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Pinnacle Biologics dépose une nouvelle indication pharmaceutique en Allemagne et en France
Date:12/5/2012

rradier la zone affectée par une lumière laser non brûlante 40 à 50 heures après l'injection de PHOTOFRIN. Après avoir été injecté, le PHOTOFRIN est attiré vers certains tissus, en particulier les cellules cancéreuses. La tumeur est détruite par l'action de réactions biochimiques, et non en raison de la chaleur. La sélectivité de la tumeur est due à une rétention préférentielle de PHOTOFRIN par la tumeur qui survient en même temps que la diffusion sélective de lumière sur le site tumoral.

En France, les indications actuellement agréées pour le PHOTOFRIN sont pour le traitement de récidives de cancers bronchiques non à petites cellules ou de cancers de l'œsophage, qui avaient été auparavant traités au niveau locorégional. En Allemagne, les indications actuellement agréées pour le PHOTOFRIN sont pour le traitement curatif de patients atteints de carcinomes précoces endobronchiaux non à petites cellules prouvés histologiquement (stade T est NO MO ou T1 NO MO) et qui, selon le médecin traitant, ne peuvent pas être traités de façon curative par la chirurgie ou la radiothérapie.

Pinnacle a récemment acquis la technologie laser et des fibres utilisée pour la PDT. Cette acquisition a permis à la société de créer un portefeuille complet de produits qui comprend aujourd'hui tous les composants thérapeutiques PDT PHOTOFRIN.

Informations importantes en matière de sécurité

Pour des informations importantes en matière de sécurité concernant les indications actuellement agréées, prière de consulter la notice PHOTOFRIN valable pour votre région.

A propos de Pinnacle

Pinnacle Biologics Inc. est un
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SOURCE Pinnacle Biologics, Inc.
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