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¤@ª½³£¦³¹ê»Ú¨Ò¤l¦b¤Wºt¡G Áú¬ü¬ì§Þ»PºX¤UÁú¬üÃÄ·~¦b§¹¦¨ªÍÀù»P¿}§¿¯fªvÀøÁ{§É¹êÅç«á¡AªÑ»ù¤À§O¤jº¦ 968% »P 699% 11/13·s»D SEOUL -- Hanmi Science subsidiary Hanmi Pharmaceutical has inked a 3.9 billion euro ($4.26 billion) licensing deal with France¡¦s Sanofi for new diabetes treatments Under the terms of the agreement, Janssen will obtain exclusive worldwide rights, except Korea and China, to develop and commercialize HM12525A. Hanmi will receive an upfront payment of $105 million, and is eligible for up to $810 million in potential clinical development, regulatory and sales milestones. ¤~n¶i¤J¤G´Á¡Hº¦¤Q¿¡Hupfront ¤@»õ¬üª÷ ¡AÁ`ȤK»õ¬üª÷±ÂÅv¡A¤¤°êÁú°ê¦Û°â ¥@¬É¼é¬y¨ÏµM¡A¦p¦U¦ì¤j¤j©Ò説¡A¤£¬OEPS¨Óµû»ù来µÛ°Õ¡I ³o¤½¥q·s»D»á¦h¡A±ÂÅv¤@Ó±µ¤@Ó⋯³o¥u¬O¨ä¤¤¤@¨Ò |
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¥xÁÞ¤j¡A¦Ñ´¤j¡A¯E«È¤j¡Aµ½¤H¤j¡ACliff¤j¡G ¸ò±zÌ»¡Án©êºp¤F¡A°²¤é«U°ÈÄñ¨¡A¨S¯à¤Î®É¶K¤W¥H¤Uªº¶K¤å¡C ¥H¤U¤p§ÌɪáÄm¦ò¡A¬O²q·Q¤j´£¨Ñªº¸ê®Æ(²q·Q¤j¥i¯à³Ìªñ¤ñ¸û¦£¡A¤p§ÌÀ°¦£¶K)¡G pȺâªk the logrank test¦³¨âºØ¡A¤@ºØ¬OCox-Mantel Logrank Test ¤½¦¡¡G X^2 = (O1 ¡V E1)^2/ E1 + (O2 ¡V E2)^2/ E2 ¨Ò¤l¦b²q·Q¤j´£¨Ñªºhttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC403858/ ¥t¤@ºØ¬OMantel-Haenszel Logrank Test ¤½¦¡¡G X^2 = (O1 ¡V E1)^2/ V ¨Ò¤l¦b²q·Q¤j´£¨Ñªºhttps://stat.ethz.ch/education/semesters/ss2011/seminar/contents/presentation_2.pdf ¦b¤£¬O¤p¼Ë¥»ªº±¡ªp¤U¡A¨âÓ¤½¦¡ªºpºâµ²ªG¬O¬Û¦Pªº¡A©Ò¥H·íµM¥Î²Ä¤@Ó¤½¦¡¤ñ¸û¦nºâ¡C Á|http://www.ncbi.nlm.nih.gov/pmc/articles/PMC403858/ùتº¨Ò¤l¡G The logrank test is used to test the null hypothesis that there is no difference between the populations in the probability of an event (here a death) at any time point. The analysis is based on the times of events (here deaths). For each such time we calculate the observed number of deaths in each group and the number expected if there were in reality no difference between the groups. The first death was in week 6, when one patient in group 1 died. At the start of this week, there were 51 subjects alive in total, so the risk of death in this week was 1/51. There were 20 patients in group 1, so, if the null hypothesis were true, the expected number of deaths in group 1 is 20 ¡Ñ 1/51 = 0.39. Likewise, in group 2 the expected number of deaths is 31 ¡Ñ 1/51 = 0.61. The second event occurred in week 10, when there were two deaths. There were now 19 and 31 patients at risk (alive) in the two groups, one having died in week 6, so the probability of death in week 10 was 2/50. The expected numbers of deaths were 19 ¡Ñ 2/50 = 0.76 and 31 ¡Ñ 2/50 = 1.24 respectively. The same calculations are performed each time an event occurs. If a survival time is censored, that individual is considered to be at risk of dying in the week of the censoring but not in subsequent weeks. This way of handling censored observations is the same as for the Kaplan-Meier survival curve.3 From the calculations for each time of death, the total numbers of expected deaths were 22.48 in group 1 and 19.52 in group 2, and the observed numbers of deaths were 14 and 28. We can now use a £q2 test of the null hypothesis. The test statistic is the sum of (O - E)2/E for each group, where O and E are the totals of the observed and expected events. Here (14 - 22.48)2 / 22.48 + (28 - 19.52)2 / 19.52 = 6.88. The degrees of freedom are the number of groups minus one, i.e. 2 - 1 = 1. From a table of the £q2 distribution we get P < 0.01, so that the difference between the groups is statistically significant. ©Ò¥H¡A 1.¥Í¦s¤ÀªR¥ÎK-M¨ç¼Æ¨Óµe¹Ï§äPFS©MOS¡A¥Îthe logrank test¨ÓpºâpÈ¡A¤]´N¬O¥ÎIntention-to-treat analysis¡FITT¡A¨CÓdropout¡A¨CÓ³]¸ê®Æ³£n¶i¤J²Îp¤ÀªR¡C 2.The degrees of freedom are the number of groups minus one, i.e. 2 - 1 = 1 3.n¦³¹ê»Úªº¼Æ¦r¥X¨Ó(¤]´N¬O¸Ñª¼)¤~¯àºâ¥XpÈ(¤]´N¬O·Q±Àºâ¬O§_p¤p©ó0.001)¡A¦ý¦pªG¥u·Qª¾¹Dp¬O§_p¤p©ó0.05¡A¥Î187©M229³o¨âӼƦr¤j²¤±À¤@¤U´N¥i¥Hª¾¹D¤F 4.¦b§PÂ_PD¼Æ¾Ú¤jP¦¨¼ô«á¡A¤£¦Pªº®É¶¡ÂI¶}ª¼©Òpºâ¥XªºpÈ®t²§·|«Ü¤p¡A¤]´N¬O¡A°²³]2015/5©Î2015/8©Î2015/11³£¶}ª¼ªº¸Ü¡ApÈ®t²§·|«Ü¤p¡F¤]´N¬O»¡¡ApȤ£·|¦]¶}ª¼®É¶¡ªº¿ï¾Ü¦Ó²£¥Í¤jªº®t²§¡C ¥H¤W½Ð°Ñ¦Ò¡C |
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