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https://www.businesswire.com/news/home/20230912387756/en
Lisata TherapeuticsÐû²¼ÔÚLSTA1(Ò»ÖÖÐÂÐÍÖ×Áö°ÐÏòºÍ´©Í¸ëÄ)µÄBOLSTERÊÔÑéÖÐÖÎÁÆÁ˵ÚÒ»ÀýÍíÆÚʵÌåÁö»¼Õß
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https://www.globenewswire.com/news-release/2023/09/12/2741590/18623/en/Lisata-Therapeutics-Announces-First-Patient-Treated-in-the-BOLSTER-Trial-of-LSTA1-a-Novel-Tumor-Targeting-and-Penetrating-Peptide-in-Patients-with-Advanced-Solid-Tumors.html
Nektar TherapeuticsÐû²¼RezpegaldesleukinÖÎÁÆÖÐÖضÈÌØÓ¦ÐÔƤÑ×µÄ1bÆÚÑо¿µÄÓÐÏ£ÍûµÄÐÂÊý¾Ý
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https://www.prnewswire.com/news-releases/nektar-therapeutics-announces-promising-new-data-from-phase-1b-study-of-rezpegaldesleukin-in-moderate-to-severe-atopic-dermatitis-301925787.html
Ojjaara(momelotinib)ÔÚÃÀ¹ú»ñÅú£¬ÊÇÊ׸öÒ²ÊÇΨÖðÒ»¸öÊÊÓÃÓÚ¹ÇËèÏËά»¯ÑªÐ黼ÕßµÄÖÎÁÆÒ©Îï
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https://www.anavex.com/post/anavex-sphase2b-3trialofblarcamesine-anavex-2-73-inpatientswithalzheimer-sdisease#:~:text=Anavex's%20lead%20drug%20candidate%2C%20ANAVEX,adult%20patients%20with%20Rett%20syndrome.
CrineticsÖðÈÕÒ»´Î¿Ú·þÅÁͼË÷Í¡ÔÚÆÀ¹ÀÖ«¶Ë·Ê´óÖ¢»¼ÕßÖÎÁƵÄ3ÆÚPATHFNDR-1Ñо¿ÖеִïÁËÖ÷ÒªºÍËùÓдÎÒªÖÕµã
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AlveoGeneÍƳöÕë¶ÔÓÐÊýºôÎüϵͳ¼²²¡µÄÆæÒìÎüÈëʽ»ùÒòÁÆ·¨
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https://www.globenewswire.com/news-release/2023/09/14/2742984/0/en/AlveoGene-Launches-to-Develop-Unique-Inhaled-Gene-Therapies-for-Rare-Respiratory-Disorders.html
NEUROBO PHARMACEUTICALSÔÚÆäÆÀ¹ÀDA-1241ÖÎÁÆNASHµÄ2AÆÚÁÙ´²ÊÔÑéÖÐÏòµÚһλ»¼Õ߸øÒ©
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https://www.neurobopharma.com/news-releases/news-release-details/neurobo-pharmaceuticals-doses-first-patient-its-phase-2a
Orchard TherapeuticsÐû²¼½ÓÊÜMLDÖÐOTL-200µÄÉúÎïÖƼÁÔÊÐíÉêÇë²¢»ñµÃÓÅÏÈÉó²é
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https://ir.orchard-tx.com/news-releases/news-release-details/orchard-therapeutics-announces-acceptance-biologics-license
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https://www.nature.com/articles/s41591-023-02572-5
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https://www.merck.com/news/fda-accepts-for-priority-review-mercks-supplemental-new-drug-application-for-welireg-belzutifan-in-certain-previously-treated-patients-with-advanced-renal-cell-carcinoma-rcc/
Relmada TherapeuticsÐû²¼REL-1017ÖÎÁÆÖضÈÒÖÓôÖ¢µÄ3ÆÚºã¾ÃÑо¿µÄÁÆЧºÍÇå¾²ÐÔЧ¹û
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https://www.relmada.com/for-investors/news/detail/285/relmada-therapeutics-announces-efficacy-and-safety-results
FDA¶ÔĬ¿Ë¹«Ë¾¹ØÓÚKEYTRUDA?(ÅÉÄ·µ¥¿¹)ÁªÌõÔ¼²½·Å»¯ÁÆÖÎÁÆÐÂÕï¶ÏµÄ¸ßΣº¦¾Ö²¿ÍíÆÚ¹¬¾±°©»¼ÕßµÄÉêÇë¸øÓèÓÅÏÈÉó²é
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https://www.businesswire.com/news/home/20230920107710/en
89bioÐû²¼FDAÒÑÊÚÓèPegozaferminÔڷǾƾ«ÐÔÖ¬·¾ÐÔ¸ÎÑ×(NASH)ÖеÄÍ»ÆÆÐÔÖÎÁÆÖ¸¶¨
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https://ir.89bio.com/news-releases/news-release-details/89bio-announces-us-fda-has-granted-breakthrough-therapy
FDAÅú×¼Jardiance?ÓÃÓÚÖÎÁƳÉÈËÂýÐÔÉö²¡
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https://www.prnewswire.com/news-releases/us-fda-approves-jardiance-for-the-treatment-of-adults-with-chronic-kidney-disease-301936176.html
Bristol Myers SquibbÐû²¼Ð¸¨ÖúOpdivo(nivolumab)ºÍ»¯ÁƵÄΧÊÖÊõÆڼƻ®£¬ËæºóÊǸ¨ÖúOpdivo£¬¿ÉÏÔÖø¸ÄÉÆ¿ÉÇгý·ÇСϸ°û·Î°©»¼ÕßµÄÎÞÊÂÎñÉúÑÄÆÚ
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https://news.bms.com/news/corporate-financial/2023/Bristol-Myers-Squibb-Announces-Perioperative-Regimen-of-Neoadjuvant-Opdivo-nivolumab-and-Chemotherapy-Followed-by-Adjuvant-Opdivo-Significantly-Improves-Event-Free-Survival-in-Patients-with-Resectable-Non-Small-Cell-Lung-Cancer/default.aspx
PADCEV?(enfortumab vedotin-ejfv)ºÍKEYTRUDA?(pembrolizumab)ÔÚÒªº¦ÐÔ3ÆÚEV-302ÊÔÑéÖÐÏÔÖø¸ÄÉƼÈÍùδ¾ÖÎÁƵÄÍíÆÚ°òë×°©»¼ÕßµÄ×ÜÉúÑÄÆÚºÍÎÞÏ£ÍûÉúÑÄÆÚ
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https://newsroom.astellas.us/2023-09-22-PADCEV-R-enfortumab-vedotin-ejfv-and-KEYTRUDA-R-pembrolizumab-Significantly-Improve-Overall-Survival-and-Progression-Free-Survival-in-Patients-With-Previously-Untreated-Advanced-Bladder-Cancer-in-Pivotal-Phase-3-EV-302-Trial
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