Interdict

Interdict

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Private Company

Funding information not available

Overview

Interdict Bio is a private, pre-clinical stage biotech founded in 2022 and based in Cambridge, USA, developing a revolutionary small molecule modality called Interdictors™. Its platform targets the ribosome to selectively inhibit the synthesis of pathogenic proteins, enabling it to address validated but elusive targets like intrinsically disordered proteins (e.g., MYC) and aggregation-prone proteins. The lead program targeting MYC-dependent cancers is in IND-enabling studies, positioning the company to potentially open new therapeutic frontiers in oncology and neurodegeneration.

OncologyNeurodegenerationRare Diseases

Technology Platform

Proprietary platform for designing 'Interdictors™' – orally bioavailable, linkerless heterobifunctional small molecules that bind the ribosomal peptidyl-transferase center (PTC) to inhibit context-dependent protein synthesis. The platform integrates AI/bioinformatics (INTERDICTionary™), structural biology, ribosome profiling, and medicinal chemistry to target specific nascent polypeptide sequences.

Opportunities

The platform offers a novel approach to target high-value, validated proteins like MYC that have been historically undruggable, representing multi-billion dollar markets in oncology and neurodegeneration.
Its oral, small molecule modality could provide significant advantages over biologic approaches (e.g., ASOs) in terms of patient convenience, brain penetration, and broader applicability.

Risk Factors

The core technology is novel and unproven in humans, with risks around achieving sufficient selectivity and a therapeutic window by modulating the ribosome.
As a pre-clinical, private company, it faces significant financing risk and intense competition from other next-generation modalities (PROTACs, molecular glues, oligonucleotides) targeting similar disease areas.

Competitive Landscape

Interdict competes with companies developing other novel modalities to address 'undruggable' targets, including PROTAC/proteolysis-targeting chimera companies (e.g., Arvinas), molecular glue developers, and oligonucleotide therapy firms (e.g., Ionis, Alnylam). Its unique differentiation is the direct, context-specific inhibition of protein synthesis at the ribosome via an oral small molecule.