Drug intelligence / Profile preview

BLU-525

Development stage
Unknown
Lead developer
Blueprint Medicines
Modality
Small Molecules
Administration
Oral
01

Overview

BLU-525 is a **small molecule, selective epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor** developed by Blueprint Medicines for the treatment of EGFR-mutant non-small cell lung cancer (NSCLC)[4][7]. It features a distinct chemical structure compared to earlier candidates (like BLU-701), offers improved kinome selectivity, differentiated metabolism, wild-type EGFR selectivity, strong coverage of EGFR mutations (including exon 19 deletions and L858R), and central nervous system (CNS) penetration[4][5][10]. The drug is designed to address resistance mutations such as EGFR C797S that emerge during treatment with third-generation EGFR inhibitors like osimertinib[4][7][8][10]. As of May 2023, the US FDA had accepted the Investigational New Drug (IND) application for BLU-525 for NSCLC, and it remains in early clinical development[7][8][4]. Blueprint Medicines is the primary developer, with licensing agreements in Greater China with Zai Lab[2].

Other names
BLU 525BLU525BLU-525
02

Targets

EGFR exon 19del (Epidermal growth factor receptor exon 19 deletion mutant)EGFR C797S (Epidermal Growth Factor Receptor C797S)EGFR L858R (Epidermal growth factor receptor L858R mutant)EGFR T790M (Epidermal growth factor receptor T790M mutant)

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