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Orathecin + Gemcitabine Versus Placebo + Gemcitabine in Chemonaive Non-Resectable Pancreatic Cancer

Primary Purpose

Pancreatic Cancer

Status
Terminated
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Rubitecan
Sponsored by
Astex Pharmaceuticals, Inc.
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pancreatic Cancer focused on measuring rubitecan, Orathecin, 9-nitrocamptothecin, gemcitabine, Gemzar, pancreatic cancer, adenocarcinoma, RFS 2000

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: The patient is at least 18 years of age. The patient has histologically or cytologically confirmed, non-resectable, Stage II-IV primary adenocarcinoma of the pancreas. The patient has had a baseline computed tomography (CT) scan, or magnetic resonance imaging (MRI), to evaluate tumor(s) within 28 days prior to randomization. The patient has never been treated with prior chemotherapy, with the exception of low-dose 5-fluorouracil (5-FU) as a radiation sensitizer. The patient has sufficiently recovered from the effects of previous surgery (no less than 3 weeks prior to randomization), radiotherapy, and/or immunotherapy (no less than 4 weeks prior to randomization). The patient's estimated life expectancy is at least 12 weeks. The patient has a Karnofsky Performance Status between 50 and 100. The patient has adequate bone marrow function. The patient has adequate hepatic and renal function. Exclusion Criteria: The patient has any active, uncontrolled infection requiring antibiotics. The patient has any serious, uncontrolled concomitant systemic disorder. The patient has surgery scheduled within 8 weeks following initiation of treatment. The patient is pregnant or nursing. The patient is not capable of consistent oral intake of at least 3 L/day of fluid and/or requires constant intravenous (IV) hydration or frequent tube feeding. The patient is receiving any investigational agent(s) or has been a participant in a clinical trial within the last 30 days.

Sites / Locations

  • Compassionate Cancer Care Medical Group
  • 11100 Warner Avenue, Ste. 200
  • The Cancer Research & Prevention Center
  • Mile High Oncology
  • Norton Healthcare, Inc.
  • Mary Bird Perkins Cancer Center
  • Medical Oncology
  • N. Mississippi Hematology & Oncology Associates
  • Kansas City Cancer Center
  • Cancer Research of Long Island
  • Charleston Hematology Oncology, PA

Outcomes

Primary Outcome Measures

survival

Secondary Outcome Measures

Full Information

First Posted
June 6, 2005
Last Updated
January 22, 2013
Sponsor
Astex Pharmaceuticals, Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT00113256
Brief Title
Orathecin + Gemcitabine Versus Placebo + Gemcitabine in Chemonaive Non-Resectable Pancreatic Cancer
Official Title
Randomized Trial of Orathecin and Gemcitabine Versus Placebo and Gemcitabine in Patients With Non-Resectable Pancreatic Cancer Who Have Not Already Received Chemotherapy
Study Type
Interventional

2. Study Status

Record Verification Date
October 2009
Overall Recruitment Status
Terminated
Study Start Date
February 2005 (undefined)
Primary Completion Date
February 2006 (Actual)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Astex Pharmaceuticals, Inc.

4. Oversight

5. Study Description

Brief Summary
Patients will be treated with gemcitabine and Orathecin (rubitecan) capsules to evaluate the current estimate of overall survival as a study endpoint prior to launching the blinded randomized phase (versus gemcitabine and placebo) of the study. Toxicity of the drug combination will also be evaluated.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pancreatic Cancer
Keywords
rubitecan, Orathecin, 9-nitrocamptothecin, gemcitabine, Gemzar, pancreatic cancer, adenocarcinoma, RFS 2000

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
39 (Actual)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Rubitecan
Primary Outcome Measure Information:
Title
survival

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: The patient is at least 18 years of age. The patient has histologically or cytologically confirmed, non-resectable, Stage II-IV primary adenocarcinoma of the pancreas. The patient has had a baseline computed tomography (CT) scan, or magnetic resonance imaging (MRI), to evaluate tumor(s) within 28 days prior to randomization. The patient has never been treated with prior chemotherapy, with the exception of low-dose 5-fluorouracil (5-FU) as a radiation sensitizer. The patient has sufficiently recovered from the effects of previous surgery (no less than 3 weeks prior to randomization), radiotherapy, and/or immunotherapy (no less than 4 weeks prior to randomization). The patient's estimated life expectancy is at least 12 weeks. The patient has a Karnofsky Performance Status between 50 and 100. The patient has adequate bone marrow function. The patient has adequate hepatic and renal function. Exclusion Criteria: The patient has any active, uncontrolled infection requiring antibiotics. The patient has any serious, uncontrolled concomitant systemic disorder. The patient has surgery scheduled within 8 weeks following initiation of treatment. The patient is pregnant or nursing. The patient is not capable of consistent oral intake of at least 3 L/day of fluid and/or requires constant intravenous (IV) hydration or frequent tube feeding. The patient is receiving any investigational agent(s) or has been a participant in a clinical trial within the last 30 days.
Facility Information:
Facility Name
Compassionate Cancer Care Medical Group
City
Corona
State/Province
California
ZIP/Postal Code
92882
Country
United States
Facility Name
11100 Warner Avenue, Ste. 200
City
Fountain Valley
State/Province
California
ZIP/Postal Code
92708
Country
United States
Facility Name
The Cancer Research & Prevention Center
City
Soquel
State/Province
California
ZIP/Postal Code
95073
Country
United States
Facility Name
Mile High Oncology
City
Denver
State/Province
Colorado
ZIP/Postal Code
80210
Country
United States
Facility Name
Norton Healthcare, Inc.
City
Louisville
State/Province
Kentucky
ZIP/Postal Code
40202
Country
United States
Facility Name
Mary Bird Perkins Cancer Center
City
Baton Rouge
State/Province
Louisiana
ZIP/Postal Code
70809
Country
United States
Facility Name
Medical Oncology
City
Baton Rouge
State/Province
Louisiana
ZIP/Postal Code
70809
Country
United States
Facility Name
N. Mississippi Hematology & Oncology Associates
City
Tupelo
State/Province
Mississippi
ZIP/Postal Code
38801
Country
United States
Facility Name
Kansas City Cancer Center
City
Kansas City
State/Province
Missouri
ZIP/Postal Code
64111
Country
United States
Facility Name
Cancer Research of Long Island
City
Great Neck
State/Province
New York
ZIP/Postal Code
11023
Country
United States
Facility Name
Charleston Hematology Oncology, PA
City
Charleston
State/Province
South Carolina
ZIP/Postal Code
29403
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Orathecin + Gemcitabine Versus Placebo + Gemcitabine in Chemonaive Non-Resectable Pancreatic Cancer

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