Drug intelligence / Profile preview

CEP-37251

Development stage
Preclinical
Lead developer
Teva Pharmaceutical Industries
Modality
Recombinant Proteins and Enzymes, Small Molecules
Administration
Intravenous, Subcutaneous
01

Overview

CEP-37251 is a biological drug developed as an osteoprotegerin (OPG) analogue and functions as a RANKL inhibitor. It was designed to inhibit the activity of the receptor activator of nuclear factor kappa-B ligand (RANKL), also known as tumor necrosis factor ligand superfamily member 11. By inhibiting RANKL, CEP-37251 aimed to prevent bone resorption and loss by blocking osteoclast activation. The drug was initially developed by Cephalon and later associated with Teva Pharmaceutical Industries following acquisition. Its primary indication was osteoporosis, particularly in postmenopausal women, but it was also investigated for potential use in bone metastases and considered for colorectal cancer. Clinical development reached Phase 1 before being discontinued due to lack of further advancement[1][2][3][4][5][9].

Other names
OPG analogueOPG variantOPG variant protein
02

Targets

RANKL (Receptor Activator for Nuclear Factor-kappa B Ligand)

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