Mozart Therapeutics Inc, a developer of CD8 Treg network modulators for the treatment of autoimmune disease, announced on Monday the presentation of clinical and preclinical data for its lead development programme, MTX-101, at the 62nd Annual Meeting of the European Association for the Study of Diabetes (EASD), held last week in Milan, Italy.
In three presentations given by Courtney Crane, Ph.D., Mozart's SVP of Translational Medicine and Biology, the company shared clinical and preclinical data supporting the continued development of MTX-101 as a promising investigational therapy for the treatment of type 1 diabetes.
The company says that collectively, the preclinical and clinical data presented support the potential of MTX-101 as a safe, well-tolerated, and selective therapeutic candidate that may restore CD8 regulatory T cell function, reduce pathogenic T cells in adults and adolescents with Stage 3 type 1 diabetes, and promote durable preservation of beta-cell function. Mozart Therapeutics is in the planning stages of a Phase 2a proof-of-concept study, with enrolment projected to begin in the first half of 2027.
MTX-101 is an antigen-agnostic bispecific antibody targeting inhibitory KIR and CD8 expressed on regulatory CD8 T cells. This autoimmune checkpoint inhibitor aims to restore the intrinsic functions of CD8 Treg, acting early in the autoimmune disease process to suppress and eliminate pathogenic T cells, halt downstream inflammation, and prevent tissue destruction.
BRC Therapeutics participates in regulators' workshop advancing botanical drug development
Ascletis reports positive results from ASC50 clinical study for treatment of plaque psoriasis
XtalPi submits US FDA IND application for KQTD-126 in chronic intestinal pain
AbbVie secures EU approval for RINVOQ in polyarticular juvenile idiopathic arthritis
Altesa BioSciences presents positive vapendavir clinical data at ERS International Congress 2026
Kali Therapeutics' KT501 Investigational New Drug application cleared by US FDA
Teva reports positive Phase 2a data for TEV '408 in celiac disease
AbbVie seeks EMA approval for subcutaneous induction of risankizumab in Crohn's disease
AstraZeneca and Amgen report Tezspire met primary endpoints in Phase III EoE trial
Oxcia receives EMA orphan designation for OXC-201 in idiopathic pulmonary fibrosis
Graviton BioScience reports positive trial results for GV101 in chronic Graft versus Host Disease
Cellenkos' CK0803 granted US FDA Fast Track designation for ALS
European Commission grants orphan designation for Vanda's imsidolimab