Pyxis Oncology Announces New Clinical Data for MICVO ADC Targeting Solid Tumors to Be Presented at ESMO 2025 and AACR-NCI-EORTC

Reuters
10/14
<a href="https://laohu8.com/S/PYXS">Pyxis Oncology</a> Announces New Clinical Data for MICVO ADC Targeting Solid Tumors to Be Presented at ESMO 2025 and AACR-NCI-EORTC

Pyxis Oncology Inc. has announced the upcoming presentation of translational data for micvotabart pelidotin (MICVO), a first-in-concept antibody-drug conjugate $(ADC)$, at two major medical meetings. The data will be shared in two posters at the European Society for Medical Oncology (ESMO) Congress 2025 in Berlin, Germany, and in six posters at the AACR-NCI-EORTC International Conference in Boston, Massachusetts. MICVO is designed to target extradomain-B of fibronectin (EDB+FN) and employs an extracellular-cleaving mechanism. The findings to be presented include MICVO's mechanism of action, which involves direct tumor cell killing, bystander effect, and immunogenic cell death, as well as its effects on tumor microenvironment remodeling and immune activation. Presentation materials will be made available on the company's website following the conclusion of each meeting.

Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Pyxis Oncology Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW9544670-en) on October 13, 2025, and is solely responsible for the information contained therein.

免责声明:投资有风险,本文并非投资建议,以上内容不应被视为任何金融产品的购买或出售要约、建议或邀请,作者或其他用户的任何相关讨论、评论或帖子也不应被视为此类内容。本文仅供一般参考,不考虑您的个人投资目标、财务状况或需求。TTM对信息的准确性和完整性不承担任何责任或保证,投资者应自行研究并在投资前寻求专业建议。

热议股票

  1. 1
     
     
     
     
  2. 2
     
     
     
     
  3. 3
     
     
     
     
  4. 4
     
     
     
     
  5. 5
     
     
     
     
  6. 6
     
     
     
     
  7. 7
     
     
     
     
  8. 8
     
     
     
     
  9. 9
     
     
     
     
  10. 10