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DRUG:

MCY-M11 IP

i
Other names: MCY M11 IP, MCY-M11 IP, mesothelin-targeting CAR intraperitoneal, MCY-M11 intraperitoneal
Associations
Trials
Company:
Johns Hopkins University, MaxCyte
Drug class:
Mesothelin-targeted CAR-T immunotherapy
Associations
Trials
over3years
[VIRTUAL] MCY-M11, a CAR-PBMC cell product transiently expressing a mesothelin targeted mRNA CAR, exhibits desirable functional and immune phenotype attributed to sustained antitumor immunity in vitro (SITC 2020)
These phenotypic changes in cell subsets of MCY-M11 transpired with simultaneous secretion of potent immunostimulatory molecules and chemokines facilitating an extended antitumor response through epitope spreading. Conclusions We demonstrated that MCY-M11 is a unique cell product possessing a complete built-in immune cellular machinery with favorable phenotype and enhanced functions specialized in mediating an effective and long-term antitumor response.
Preclinical • IO biomarker
|
CD8 (cluster of differentiation 8) • MSLN (Mesothelin) • CD27 (CD27 Molecule) • NKG2D (killer cell lectin like receptor K1)
|
MCY-M11 IP
over3years
[VIRTUAL] MCY-M11, a CAR-PBMC cell product transiently expressing a mesothelin targeted mRNA CAR, exhibits desirable functional and immune phenotype attributed to sustained antitumor immunity in vitro (SITC 2020)
These phenotypic changes in cell subsets of MCY-M11 transpired with simultaneous secretion of potent immunostimulatory molecules and chemokines facilitating an extended antitumor response through epitope spreading. Conclusions We demonstrated that MCY-M11 is a unique cell product possessing a complete built-in immune cellular machinery with favorable phenotype and enhanced functions specialized in mediating an effective and long-term antitumor response.
Preclinical • IO biomarker
|
CD8 (cluster of differentiation 8) • MSLN (Mesothelin) • CD27 (CD27 Molecule) • NKG2D (killer cell lectin like receptor K1)
|
MCY-M11 IP
4years
[VIRTUAL] Feasibility and preliminary safety and efficacy of first-in-human intraperitoneal delivery of MCY-M11, anti-human-mesothelin CAR mRNA transfected into peripheral blood mononuclear cells, for ovarian cancer and malignant peritoneal mesothelioma. (ASCO 2020)
Feasibility of 1-day manufacturing of MCY-M11 for ip delivery is demonstrated. Treatment has been safe. Initial SD observed in DL2 and DL3 with one-cycle infusions is encouraging and supports exploration of additional strategies such as the addition of preconditioning chemotherapy and multiple cycles to increase efficacy.
Clinical • P1 data
|
MSLN (Mesothelin)
|
MCY-M11 IP