The president and chief operating officer of Agenus discussed the cell therapies the company is developing for the treatment of multiple myeloma.
“We've engineered [CTLA4] to broaden the patient population who respond. We identified that there are patients who don't respond to first generation therapies, because of a genetic predisposition, and we've designed a molecule that will address that population. And that's about 40% of the population.”
Agenus is exploring many different avenues in treating cancer, including cell therapies, which are developed under their subsidiary Mink Therapeutics (formerly AgenTus Therapeutics). One such therapy being developed is agenT-797, an allogeneic unmodified invariant natural killer TT cell therapy.
AgenT-797 is being evaluated in a phase 2 clinical trial (NCT04754100) that dosed its first patient with relapsed/refractory multiple myeloma in April 2021. The trial is evaluating the safety, tolerability, and preliminary clinical activity of agenT-797, with the 3 primary outcomes focusing on safety, dose correlation to adverse events, and aiming to find a recommended dose. The therapy is also being looked at for the treatment of COVID-19.
GeneTherapyLive spoke with Agenus’ president and chief operating officer, Jennifer Buell, PhD, to learn more about the different cell therapies the company is developing. She also discussed the company’s background as a player in the cell therapy and cancer spaces.
Autologous HCT Shows No Benefit for Patients With MCL in First Complete Remission
December 10th 2024Among those who had undetectable minimal residual disease, autologous hematopoietic cell transplantation showed signs of benefit only for those who remained MRD-positive following induction therapy.
Bendamustine Is an Effective Alternative to Fludarabine-Based Lymphodepletion in LBCL
December 7th 2024In the wake of fludarabine shortages, lemphodepletion with bendamustine was found to be an effective alternative compared for patients with large B-cell lymphoma being treated with a CD19-directed CAR T-cell therapy.