XILIO THERAPEUTICS, INC.

We are advancing a number of geographically precise, or tumor-selective, agents through various stages of development. Our most advanced product candidates are:
-XTX101, an anti-cytotoxic T-lymphocyte-associated protein 4, or anti-CTLA-4, monoclonal antibody, or mAb, which received IND (investigational new drug) clearance from the FDA in June 2021; we recently initiated a Phase 1/2 trial to evaluate XTX101 in patients with solid tumors, and
-XTX202, -an interleukin 2, or IL-2, therapy, which received IND clearance from the FDA in October 2021, and we anticipate initiating a Phase 1/2 trial in the first quarter of 2022 to evaluate XTX202 in patients with multiple solid tumor types.
We are also advancing our tumor-selective IL-12 product candidate, XTX301, with the goal of submitting an IND in the second half of 2022, and we are currently pursuing preclinical studies for our tumor-selective IL-15 product candidate, XTX401. We also plan to continue to leverage our GPS platform to develop additional immunotherapies, including product candidates with a range of tumor-targeting approaches.