Methods for the treatment of arthritis using phosphonates...

A - Human Necessities – 61 – K

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A61K 31/675 (2006.01)

Patent

CA 2138366

Image (see fig.1) The present invention provides methods of treating a human or other animal subject afflicted with arthritis, including rheumatoid, arthritis and osteoarthritis, comprising a sixty (60)-day treatment period, comprised of an optional NSAID administration regimen and a phosphonate administration regimen, wherein (a) said optional NSAID administration regimen which comprises the administration to said subject of NSAIDs at a level of from 20% to 80%, preferably 20% to 70%, most preferably 20% to 50% of the conventionally prescribed daily dose on each day that said NSAID is administered; provided that said NSAID is administered in sufficient quantities and on a sufficient number of days to alleviate symptoms of inflammation, and wherein (b) said phosphonate administration regimen comprises the administration to said subject of a phosphonate at a dose equivalent to a systemic level of from about 0.0005 mgP/kg to about 1.0 mgP/kg per day that said phosphonate is administered; provided that said phosphonate is administered at least 1 day of every said sixty (60)-day treatment period.

Image (voir fig. 1) La présente invention porte sur des méthodes pour le traitement de sujets humains ou animaux atteints d'arthrite, dont la polyarthrite rhumatoïde, l'arthrite et l'arthrose, prévoyant une période de traitement de soixante (60) jours et l'administration d'un régime thérapeutique optionnel d'AINS et un régime d'administration de phosphonate, dans lequel (a) ledit régime optionnel d'administration d'AINS qui prévoit l'administration au sujet d'AINS à un niveau variant entre 20 % et 80 %, de préférence entre 20 % et 70 %, idéalement entre 20 % et 50 % de la dose quotidienne habituellement prescrite chaque jour que l'AINS est administré; à condition que l'AINS en question soit administré en quantité suffisante et pendant un nombre de jours suffisants pour soulager les symptômes de l'inflammation, et dans lequel ledit régime d'administration de phosphonate prévoit l'administration au sujet d'un phosphonate à une dose équivalente à un niveau systémique d'environ 0,0005 mgP/kg à environ 1 mgP/kg par jour que ledit phosphonate est administré; à condition que ledit phosphonate soit administré pendant au moins 1 jour au cours de la période de traitement de soixante (60) jours.

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