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| Sponsor: | Washington University School of Medicine |
|---|---|
| Information provided by (Responsible Party): | Washington University School of Medicine |
| ClinicalTrials.gov Identifier: | NCT00732082 |
Purpose
The overall purpose of this research is to evaluate the safety and toxicity of an investigational medication, IMP321, in patients being treated with gemcitabine. IMP321 is a synthetic protein (made in the laboratory to simulate a protein that your body makes on its own) and was designed to stimulate the immune system with the overall objective of improving the body's capacity to react to your pancreas cancer.
| Condition | Intervention | Phase |
|---|---|---|
|
Pancreatic Neoplasms |
Drug: Gemcitabine Drug: LAG-3 and Gemcitabine Drug: LAG-3 and gemcitabine |
Phase I |
| Study Type: | Interventional |
| Study Design: | Allocation: Non-Randomized Endpoint Classification: Safety Study Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Phase I Study of Soluble LAG-3 (IMP321) and Gemcitabine in Patients With Advanced Pancreas Cancer |
| Estimated Enrollment: | 30 |
| Study Start Date: | February 2009 |
| Estimated Study Completion Date: | February 2015 |
| Primary Completion Date: | June 2010 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
| Active Comparator: 1 |
Drug: Gemcitabine
Gemcitabine 1 gm/m2
|
| Experimental: 2 |
Drug: LAG-3 and Gemcitabine
Gemcitabine 1 gm/m2 and IMP321 3 mg
|
| Experimental: 3 |
Drug: LAG-3 and gemcitabine
gemcitabine 1 gm/m2 and IMP321 6.5 mg
|
| Experimental: 4 |
Drug: LAG-3 and gemcitabine
gemcitabine 1 gm/m2 and IMP321 13 mg
|
| Experimental: 5 |
Drug: LAG-3 and gemcitabine
gemcitabine 1 gm/m2 and IMP321 26 mg
|
This is a phase I, single center, open label, non-randomized, dose-escalation phase I study performed in the ambulatory setting in patients receiving first line chemotherapy for unresectable pancreas cancer with gemcitabine weekly and the investigational agent IMP321. IMP321 will be given at D2 and D16 of a 4-week cycle, for a period of 6 months. The hypothesis of this study is that IMP321 is safe for human administration. Additionally we hypothesize that IMP321 elicits an immunomodulatory effect that is therapeutic in the treatment of pancreas cancer.
Primary Objectives
Secondary Objectives
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
The patient with previous history of malignancy is eligible for this study only if the patient meets the following criteria for cancer survivor:
Exclusion Criteria:
Contacts and Locations| United States, Missouri | |
| Washington University | |
| St. Louis, Missouri, United States, 63110 | |
| Principal Investigator: | William G. Hawkins, M.D. | Washington Univerisity |
More Information
| Responsible Party: | Washington University School of Medicine |
| ClinicalTrials.gov Identifier: | NCT00732082 History of Changes |
| Other Study ID Numbers: | 07-0265 |
| Study First Received: | August 6, 2008 |
| Last Updated: | September 23, 2011 |
| Health Authority: | United States: Food and Drug Administration |
|
LAG-3 and gemcitabine treatment for advanced pancreas cancer |
|
Neoplasms Pancreatic Neoplasms Digestive System Neoplasms Neoplasms by Site Endocrine Gland Neoplasms Digestive System Diseases Pancreatic Diseases Endocrine System Diseases Pancrelipase Gemcitabine Gastrointestinal Agents Therapeutic Uses |
Pharmacologic Actions Antimetabolites, Antineoplastic Antimetabolites Molecular Mechanisms of Pharmacological Action Antineoplastic Agents Antiviral Agents Anti-Infective Agents Enzyme Inhibitors Immunosuppressive Agents Immunologic Factors Physiological Effects of Drugs Radiation-Sensitizing Agents |