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A Randomized Controlled Study of Suizenji in Patients with Unresectable Pancreatic Cancer

A Randomized Controlled Study of Suizenji in Patients with Unresectable Pancreatic Cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT2032220428
Enrollment
90
Registered
2022-10-29
Start date
2023-01-31
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Unresectable pancreatic cancer

Interventions

- HIFU (High-Intensity Focused Ultrasound) + chemotherapy group: HIFU treatment with Suizenji: up to 2 times per week (1 course) for pancreatic primary lesions
the second course should be at least 60 days apart, up to a maximum of 5 courses. Chemotherapy (physician's choice): Nal-IRI/FL, mFOLFIRINOX or Gem/nab-PTX - Chemotherapy group: Chemothe

Sponsors

Iwasaki Seinori
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Ages 20 years and over. (2) Unresectable pancreatic cancer (including metastatic pancreatic cancer) who are refractory or intolerant to first-line chemotherapy. Any first-line chemotherapy is acceptable. (3) Target treatment tumor is located in the pancreas, and the target tumor can be visualized with ultrasound echography and can also be treated by high-intensity focused ultrasound. (4) Has primary tumor site of measurable lesion according to RECIST guidelines version 1.1 (5) ECOG performance status of 0 to 2.

Exclusion criteria

Exclusion criteria: (1) Active multiple cancers that require treatment. (2) Suspected gastrointestinal invasion of the primary tumor based on CT scan. (3) Obstructive jaundice. However, patients who have a bile duct stent placed for obstructive jaundice by the time of allocation may be enrolled. (4) Child-Pugh Classification B or C liver failure due to liver metastases. (5) Tumor embolization in the veins surrounding the pancreas. (6) Cystic component within the pancreatic cancer. (7) Peritoneal dissemination. (8) Pleural effusion or ascites with poorly controlled (9) Contraindications to the use of secondary chemotherapy used in this study.

Design outcomes

Primary

MeasureTime frame
Overall Survival

Secondary

MeasureTime frame
Progression-free survival (PFS), 1-year survival rate, objective response rate (ORR), disease control rate (DCR), Adverse Events (AEs), etc.

Contacts

Public ContactIwasaki

SONIRE Therapeutics Inc.

seinori_iwasaki@sonire-t.com+81-3-5843-6764

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026