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Study identifier: NCT07575191 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Safety and Performance of a Novel Infusion Catheter System for Peri/Intratumoral Gemcitabine Delivery in Patients With Pancreatic Cancer

Condition: Pancreatic Cancer Non-resectable  ·  Sponsor: Smartwise Sweden AB

PhasePhase 1/Phase 2
Planned participants9
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This study is testing a new way to deliver the chemotherapy drug Gemcitabine in pancreatic tumors using the catheter Extroducer® Infusion Catheter System. The study will include patients with Locally Advanced Pancreatic Cancer that cannot be removed with surgery. Patients will receive four treatment sessions, given every two weeks, in which Gemcitabine is infused directly into or near the tumor. The study will test up to three increasing dose levels of Gemcitabine (200 mg, 400 mg, and 100 mg). The study will enroll three groups of three patients each. After each group completes treatment, an independent safety committee will review the results to decide whether it is safe to move to the next dose per predefined study criteria. After finishing treatment, patients will be followed for six months. Each patient's total participation in the study will last about 8-9 months. The main goal of the study is to evaluate the safety and feasibility of this treatment approach.

This description comes directly from the study's public registry record.

Talk to the study team

Ulrik Birgersson, PhD, MSc  ·  +46 70 842 10 54  ·  Ulrik.Birgersson@smartcella.com

Always discuss trial participation with your own doctor first.

Locations (1)

Karolinska University HospitalSolna, SwedenRecruiting

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Source record: clinicaltrials.gov/study/NCT07575191