Drug intelligence / Profile preview

TJ101

Development stage
Unknown
Lead developer
Phrontline Biopharma
Modality
Bispecific Antibodies → Multispecific Antibodies → Engineered Antibody Formats → Antibody-Based Therapeutics, Cytotoxic ADCs → Antibody-Drug Conjugates (ADCs) → Antibody Conjugates → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

TJ101 is a first-in-class bispecific antibody-drug conjugate (ADC) developed by Phrontline Biopharma, targeting both Epidermal Growth Factor Receptor (EGFR) and B7-H3 (CD276). It utilizes a proprietary cleavable linker to attach a novel topoisomerase I inhibitor payload. By targeting two distinct tumor-associated antigens, TJ101 is designed to enhance tumor selectivity and overcome resistance mechanisms associated with single-target ADCs. Upon binding and internalization into tumor cells, the payload is released via enzymatic cleavage in lysosomes, leading to DNA damage and cell death, while also exerting a bystander effect on neighboring tumor cells. It is currently being evaluated in Phase 1 clinical trials for advanced solid tumors, including non-small cell lung cancer, prostate cancer, and esophageal cancer.

02

Targets

EGFR T790M (Epidermal growth factor receptor T790M mutant)B7-H3TOP1 (DNA Topoisomerase I)

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