
Wugen Secures $115M to Advance Allogeneic CAR-T Therapy for T Cell Malignancies
ST. LOUIS, Missouri – Wugen, a clinical-stage biotechnology company, announced today the first close of a $115 million Series C funding round, led by existing investor Fidelity Management & Research Company. The financing will be used to advance the company’s lead program, WU-CART-007, an allogeneic (off-the-shelf) CAR-T cell therapy for T cell malignancies.
The funding provides a significant boost to Wugen as it navigates a shifting market and forges ahead with its allogeneic approach. Unlike autologous cell therapies, which are personalized and costly, Wugen’s off-the-shelf therapy is being developed to offer a more accessible treatment option. The company recently entered a pivotal clinical trial for WU-CART-007 and, if successful, anticipates filing for regulatory approval in 2027.
The Series C funding follows Wugen’s decision last fall to pause development of its natural killer (NK) cell therapy program, WU-NK-101, due to a decline in investor interest in that niche of the cell therapy landscape.
Wugen CEO Kumar Srinivasan stated that the new funding validates the promise of their allogeneic CAR-T platform. The company expects to use the capital to complete its pivotal study and engage in regulatory discussions with the FDA and European Medicines Agency.
Source:
https://endpoints.news/wugen-collects-115m-as-it-runs-pivotal-allogeneic-car-t-trial/?utm_source=dlvr.it&utm_medium=linkedin
About PackGene
PackGene Biotech is a world-leading CRO and CDMO, excelling in AAV vectors, mRNA, plasmid DNA, and lentiviral vector solutions. Our comprehensive offerings span from vector design and construction to AAV, lentivirus, and mRNA services. With a sharp focus on early-stage drug discovery, preclinical development, and cell and gene therapy trials, we deliver cost-effective, dependable, and scalable production solutions. Leveraging our groundbreaking π-alpha 293 AAV high-yield platform, we amplify AAV production by up to 10-fold, yielding up to 1e+17vg per batch to meet diverse commercial and clinical project needs. Moreover, our tailored mRNA and LNP products and services cater to every stage of drug and vaccine development, from research to GMP production, providing a seamless, end-to-end solution.
