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Clinical Trials in France / NCT07811193
Recruiting Phase 2

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

NCT07811193 · tracked via the Priya Life Science France tracker
Phase
Phase 2
Started
2026-09-11
Last updated
2026-09-16

Condition(s) studied

Colorectal Adenocarcinoma

Investigational drug(s) / intervention(s)

VVD-133214 →Pembrolizumab →

VVD-133214: VVD-133214 will be administered orally

Pembrolizumab: Pembrolizumab will be administered by intravenous infusion (IV) every three weeks

Study summary

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

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.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * 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 Exclusion Criteria: * 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 * 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 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 * Participants with active hepatitis B, hepatitis C or HIV * Participants with known Werner Syndrome (WRN) * Prior treatment with any WRN helicase inhibitor

Primary outcome measure(s)

Trial sites (122)

FacilityCityRegionStatus
University of Arizona Cancer Center - North Campus Tucson Arizona Not Yet Recruiting
University of Michigan Rogel Cancer Center Ann Arbor Michigan Not Yet Recruiting
Brigette Harris Cancer Pavilion at Henry Ford Cancer Center - Detroit Detroit Michigan Not Yet Recruiting
Mary Babb Randolph Cancer Center Morgantown West Virginia Not Yet Recruiting
Hospital Italiano de Buenos Aires Buenos Aires Buenos Aires Not Yet Recruiting
Centro Medico Fleischer Buenos Aires Buenos Aires Not Yet Recruiting
Instituto Alexander Fleming Buenos Aires Buenos Aires Not Yet Recruiting
Sanatorio Allende | Departamento de Investigación Clínica Córdoba Córdoba Province Not Yet Recruiting
Fundación Intecnus Bariloche Río Negro Province Not Yet Recruiting
Sanatorio Parque - Oncology Rosario Santa Fe Province Not Yet Recruiting
Investigaciones Oncológicas C Colón Mar Del Plata, Buenos Aires, Argentina Not Yet Recruiting
Institut Jules Bordet - Clinique D'Oncology Brussels Brussels Capital Not Yet Recruiting
UZ Leuven - Digestive oncology Leuven Flemish Brabant Not Yet Recruiting
CHU Helora - Hopital de La Louvière - Site Jolimont - Oncology department La Louvière Hainaut Not Yet Recruiting
UZ Gent - Digestive Oncology Ghent Belgium Not Yet Recruiting
AZ Delta - Digestive oncology Roeselare Belgium Not Yet Recruiting
Hospital Evangélico de Cachoeiro de Itapemirim Vitória Espírito Santo Not Yet Recruiting
Hospital Araujo Jorge Associaçao de Combate ao Cancer em Goias Goiânia Goiás Not Yet Recruiting
Nucleo de Ensino e Pesquisa do Hospital de Clinicas de Ijuí Ijuí Rio Grande do Sul Not Yet Recruiting
Unidade de Pesquisas Clinicas em Oncologia Pelotas Rio Grande do Sul Not Yet Recruiting
NAIC - Instituto do Cancer Bauru São Paulo Not Yet Recruiting
Fundacao Pio XII - Hospital de Cancer de Barretos Jaú São Paulo Not Yet Recruiting
Instituto do Cancer do Estado de Sao Paulo São Paulo São Paulo Not Yet Recruiting
Hospital Sirio Libanes - Oncology_Sao Paulo São Paulo São Paulo Not Yet Recruiting
The First Affiliated Hospital of Bengbu Medical College Bengbu Anhui Not Yet Recruiting
Beijing Cancer Hospital - Oncology Department Beijing Beijing Municipality Not Yet Recruiting
Fujian Cancer Hospital Fuzhou Fujian Not Yet Recruiting
The Sixth Affiliated Hospital, Sun Yat-sen University Guangzhou Guangdong Not Yet Recruiting
Harbin Medical University Cancer Hospital Harbin Heilongjiang Not Yet Recruiting
Tongji Hospital affiliated to Tongji Medical College of Huazhong University of Science & Technology Wuhan Hubei Not Yet Recruiting
Shandong University - Shandong Cancer Hospital Jinan Shandong Not Yet Recruiting
Zhongshan Hospital, Fudan University Shanghai Shanghai Municipality Not Yet Recruiting
West China Hospital Sichuan University Chengdu Sichuan Not Yet Recruiting
Yunnan Cancer Hospital Kunming Yunnan Not Yet Recruiting
Sir Run Run Shaw Hospital, Zhejiang Univ. School of Medicine - Oncology Department Hangzhou Zhejiang Not Yet Recruiting
Zhejiang Cancer Hospital Hangzhou Zhejiang Not Yet Recruiting
CHU Brest - Hopital La Cavale Blanche - service oncologie medicale Brest Brittany Region Not Yet Recruiting
CHRU de Besancon - Hopital Jean Minjoz - Medical Oncology Besançon France Not Yet Recruiting
Unicancer Dijon - Centre Georges Francois Leclerc - Oncologie medicale Dijon France Not Yet Recruiting
Unicancer Marseille - Institut Paoli-Calmettes - Oncologie medicale Marseille France Not Yet Recruiting

+ 82 more sites — see the full list on the official registry below.

On this site

📄 Keytruda (pembrolizumab) drug profile →

More Vividion Therapeutics, Inc. trials in France

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07811193 on ClinicalTrials.gov ↗ ← All trials in France