Samuraciclib for the Treatment of Patients With Resectable, Borderline Resectable, or Locally Advanced Basal Pancreatic Cancer
Part of paid clinical trials in Seattle, Washington.
- Sponsor
- University of Washington
- Study ID
- NCT07645651
- Phase
- PHASE1
- Status
- Recruiting
Conditions
- Borderline Resectable Pancreatic Ductal Adenocarcinoma
- Locally Advanced Pancreatic Ductal Adenocarcinoma
- Resectable Pancreatic Ductal Adenocarcinoma
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Samuraciclib — DRUGGiven PO
- Computed Tomography — PROCEDUREUndergo CT
- Endoscopic Ultrasound Biopsy — PROCEDUREUndergo EUS/FNB
- Biospecimen Collection — PROCEDUREUndergo blood sample collection
Study Details
The purpose of this study is to evaluate the safety and efficacy of samuraciclib in patients with localized pancreatic cancer.
Key Dates
- First listed
- Jun 12, 2026
- Start date
- Sep 15, 2026
- Status verified
- Aug 2026
- Primary completion
- Jul 14, 2027
- Completion
- Nov 1, 2027
Study Design
- Enrollment
- 15 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- 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.
Primary Outcome Measure
Change in ribonucleic acid polymerase II serine levels [ Time Frame: Within 72 hours post versus pre-samuraciclib treatment ]
Central Contacts
- Rachael Safyan, MD206-606-2038
- Isabel Blanco206-606-5864
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Fred Hutch/University of Washington Cancer Consortium | Seattle | Washington | 98109 | Rachael Safyan, MD (PRINCIPAL_INVESTIGATOR) |
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