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NCT07811193

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

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Aún no reclutando Fase 2

Descripción

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.

Evidencia de la diana molecular en cáncer colorrectal

Aún no hay evidencia documentada en nuestra base para la diana o el fármaco de este ensayo. Esta sección crece a medida que se procesan nuevas publicaciones.

Criterios de Elegibilidad

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

Información del Ensayo

NCT07811193
Aún no reclutando
Fase 2
140 participantes
Sep 2026
Jun 2028

Ubicaciones121

Argentina (7)
Fundación Intecnus
Bariloche
Centro Medico Fleischer
Buenos Aires
Hospital Italiano de Buenos Aires
Buenos Aires
Instituto Alexander Fleming
Buenos Aires
Sanatorio Allende | Departamento de Investigación Clínica
Córdoba
Investigaciones Oncológicas C Colón
Mar Del Plata, Buenos Aires,
Sanatorio Parque - Oncology
Rosario
Belgium (5)
Institut Jules Bordet - Clinique D'Oncology
Brussels
UZ Gent - Digestive Oncology
Ghent
CHU Helora - Hopital de La Louvière - Site Jolimont - Oncology department
La Louvière
UZ Leuven - Digestive oncology
Leuven
AZ Delta - Digestive oncology
Roeselare
Brazil (8)
NAIC - Instituto do Cancer
Bauru
Hospital Araujo Jorge Associaçao de Combate ao Cancer em Goias
Goiânia
Nucleo de Ensino e Pesquisa do Hospital de Clinicas de Ijuí
Ijuí
Fundacao Pio XII - Hospital de Cancer de Barretos
Jaú
Unidade de Pesquisas Clinicas em Oncologia
Pelotas
Hospital Sirio Libanes - Oncology_Sao Paulo
São Paulo
Instituto do Cancer do Estado de Sao Paulo
São Paulo
Hospital Evangélico de Cachoeiro de Itapemirim
Vitória
China (12)
Beijing Cancer Hospital - Oncology Department
Beijing
The First Affiliated Hospital of Bengbu Medical College
Bengbu
West China Hospital Sichuan University
Chengdu
Fujian Cancer Hospital
Fuzhou
The Sixth Affiliated Hospital, Sun Yat-sen University
Guangzhou
Sir Run Run Shaw Hospital, Zhejiang Univ. School of Medicine - Oncology Department
Hangzhou
Zhejiang Cancer Hospital
Hangzhou
Harbin Medical University Cancer Hospital
Harbin
Shandong University - Shandong Cancer Hospital
Jinan
Yunnan Cancer Hospital
Kunming
Zhongshan Hospital, Fudan University
Shanghai
Tongji Hospital affiliated to Tongji Medical College of Huazhong University of Science & Technology
Wuhan
France (4)
CHRU de Besancon - Hopital Jean Minjoz - Medical Oncology
Besançon
CHU Brest - Hopital La Cavale Blanche - service oncologie medicale
Brest
Unicancer Dijon - Centre Georges Francois Leclerc - Oncologie medicale
Dijon
Unicancer Marseille - Institut Paoli-Calmettes - Oncologie medicale
Marseille
Germany (7)
DRK Kliniken Berlin-Köpenick - Darmzentrum
Berlin
Universitaetsklinikum Essen - Innere Klinik (Tumorforschung)
Essen
Krankenhaus Nordwest GmbH - Institut Fuer Klinisch-Onkologische Forschung (IKF)
Frankfurt am Main
Asklepios Klinik Altona - Onkologie, Hämatologie, Palliativmedizin, Rheumatologie und Pneumologie
Hamburg
Klinikum Oldenburg - Klinik für Onkologie und Hämatologie
Oldenburg
Leopoldina-Krankenhaus der Stadt Schweinfurt GmbH-Medizinische Klinik 2
Schweinfurt
Universitätsklinikum Ulm - Klinik für Innere Medizin I
Ulm
Greece (6)
General Hospital Of Athens Alexandra-Plasma Cell Dyscrasias Unit, Department of Clinical Therapeutics, N.K.U.A
Athens
Laiko General Hospital Of Athens- Oncology Department
Athens
Saint Savvas Oncology Hospital -1st Internal Medicine - Oncology Department
Athens
Metropolitan General Hospital -Oncologic Clinical Trials and Research Clinic
Cholargos/ Athens
General University Hospital Of Patras- Division of Oncology, Department of Medicine
Pátrai
Athens Medical Center S.A./ European Interbalkan Medical Center - 4th Department of Medical Oncology
Pylaia
Hong Kong (3)
Queen Mary Hospital
Hong Kong
Hong Kong United Oncology Centre
Kowloon
Prince of Wales Hospital
Shatin
Italy (5)
ASST Grande Ospedale Metropolitano Niguarda - Oncologia Falck
Milan
Istituto Europeo di Oncologia s.r.l - Sviluppo di nuovi farmaci per Terapie Innovative
Milan
A.O.U. Universita' Degli Studi Della Campania Luigi Vanvitelli - Oncoematologia
Naples
Fondazione Policlinico Universitario Agostino Gemelli IRCCS - UOC Oncologia Medica
Roma
Humanitas Mirasole S.p.A. - Oncologia Medica ed Ematologia
Rozzano
Malaysia (6)
Hospital Wanita Dan Kanak Kanak Sabah - Oncology and Radiotherapy
Kota Kinabalu
Cengild G.I. Medical Centre - Curie Oncology KL
Kuala Lumpur
Universiti Malaya Medical Centre - Clinical Oncology Department
Kuala Lumpur
Hospital Umum Sarawak (Sarawak General Hospital) SGH
Kuching
Sunway Medical Centre Penang - Department of Clinical Oncology
Perai
Sunway Medical Centre - Medical Oncology
Subang Jaya
Mexico (6)
Grupo Medico ASSET S.C
Benito Juárez
Renati Innovation SAPI de CV
Guadalajara
Instituto Nacional de Cancerología
Mexico City
Oncare Viaducto Nápoles
Mexico City
Hospital Universitrio Dr. José Eleuterio González. Servicio de Oncologia
Monterrey
Hospital Zambrano Hellion
Monterrey
Netherlands (1)
HagaZiekenhuis - Oncologie Interne Geneeskunde
The Hague
Poland (11)
Białostockie Centrum Onkologii im. M. Skłodowskiej-Curie w Białymstoku Oddział Onkologii Klinicznej
Bialystok
Comarch Healthcare SA Centrum Medyczne iMed24
Krakow
Pratia McM Kraków
Krakow
Wojewódzkie Wielospecjalistyczne Centrum Onkologii i Traumatologii im. M. Kopernika w Łodzi
Lodz
Opolskie Centrum Onkologii
Opole
Europejskie Centrum Zdrowia Otwock, Szpital im. F. Chopina
Otwock
Wojewodzki Szpital im. Sw. Ojca Pio w Przemyslu Oddział Onkologiczny z Pododdziałem Dziennej Chemioterapii
Przemyśl
Mazowiecki Szpital Wojewódzki Siedleckie Centrum Onkologii Oddział Onkologii Klinicznej i Radioterapii
Siedlce
Centrum Medyczne Pratia Poznan
Skorzewo
Narodowy Instytut Onkologii im. Marii Skłodowskiej Curie Państwowy Instytut Badawczy- Oddział Warszawa Wawelska
Warsaw
Pratia Wroclaw
Wroclaw
Portugal (5)
Unidade Local de Saúde de Coimbra, E.P.E. - Hospitais da Universidade de Coimbra - Serviço de Oncologia
Coimbra
Instituto Português de Oncologia de Lisboa Francisco Gentil, E.P.E. - Serviço de Oncologia Médica
Lisbon
START Research Portugal - ULSS Maria - Unidade de Ensaios de Fase I Start Lisbon
Lisbon
Unidade Local de Saúde de São José, E.P.E - Hospital dos Capuchos - Serviço de Oncologia Médica
Lisbon
Instituto Português de Oncologia do Porto Francisco Gentil, E.P.E. - Serviço de Oncologia Médica
Porto
Singapore (4)
Curie Oncology | Farrer
Singapore
National Cancer Center Singapore - Oncology Department
Singapore
National University Cancer Institute (NCIS)
Singapore
OncoCare Cancer Centre | Gleneagles Medical Centre
Singapore
South Korea (5)
Seoul National University Hospital | Oncology
Jongno -Gu
Seoul National University Bundang Hospital | Oncology
Seongnam-si, Gyeonggi-do
Asan Medical Center | Oncology
Seoul
Samsung Medical Center | Oncology
Seoul
Severance Hospital | Oncology
Seoul
Spain (6)
Hospital del Mar | Oncologia
Barcelona
Hospital Universitari Vall D Hebron | Oncologia
Barcelona
Hospital Universitario Ramon Y Cajal | Oncologia Medica
Madrid
Hospital Universitario Virgen De La Victoria | Oncologia Medica
Málaga
Complexo Hospitalario Universitario De Santiago | Oncologia
Santiago de Compostela
Hospital Clinico Universitario De Valencia | Oncologia
Valencia
Taiwan (7)
Chang Gung Memorial Hospital Kaohsiung
Kaohsiung City
Keelung Chang Gung Memorial Hospital - Division of Hematology and Oncology
Keelung
Taichung Veterans General Hospital | Division of Colorectal Surgery
Taichung
Chi Mei Medical Center, Yongkang Branch
Tainan
National Cheng Kung University Hospital
Tainan
Chang Gung Memorial Hospital at Linkou
Taipei
Taipei Veterans General Hospital
Taipei
Turkey (Türkiye) (7)
Ankara Bilkent Sehir Hastanesi
Bilkent Çankaya
Trakya Univ. Tip Fak.
Edirne
Gaziantep Sehir Hastanesi -Medical Oncology Department
Gaziantep
Kartal Dr Lutfi Kirdar Sehir Hastanesi- Medical Oncology
Istanbul
İstanbul Medeniyet Üniversitesi Göztepe Süleyman Yalçın Şehir Hastanesi
Kadıköy
VM Medical Park Samsun Hospital Medical Oncology Department
Samsun
Ankara Etlik Sehir Hastanesi
Yenimahalle
United Kingdom (2)
University Hospital Coventry | Oncology
Coventry
University College Hospital | Cancer Clinical Trials Unit
London
United States (4)
University of Michigan Rogel Cancer Center
Ann Arbor
Brigette Harris Cancer Pavilion at Henry Ford Cancer Center - Detroit
Detroit
Mary Babb Randolph Cancer Center
Morgantown
University of Arizona Cancer Center - North Campus
Tucson