Xenetic Biosciences Expands Research Collaboration with Scripps Research to Advance DNase Platform for Lymphoma and Leukemia Models

Reuters
07/23
Xenetic Biosciences Expands Research Collaboration with Scripps Research to Advance DNase Platform for Lymphoma and Leukemia Models

Xenetic Biosciences, Inc. has announced an expansion of its research and development collaboration with The Scripps Research Institute to advance its DNase platform. This collaboration will now include additional models of lymphoma and leukemia in order to further validate the promising DNase-I data observed to date. Xenetic's DNase-based oncology platform targets neutrophil extracellular traps (NETs), which are implicated in cancer spread and immunosuppression. Preclinical studies have shown that co-administration of DNase I with CAR-T cell therapy significantly improves therapeutic outcomes in models of lymphoma and metastatic melanoma. This has prompted the expansion of the research program to include further models to validate these findings. The company is moving towards Phase 1 clinical development for treating pancreatic carcinoma and other solid tumors with its systemic DNase I candidate, XBIO-015, though no specific results from these trials have been presented yet.

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. Xenetic Biosciences Inc. published the original content used to generate this news brief via ACCESS Newswire (Ref. ID: 1051661) on July 23, 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