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Vividion Therapeutics

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uuid0000wgi

Namestring
Vividion Therapeutics
Legal namestring
Vividion Therapeutics, Inc.
Websiteurl
vividion.com
Company typeenum
Private
Founded yearint
2016
Descriptiontext

Vividion Therapeutics is a clinical-stage biopharmaceutical company developing first-in-class covalent small molecule therapeutics against disease-causing proteins historically considered undruggable. The company was founded in 2016 based on foundational research from Scripps Research scientists Ben Cravatt, Phil Baran, and Jin-Quan Yu, and was acquired by Bayer AG in August 2021 for approximately $2 billion, becoming a wholly-owned and independently operated subsidiary headquartered in San Diego, California.

Vividion's core asset is a proprietary chemoproteomics discovery platform that combines a custom covalent fragment library of over 50,000 small molecules, high-resolution high-throughput mass spectrometry screening against thousands of proteins in their native cellular state, and an integrated data portal that overlays approximately 250,000 new data points per day with public human genetics and structural biology resources. The platform has produced three clinical-stage programs: VVD-214 (covalent allosteric WRN helicase inhibitor for MSI-high solid tumors, Phase Ib), VVD-037 (first-in-class KEAP1 activator for NRF2-activated cancers, Phase I), and VVD-642 (RAS-PIK3CA interaction inhibitor for RAS-driven cancers, Phase I), plus undisclosed early-stage immunology programs. Recent platform publications have appeared in Journal of Medicinal Chemistry and Science.

Vividion is pre-revenue with no commercialized products; pricing for investigational drugs is not publicly disclosed. The company is funded entirely through Bayer as its parent company and leverages Bayer's global clinical development infrastructure (current Phase Ib trial enrolls across 11 countries) and commercial capabilities for eventual product launch. The go-to-market model is effectively enterprise partnership via Bayer rather than independent commercialization, and clinical operations function through Bayer's clinical trial site network globally. Headcount of 251–500 employees supports a maturing clinical-stage organization spanning discovery, translational research, CMC, and clinical development.

Short descriptiontext

Vividion Therapeutics is a clinical-stage biopharmaceutical company and Bayer AG subsidiary that uses a proprietary chemoproteomics platform to develop covalent small molecule therapeutics against previously undruggable proteins in oncology and immunology. It has three Phase I clinical programs—VVD-214 (WRN), VVD-037 (KEAP1), and VVD-642 (RAS-PIK3CA)—and is pre-revenue.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
251–500
akta.pro rankint
HeadquartersSan Diego, United States
HQ citystring
San Diego
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices1 record

Each record includes

City, Country, Type, Description, Source

Keyword5 values
small molecule therapeutics, chemoproteomics drug discovery, covalent inhibitor development, oncology drug discovery, precision medicine development
Industry3 codes
1Rare Oncology & Hematologic Malignancy Therapies
CodeHLAIAIACPrimaryYes
2Drug Discovery (Target ID/Validation & Hit Discovery)
CodeHLAIALAAPrimaryNo
3Clinical Development (Phase I–III Trial Design & Execution)
CodeHLAIALAEPrimaryNo
NAICS code2 codes
  • Research and Development in Biotechnology (except Nanobiotechnology)541714
  • Scientific Research and Development Services5417
SIC code1 code
  • Services-Commercial Physical & Biological Research8731
Product category
Clinical-stage Biopharmaceuticals
Social media profiles2 records
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model1 record
1Pharmaceutical Product Revenue
TypeLicensing Royalties
Description

Vividion is a clinical-stage biopharmaceutical company with multiple drug candidates in Phase I clinical trials. No commercial products or revenue currently. As a wholly-owned subsidiary of Bayer AG, the company is funded through Bayer's investment for drug development activities.

vividion.com
Marketing channels4 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels1 record

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components5 values
Technology or R&D, Personnel, Operations, Infrastructure, Others
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Core offering1 text field

Vividion Therapeutics is a clinical-stage biopharmaceutical company that discovers and develops first-in-class covalent small molecule therapeutics using a proprietary chemoproteomics platform. The company is advancing three clinical-stage candidates (VVD-214 WRN inhibitor, VVD-037 KEAP1 activator, VVD-642 RAS-PIK3CA inhibitor) for oncology indications and earlier-stage immunology programs, targeting protein classes previously considered undruggable.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 3 values shown
  • VVD-214 showed robust tumor regression in multiple patient-derived xenograft mouse models of MSI-high colorectal cancer in preclinical studies
+2 more records
Product overview1 text field

Vividion Therapeutics is a clinical-stage biopharmaceutical company developing a diversified pipeline of first-in-class small molecule therapeutics for previously undruggable disease targets in oncology and immunology. The company's core offerings include three clinical-stage programs: VVD-037 (KEAP1 Activator) for NRF2-activated solid tumors, VVD-214 (WRN Inhibitor) for MSI-high cancers, and VVD-642 (RAS-PIK3CA Inhibitor) for RAS-driven cancers. These programs are enabled by Vividion's proprietary chemoproteomics discovery platform, which combines a covalent fragment library (50,000+ molecules), high-throughput mass spectrometry screening, and an integrated data portal to identify and develop highly selective small molecule drugs against challenging protein targets.

Product and service4 records
1VVD-214 (WRN Inhibitor)
CategoryOncology Drug Candidate (Phase I)
Description

An investigational oral covalent inhibitor of Werner helicase (WRN) designed to treat MSI-high solid tumors including colorectal, endometrial, ovarian, and gastric cancers by exploiting the dependency of MSI-high cancer cells on WRN-mediated DNA repair while sparing healthy tissue.

2VVD-037 (KEAP1 Activator)
CategoryOncology Drug Candidate (Phase I)
Description

A first-in-class small molecule KEAP1 activator that allosterically enhances KEAP1's ability to degrade NRF2, designed to treat solid tumors with NRF2 pathway activation including non-small cell lung cancer, esophageal squamous cell carcinoma, and head and neck squamous cell carcinoma.

3VVD-642 (RAS-PIK3CA Inhibitor)
CategoryOncology Drug Candidate (Phase I)
Description

A small molecule inhibitor that blocks RAS-dependent PIK3CA oncogenic signaling by specifically inhibiting the interaction between RAS and PIK3CA without disrupting homeostatic signaling, designed for use in combination with MAPK pathway inhibitors for RAS-driven cancers.

4Multiple Undisclosed Immunology Programs
CategoryImmunology Drug Candidates (Discovery/Preclinical)
Description

Early-stage immunology programs leveraging Vividion's covalent-first chemoproteomics platform to identify and characterize functional sites on proteins linked to immune diseases with high unmet need.

Scale indicator2 records

Each record includes

Type, Value, Description, Source

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight5 records

Each record includes

Type, Description

Peers10 records
TypeEmerging player
Description

Clinical-stage company pioneering targeted protein degradation using covalent ligand technology (PROTACs), overlapping with Vividion's covalent chemistry expertise and undruggable target focus. Applicable to similar oncology and immunology indications.

TypeDirect peer
Description

Clinical-stage precision oncology company developing synthetic lethality-based therapeutics, including a WRN inhibitor program (similar mechanism to Vividion's VVD-214) for MSI-high cancers. Most direct mechanistic competitor in the WRN inhibitor space.

TypeDirect peer
Description

Clinical-stage oncology company developing precision small molecule therapies for previously undruggable targets, including programs against cancer-relevant proteins. Closely comparable in stage, modality, and target class philosophy to Vividion.

TypeDirect peer
Description

Clinical-stage precision oncology company focused on the RAS/MAPK pathway, directly relevant to Vividion's RAS-PIK3CA program (VVD-642). Competes in RAS-driven cancer space with similar target patient populations.

TypeDirect peer
Description

Clinical-stage biotechnology company developing synthetic lethality-based precision oncology medicines targeting cancer-specific vulnerabilities, overlapping with Vividion's chemoproteomics-driven target identification approach.

TypeDirect peer
Description

Clinical-stage oncology company developing medicines targeting the chromatin regulatory system using a proprietary platform, paralleling Vividion's platform-based approach to previously undruggable cancer targets.

TypeDirect peer
Description

Clinical-stage precision oncology company using motion-based protein design to drug previously undruggable targets, including RAS-driven cancers. Comparable in targeting intractable oncology targets with a platform-enabled approach.

TypeBroad incumbent
Description

Established precision oncology company with multiple approved and clinical-stage kinase-targeted therapies, including covalent inhibitors. Comparable target class and indication overlap, with greater commercial maturity.

TypeBroad incumbent
Description

Commercial-stage precision oncology company (acquired by Bristol-Myers Squibb) with approved KRAS inhibitors (Krazati), directly competitive with Vividion's RAS pathway program (VVD-642). Provides established commercial benchmark in the space.

TypeEmerging player
Description

Clinical-stage biotech using targeted protein degradation (degraders/covalent modality) to drug previously undruggable targets in oncology and immunology. Comparable in modality innovation and target-class ambition.

Market position
Strengths4 records

Each record includes

Headline, Details, Source

Weaknesses4 records

Each record includes

Headline, Details, Source

Competitive moat5 records

Each record includes

Type, Details

Key risks6 records

Each record includes

Headline, Details, Source

Key highlights6 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Segment3 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile1 record

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
Yes
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature6 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles16 records

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

No data
No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds5 records

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors23 records

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A1 record

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment1 record

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Vividion Therapeutics

Clinical-stage Biopharmaceuticalsvividion.com

Vividion Therapeutics is a clinical-stage biopharmaceutical company and Bayer AG subsidiary that uses a proprietary chemoproteomics platform to develop covalent small molecule therapeutics against previously undruggable proteins in oncology and immunology. It has three Phase I clinical programs—VVD-214 (WRN), VVD-037 (KEAP1), and VVD-642 (RAS-PIK3CA)—and is pre-revenue.

What Vividion Therapeutics does

Vividion Therapeutics is a clinical-stage biopharmaceutical company developing first-in-class covalent small molecule therapeutics against disease-causing proteins historically considered undruggable. The company was founded in 2016 based on foundational research from Scripps Research scientists Ben Cravatt, Phil Baran, and Jin-Quan Yu, and was acquired by Bayer AG in August 2021 for approximately $2 billion, becoming a wholly-owned and independently operated subsidiary headquartered in San Diego, California.

Vividion's core asset is a proprietary chemoproteomics discovery platform that combines a custom covalent fragment library of over 50,000 small molecules, high-resolution high-throughput mass spectrometry screening against thousands of proteins in their native cellular state, and an integrated data portal that overlays approximately 250,000 new data points per day with public human genetics and structural biology resources. The platform has produced three clinical-stage programs: VVD-214 (covalent allosteric WRN helicase inhibitor for MSI-high solid tumors, Phase Ib), VVD-037 (first-in-class KEAP1 activator for NRF2-activated cancers, Phase I), and VVD-642 (RAS-PIK3CA interaction inhibitor for RAS-driven cancers, Phase I), plus undisclosed early-stage immunology programs. Recent platform publications have appeared in Journal of Medicinal Chemistry and Science.

Vividion is pre-revenue with no commercialized products; pricing for investigational drugs is not publicly disclosed. The company is funded entirely through Bayer as its parent company and leverages Bayer's global clinical development infrastructure (current Phase Ib trial enrolls across 11 countries) and commercial capabilities for eventual product launch. The go-to-market model is effectively enterprise partnership via Bayer rather than independent commercialization, and clinical operations function through Bayer's clinical trial site network globally. Headcount of 251–500 employees supports a maturing clinical-stage organization spanning discovery, translational research, CMC, and clinical development.

Vividion Therapeutics firmographics

Firmographics
Name
Vividion Therapeutics
Legal name
Vividion Therapeutics, Inc.
Website
https://vividion.com
Company type
Private
Founded year
2016
Operating status
Operating
Headcount range
251–500 employees
Short description
Vividion Therapeutics is a clinical-stage biopharmaceutical company and Bayer AG subsidiary that uses a proprietary chemoproteomics platform to develop covalent small molecule therapeutics against previously undruggable proteins in oncology and immunology. It has three Phase I clinical programs—VVD-214 (WRN), VVD-037 (KEAP1), and VVD-642 (RAS-PIK3CA)—and is pre-revenue.
Ownership category
akta.pro rank

Vividion Therapeutics industry classification

Industry
Product category
Clinical-stage Biopharmaceuticals
NAICS
Research and Development in Biotechnology (except Nanobiotechnology) (541714), Scientific Research and Development Services (5417)
SIC
Services-Commercial Physical & Biological Research (8731)
akta.pro primary industry
Rare Oncology & Hematologic Malignancy Therapies (HLAIAIAC)
akta.pro secondary industries
Drug Discovery (Target ID/Validation & Hit Discovery) (HLAIALAA), Clinical Development (Phase I–III Trial Design & Execution) (HLAIALAE)

Keywords

  • Small molecule therapeutics
  • Chemoproteomics drug discovery
  • Covalent inhibitor development
  • Oncology drug discovery
  • Precision medicine development

Where Vividion Therapeutics is headquartered

Location

Headquarters

HQ city
San Diego
HQ country
United States
HQ region
North America

Offices1 record

Markets served

Vividion Therapeutics business model

Business model
GTM type
B2B
Offering type
Hardware or Manufacturing
Cost components
Technology or R&D, Personnel, Operations, Infrastructure, Others

Revenue model

  1. Pharmaceutical Product Revenue: Vividion is a clinical-stage biopharmaceutical company with multiple drug candidates in Phase I clinical trials. No commercial products or revenue currently. As a wholly-owned subsidiary of Bayer AG, the company is funded through Bayer's investment for drug development activities.

Go-to-market motion1 record

Distribution channels1 record

Marketing channels4 records

Vividion Therapeutics product offering

Product offering

Core offering

Vividion Therapeutics is a clinical-stage biopharmaceutical company that discovers and develops first-in-class covalent small molecule therapeutics using a proprietary chemoproteomics platform. The company is advancing three clinical-stage candidates (VVD-214 WRN inhibitor, VVD-037 KEAP1 activator, VVD-642 RAS-PIK3CA inhibitor) for oncology indications and earlier-stage immunology programs, targeting protein classes previously considered undruggable.

Product overview

Vividion Therapeutics is a clinical-stage biopharmaceutical company developing a diversified pipeline of first-in-class small molecule therapeutics for previously undruggable disease targets in oncology and immunology. The company's core offerings include three clinical-stage programs: VVD-037 (KEAP1 Activator) for NRF2-activated solid tumors, VVD-214 (WRN Inhibitor) for MSI-high cancers, and VVD-642 (RAS-PIK3CA Inhibitor) for RAS-driven cancers. These programs are enabled by Vividion's proprietary chemoproteomics discovery platform, which combines a covalent fragment library (50,000+ molecules), high-throughput mass spectrometry screening, and an integrated data portal to identify and develop highly selective small molecule drugs against challenging protein targets.

Differentiator

Problem solved

Functional benefit

Products and services

  • VVD-214 (WRN Inhibitor) An investigational oral covalent inhibitor of Werner helicase (WRN) designed to treat MSI-high solid tumors including colorectal, endometrial, ovarian, and gastric cancers by exploiting the dependency of MSI-high cancer cells on WRN-mediated DNA repair while sparing healthy tissue.
  • VVD-037 (KEAP1 Activator) A first-in-class small molecule KEAP1 activator that allosterically enhances KEAP1's ability to degrade NRF2, designed to treat solid tumors with NRF2 pathway activation including non-small cell lung cancer, esophageal squamous cell carcinoma, and head and neck squamous cell carcinoma.
  • VVD-642 (RAS-PIK3CA Inhibitor) A small molecule inhibitor that blocks RAS-dependent PIK3CA oncogenic signaling by specifically inhibiting the interaction between RAS and PIK3CA without disrupting homeostatic signaling, designed for use in combination with MAPK pathway inhibitors for RAS-driven cancers.
  • Multiple Undisclosed Immunology Programs Early-stage immunology programs leveraging Vividion's covalent-first chemoproteomics platform to identify and characterize functional sites on proteins linked to immune diseases with high unmet need.

Quantifiable outcome

  • VVD-214 showed robust tumor regression in multiple patient-derived xenograft mouse models of MSI-high colorectal cancer in preclinical studies
  • +2 more outcomes

Companies that use Vividion Therapeutics

Customer profile

Segments3 records

Ideal customer profiles1 record

Vividion Therapeutics technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature6 records

Vividion Therapeutics partnerships and signals

Strategic signal

Scale indicators2 records

Recent moves6 records

Expansion highlights5 records

Vividion Therapeutics competitors and assessment

Company assessment

Emerging players

  • Arvinas: Clinical-stage company pioneering targeted protein degradation using covalent ligand technology (PROTACs), overlapping with Vividion's covalent chemistry expertise and undruggable target focus. Applicable to similar oncology and immunology indications.
  • Kymera Therapeutics: Clinical-stage biotech using targeted protein degradation (degraders/covalent modality) to drug previously undruggable targets in oncology and immunology. Comparable in modality innovation and target-class ambition.

Direct peers

  • Repare Therapeutics: Clinical-stage precision oncology company developing synthetic lethality-based therapeutics, including a WRN inhibitor program (similar mechanism to Vividion's VVD-214) for MSI-high cancers. Most direct mechanistic competitor in the WRN inhibitor space.
  • Scorpion Therapeutics: Clinical-stage oncology company developing precision small molecule therapies for previously undruggable targets, including programs against cancer-relevant proteins. Closely comparable in stage, modality, and target class philosophy to Vividion.
  • Erasca: Clinical-stage precision oncology company focused on the RAS/MAPK pathway, directly relevant to Vividion's RAS-PIK3CA program (VVD-642). Competes in RAS-driven cancer space with similar target patient populations.
  • Tango Therapeutics: Clinical-stage biotechnology company developing synthetic lethality-based precision oncology medicines targeting cancer-specific vulnerabilities, overlapping with Vividion's chemoproteomics-driven target identification approach.
  • Foghorn Therapeutics: Clinical-stage oncology company developing medicines targeting the chromatin regulatory system using a proprietary platform, paralleling Vividion's platform-based approach to previously undruggable cancer targets.
  • Relay Therapeutics: Clinical-stage precision oncology company using motion-based protein design to drug previously undruggable targets, including RAS-driven cancers. Comparable in targeting intractable oncology targets with a platform-enabled approach.

Broad incumbents

  • Blueprint Medicines: Established precision oncology company with multiple approved and clinical-stage kinase-targeted therapies, including covalent inhibitors. Comparable target class and indication overlap, with greater commercial maturity.
  • Mirati Therapeutics: Commercial-stage precision oncology company (acquired by Bristol-Myers Squibb) with approved KRAS inhibitors (Krazati), directly competitive with Vividion's RAS pathway program (VVD-642). Provides established commercial benchmark in the space.

Market position

Strengths4 records

Weaknesses4 records

Competitive moat5 records

Key risks6 records

Key highlights6 records

Customer concentration

Vividion Therapeutics social profiles

Digital presence

Vividion Therapeutics financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Vividion Therapeutics leadership team

Management profile

Number of profiles

Profiles16 records

Vividion Therapeutics funding detail

Funding detail

Funding overview

Funding rounds5 records

Investors23 records

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

Vividion Therapeutics M&A and investment

M&A and investment

M&A1 record

Investments1 record

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about Vividion Therapeutics

What does Vividion Therapeutics do?

Vividion Therapeutics is a clinical-stage biopharmaceutical company that discovers and develops first-in-class covalent small molecule therapeutics using a proprietary chemoproteomics platform. The company is advancing three clinical-stage candidates (VVD-214 WRN inhibitor, VVD-037 KEAP1 activator, VVD-642 RAS-PIK3CA inhibitor) for oncology indications and earlier-stage immunology programs, targeting protein classes previously considered undruggable.

Is Vividion Therapeutics a public or private company?

Vividion Therapeutics is a private company. It is classified as corporate owned and is currently operating.

When was Vividion Therapeutics founded?

Vividion Therapeutics was founded in 2016. It employs 251 to 500 people.

Where is Vividion Therapeutics based?

Vividion Therapeutics is headquartered in San Diego, United States, in the North America region.

How does Vividion Therapeutics make money?

One revenue line is on record: pharmaceutical Product Revenue.

Who are Vividion Therapeutics's main competitors?

Emerging players on record are Arvinas and Kymera Therapeutics. Direct peers are Repare Therapeutics, Scorpion Therapeutics, Erasca, Tango Therapeutics, Foghorn Therapeutics and Relay Therapeutics. Broad incumbents are Blueprint Medicines and Mirati Therapeutics.

Does Vividion Therapeutics have an API?

No public API is recorded for Vividion Therapeutics.

What industry is Vividion Therapeutics in?

Vividion Therapeutics's product category is Clinical-stage Biopharmaceuticals. Its primary akta.pro industry code is HLAIAIAC, Rare Oncology & Hematologic Malignancy Therapies, with a secondary code of HLAIALAA, Drug Discovery (Target ID/Validation & Hit Discovery). Its NAICS code is 541714 and its SIC code is 8731.

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Live signals
BioSpaceVividion Announces Publication of Clinical Data for VVD-214 in Nature Medicine, Highlighting Potential in Colorectal CancerVividion published Phase 1 data for VVD-214 in Nature Medicine, showing an 80.5% disease control rate and 7.3-month median progression-free survival in MSI-high colorectal cancer. The findings support ongoing Phase 1b and Phase 2 combination studies with bevacizumab and pembrolizumab.Law360Vividion Investor Wants IP Suit Over $2B Bayer Deal RevivedCHP III LP urged the Delaware Supreme Court to revive its suit over allegedly diverted intellectual property in Vividion Therapeutics' $2 billion sale to Bayer Corp. The defendants argued the investor is trying to turn a corporate injury into a direct stockholder claim that did not survive the merger.openPR.comFunctional Genomics Market Demonstrates Long-Term Growth Potential At 14.1% CAGRThe Business Research Company released a market report forecasting the functional genomics sector to reach $28.71 billion by 2030, driven by precision medicine adoption and genomic data analytics investments. Key industry developments include Vividion Therapeutics' acquisition of Tavros Therapeutics in January 2025 to enhance drug discovery capabilities and Roche's February 2025 launch of its SBX sequencing technology.FinancialContent Business PageVividion Therapeutics Doses First Patient in Phase Ib Combination Study of WRN Inhibitor VVD-214 in Patients with Advanced Colorectal CancerVividion Therapeutics announced that the first patient has been dosed in a Phase Ib combination clinical trial evaluating VVD-214, an investigational oral inhibitor of Werner helicase (WRN), in combination with bevacizumab for patients with microsatellite instability-high or deficient mismatch repair colorectal cancer whose disease has progressed following prior therapy. The global trial is enrolling patients at clinical sites across 11 countries including the U.S., Australia, Belgium, Canada, China, Denmark, France, Malaysia, South Korea, Spain, and the U.K. Preliminary data from the Phase Ia study presented at AACR 2025 showed VVD-214 was well tolerated with early signals of activity.BioSpaceVividion Therapeutics Doses First Patient in Phase Ib Combination Study of WRN Inhibitor VVD-214 in Patients with Advanced Colorectal CancerVividion Therapeutics and Bayer announced the first patient was dosed in a Phase Ib trial of VVD-214, an oral WRN inhibitor, combined with bevacizumab in patients with MSI-high or dMMR colorectal cancer. The global trial will enroll patients across multiple countries, building on Phase Ia data showing tolerability and early activity signals.MorningstarVividion Therapeutics Doses First Patient in Phase Ib Combination Study of WRN Inhibitor VVD-214 in Patients with Advanced Colorectal CancerVividion Therapeutics dosed the first patient in a Phase Ib trial of VVD-214, a WRN inhibitor, combined with bevacizumab in patients with MSI-high or dMMR colorectal cancer. The global trial will enroll patients across multiple countries, building on Phase Ia data showing tolerability and early activity signals.openPR.comPI3K Inhibitor Treatment Pipeline Shows Strong Momentum as 20+ Pharma Companies in the Race | DelveInsightDelveInsight's "PI3K Inhibitor Pipeline Insight 2026" report identifies over 20 pharmaceutical companies developing more than 25 PI3K inhibitor therapies targeting cancer. On March 20, 2026, Eli Lilly initiated a Phase 3 study to assess Tersolisib (LY4064809/STX-478) in combination with other anti-cancer drugs as a first-line treatment for advanced HR+/HER2- breast cancer. On March 18, 2026, Vividion Therapeutics announced a Phase 1 study evaluating VVD-159642, a RAS-PI3K inhibitor, for advanced solid tumors both as monotherapy and in combination with sotorasib or trametinib.Business Wire BlogVividion Publishes Discovery of First-in-Class KEAP1 Activator, Supporting Ongoing Clinical Program in OncologyVividion Therapeutics published research describing the discovery of first-in-class small molecule KEAP1 activators that use a novel covalent allosteric molecular glue mechanism to drive NRF2 degradation in cancer cells. The study establishes KEAP1 activation as a promising therapeutic approach for NRF2-activated cancers including non-small cell lung cancer, esophageal squamous cell carcinoma, and head and neck squamous cell carcinoma. VVD-037, the company's lead KEAP1 activator, is currently being evaluated in a Phase I clinical trial in patients with solid tumors characterized by NRF2 pathway activation.The Times of IndiaCould cancer finally have a targeted cure? Groundbreaking study reveals potential pathway to stop tumor growth without harming healthy cells - The Economic TimesScientists from the Francis Crick Institute and Vividion Therapeutics have developed new chemical compounds capable of stopping tumor growth without damaging healthy cells, with the experimental therapy now advancing to its first human clinical trial. The compounds target the RAS gene, which is mutated in approximately one in five cancers, and the study was published in Science on October 9. The researchers used chemical screening and biological assays to identify compounds that block the interaction between RAS and PI3K while preserving normal cellular activity, and testing in mice showed tumor growth was suppressed even without RAS involvement.BioSpaceVividion Announces Publication in Science of Preclinical Data on Covalent Inhibitors of RAS-PI3K that Block Tumor GrowthVividion Therapeutics, a clinical-stage biopharmaceutical company and subsidiary of Bayer AG, published preclinical data in Science describing novel covalent inhibitors that selectively block RAS-mediated activation of PI3Kα, demonstrating tumor growth inhibition in RAS-mutant and HER2 over-expressing models without causing hyperglycemia. The research, conducted in collaboration with the Francis Crick Institute, identified compounds that simultaneously target both the RAS-PI3K and HER2 pathways through the same binding site, overcoming a historical limitation of dual-pathway inhibition approaches. The investigational therapy is currently in Phase I clinical trials, representing a potential new treatment class for RAS-driven cancers, which account for approximately 20% of human malignancies.