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Phase 2 Study of Irinotecan Liposome Injection, Oxaliplatin, 5-fluorouracil/Levoleucovorin in Japanese Participants Not Previously Treated for Metastatic Adenocarcinoma of the Pancreas
Sponsor: Institut de Recherches Internationales Servier
Summary
This study is to assess the anti-tumour activity, safety and tolerability of irinotecan liposome injection (S095013) in combination with oxaliplatin, 5-Fluorouracil (5-FU) and levoisomer form of leucovorin (LLV). S095013, oxaliplatin, 5-FU and LLV will be administered on days 1 and 15 of each 28-day cycle. Cycles will continue until clinical or radiological progressive disease, unacceptable study medication-related toxicity or withdrawal from study. During the treatment period participants will have study visits on day 1, 3, 15, and 17 of each cycle, some of which may occur as a home visit. At least 30 days after treatment has ended a end of treatment visit will occur and then participants will be followed for survival every month via telephone or email until death or end of the study. Study visits may include questionnaires, blood and urine tests, ECG, vital signs, physical examination, and administration of study treatment.
Official title: A Single-arm Multicentre Phase 2 Study of Irinotecan Liposome Injection, Oxaliplatin, 5-fluorouracil/Levoleucovorin in Japanese Participants Who Have Not Previously Received Therapy for Metastatic Adenocarcinoma of the Pancreas
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
41
Start Date
2024-04-25
Completion Date
2026-01-01
Last Updated
2024-10-08
Healthy Volunteers
No
Interventions
Irinotecan liposome injection (S095013)
Irinotecan liposome injection (S095013) will be administered via intravenous (IV) infusion on days 1 and 15 of each 28-day cycle.
Oxaliplatin
Oxaliplatin will be administered via intravenous (IV) infusion on days 1 and 15 of each 28-day cycle.
LLV (levoisomer form of leucovorin)
LLV will be administered via intravenous (IV) infusion on days 1 and 15 of each 28-day cycle.
5- FU (5-Fluorouracil)
5-FU will be administered via intravenous (IV) infusion on days 1 and 15 of each 28-day cycle.
Locations (14)
National Cancer Center Hospital East (003)
Kashiwa, Chiba, Japan
Chiba University Hospital (015)
Chiba, Japan
Chiba Cancer Center (011)
Chiba, Japan
National Hospital Organization Shikoku Cancer Center (013)
Ehime, Japan
National Hospital Organization Kyushu Cancer Center (005)
Fukuoka, Japan
Kanazawa University Hospital (008)
Ishikawa, Japan
Kanagawa Cancer Center (002)
Kanagawa, Japan
Aichi Cancer Center (007)
Nagoya, Japan
Osaka International Cancer Institute (009)
Osaka, Japan
Saitama Cancer Center (012)
Saitama, Japan
Hokkaido University Hospital (004)
Sapporo, Japan
National Cancer Center Hospital (001)
Tokyo, Japan
The Cancer Institute Hospital of JFCR (006)
Tokyo, Japan
Yamaguchi University Hospital (010)
Yamaguchi, Japan