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http://www.hematology.org.tw/web2/project/img/mPurpose-logo.png ¦^À³¤ÑYÀº¡G1¤ë9¤é¬ã°Q·|¡A¤¤µØ¥Á°ê¦å²G¯f¾Ç·|ºô¯¸¦³¤½¥¬°Ñ¥[¤è¦¡¡G½Ð°Ñ¾\¡G ¤¤µØ¥Á°ê¦å²G¯f¾Ç·| The Hematology Society of Taiwan ¦a§}¡G¥x¥_¥«±`¼wµó¤@¸¹¥x¤j´ººÖÀ]¤G¼Ó203D«Ç ¹q¸Ü¡G02-23751091 ¶Ç¯u¡G02-23751092 Email:hema.taiwan@gmail.com / hema@seed.net.tw 09 Jan MPN°ê»Ú¬ã°Q·| ¬¡°Êºô¯¸¶±³sµ²¡Ghttp://www.contentednet.url.tw/mpnAsia/Agenda.html ³ø¦W®É¶¡: 1¡^²Ä¤@ªi³ø¦W 12/10-12/23¡A¶È¶}©ñµ¹¦å²G¯f¾Ç·|·|û³ø¦W 2¡^²Ä¤Gªi³ø¦W 12/24-12/30¡AµøªÅ¦ì±¡ªp¶}©ñµ¹«D·|û³ø¦W ✏ ³ø¦W/¸`¥Øªí MPN°ê»Ú¬ã°Q·| MPN Asia The 1st International Congress on Myeloproliferative Neoplasms úc105¦~1¤ë09¤é(¤»)09:30:00 ¶µ¥Ø ¤º®e ®É¶¡ 2016-01-09ªº09:30¦Ü16:30 Ãþ«¬ ¥ÒÃþ ¿n¤À 5.75 ¥D¿ì³æ¦ì ÃĵØÂåÃĪѥ÷¦³¤½¥q¡B¦å²G¯f¾Ç·| ·|ij¦aÂI Humble House Taipei, Taiwan(No.18, Songgao Rd., Xinyi Dist., Taipei City 110, Taiwan) / ´HªÙ¦ãÄR¶º©±(¥x¥_¥««H¸q°ÏªQ°ª¸ô18¸¹) ³ø¦W®É¶¡: 1¡^²Ä¤@ªi³ø¦W 12/10-12/23¡A¶È¶}©ñµ¹¦å²G¯f¾Ç·|·|û³ø¦W 2¡^²Ä¤Gªi³ø¦W 12/24-12/30¡AµøªÅ¦ì±¡ªp¶}©ñµ¹«D·|û³ø¦W Time Topic Faculty Speaker Moderator 09:30 Registration 09:50 Welcome Remarks Dr. Dong-Tsamn Lin 09:55 Opening Remarks Dr. Lee-Yung Shih Unmet Needs in Essential Thrombocythemia and Polycythemia Vera 10:00 Unmet Needs in Essential Thrombocythemia Dr. Ruben A. Mesa Dr. Heinz Gisslinger 10:40 Treatment/Unmet Needs in Polycythemia Vera Dr. Srdan Verstovsek 11:20 Myeloproliferative Neoplasms in Taiwan Dr. Lee-Yung Shih Dr. Dong-Tsamn Lin 11:50 Lunch 12:30 The status of MPN treatments in Asia Dr. Jong Jin Seo Dr. Dong-Tsamn Lin Dr. Lee-Yung Shih Dr. Qian Jiang Dr. Norio Komatsu Genetic Causes of MPN and can Interferon be a Solution? 13:45 Genetic Basis of Myeloproliferative Neoplasms Dr. Robert Kralovics Dr. Richard T. Silver 14:15 Interferon alpha for the Therapy of Myeloproliferative Neoplasms: Targeting the Malignant Clone Dr. Jean-Jacques Kiladjian 14:45 Coffee Break Current Status of Interferon Treatment in PV 15:00 Is Polycythemia Vera Curable? Dr. Richard T. Silver Dr. Ruben A. Mesa 15:30 The Added Value of Ropeginterferon alfa-2b in the Treatment of Polycythemia Vera Dr. Heinz Gisslinger Panel Discussion: Current Status of The Effect of Treatment on Mutations in MPNs 16:00 Chair: Dr. Richard T. Silver Dr. Heinz Gisslinger Dr. Jean-Jacques Kiladjian Dr. Robert Kralovics Dr. Ruben Mesa Dr. Lee-Yung Shih Dr. Srdan Verstovsek 17:00 Closing Remarks Dr. Lee-Yung Shih Adjourn |
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http://www.biodriven.taipei/tw/awards_3.html 2015¥x¥_¥Í§Þ¼ú±o¥D4174, ±o¼ú¼Ðªº Àù¯g§K¬ÌÀøªk OBI-822§ÜÀù¬Ì]·sÃÄ ±o¼ú³æ¦ì ¥xÆW¯E¹©¥Í§ÞªÑ¥÷¦³¤½¥q ±o¼ú¼Ðªº±Ôz ¥xÆW¯E¹©ªºOBI-822Àù¯gªvÀø©Ê¬Ì]¡A¬ð¯}¶Ç²ÎÁÞÃþ¦X¦¨²~ÀV¡A¥H¿W¨B¥þ²yªºÁÞÃþ¤@Áç¦X¦¨ªk¡A°w¹ïÀù²ÓMªí±¤j¶qªí²{ªºGlobo HÁÞ§Ü쬰¼Ðªº¡A¤Þµo§K¬Ì²ÓM²£¥Í§ÜÅé¡A¶i¦ÓºR·´Àù²ÓM¡A¬O¥þ²y°ß¤@¶}µoGlobo H ÁÞ§Üì¶i¤J¤¤±ß´ÁÁ{§É¸ÕÅ綥¬qªº¥Í§Þ¤½¥q¡C 2013¥x¥_¥Í§Þ¼ú±o¥Dª÷¼ú6446 ¬ãµo³Ð·s¼ú ª÷¼ú ÃĵØÂåÃĪѥ÷¦³¤½¥q ·s¤@¥Nªø®Ä«¬¤zÂZ¯À£\P1101 |
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·|û¡GCliff10135274 µoªí®É¶¡:2015/12/23 ¤W¤È 12:25:16²Ä 384 ½g¦^À³
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°Ñ¦Ò ¡uMerck Announces U.S. Food and Drug Administration Acceptance of New Drug Application for Grazoprevir/Elbasvir, an Investigational Therapy for Treatment of Chronic Hepatitis C Genotypes 1, 4 and 6 Infection¡v¡]http://hepatitiscnewdrugresearch.com/grazoprevirelbasvir.html ¡^ ºC©ÊC«¬¨xª¢ªvÀø¥ÎÃÄ¡A¨C¤éªA¥Î¤@¿õ¡A¹wp2016/01/28«e§¹¦¨´`¡uÀu¥ý¼f¬d¡v¸ô®|§¹¦¨ÃÄÃÒ¼f®Ö¡C¡]PDUFA¡G2016/01/28¡^ ¾A¥Î¹ï¶H¡GºC©ÊC«¬¨xª¢¡AGenotype 1¡A4¡A6¡C§t¨ÖµoºC©ÊµÇ°IºÜ¬~µÇ±wªÌ¡B¨xµw¤Æ¡B¦X¨ÖHIV·P¬VªÌµ¥¡C 2015/4¤ëÀò±o¨âÓ¡u¬ð¯}©ÊªvÀø¡v»{ÃÒ¡G 1.ºC©ÊC«¬¨xª¢¡]Genotype 1¡^¦X¨ÖºC©ÊµÇ°IºÜ¬~µÇ±wªÌ¡C 2.ºC©ÊC«¬¨xª¢¡]Genotype 4¡^¡C ¡uOverall SVR12 rates were 92% in the 12-week arm without ribavirin, 94% in the 12-week arm with ribavirin, 92% for the 16-week arm without ribavirin and 97% for the 16-week arm with ribavirin. For genotype 1a disease, SVR12 rates were 90% without ribavirin for 12 weeks, 93% for 12 weeks with ribavirin, 94% for the non-ribavirin 16-week arm and 95% for the ribavirin 16-week arm. One hundred percent SVR12 rates were reported for two groups of genotype 1b patients (12 weeks without ribavirin, 16 weeks with ribavirin) and greater than 94% for the other two groups. Responses in genotype 4 disease were slightly lower, with 78% of those in the 12-week, non-ribavirin arm responding; 93% of those in the 12-week ribavirin arm responding; 80% of 16-week non-ribavirin patients but 100% of those treated for 16 weeks with ribavirin. Responses ranged from 87% to 98% for prior null responders and from 95% to 100% for partial responders and previous treatment relapsers. In a subgroup analysis, the lowest sustained response rate in cirrhotics was 89% (12 weeks with ribavirin) with the 16 week arm with ribavirin achieving a 100% sustained response rate in cirrhotic patients. All other responses in patients with cirrhosis were higher than 90%.¡v ¡uFatigue was reported in 23% of patients, while headache occurred in 20% and nausea occurred in 11%. ¡§The regimen was well tolerated,¡¨ Kwo said. ¡§The SAE rate was very low. Discontinuation was uncommon and not related to therapy¡v |
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