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Taking peoplePhase 2

Tests VVD-133214 with pembrolizumab in advanced colorectal cancer

Tests VVD-133214 plus pembrolizumab in adults with advanced colorectal cancer with MSI or dMMR.

Key facts

Who runs it
Vividion Therapeutics, Inc.
Where
Besançon, Brest, Dijon, and Marseille, FranceSee the 4 sitesAlso in 21 other countries, 118 sites
Registry title
A Study to Evaluate the Efficacy of VVD-133214 in Combination With Pembrolizumab Compared With Pembrolizumab Alone in Participants With Advanced Cancer of the Colon or Rectum
Status
Recruiting
Phase
Phase 2
People taking part
140 people, planned
Started
11 Sept 2026
Expected to end
31 Dec 2030
Type of study
Interventional, 3 groupsOne group gets an existing treatment, for comparison.
Treatments tested
  • VVD-133214
  • Pembrolizumab
Record updated
21 October 2026

Who can take part

AI summary

From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for adults with advanced colorectal cancer that has MSI and/or dMMR, who have not yet had treatment for the advanced disease.

Age
18 years or older
Sex
All sexes can join
Disease stage
Advanced colorectal adenocarcinoma that cannot be removed by surgery and/or has spread, with measurable disease (RECIST v1.1). Tumor must have MSI and/or dMMR status confirmed.
Earlier treatment
No earlier systemic treatment for advanced or metastatic disease. Earlier adjuvant chemotherapy is allowed if the disease progressed at least 12 months after the last dose. No earlier adjuvant immunotherapy and no earlier WRN helicase inhibitor.
Biomarker or test result
Known MSI (microsatellite instability) and/or dMMR (deficient mismatch repair) tumor status, confirmed in a certified laboratory. Archival tumor tissue must be available.

Main reasons for not taking part

  • Active or uncontrolled brain or central nervous system metastases
  • Active autoimmune disease or immune deficiency that needed treatment in the past 2 years
  • Another cancer in the past 5 years (Lynch syndrome is not excluded)
  • Active hepatitis B, hepatitis C or HIV
  • Known Werner Syndrome

The registry criteria, word for word

Show all 17 criteriaShow less

Who can take part

  • Eastern Cooperative Oncology Group (ECOG) performance-status score of 0 or 1
  • Have a known microsatellite instability (MSI) and/or deficient mismatch repair (dMMR) tumor status confirmed per local standard of care (SoC), and have histologically or cytologically documented advanced (unresectable and/or metastatic) colorectal adenocarcinoma (CRC)
  • No prior systemic treatment for metastatic disease and not amenable to curative resection
  • Participants must have documented MSI and/or dMMR tumor status determined as part of the routine diagnostic workup in a certified laboratory
  • Availability of formaldehyde-fixed paraffin-embedded (FFPE) archival tumor tissue for submission to Sponsor/central laboratory for retrospective central testing including a copy of a redacted pathology report if available
  • Presence of measurable disease according to RECIST v1.1
  • Adequate hematologic and end-organ function, defined using laboratory results obtained within 14 days prior to first dose of study treatment
  • Females of childbearing potential must have negative serum pregnancy test before starting study treatment

Who cannot take part

  • Prior systemic treatment for advanced CRC. Participants may have received prior adjuvant chemotherapy as long as disease progression occurred at least 12 months after the last dose of adjuvant treatment
  • Prior treatment with adjuvant immunotherapy (e.g., anti-PD-1, anti-PD-L1, anti-PD-L2 agent, or anti-CTLA-4 agent, or any other antibody or drug specifically targeting T cell co-stimulation or immune checkpoint pathways, including prior therapy with anti-tumor vaccines or other immuno-stimulatory antitumor agents, etc.)
  • Known active or uncontrolled central nervous system (CNS) or brain metastases (progressing or requiring anticonvulsants or corticosteroids for symptomatic control) and/or carcinomatous meningitis
  • Participants requiring treatment with systemic immunosuppressive medication (such as corticosteroids) within 2 weeks prior to initiation of study treatment, or anticipation of need for systemic immunosuppressive medication during study treatment
  • Prior treatment with any WRN helicase inhibitor
  • Patients with active or history of autoimmune disease or immune deficiency that has required treatment in past 2 years
  • History of malignancy other than CRC, within 5 years prior to screening. Participants with Lynch syndrome are not excluded
  • Participants with active hepatitis B, hepatitis C or HIV
  • Participants with known Werner Syndrome (WRN)

Where in France

Also in 21 other countries, 118 sites

  • CHRU de Besancon - Hopital Jean Minjoz - Medical OncologyBesançon, FranceNot yet recruiting
  • CHU Brest - Hopital La Cavale Blanche - service oncologie medicaleBrest, FranceNot yet recruiting
  • Unicancer Dijon - Centre Georges Francois Leclerc - Oncologie medicaleDijon, FranceNot yet recruiting
  • Unicancer Marseille - Institut Paoli-Calmettes - Oncologie medicaleMarseille, FranceNot yet recruiting

About the trial

What the trial wants to find out

Researchers are looking for a better way to treat people with advanced colorectal cancer.

Read full original descriptionShow less

Colorectal cancer (cancer of the colon or rectum) is one of the most common cancers worldwide. Treatments include surgery, chemotherapy, radiotherapy, and immunotherapy; however, these treatments do not work for everyone, may cause serious adverse events or may stop working eventually. New treatments and treatment combinations are needed, especially for cancers that cannot be removed with surgery or that have spread to other parts of the body (called advanced or metastatic cancer).

Cells normally repair themselves when mistakes happen as they divide. But in some people with cancer, the repair system does not work properly because of a problem called dMMR (deficient mismatch repair). As a result, mistakes build up in the cell's DNA, leading to a condition called MSI (microsatellite instability). Over time, these changes can cause cells to grow and behave abnormally, contributing to the development and growth of cancer.

To survive, some cancer cells with dMMR or MSI rely on a protein called Werner helicase. This protein helps repair some of the DNA damage allowing them to keep growing. Because these cancer cells depend more on Werner helicase than healthy cells, blocking this protein may help stop cancer cells from surviving while having less effect on healthy cells.

The study drug, VVD-133214, is designed to block the Werner helicase protein. Blocking this protein may help stop cancer cells from growing, while causing less harm to healthy cells. VVD-133214 is being studied in combination with pembrolizumab, an approved immunotherapy that helps the immune system recognize and attack cancer cells.

This study will test the combination of VVD-133214 and pembrolizumab in people with advanced colorectal cancer with MSI and/or dMMR who have not yet received treatment for their advanced disease. The study aims to find the best dose of VVD-133214 in combination with pembrolizumab and to test whether the combination is more effective than pembrolizumab alone.

Participants will receive treatment with VVD-133214 for as long as it can help them and does not cause serious adverse events. Treatment with pembrolizumab will stop after two years. Participants can also stop treatment at any time.

During the study, participants will have regular visits with the study doctor for tests, scans, and check-ups. These visits help check how well the cancer is responding to the treatment and monitor the participants' health.

The study will also monitor adverse events, which are any new or worsening medical problems that can happen during the study. Doctors record all adverse events, irrespective of whether the study doctor believes they are related to the study treatments, to help ensure participants' safety throughout the study.

After stopping treatment, participants will return for follow-up visits: 30 days after their last dose of VVD-133214 and/or 100 days after their last dose of pembrolizumab. After that, participants will have long-term follow-up visits every 90 days for as long as they agree to continue participating in follow-up.

The 3 groups in the trial

  • VVD-133214 Dose 1 + PembrolizumabTreatment being tested

    Participants will receive VVD-133214 in combination with pembrolizumab

    Treatment: VVD-133214 and Pembrolizumab

  • VVD-133214 Dose 2 + PembrolizumabTreatment being tested

    Participants will receive VVD-133214 in combination with pembrolizumab

    Treatment: VVD-133214 and Pembrolizumab

  • PembrolizumabExisting treatment, for comparison

    Participants will receive pembrolizumab only (monotherapy)

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Data and sources

Registry record
Listed on ClinicalTrials.gov and on the EU's official list of trials (CTIS).
Official title
A Phase 2, Randomized, Open-label Study of VVD-133214 in COmbination With Pembrolizumab Compared to Pembrolizumab Monotherapy in Participants With Advanced Colorectal Adenocarcinoma (CRC) Harboring Microsatellite Instability (MSI) and/or Deficient Mismatch Repair (DMMR)
Plain-language title
Tests VVD-133214 with pembrolizumab in advanced colorectal cancerGenerated from the registry record. The registry title is the official one.
AI summary
From the trial's eligibility criteria. Read by machine on 12 November 2026.
Record updated
21 October 2026