Daily Newsletter

16 November 2023

Daily Newsletter

16 November 2023

Cambridge University spinout raises £48m to advance T-cell therapies

T-Therapeutics plans to use the Series A funds to develop T-cell therapies for cancer and auto-immune disorders.

Phalguni Deswal November 15 2023

A University of Cambridge spinout T-Therapeutics has raised £48m ($59.7m) in Series A financing to develop T cell receptor (TCR) therapies.

The Series A financiers include the University of Cambridge Venture Fund, Sanofi Ventures, Sofinnova Partners, F-Prime Capital, Digitalis Ventures, and Cambridge Innovation Capital (CIC).

Cell therapies are a growing area of interest in the immuno-oncology (IO) field, with multiple companies investing in developing TCR therapies. To address this growing interest, Twist Biosciences launched Twist TCR libraries to aid in developing these therapies in April.

Aong with the financing, Sofinnova Partners’ Graziano Seghezzi, F-Prime’s Nihal Sinha, Digitalis’ Samuel Bjork and CIC’s Robert Tansley will join the board of directors at T-Therapeutics, as per a 15 November press release.

The UK-based company plans to develop TCR therapies to treat cancers and auto-immune diseases. T-Therapeutics has developed a proprietary transgenic mouse platform, OpTiMus, based on a fully humanised mouse to develop these antigen specific human TCR therapies.

“We intend to replicate the success of therapeutic antibodies but build on this in a new dimension, by using the targeting domains of TCR receptors to take advantage of their much greater specificity for cancer cells compared to normal cells,” said T-Therapeutics’ CEO Professor Allan Bradley in the 15 November press release.

“The same logic can be used to target immunosuppressive biologics to tissues impacted by autoimmune disorders. By engineering a mouse that makes human TCRs, we are able to discover anti-cancer TCRs that are quantitatively and qualitatively better than those that can currently be isolated from humans or using display technologies.”

Cell & Gene Therapy coverage on Pharmaceutical Technology is supported by Cytiva

Editorial content is independently produced and follows the highest standards of journalistic integrity. Topic sponsors are not involved in the creation of editorial content.

Disease-modifying therapies (DMTs) entering the PD market pose significant opportunities and risks

As PD therapy currently centers on symptomatic treatment, the need for DMTs is one of the greatest unmet needs. Several companies within the late-stage PD pipeline are developing drugs that target PD via novel MOAs. Targeting α-synuclein and other neurotoxic proteins is a key strategy in the late-stage pipeline for DMTs. However, the lack of validated predictive biomarkers of PD progression have made the development of DMTs and neuroprotective agents challenging.

Newsletters by sectors

close

Sign up to the newsletter: In Brief

Visit our Privacy Policy for more information about our services, how we may use, process and share your personal data, including information of your rights in respect of your personal data and how you can unsubscribe from future marketing communications. Our services are intended for corporate subscribers and you warrant that the email address submitted is your corporate email address.

Thank you for subscribing

View all newsletters from across the GlobalData Media network.

close