Drug intelligence / Profile preview

OBT076

Development stage
Phase 1
Lead developer
Oxford BioTherapeutics
Modality
Cytotoxic ADCs → Antibody-Drug Conjugates (ADCs) → Antibody Conjugates → Antibody-Based Therapeutics, Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
Administration
Intravenous
01

Overview

OBT076 is an antibody-drug conjugate (ADC) composed of a fully human IgG1 monoclonal antibody targeting the CD205 (also known as DEC205 or Ly75) receptor, which is overexpressed on the surface of various solid and liquid tumor cells as well as immunosuppressive dendritic cells. The antibody is conjugated via a cleavable linker to DM4 (ravtansine), a potent maytansinoid microtubule inhibitor. OBT076 selectively binds to CD205-positive cancer cells, delivering the cytotoxic payload directly into these cells, leading to their death while minimizing damage to healthy tissue. Additionally, OBT076 may deplete immunosuppressive CD205+ cells in the tumor microenvironment and promote immune system reactivation against tumors—a potential dual mechanism of action. It is being developed primarily for advanced or refractory solid tumors with high CD205 expression, including gastric cancer, non-small cell lung cancer, endometrial cancer, ovarian cancer, breast cancers (including triple-negative), bladder cancer, pancreatic cancers and certain lymphomas such as diffuse large B-cell lymphoma[1][2][3][4][5][6][7][8].

Other names
CD205-ADCCD-205-ADCCD 205-ADC
02

Targets

LY75 (Dendritic cell receptor DEC–205)

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