CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 50 enrolled
Drug / intervention
Curcumindrug
Likely dose
Curcumin 8 gm orally per dayAI-extracted
Key inclusion· 4
  • Pathologically confirmed adenocarcinoma of pancreas not amenable to curative surgery (locally advanced, metastatic, or recurrent)
  • Karnofsky Performance Status ≥60
  • Measurable disease
  • Age ≥18 years
Key exclusion· 4
  • History of treated or active brain metastases, carcinomatous meningitis, uncontrolled seizure disorder, or active neurological disease
  • Unstable medical condition including uncontrolled diabetes, hypertension, active infections, unstable CHF, uncontrolled arrhythmias, or coagulation disorders
  • Pregnant or breast feeding
  • Investigational agent within 4 weeks of study entry

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00094445
NCT00094445Phase 2Completed

Phase II Trial of Curcumin in Patients With Advanced Pancreatic Cancer

M.D. Anderson Cancer Center·interventional·Posted Oct 19, 2004·Updated Aug 28, 2020

In Brief

A Phase 2 clinical trial evaluating Curcumin for Pancreatic Neoplasms and Adenocarcinoma. Completed, enrolled 50 participants across 1 site.

Detailed Summary

The goal of this clinical research study is to learn if treatment with curcumin can help shrink or slow the growth of pancreatic cancers. The effect of curcumin on the way pancreatic cancer cells function and the safety of treatment with curcumin will also be studied.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
CollaboratorsSabinsa Corporation

Timeline

Phase 2CompletedFinished
20052006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedOct 19, 2004
Enrollment StartNov 1, 2004
Primary CompletionApr 1, 2014
TodayJul 2, 2026
Enrollment to primary: 9.4 yearsPosted 21.7 years ago

Interventions

Curcumindrug

Starting dose 8 gm orally per day for 8 weeks. If patient experiences grade III toxicity, dose held and restarted with a 50% dose reduction after resolution of toxicity to \</= Grade I. Patients with grade IV toxicity will discontinue treatments. Patients with \</= grade I toxicity may have a 25% dose increase at each four-week period. Patients will continue on treatment until disease progresses, unless Grade III toxicity supervenes.