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
調査の概要
状態
詳細な説明
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.
研究の種類
入学 (推定)
段階
- フェーズ 1
連絡先と場所
研究連絡先
- 名前:Rachael Safyan, MD
- 電話番号:206-606-2038
- メール:rsafyan@uw.edu
研究連絡先のバックアップ
- 名前:Isabel Blanco
- 電話番号:206-606-5864
- メール:giresearch@fredhutch.org
研究場所
-
-
Washington
-
Seattle、Washington、アメリカ、98109
- 募集
- Fred Hutch/University of Washington Cancer Consortium
-
主任研究者:
- Rachael Safyan, MD
-
コンタクト:
- Rachael Safyan, MD
- 電話番号:206-606-2038
- メール:rsafyan@uw.edu
-
コンタクト:
- Isabel Blanco
- 電話番号:206-606-5864
- メール:giresearch@fredhutch.org
-
-
参加基準
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
説明
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
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:処理
- 割り当て:なし
- 介入モデル:単一グループの割り当て
- マスキング:なし(オープンラベル)
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
実験的: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.
|
CTを受ける
他の名前:
採血を受ける
他の名前:
Given PO
他の名前:
Undergo EUS/FNB
|
この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Change in ribonucleic acid polymerase II serine levels
時間枠: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
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Incidence of samuraciclib-related adverse events
時間枠: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)
時間枠: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)
時間枠: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)
時間枠: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)
時間枠:Up to 90 days
|
Will be estimated using the Kaplan Meier method.
|
Up to 90 days
|
|
Incidence of schedule delays attributable to study drug
時間枠:Up to 90 days
|
Will be summarized by proportions and 90% confidence intervals using the Wilson score method.
|
Up to 90 days
|
協力者と研究者
スポンサー
捜査官
- 主任研究者:Rachael Safyan, MD、Fred Hutch/University of Washington Cancer Consortium
研究記録日
主要日程の研究
研究開始 (推定)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
その他の研究ID番号
- RG1126054
- NCI-2026-01733 (レジストリ識別子:CTRP (Clinical Trial Reporting Program))
- 21300 (その他の識別子:Fred Hutch/University of Washington Cancer Consortium)
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
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