Drug intelligence / Profile preview

DYP688

Development stage
Phase 2
Lead developer
Novartis
Modality
Small Molecules, Cytotoxic ADCs → Antibody-Drug Conjugates (ADCs) → Antibody Conjugates → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

DYP688 is a novel antibody-drug conjugate (ADC) developed for the treatment of metastatic uveal melanoma (MUM) and other melanomas harboring GNAQ/11 mutations. The drug consists of an antibody targeting the protein PMEL17, which is present on GNAQ/11 mutant cancer cells. Upon binding to PMEL17, DYP688 delivers its cytotoxic payload—FR900359, a signaling protein inhibitor—directly to the tumor cell. The payload undergoes unique on-antibody inactivation in plasma but remains active within tumors, resulting in complex pharmacology and potentially improved safety and efficacy profiles. Currently, DYP688 is being evaluated as a single agent in a first-in-human phase I/II clinical trial to determine its safety, tolerability, and anti-tumor activity. Novartis is developing this therapy primarily for patients with metastatic uveal melanoma and other melanomas with GNAQ/11 mutations.

02

Targets

GNAQ (G protein subunit alpha q)GNA11 (Guanine nucleotide-binding protein subunit alpha-11)PMEL (Melanocyte Protein PMEL)

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