Vividion Therapeutics


Clinical-stage biopharmaceutical company using a covalent-first chemoproteomics discovery platform to identify ligandable pockets across the human proteome and develop selective small-molecule therapeutics for oncology and immunology. Operates an industrialized screening engine, a large covalent fragment library, integrated multi-omic data systems for proteomics/genetics/structural biology, and global clinical development programs.

Industries

Biotechnology
Health Care
Therapeutics
Biotech & Pharmaceuticals
Pharmaceutical and biotechnology
Biotechnology Research

Nr. of Employees

large (251-1000)

Vividion Therapeutics


Patents

Inhibitors and uses thereof

US-12740991-B2

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Pharmaceutical compositions comprising WRN helicase inhibitors

US-12187685-B2

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Cereblon modulators and uses thereof

US-11771689-B2

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Cereblon modulators and uses thereof

US-10869860-B2

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In vivo engineered cereblon protein

US-10781239-B2

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Products

Oral WRN inhibitor — clinical program

Covalent small-molecule inhibitor targeting WRN dependency in MSI-high/dMMR tumors; progressed through discovery and preclinical models into Phase I/IB and Phase II clinical trials.

KEAP1 activator — clinical program

Small molecule that allosterically modulates KEAP1 to promote degradation of NRF2; progressed from preclinical validation into Phase I clinical evaluation.

Inhibitors of RAS–PI3Kα interaction — clinical program

Covalent small molecules that disrupt RAS-dependent activation of PI3Kα (PIK3CA) with demonstrated preclinical tumor growth inhibition and progression to Phase I clinical evaluation.

Multiple undisclosed early-stage discovery programs

Platform-driven discovery and preclinical-stage small-molecule programs in oncology and immunology identified via chemoproteomics and covalent chemistry approaches.

VVD-037

A highly selective, first-in-class small molecule activator of KEAP1 that allosterically enhances the ability of this E3 ligase to degrade its natural cellular target, NRF2, to inhibit tumor growth in NRF2-hyperactivated solid tumors.

VVD-642

A small molecule RAS-PIK3CA inhibitor that specifically blocks the interaction between RAS and PIK3CA to inhibit oncogenic signaling without disrupting homeostatic signaling.

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Expertise Areas

  • Chemoproteomics-driven drug discovery
  • Covalent small-molecule discovery
  • Medicinal chemistry and SAR optimization
  • Preclinical pharmacology and translational in vivo models
  • Show More (6)

Key Technologies

  • Chemoproteomics
  • Covalent fragment libraries
  • High-resolution high-throughput mass spectrometry
  • Integrated proteomics–genetics–structural data integration
  • Show More (5)

News & Updates

Announcement that the head of R&D assumed the role of President and Chief Executive Officer and joined the Board; prior CEO transitioned to Chairman of the Board.

Announcement of a new Chief Medical Officer joining the company to lead clinical development and translational strategy.

Collaboration agreement to discover targets and co-develop targeted oncology programs, including option/rights terms for multiple programs.

Description of an 'arm's-length' operating model that preserves independent R&D while leveraging resources from a parent pharmaceutical company and notes site expansion to support growth.

Announcement of a scientific advisory board composed of external leaders in chemical biology, oncology, immunology and drug discovery to advise on research and development strategy.

Manuscript describing discovery and optimization of a covalent allosteric WRN inhibitor and its selection for clinical development.

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