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- Ensaio Clínico NCT07645651
Samuraciclib for the Treatment of Patients With Resectable, Borderline Resectable, or Locally Advanced Basal Pancreatic Cancer
Phase 1b Window-of-Opportunity Study Evaluating CDK7 Inhibition in Patients With Localized Basal Pancreatic Cancer
Visão geral do estudo
Status
Condições
Descrição detalhada
This is a single-institution, single-arm, open-label, Phase 1 study designed to evaluate whether samuraciclib, a cyclin dependent kinase 7 inhibitor (CDK7), alters the cellular functioning of the pancreatic tumor cells.
OUTLINE:
Patients will receive samuraciclib orally (PO) once daily (QD) for 14 days on study following their diagnosis of pancreatic cancer and before starting chemotherapy or undergoing surgery for their cancer. Patients will undergo an endoscopic ultrasound (EUS) with fine needle biopsy (FNB) while on study.
After completion of study treatment, patients are followed up at 30 and 90 days.
Tipo de estudo
Inscrição (Estimado)
Estágio
- Fase 1
Contactos e Locais
Contato de estudo
- Nome: Rachael Safyan, MD
- Número de telefone: 206-606-2038
- E-mail: rsafyan@uw.edu
Estude backup de contato
- Nome: Isabel Blanco
- Número de telefone: 206-606-5864
- E-mail: giresearch@fredhutch.org
Locais de estudo
-
-
Washington
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Seattle, Washington, Estados Unidos, 98109
- Recrutamento
- Fred Hutch/University of Washington Cancer Consortium
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Investigador principal:
- Rachael Safyan, MD
-
Contato:
- Rachael Safyan, MD
- Número de telefone: 206-606-2038
- E-mail: rsafyan@uw.edu
-
Contato:
- Isabel Blanco
- Número de telefone: 206-606-5864
- E-mail: giresearch@fredhutch.org
-
-
Critérios de participação
Critérios de elegibilidade
Idades elegíveis para estudo
- Adulto
- Adulto mais velho
Aceita Voluntários Saudáveis
Descrição
Inclusion Criteria:
Histologically or cytologically proven basal pancreatic adenocarcinoma. Histologies other than adenocarcinoma, or any mixed histologies, will NOT be eligible.
- Basal tumors are defined as GATA6- and HMGA2+. Tumor cores are considered positive for GATA6 or HMGA2 if greater than 10% of tumor epithelial cells had positive nuclei
Resectable, borderline resectable, or locally advanced pancreatic ductal adenocarcinoma (PDA) at diagnosis based on contrast-enhanced CT or magnetic resonance imaging (MRI) (CT or MRI without contrast as part of positron emission tomography (PET)/CT or PET/MRI is NOT acceptable; CT or MRI with contrast as part PET/CT or PET/MRI is acceptable) of the chest, abdomen, and pelvis. The institutional radiologist must review the scans. Resectable, borderline resectable, and locally advanced will be defined by National Comprehensive Cancer Network (NCCN) guidelines version 2.2025.
- There must be no evidence of metastatic disease
- Must be 18 years or older
- Ability to understand and willingness to sign a written informed consent document
- Archival biopsy specimen collected within 3 months must be available. If not available, a diagnostic EUS/FNB will be performed during screening
- Eastern Cooperative Oncology Group (ECOG) performance status 0-1
- Absolute neutrophil count (ANC) ≥ 1,500/mcL (within 14 days prior to study drug)
- Platelets ≥ 100,000/mcL (within 14 days prior to study drug)
- Hemoglobin ≥ 9 g/dL (within 14 days prior to study drug)
- Creatinine clearance ≥ 50 ml/min by Cockcroft-Gault
- Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) both ≤ 2.5X ULN (within 14 days prior to study drug)
- Total bilirubin ≤ 1.5X ULN (within 14 days prior to study drug)
- Participants must not be pregnant or nursing. Women of childbearing potential (WOCBP) must have a negative urine pregnancy test within 72 hours of treatment initiation, where WOCBP are defined as all female participants between 18 - 55 years of age. Participants of child-bearing potential must be willing to employ two highly effective and acceptable forms of contraception for up to 6 months after the final administered dose of investigational agent. A woman is considered to be of reproductive potential if she has had menses at any time in the preceding 12 consecutive months
- HIV-infected patients on effective anti-retroviral therapy with undetectable viral load within 6 months are eligible for this trial
Exclusion Criteria:
- Prior radiation
- Unable to tolerate oral medication, per assessment of the principal investigator (PI)
- Participants who are receiving other investigational agents
- Concomitant mediation use should only exclude patients from trial participation when clinically relevant known or predicted drug-drug interactions or potential overlapping toxicities will impact safety or efficacy
- Uncontrolled or concurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements
- Refractory nausea and vomiting, chronic gastrointestinal diseases or previous significant bowel resection with clinically significant sequelae that precluded adequate absorption of samuraciclib
- Uncontrolled seizures
- Active infection
- Active bleeding diatheses
- Known active hepatitis B or hepatitis C infection
- Breastfeeding or pregnancy
- Receipt of systemic corticosteroids within 14 days before the first dose of study medication
- Receipt of St. John's Wort within 21 days before the first dose of study medication or of another concomitant medication, herbal supplement, or food that was a strong inhibitor or inducer of CYP3A4, CYP2C19, CYP2D6, or P-glycoprotein activity within 21 days before the first dose of samuraciclib
- Known hypersensitivity to samuraciclib or any excipient of the product
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Tratamento
- Alocação: N / D
- Modelo Intervencional: Atribuição de grupo único
- Mascaramento: Nenhum (rótulo aberto)
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
|---|---|
|
Experimental: Treatment (Samuraciclib)
Patients receive samuraciclib PO QD for 14 days on study.
Treatment continues in the absence of disease progression or unacceptable toxicity.
Patients will have a research EUS/FNB on study.
Patients also undergo CT scans during screening and blood sample collection on study.
|
Submeter-se a TC
Outros nomes:
Realizar coleta de sangue
Outros nomes:
Given PO
Outros nomes:
Undergo EUS/FNB
|
O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Change in ribonucleic acid polymerase II serine levels
Prazo: Within 72 hours post versus pre-samuraciclib treatment
|
Will be assessed by pharmacodynamic changes in primary tumor cells.
Pre and post measurements will be compared using a paired t-test at the 2-sided 5% level.
Data will be transformed as necessary (e.g. using log-transformation).
|
Within 72 hours post versus pre-samuraciclib treatment
|
Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Incidence of samuraciclib-related adverse events
Prazo: Within 30 days of the last dose of samuraciclib
|
Will be measured by Common Terminology Criteria for Adverse Events version 6.
|
Within 30 days of the last dose of samuraciclib
|
|
Completion of 14 days of study drug (Feasibility)
Prazo: Up to 90 days
|
Will be summarized by proportions and 90% confidence intervals using the Wilson score method.
|
Up to 90 days
|
|
Completion of the on-protocol research endoscopic ultrasound/fine needle biopsy (Feasibility)
Prazo: Up to 90 days
|
Will be summarized by proportions and 90% confidence intervals using the Wilson score method.
|
Up to 90 days
|
|
Adequate biopsy (≥ 3 cores with ≥30% tumor cellularity) (Feasibility)
Prazo: Up to 90 days
|
Will be summarized by proportions and 90% confidence intervals using the Wilson score method.
|
Up to 90 days
|
|
Time (days) from last dose of study drug to first definitive therapy (surgery or cycle 1 day 1 of neoadjuvant chemotherapy)
Prazo: Up to 90 days
|
Will be estimated using the Kaplan Meier method.
|
Up to 90 days
|
|
Incidence of schedule delays attributable to study drug
Prazo: Up to 90 days
|
Will be summarized by proportions and 90% confidence intervals using the Wilson score method.
|
Up to 90 days
|
Colaboradores e Investigadores
Patrocinador
Colaboradores
Investigadores
- Investigador principal: Rachael Safyan, MD, Fred Hutch/University of Washington Cancer Consortium
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo (Estimado)
Conclusão Primária (Estimado)
Conclusão do estudo (Estimado)
Datas de inscrição no estudo
Enviado pela primeira vez
Enviado pela primeira vez que atendeu aos critérios de CQ
Primeira postagem (Real)
Atualizações de registro de estudo
Última Atualização Postada (Real)
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última verificação
Mais Informações
Termos relacionados a este estudo
Termos MeSH relevantes adicionais
Outros números de identificação do estudo
- RG1126054
- NCI-2026-01733 (Identificador de registro: CTRP (Clinical Trial Reporting Program))
- 21300 (Outro identificador: Fred Hutch/University of Washington Cancer Consortium)
Plano para dados de participantes individuais (IPD)
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