Drug intelligence / Profile preview

SDF-061390E + MMAF

Development stage
Preclinical
Lead developer
Synthetic Design Lab
Modality
Cytotoxic ADCs → Antibody-Drug Conjugates (ADCs) → Antibody Conjugates → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

SDF-061390E + MMAF is a multivalent, multispecific antibody-drug conjugate (ADC) developed by Synthetic Design Lab using their proprietary Synthbody™ platform. It is designed to target three distinct antigens commonly expressed on human multiple myeloma cells: B-cell maturation antigen (BCMA), G protein-coupled receptor class C group 5 member D (GPRC5D), and CD38. The Synthbody™ architecture incorporates 6-12 tumor antigen-binding domains, enabling logic-gated targeting and enhanced internalization. The drug is conjugated to the cytotoxic payload monomethyl auristatin F (MMAF), a tubulin inhibitor. In preclinical studies, SDF-061390E + MMAF demonstrated significantly greater potency and internalization compared to the BCMA-targeting ADC belantamab mafodotin, and it remained effective even in the presence of soluble BCMA or in cells with low target expression.

02

Targets

TUBB (Tubulin (alpha and beta subunits))CD38 (Cluster of Differentiation 38)BCMA (B-cell maturation antigen)GPRC5D

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