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罗斯他泊芬:光动力点(PhotoPoint)SnET2、普立汀(Purlytin)、四价锡原卟啉、SnET2、乙基锡原卟啉。

Rostaporfin: PhotoPoint SnET2, Purlytin, Sn(IV) etiopurpurin, SnET2, tin ethyl etiopurpurin.

出版信息

Drugs R D. 2004;5(1):58-61. doi: 10.2165/00126839-200405010-00013.

Abstract

The photosensitiser rostaporfin [Purlytin trade mark, SnET2, tin ethyl etiopurpurin, Sn(IV) etiopurpurin, PhotoPoint SnET2] was developed by Miravant Medical Technologies (USA) for use in the company's PhotoPoint trade mark photodynamic therapy. The therapy relies on low power, non-thermal light produced by a solid-state diode laser, sourced from the device co-developing partner, Iredex Corporation. Mirvant is currently undergoing discussions for potential licensing agreements with leading ophthalmology companies for rostaporfin. In June 2002, Miravant and Bausch & Lomb signed a non-binding letter on intent. The companies are expected to jointly review phase III clinical data concerning rostaporfin. Following the review Bausch & Lomb may negotiate an exclusive worldwide license to develop and commercialise the agent for ophthalmological indications. Previously, in June 1995, Miravant granted Pharmacia & Upjohn (now Pfizer) an exclusive worldwide license for development and marketing of rostaporfin. However, this agreement was terminated in March 2002, at which time Miravant regained the rights to all assets related to rostaporfin. In April 2000, Monsanto merged with Pharmacia & Upjohn to form Pharmacia Corporation. Subsequently, on 16 April 2003, Pharmacia Corporation was acquired by, and merged into, Pfizer. Preclinical studies had been underway for other vision-threatening eye diseases, as it also has potential in the treatment of diabetic retinopathy and glaucoma. The US FDA had granted fast-track status to rostaporfin for the treatment of age-related macular degeneration in 1998.

摘要

光敏剂罗斯塔泊芬[Purlytin商标,SnET2,二乙锡卟吩,四价锡卟吩,PhotoPoint SnET2]由美国Miravant医疗技术公司开发,用于该公司PhotoPoint商标的光动力疗法。该疗法依靠固态二极管激光器产生的低功率、非热光,激光器由共同开发伙伴Iredex公司提供。Miravant目前正在与领先的眼科公司就罗斯塔泊芬的潜在许可协议进行商讨。2002年6月,Miravant与博士伦签署了一份无约束力的意向书。预计两家公司将共同审查有关罗斯塔泊芬的III期临床数据。审查之后,博士伦可能会谈判获得一项全球独家许可,以开发该药物并将其商业化用于眼科适应症。此前,1995年6月,Miravant授予法玛西亚普强公司(现为辉瑞公司)一项全球独家许可,用于罗斯塔泊芬的开发和营销。然而,该协议于2002年3月终止,当时Miravant重新获得了与罗斯塔泊芬相关的所有资产的权利。2000年4月,孟山都与法玛西亚普强公司合并,成立了法玛西亚公司。随后,2003年4月16日,法玛西亚公司被辉瑞收购并并入辉瑞。针对其他威胁视力的眼部疾病的临床前研究一直在进行,因为它在治疗糖尿病性视网膜病变和青光眼方面也具有潜力。1998年,美国食品药品监督管理局授予罗斯塔泊芬治疗年龄相关性黄斑变性的快速通道地位。

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