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Phase II Clinical Trial of Gemcitabine and Irinotecan for Unresectable and Recurrent Pancreatic Cancer

Phase II Clinical Trial of Gemcitabine and Irinotecan for Unresectable and Recurrent Pancreatic Cancer - Phase II Tial of Gem+CPT-11 for Unresectable PC

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000009963
Enrollment
40
Registered
2013-02-05
Start date
2004-04-01
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 or Recurrent Pancreatic Cancer (PC)

Interventions

Gemcitabine 1,000mg/m2 and Irinotecan 100mg/m2 are administered with intravenous infusion on day 1 and 15 every 4 weeks.

Sponsors

Osaka Medical Center for Cancer and CVD
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Histologically confirmed pancreatic ductal carcinoma. 2) Patients of age =>20 and 80> 3) Performance Status:0-2(ECOG) 4) Life expectancy more than 1 months. 5) Adequate organ functions. neutrophils >=2,000/mm3 leukocytes =>4,000 and 12,000/mm3> platelets >=100,000/mm3 hemoglobin >=9.5g/dl AST(GOT)/ALT(GPT) <=LLN x2.5 total bilirubin <=LLN x2 serum creatinine <= LLN BUN <= LLN PaO2 >= 70 torr 6) Written informed consent.

Exclusion criteria

Exclusion criteria: 1) Lung fibrosis or intestinal pneumoni, and anamnesis or imaging findings. 2) Severe infection. 3) Severe complication. (heart failure, angina pectoris, arrhythmia, diabetes , intestines paralysis, ileus, myocardial infarction within 6 months after the onset.) 4) Pregnant or lactation women, or women with known or suspected pregnancy and men who want let to pregnancy. 5) Watery diarrhea. 6) Jaundice. 7) Uncontrolled pleural or abdominal effusion. 8) Severe drug hypersensitivity. 9) History of other active malignancy. 10) Severe mental illness 11) Patients who are judged inappropriate for the entry into the study by the investigater.

Design outcomes

Primary

MeasureTime frame
Response Rate

Secondary

MeasureTime frame
Safety PFS OS

Countries

Japan

Contacts

Public ContactTatsya Ioka

Osaka Medical Center for Cancer and CVD Hepatobiliary and Pancreatic Oncology

ioka_ta@hotmail.com06-6972-1181

Outcome results

None listed

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