Denna sida har översatts automatiskt och översättningens korrekthet kan inte garanteras. Vänligen se engelsk version för en källtext.

Samuraciclib for the Treatment of Patients With Resectable, Borderline Resectable, or Locally Advanced Basal Pancreatic Cancer

19 augusti 2026 uppdaterad av: University of Washington

Phase 1b Window-of-Opportunity Study Evaluating CDK7 Inhibition in Patients With Localized Basal Pancreatic Cancer

The purpose of this study is to evaluate the safety and efficacy of samuraciclib in patients with localized pancreatic cancer.

Studieöversikt

Detaljerad beskrivning

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.

Studietyp

Interventionell

Inskrivning (Beräknad)

15

Fas

  • Fas 1

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studiekontakt

  • Namn: Rachael Safyan, MD
  • Telefonnummer: 206-606-2038
  • E-post: rsafyan@uw.edu

Studera Kontakt Backup

Studieorter

    • Washington
      • Seattle, Washington, Förenta staterna, 98109
        • Rekrytering
        • Fred Hutch/University of Washington Cancer Consortium
        • Huvudutredare:
          • Rachael Safyan, MD
        • Kontakt:
          • Rachael Safyan, MD
          • Telefonnummer: 206-606-2038
          • E-post: rsafyan@uw.edu
        • Kontakt:

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

  • Vuxen
  • Äldre vuxen

Tar emot friska volontärer

Nej

Beskrivning

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

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Behandling
  • Tilldelning: N/A
  • Interventionsmodell: Enskild gruppuppgift
  • Maskning: Ingen (Open Label)

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Experimentell: 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.
Genomgå CT
Andra namn:
  • CT
  • KATT
  • Datortomografi
  • Beräknad axiell tomografi
  • Datoriserad axialtomografi
  • tomografi
  • Datoriserad axiell tomografi (förfarande)
  • Datortomografi (CT) skanning
  • Diagnostisk kattskanning
  • Diagnostisk kattskanningstjänsttyp
Genomgå blodprovtagning
Andra namn:
  • Biologisk provsamling
  • Bioprov insamlat
  • Provsamling
Given PO
Andra namn:
  • CT7001
  • CDK7 Inhibitor CT7001
  • CT 7001
  • CT-7001
Undergo EUS/FNB

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Change in ribonucleic acid polymerase II serine levels
Tidsram: 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

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Incidence of samuraciclib-related adverse events
Tidsram: 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)
Tidsram: 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)
Tidsram: 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)
Tidsram: 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)
Tidsram: Up to 90 days
Will be estimated using the Kaplan Meier method.
Up to 90 days
Incidence of schedule delays attributable to study drug
Tidsram: Up to 90 days
Will be summarized by proportions and 90% confidence intervals using the Wilson score method.
Up to 90 days

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Utredare

  • Huvudutredare: Rachael Safyan, MD, Fred Hutch/University of Washington Cancer Consortium

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Beräknad)

15 september 2026

Primärt slutförande (Beräknad)

14 juli 2027

Avslutad studie (Beräknad)

1 november 2027

Studieregistreringsdatum

Först inskickad

5 juni 2026

Först inskickad som uppfyllde QC-kriterierna

8 juni 2026

Första postat (Faktisk)

12 juni 2026

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

20 augusti 2026

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

19 augusti 2026

Senast verifierad

1 augusti 2026

Mer information

Termer relaterade till denna studie

Andra studie-ID-nummer

  • RG1126054
  • NCI-2026-01733 (Registeridentifierare: CTRP (Clinical Trial Reporting Program))
  • 21300 (Annan identifierare: Fred Hutch/University of Washington Cancer Consortium)

Plan för individuella deltagardata (IPD)

Planerar du att dela individuella deltagardata (IPD)?

NEJ

Läkemedels- och apparatinformation, studiedokument

Studerar en amerikansk FDA-reglerad läkemedelsprodukt

Ja

Studerar en amerikansk FDA-reglerad produktprodukt

Nej

Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .

Prenumerera