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Phase I study using pulverized curcumin for pancreatic/biliary tract cancer patients who get resistant to gemcitabine-based chemotherapy

Phase I study using pulverized curcumin for pancreatic/biliary tract cancer patients who get resistant to gemcitabine-based chemotherapy - Phase I study using pulverized curcumin for pancreatic/biliary tract cancer patients

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000002950
Enrollment
12
Registered
2010-12-01
Start date
2010-01-01
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

Advanced pancreatic/biliary tract cancer patients who get resistant to gemcitabine-based chemotherapy

Interventions

pulverized curcumin

Sponsors

Kyoto University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients who have histologically or radiologically comfirmed pancreatic/biliary tract cancer 2. Patients who get resistant to gemcitabine based chemotherapy 3. Age >/=20 4. ECOG performance status </=2 5. Adequate oral intake 6. Adequate organ and bone marrow function 7. Provided written informed consent

Exclusion criteria

Exclusion criteria: 1. Patients with active interstitial pneumonia or pulmonary fibrosis 2. Patients with uncontrollable diabetes mellitus, liver disease, angina pectoris or a new onset of myocardial infarction within 3 months 3. Patients with severe infection 4. Patients with severe drug allergy 5. Patients with other serious comorbid diseases 6. Pregnant women or patients who wish pregnanct 7. Patients with mental diseases 8. Patients who are judged inappropriate for the entry into the study by the investigator

Design outcomes

Primary

MeasureTime frame
Phase I; To find a recommended dose of pulverized curcumin

Countries

Japan

Contacts

Public ContactMasashi Kanai

Kyoto University Hospital Outpatient Oncology Unit

075-751-4770

Outcome results

None listed

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