamada|first4=T|last5=Arjona Ferreira|first5=JC|title=Naldemedine versus placebo for opioid-induced constipation (COMPOSE-1 and COMPOSE-2): two multicentre, phase 3, double-blind, randomised, parallel-group trials.|journal=The Lancet. Gastroenterology & Hepatology|date=August 2017|volume=2|issue=8|pages=555–564|doi=10.1016/S2468-1253(17)30105-X|pmid=28576452}} 8 : Carboxamides|Cyclopropanes|Morphinans|Opioids|Opioid antagonists|Oxadiazoles|Peripherally selective drugs|Experimental drugs |
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