Xenetic Biosciences Extends Research Collaboration with Scripps Research to Advance DNase Platform

Reuters

Nov 19

Xenetic Biosciences Extends Research Collaboration with Scripps Research to Advance DNase Platform

Xenetic Biosciences Inc. has extended its research and development collaboration with The Scripps Research Institute and Dr. Alexey Stepanov's laboratory. The partnership will continue for an additional four months starting November 1, 2025, focusing on advancing Xenetic's DNase I platform in combination with CAR T-cell therapies. The collaboration aims to further evaluate the therapeutic potential of systemic DNase I, particularly in improving responses to CAR-T cell therapy for both hematologic and solid tumors. Preclinical studies have shown promising results, and the program is being advanced toward Phase 1 clinical development.

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: 1103941) on November 19, 2025, and is solely responsible for the information contained therein.

Disclaimer: Investing carries risk. This is not financial advice. The above content should not be regarded as an offer, recommendation, or solicitation on acquiring or disposing of any financial products, any associated discussions, comments, or posts by author or other users should not be considered as such either. It is solely for general information purpose only, which does not consider your own investment objectives, financial situations or needs. TTM assumes no responsibility or warranty for the accuracy and completeness of the information, investors should do their own research and may seek professional advice before investing.

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Xenetic Biosciences Inc. published the original content used to generate this news brief via ACCESS Newswire (Ref. 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