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ACTIVE NOT RECRUITING
NCT06225999
PHASE2

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

View on ClinicalTrials.gov

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

DRUG

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.

DRUG

Oxaliplatin

Oxaliplatin will be administered via intravenous (IV) infusion on days 1 and 15 of each 28-day cycle.

DRUG

LLV (levoisomer form of leucovorin)

LLV will be administered via intravenous (IV) infusion on days 1 and 15 of each 28-day cycle.

DRUG

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