Biotechnology company Transgene (Euronext Paris: TNG) and NEC Corporation (NEC; TSE: 6701), an IT and network technology company, on Tuesday reported the presentation of new immunological data on TG4050, an individualised cancer vaccine, at the ASCO 2023 Annual Meeting.
TG4050 was developed using Transgene's myvac platform and NEC's AI capabilities. The vaccine induces specific immune responses against head and neck carcinoma in patients. It leverages viral vector technology to stimulate the patient's immune system and target solid tumours.
NEC's AI-driven Neoantigen Prediction System is used to identify and select immunogenic sequences for TG4050.
The data shows that all patients treated with TG4050 in an ongoing Phase I trial have developed a specific immune response and remain in remission. This indicates the potential of TG4050 as an adjuvant treatment for head and neck cancer.
Also, the data demonstrates that TG4050 induces strong immune responses against targeted antigens, even in patients with unfavorable systemic immunity and tumour micro-environment.
All patients who received TG4050 in the trial remain disease-free, showcasing its efficacy compared to the control arm.
Transgene and NEC are preparing for a Phase II trial in head and neck cancer, aiming to initiate it in the second half of 2023.
In addition, TG4050 is also being evaluated in a Phase I trial for ovarian cancer.
SCG releases SCG101 late-breaking clinical data in HBV-related hepatocellular carcinoma
Genprex signs new research agreement with University of Pittsburgh to advance diabetes gene therapy
AstraZeneca and Daiichi Sankyo's Enhertu shows strong results in early-stage breast cancer trial
Adcentrx's ADRX-0706 granted US FDA Fast Track designation to treat advanced cervical cancer
Ajinomoto and RIBOMIC announce successful extension of nucleic acid aptamer pharmacokinetics
AstraZeneca secures EU approval for Calquence combo as first-line treatment in mantle cell lymphoma
Odylia Therapeutics undertakes gene replacement therapy project for NPHP1 retinal dystrophy
Phanes Therapeutics doses first patient in peluntamig-atezolizumab combination clinical study
FDA accepts Novo Nordisk's filing application for oral semaglutide 25 mg
Nutshell Therapeutics' NTS071 p53 allosteric reactivator cleared for US clinical trial