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¬Ý¾§r, ¬O§_ı±o©t¨àÃÄ©eû·|«ÜÁcº¾©O? ¬O§_¥i¥H²z¸Ñ¸Û¦pAOP»P«Ü¦h¨ä¥Lì¥ý©t¨àÃĦbÃÄÃÒ®Öµo«e©Î¦æ¾P¤@¬q®É¶¡«á¤]¥Ó½Ð¸ê®æ°h¥X©O? (¦]¬°¾Ö¦³³oÓorphan¸ê®æ»Ýn«Ü¦h,«Ü¦h,«Ü¦hªº©w´Á³ø§i/¸ê®Æ¦^õX¡K..©Ò¥H, °£«D¸ÓÃįuªºÁÙ¦³«áÄò²`¤J¶}µo»P¬ã¨s§ë¤J®É¤]»Ýn©eû·|ªº¬ÛÃö«ü¾É»P¸ê·½, §_«h½Ö¦³¤Ó¦h¸ê·½¥h·d³o¨Ç?)
¬Ý§¹¤FºM°h©t¨àÃÄ¸ê®æªº³ø§iì¤å»P¤¤¤åºKn, §Ú¥i¥H±µ¨üAOP/Ãĵج°¤F·m®É¶¡¤W¥«¾P°â¦Ó¥Ó½ÐºM¾Porphan¸ê®æ. Áö¦p¦¹, §A·|ı±o5/13¤½§i«Ü¸Ô¹ê©P¥þ? ¦³«OÅ@§ë¸ê¤H?
¤Wz½Ķ¤§ì¤åÁÙìºK¿ý: The sponsor also includes an argument of improved safety, but this is not quantified nor examined in the context of the broader safety profile. It is argued that the overall safety profile was consistent with class effects of other interferons used (interferon alfa-2a and 2b), and that during AOP¡¦s clinical development, no leukaemogenic transformations have been observed in ropegIFN alfa-2b treated patients, whereas two acute leukaemia were observed in the control arm (i.e. HU-treated patients). The Committee considered that an improved safety argument would require further elaboration.
Withdrawal Assessment Report ¡V Orphan Maintenance EMA/47444/2019 Page 7/7 Moreover, the other arguments discussed above have to be interpreted with caution taking into consideration that to establish non-inferiority, post-hoc modifications were introduced in the primary endpoint and non-inferiority margin. It was also pointed out that a non-inferiority conclusion by itself would not suffice to justify significant benefit. A list of issues was raised to the applicant. 4. COMP list of issues Significant benefit Significant benefit is argued on the basis of improved efficacy and safety versus hydroxyurea. The sponsor is requested to further elaborate on the issue taking into consideration the following points: • Provide a discussion versus all authorised counterparts, indicated for the updated indication as discussed with the CHMP; • Further elaborate on the issue of improved efficacy versus hydroxyurea, taking into consideration that to establish non-inferiority, post-hoc modifications were introduced in the primary endpoint and non-inferiority margin; • Further elaborate on the argument of improved safety, in the context of the broader safety profile of the proposed product and the comparator(s);
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