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Updated: Jun 29, 2025

Characterize Disease-related Mutants of RAF Family Kinases by Using a Set of Practical and Feasible Methods
Published on: July 17, 2019
The Pan-RAF-MEK Nondegrading Molecular Glue NST-628 Is a Potent and Brain-Penetrant Inhibitor of the RAS-MAPK Pathway
Meagan B Ryan1, Bradley Quade1, Natasha Schenk1
1Nested Therapeutics, Cambridge, Massachusetts.
Abstract:
Alterations in the RAS-MAPK signaling cascade are common across multiple solid tumor types and are a driver for many cancers. NST-628 is a potent pan-RAF-MEK molecular glue that prevents the phosphorylation and activation of MEK by RAF, overcoming the limitations of traditional RAS-MAPK inhibitors and leading to deep durable inhibition of the pathway. Cellular, biochemical, and structural analyses of RAF-MEK complexes show that NST-628 engages all isoforms of RAF and prevents the formation of BRAF-CRAF heterodimers, a differentiated mechanism from all current RAF inhibitors. With a potent and durable inhibition of the RAF-MEK signaling complex as well as high intrinsic permeability into the brain, NST-628 demonstrates broad efficacy in cellular and patient-derived tumor models harboring diverse MAPK pathway alterations, including orthotopic intracranial models. Given its functional and pharmacokinetic mechanisms that are differentiated from previous therapies, NST-628 is positioned to make an impact clinically in areas of unmet patient need. Significance: This study introduces NST-628, a molecular glue having differentiated mechanism and drug-like properties. NST-628 treatment leads to broad efficacy with high tolerability and central nervous system activity across multiple RAS- and RAF-driven tumor models. NST-628 has the potential to provide transformative clinical benefits as both monotherapy and vertical combination anchor.
Insights
NST-628 is a novel molecular glue that effectively inhibits the RAS-MAPK pathway by targeting RAF-MEK complexes. This new therapy shows broad efficacy and central nervous system activity in various cancer models.
Area of Science:
- Oncology
- Molecular Biology
- Pharmacology
Background:
- RAS-MAPK pathway alterations are prevalent drivers in numerous solid tumors.
- Existing RAS-MAPK inhibitors face limitations in achieving deep and durable pathway inhibition.
Purpose of the Study:
- To introduce and characterize NST-628, a novel pan-RAF-MEK molecular glue.
- To evaluate the mechanism of action, efficacy, and pharmacokinetic properties of NST-628.
Main Methods:
- Utilized cellular, biochemical, and structural analyses to investigate RAF-MEK complexes.
- Assessed efficacy in diverse cellular and patient-derived tumor models, including intracranial models.
Main Results:
- NST-628 engages all RAF isoforms and prevents BRAF-CRAF heterodimer formation, a novel mechanism.
- Demonstrated potent, durable RAF-MEK pathway inhibition and high brain penetrance.
- Showcased broad anti-tumor efficacy across various MAPK pathway alterations.
Conclusions:
- NST-628 represents a differentiated therapeutic approach with unique drug-like properties.
- Exhibits broad efficacy, tolerability, and CNS activity in preclinical models.
- Has the potential for significant clinical impact as monotherapy or in combination therapies.
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