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KOL Insight - Myelofibrosis

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  • 2023³â FDA, Ç÷¼ÒÆÇ ¼ö 50x109/L ¹Ì¸¸ÀÇ °ñ¼ö¼¶À¯Áõ(MF) ȯÀÚ¿¡ ´ëÇÑ Enpaxiq (Pacritinib, CTI Biopharma)ÀÇ Èñ±ÍÀǾàǰ(Èñ±ÍÁúȯ Ä¡·áÁ¦) »ç¿ë ½ÂÀÎÀº Ä¡·á¿¡ ¾î¶² ¿µÇâÀ» ¹ÌÄ¥±î?
  • Jakafi(Ruxolitinib, Incyte Corporation/Novartis)ÀÇ Áö³­ 12°³¿ù°£ »ç¿ë·® º¯È­ ÃßÀÌ
  • 2024³â 10¿ù¿¡ ¹ßÇ¥µÈ FREEDOM2 ÀÓ»ó 3»ó ½ÃÇè¿¡¼­ MF ȯÀÚ(Ruxolitinib ÀÌÀü Ä¡·á °æÇèÀÌ Àִ ȯÀÚ)¿¡¼­ »ç¿ë °¡´ÉÇÑ ÃÖ¼±ÀÇ Ä¡·á¹ý ´ëºñ È¿´ÉÀÌ °³¼±µÈ °ÍÀ¸·Î º¸°íµÈ °¡¿îµ¥, ÀÌ ½ÃÇèÀÌ Æäµå¶õƼ´Õ »ç¿ë¿¡ ¾î¶² ¿µÇâÀ» ¹ÌÄ¥ °ÍÀΰ¡?
  • Ojjaara°¡ ºóÇ÷ ȯÀÚ¿¡°Ô ruxolitinibÀ̳ª ´Ù¸¥ Ä¡·áÁ¦¸¦ ´ëüÇÒ ¼ö ÀÖ´Â °¡´É¼ºÀº ¾î´À Á¤µµÀΰ¡?
  • °ñ¼ö¼¶À¯Áõ Ä¡·á¿¡¼­ ÅڷθӶó¾ÆÁ¦ ¾ïÁ¦Á¦ÀÇ °¡´É¼º°ú JAK ¾ïÁ¦Á¦ Ä¡·á¿¡ ¹ÝÀÀÇÏÁö ¾Ê´Â ȯÀÚ¿¡°Ô ÅڷθӶó¾ÆÁ¦ ¾ïÁ¦Á¦°¡ ÁÁÀº ¼±ÅÃÀÌ µÉ ¼ö Àִ°¡?
  • °ñ¼ö¼¶À¯Áõ Ä¡·á¿¡¼­ ¹ÌÃæÁ· ¼ö¿ä´Â ¹«¾ùÀ̸ç, ÀΰøÁö´É(AI) µµ±¸¿Í µðÁöÅÐ ±â¼úÀÌ ÀÌ·¯ÇÑ ¿ì·Á¿¡ ´ëÀÀÇÒ ¼ö ÀÖÀ»±î?
  • ÀÓ»ó 2»óÀÎ SENTRY-2´Â JAK ¾ïÁ¦Á¦ ¼øÀÀ±º °ñ¼ö¼¶À¯Áõ ȯÀÚ¸¦ ´ë»óÀ¸·Î XpovioÀÇ À¯È¿¼º°ú ¾ÈÀü¼ºÀ» Æò°¡Çϰí, ºñÀå Ãà¼Ò¸¦ ÁÖ¿ä °á°ú·Î ½ÂÀÎµÈ JAK ¾ïÁ¦Á¦¿Í ºñ±³ÇÏ´Â ÀÓ»ó 2»ó ½ÃÇè ÁßÀε¥, ÀÌ ½ÃÇè¿¡ ´ëÇÑ ±â´ë´Â ¹«¾ùÀΰ¡?
  • Syntara´Â 2»ó SNT-5505 ¿¬±¸¿¡¼­ ±àÁ¤ÀûÀÎ µ¥ÀÌÅ͸¦ ¹ßÇ¥Çߴµ¥, 12ÁÖ°¿¡ ȯÀÚÀÇ 46%°¡ ÃÑ ½Ã½ºÅÛ Á¡¼ö°¡ 50% °¨¼ÒÇßÀ¸¸ç 38ÁÖ°¿¡´Â 80%·Î Áõ°¡Çß´Ù´Â °á°ú°¡ ³ª¿Ô´Ù. ÀÌ µ¥ÀÌÅͰ¡ ¾ó¸¶³ª ¼³µæ·ÂÀÌ ÀÖÀ¸¸ç, ´Ù¸¥ ¾àÁ¦¿Í ºñ±³ÇÏ¸é ¾î¶°ÇѰ¡?
  • luspatercept¿Í °°Àº À¯»ç ¾à¹°°ú ºñ±³ÇßÀ» ¶§ KER050ÀÇ È¿´ÉÀº ¾î´À ÂÊÀÌ ´õ ¿ì¼öÇÒ °ÍÀ¸·Î ¿¹»óµÇ´Â°¡?
  • ÇâÈÄ °ñ¼ö¼¶À¯Áõ Ä¡·á¿¡¼­ º´¿ë¿ä¹ýÀÇ ¿ªÇÒÀº ¾î¶»°Ô µÉ °ÍÀΰ¡?
LSH 25.03.31

Drawing on the expertise of the world's foremost KOLs, this report provides impartial and balanced insights into the myelofibrosis treatment landscape, highlighting the critical battlegrounds shaping market dynamics. Gain a deeper understanding of current and future treatment paradigms as KOLs critically evaluate the potential of launched and pipeline therapies, offering actionable intelligence to guide strategic decision-making on product positioning and competitiveness.

Key Questions Answered:

  • In 2023, the FDA granted orphan drug status Enpaxiq (Pacritinib; CTI Biopharma for use in Myelofibrosis (MF) in patients with platelet counts of below 50 x 109 /L. How has this impacted utilisation?
  • How has the use of Jakafi (Ruxolitinib; Incyte Coorporation/Novartis changed over the last 12 months?
  • The Phase III FREEDOM2 trial was published in October 2024and reported efficacy gains in MF patients (previously treated with ruxolitinib) vs the best available therapy. What do you see as the impact of this trial on fedrantinib use?
  • To what extent do you see Ojjaara replacing ruxolitinib or other therapies for patients with anaemia?
  • What do you think is the potential of telomerase inhibitors in the treatment of myelofibrosis? Do you think they offer a good alternative to those patients who have not responded to JAK-inhibitor treatment?
  • What are the key unmet needs in the treatment of myelofibrosis? Can artificial intelligence (AI) tools or digital technology address any of these concerns?
  • The Phase II SENTRY-2 is assessing efficacy and safety of Xpovio in JAK-inhibitor Naive MF patients, and comparing against approved JAK inhibitors with spleen reduction the primary outcomes. What are your expectations for this trial?
  • Syntara released positive data from its Phase II SNT-5505 study, indicating 46% of patients received a 50% decrease in their total system score at 12 weeks, increasing to 80% at 38 weeks How compelling is this data, how would you say this compares to other agents?
  • How would you say KER050 compares with similar agents such as luspatercept, which do you expect to be more efficacious?
  • What do you think the role of combinations will be in myelofibrosis treatment in the future?

Methodology

Therapy Trend reports are developed through in-depth interviews with the world's foremost Key Opinion Leaders (KOLs) on the current and future treatment landscapes in major disease areas. KOLs are carefully selected based on strict screening criteria, including their global reputation, clinical expertise, and influence within their therapeutic area. Each interview is guided by a meticulously crafted discussion guide. These guides are developed in collaboration with KOLs and peer-reviewed by industry experts to ensure that the questions are comprehensive and pertinent to current market dynamics. Through continuous market monitoring over a 12-month period following the publication of each report, we provide timely updates from KOLs on key news events, market shifts, and clinical developments.

What makes our reports different?

FirstWord Reports, a trusted industry leader with an exclusive focus on the pharmaceutical sector, delivers in-depth, actionable insights for biopharma professionals and decision-makers. Our deep industry knowledge enables us to provide relevant and valuable insights that help you identify emerging trends and navigate complex challenges effectively. Backed by extensive research and independent, impartial insights from leading experts and KOLs, our reports deliver the accuracy and reliability you need. With exclusive access to interviews and data unavailable elsewhere, along with ongoing market monitoring, we give you a comprehensive view of market dynamics. Covering over 40 dynamic disease areas and providing physician intelligence, including KOL insights and quantitative physician surveys, as well as industry expert views on issues in medical affairs, digital health, sales & marketing, market access, and other areas, our reports empower you to make smarter, data-driven decisions and maintain a competitive edge in a fast-moving industry.

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