Search engine for discovering works of Art, research articles, and books related to Art and Culture
ShareThis
Javascript must be enabled to continue!

Abstract 2652: MGT-1142, an antibody-drug conjugate targeting a novel glycan for small-cell lung cancer

View through CrossRef
Abstract Background: Aberrant glycosylation is a hallmark of many malignancies, driving tumor growth, immune evasion, and metastasis. Certain tumor-associated glycans are highly expressed in small-cell lung cancer (SCLC) but minimally present in normal tissues, making them attractive yet underexplored targets for antibody-drug conjugates (ADCs). MGT-1142 is an exatecan-based ADC engineered with an optimized Fc domain to recognize a tumor-specific glycosylation pattern and selectively deliver a potent topoisomerase I inhibitor payload. Methods: Comprehensive in vitro and in vivo evaluations were performed to characterize MGT-1142. Binding affinity, internalization, and cytotoxicity were examined across multiple SCLC cell lines. Anti-tumor efficacy was assessed in both cell line-derived xenograft (CDX) and patient-derived xenograft (PDX) models. Pharmacokinetic (PK) and dose-range-finding (DRF) studies were conducted in cynomolgus monkeys to determine systemic exposure, half-life, and tolerability. Results: MGT-1142 exhibited high target specificity with no detectable cross-reactivity to structurally related glycans. It demonstrated strong binding and rapid internalization in glycan-positive cells, resulting in potent inhibition of antigen-positive tumor cell proliferation. In vivo, MGT-1142 achieved dose-dependent tumor growth inhibition across multiple CDX and PDX models. Cynomolgus PK studies revealed linear, dose-proportional exposure and a favorable terminal half-life. Dose range finding studies indicated good tolerability and a wide therapeutic window. Conclusions: MGT-1142 shows potent and selective anti-tumor activity, favorable pharmacokinetics, and an encouraging safety profile in preclinical studies. These findings support MGT-1142 as a potential first-in-class glycan-targeting ADC for the treatment of small-cell lung cancer. Citation Format: Su-Yu Tsai, Maomao He, Ju-Mei Li, Ping Chao, Ting-Chun Hung, Mei-Hsuan Tsai, Charng-Sheng Tsai. MGT-1142, an antibody-drug conjugate targeting a novel glycan for small-cell lung cancer [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 2652.
Title: Abstract 2652: MGT-1142, an antibody-drug conjugate targeting a novel glycan for small-cell lung cancer
Description:
Abstract Background: Aberrant glycosylation is a hallmark of many malignancies, driving tumor growth, immune evasion, and metastasis.
Certain tumor-associated glycans are highly expressed in small-cell lung cancer (SCLC) but minimally present in normal tissues, making them attractive yet underexplored targets for antibody-drug conjugates (ADCs).
MGT-1142 is an exatecan-based ADC engineered with an optimized Fc domain to recognize a tumor-specific glycosylation pattern and selectively deliver a potent topoisomerase I inhibitor payload.
Methods: Comprehensive in vitro and in vivo evaluations were performed to characterize MGT-1142.
Binding affinity, internalization, and cytotoxicity were examined across multiple SCLC cell lines.
Anti-tumor efficacy was assessed in both cell line-derived xenograft (CDX) and patient-derived xenograft (PDX) models.
Pharmacokinetic (PK) and dose-range-finding (DRF) studies were conducted in cynomolgus monkeys to determine systemic exposure, half-life, and tolerability.
Results: MGT-1142 exhibited high target specificity with no detectable cross-reactivity to structurally related glycans.
It demonstrated strong binding and rapid internalization in glycan-positive cells, resulting in potent inhibition of antigen-positive tumor cell proliferation.
In vivo, MGT-1142 achieved dose-dependent tumor growth inhibition across multiple CDX and PDX models.
Cynomolgus PK studies revealed linear, dose-proportional exposure and a favorable terminal half-life.
Dose range finding studies indicated good tolerability and a wide therapeutic window.
Conclusions: MGT-1142 shows potent and selective anti-tumor activity, favorable pharmacokinetics, and an encouraging safety profile in preclinical studies.
These findings support MGT-1142 as a potential first-in-class glycan-targeting ADC for the treatment of small-cell lung cancer.
Citation Format: Su-Yu Tsai, Maomao He, Ju-Mei Li, Ping Chao, Ting-Chun Hung, Mei-Hsuan Tsai, Charng-Sheng Tsai.
MGT-1142, an antibody-drug conjugate targeting a novel glycan for small-cell lung cancer [abstract].
In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA.
Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 2652.

Related Results

Abstract 2662: MGT-1141, an antibody-drug-conjugate targeting DLL3 positive cancers
Abstract 2662: MGT-1141, an antibody-drug-conjugate targeting DLL3 positive cancers
Abstract Background: Delta-like ligand 3 (DLL3) is highly expressed on the cell surface of small cell lung cancer (SCLC) ...
Complex Collision Tumors: A Systematic Review
Complex Collision Tumors: A Systematic Review
Abstract Introduction: A collision tumor consists of two distinct neoplastic components located within the same organ, separated by stromal tissue, without histological intermixing...
Abstract 2664: MGT-1143, a novel CDH17-targeting ADC for gastrointestinal cancers
Abstract 2664: MGT-1143, a novel CDH17-targeting ADC for gastrointestinal cancers
Abstract Background: Pan-gastrointestinal cancers represent a heterogeneous group of malignancies arising from the gastro...
Small Cell Lung Cancer and Tarlatamab: A Meta-Analysis of Clinical Trials
Small Cell Lung Cancer and Tarlatamab: A Meta-Analysis of Clinical Trials
Abstract Introduction Tarlatamab is a Delta-like ligand 3 (DLL3) -directed bispecific T-cell engager recently approved for use in patients with advanced small cell lung cancer (SCL...
Glycan profiling of the gut microbiota by Glycan-seq
Glycan profiling of the gut microbiota by Glycan-seq
Abstract Bacterial glycans modulate the cross talk between the gut microbiota and its host. However, little is known about these glycans because of the lack of appro...
Neuroprotective Effects of Magnesium L-threonate in a Hypoxic Zebrafish Model
Neuroprotective Effects of Magnesium L-threonate in a Hypoxic Zebrafish Model
Abstract Background: Hypoxia inhibits the uptake of glutamate (a major neurotransmitter in the brain closely related to cognitive function) into brain cells, and the initia...

Back to Top