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(2009-07-02 12:24:20) ²Æ¸»(751899926) Pharmaprojects Accession No: 1852 Main Details Drug Name World Status Pharma Status pirmenol Launched Fully Launched CI-845 Pimenol pirmavar Latest Change Updated On By Latest Change 6 Oct 2005 IL Dainippon Sumitomo Pharma merger reported Company Status Data Originator Country Development Stage Pfizer USA Launched Activity Data Therapy Description Code Status Antiarrhythmic C1B Launched Pharmacology Description Code Sodium channel antagonist CHA-NA- Therapy Code Pharmacology Code C1B CHA-NA- Route of Administration Route of Administration Code Alimentary, po A-PO Indication Status Tachycardia, supraventricular Launched Chemical Data Origin of Material Code Description CH-SY Chemical, synthetic CAS Registry Number Molecular Weight Molecular Formula 61477-94-9 68252-19-7 338.50 C22H30N2O Chemical Name (2-Pyridinemethanol, alpha-[3-(2,6-dimethyl-1-piperidinyl)propyl]-.alpha.phenyl-, cis-(+)- [CAS] Structure Patent Data Country Number Priority Country Priority Date US 4112103 US 15 April 1976 Country Data Country Name Status Year Launched Licensing Op. Argentina - No Australia - No Austria - No Belgium - No Brazil - No Canada - No Chile - No China - No Colombia - No Denmark - No Finland - No France - No Germany - No Greece - No Hong Kong - No India - No Ireland - No Israel - No Italy - No Japan Launched 1995 No Luxembourg - No Malaysia - No Mexico - No Netherlands - No New Zealand - No Norway - No Peru - No Philippines - No Portugal - No Russian Federation - No South Africa - No South Korea - No Spain - No Sweden - No Switzerland - No Thailand - No Turkey - No UK - No USA - No Venezuela - No Major Events Event Date Act/Est Event Details 15 May 1997 Est Licences Discontinued Dainippon 15 Mar 1996 Est New Licensees Dainippon 15 Mar 1996 Est First Launches Japan 15 Sep 1992 Est Registration Submissions Japan Ratings Novelty Market Size Speed Total Established Strategy (2) US$ 501-2000 million (2) Not available (0) Not available Detailed Information Pirmenol is a long-acting class Ia antiarrhythmic, developed by Parke-Davis (Pfizer). It has similar antiarrhythmic efficacy to procainamide (qv) (Pacing Clin Electrophysiol, 1988, 11, 308). Marketing It is launched in Japan (1995) (Scrip, 1992, 1741, 23; Company communications, Parke-Davis, Dec 1993 & Jan 1996). It was previously developed with Dainippon (now Dainippon Sumitomo Pharma) (Company communication, Warner-Lambert, Jan 1996), but is no longer under joint-development (Company communication, Dainippon, Feb 1997). Clinical In 17 patients with frequent ventricular ectopic depolarizations, 100-200mg/day pirmenol prolonged the QRS and QT intervals without affecting the JT, QTc and JTc intervals. All pirmenol recipients achieved 75% suppression of arrhythmias (Clin Cardiol, 1991, 14, 25). In 20 patients with paroxysmal supraventricular tachycardia (PSVT) and paroxysmal atrial fibrillation, 200mg pirmenol po significantly increased heart rate and total systemic resistance, and reduced the stroke volume index. It restored sinus rhythm during tachyarrhythmia in 4/7 patients with PSVT and 4/9 patients with paroxysmal atrial fibrillation. It was well tolerated (J Cardiovasc Pharmacol, 1996, 27, 556). Updated by PA on 27/5/1998. Additional Clinical Information Phase II In patients with supraventricular tachycardia, 200mg po inhibited induction of tachycardia in 5/11 at 60min post-dose and in 7/11 at 120min; no side-effects were seen (3rd Cardiovasc Pharmacother Int Symp (Kyoto), 1989, Abs P575, 0). 2008 1¡ä7 29 -£¤ Copyright Informa UK Ltd 2008 |
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