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Global • 2026-10-28, 14:27 GMT • ~1 min read

Nxera wins Japan and Asia-Pacific rights to rare-disease drug lucerastat

نیکسیرا کو جاپان اور ایشیا پیسیفک میں نایاب بیماری کی دوا لوسیراسٹیٹ کے حقوق مل گئے

नेक्सेरा को जापान और एशिया-प्रशांत में दुर्लभ बीमारी की दवा ल्यूसेरास्टैट के अधिकार मिले

Nxera wins Japan and Asia-Pacific rights to rare-disease drug lucerastat

Key points

اہم نکات

मुख्य बातें

  • Nxera Pharma has secured exclusive rights to develop and sell lucerastat, an oral therapy for the rare inherited condition Fabry disease, in Japan, South Korea, Taiwan and selected other Asia-Pacific markets, excluding China.
  • The drug is designed to reduce the build-up of a fatty substance that damages the kidneys, heart and nervous system.
  • Drugmaker Idorsia has started a pivotal Phase 3 study, with a regulatory filing expected as early as 2029, and Nxera will run clinical development in Japan, paying an upfront 7 million Swiss francs.
  • نیکسیرا فارما نے نایاب موروثی بیماری فیبری کی زبانی دوا لوسیراسٹیٹ کو جاپان، جنوبی کوریا، تائیوان اور ایشیا پیسیفک کے دیگر منتخب ممالک میں، چین کے علاوہ، تیار کرنے اور بیچنے کے خصوصی حقوق حاصل کر لیے ہیں۔ یہ دوا اس چربی دار مادے کے جمع ہونے کو کم کرنے کے لیے بنائی گئی ہے جو گردوں، دل اور اعصابی نظام کو نقصان پہنچاتا ہے۔ دوا ساز ادارے آئیڈورسیا نے فیز 3 کا اہم مطالعہ شروع کر دیا ہے، اور 2029 کے اوائل میں ہی منظوری کی درخواست کی توقع ہے، جبکہ نیکسیرا جاپان میں کلینیکل ترقی چلائے گی اور 70 لاکھ سوئس فرانک پیشگی ادا کرے گی۔
  • नेक्सेरा फ़ार्मा ने दुर्लभ वंशानुगत बीमारी फ़ैब्री की मौखिक दवा ल्यूसेरास्टैट को जापान, दक्षिण कोरिया, ताइवान और एशिया-प्रशांत के अन्य चुनिंदा बाज़ारों में, चीन को छोड़कर, विकसित करने और बेचने के विशेष अधिकार हासिल कर लिए हैं। यह दवा उस वसायुक्त पदार्थ के जमाव को कम करने के लिए बनाई गई है जो गुर्दों, हृदय और तंत्रिका तंत्र को नुकसान पहुँचाता है। दवा निर्माता इडोर्सिया ने चरण 3 का महत्वपूर्ण अध्ययन शुरू कर दिया है, और 2029 की शुरुआत में ही नियामक आवेदन की उम्मीद है, जबकि नेक्सेरा जापान में नैदानिक विकास चलाएगी और 70 लाख स्विस फ़्रैंक अग्रिम देगी।

Nxera Pharma has secured exclusive rights to develop and sell lucerastat, an oral therapy for the rare inherited condition Fabry disease, in Japan, South Korea, Taiwan and selected other Asia-Pacific markets, excluding China. The drug is designed to reduce the build-up of a fatty substance that damages the kidneys, heart and nervous system. Drugmaker Idorsia has started a pivotal Phase 3 study, with a regulatory filing expected as early as 2029, and Nxera will run clinical development in Japan, paying an upfront 7 million Swiss francs.

نیکسیرا فارما نے نایاب موروثی بیماری فیبری کی زبانی دوا لوسیراسٹیٹ کو جاپان، جنوبی کوریا، تائیوان اور ایشیا پیسیفک کے دیگر منتخب ممالک میں، چین کے علاوہ، تیار کرنے اور بیچنے کے خصوصی حقوق حاصل کر لیے ہیں۔ یہ دوا اس چربی دار مادے کے جمع ہونے کو کم کرنے کے لیے بنائی گئی ہے جو گردوں، دل اور اعصابی نظام کو نقصان پہنچاتا ہے۔ دوا ساز ادارے آئیڈورسیا نے فیز 3 کا اہم مطالعہ شروع کر دیا ہے، اور 2029 کے اوائل میں ہی منظوری کی درخواست کی توقع ہے، جبکہ نیکسیرا جاپان میں کلینیکل ترقی چلائے گی اور 70 لاکھ سوئس فرانک پیشگی ادا کرے گی۔

नेक्सेरा फ़ार्मा ने दुर्लभ वंशानुगत बीमारी फ़ैब्री की मौखिक दवा ल्यूसेरास्टैट को जापान, दक्षिण कोरिया, ताइवान और एशिया-प्रशांत के अन्य चुनिंदा बाज़ारों में, चीन को छोड़कर, विकसित करने और बेचने के विशेष अधिकार हासिल कर लिए हैं। यह दवा उस वसायुक्त पदार्थ के जमाव को कम करने के लिए बनाई गई है जो गुर्दों, हृदय और तंत्रिका तंत्र को नुकसान पहुँचाता है। दवा निर्माता इडोर्सिया ने चरण 3 का महत्वपूर्ण अध्ययन शुरू कर दिया है, और 2029 की शुरुआत में ही नियामक आवेदन की उम्मीद है, जबकि नेक्सेरा जापान में नैदानिक विकास चलाएगी और 70 लाख स्विस फ़्रैंक अग्रिम देगी।

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