[Stockholm, Sweden, November 8, 2007.] The World Health Organization’s INN programme for identification of pharmaceutical substances has approved OxyPharma’s name Rabeximod for the company’s drug for treatment of Rheumatoid Arthritis (RA). Rabeximod is an orally administered compound for treatment of moderate or severe active RA that is currently undergoing phase II clinical testing in eight European countries. OxyPharma’s disease-modifing antirheumatic drug (DMARD) Rabeximod
is included in the new list (List 59) of recommended names, INN’s
(International Nonproprietary Names), published by WHO Drug Information.
The WHO’s INN programme facilitates the identification of pharmaceutical
substances or active pharmaceutical ingredients. Each INN is a unique
name that is globally recognized and is public property. A nonproprietary
name is also known as a generic name. Rabeximod (formerly known as Rob 803) is currently undergoing a phase II clinical testing in patients with moderate to severe active RA. The phase II study is carried out in Belgium, Bulgaria, Latvia, Lithuania, Romania, Serbia, Sweden and the UK by Pharm-Olam International, a multi-national contract research organization. Principal Investigator is Prof. Lars Klareskog, Head of Rheumatology Unit at Karolinska Hospital, Stockholm, Sweden. The trial is expected to be completed by Q2, 2008. The aim of the INN system is to provide health professionals with a unique and universally available designated name to identify each pharmaceutical substance. The existence of an international nomenclature for pharmaceutical substances, in the form of INN, is important for the clear identification, safe prescription and dispensing of medicines to patients and for communication and exchange of information among health professionals and scientists worldwide. About OxyPharma: For additional information please contact: |
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