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Neuropathic Pain in Patients With Cancer

Primary Purpose

Neuropathic Pain

Status
Completed
Phase
Phase 2
Locations
International
Study Type
Interventional
Intervention
KRN5500
Placebo
Sponsored by
DARA Therapeutics
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Neuropathic Pain focused on measuring Neuropathic pain, Cancer

Eligibility Criteria

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

Inclusion Criteria:

  • 18 years or older
  • Diagnosis of advanced or recurrent cancer
  • No options for curative chemotherapy, but palliative chemotherapy allowed under certain conditions
  • Refractory neuropathic pain rated 4 or greater on 0-10 scale and failure to respond to 2 commonly used treatments
  • If taking opioids for pain, stable regimen over past week before enrolling
  • Karnofsky performance status of 40 or more
  • Females must be sterile or post-menopausal

Exclusion Criteria:

  • Radiation to site of neuropathic pain for past 4 weeks
  • Major surgery within past 2 weeks
  • Liver function and other key labs outside normal parameters
  • ECG showing significant abnormality
  • Myocardial Infarction (heart attack) within past 6 months
  • History of interstitial lung disease
  • History of severe allergic reaction to drugs containing polysorbate 80
  • Other investigational drug within 2 weeks or 5 half-lives (whichever is longer

Sites / Locations

  • Cancer Institute Medical Group
  • Ghassan Al-Jazayrly, M.D., Inc.
  • University of California / Irvine Chao Family Comprehensive Cancer Center
  • Keog Pharma, Inc.
  • Hematology and Oncology Specialists, LLC
  • St. Agnes Healthcare, Inc
  • Massachusetts General Hospital
  • East Orange VA Medical Center
  • Duke University Medical Center
  • Carolina Pain Institute, PA
  • Huntsman Cancer Institute
  • Dr. Rivera-Colon

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

KRN5500

Normal Saline

Arm Description

KRN5500 escalating dose of .6, 1.2, 1.8, or 2.2 mg/m2 in IV infusion of normal saline

Placebo consists of IV infusion of normal saline

Outcomes

Primary Outcome Measures

Average pain intensity over the previous 24 hours as measured by a numeric rating scale (NRS) ranging from 0 to 10 where 0 represents "no pain" and 10 represents the "worst possible pain."

Secondary Outcome Measures

Physical Examination, Vital signs and body weight, Electrocardiogram, Laboratory parameters, Adverse events, Clinical Opiate Withdrawal Scale, rescue medication, Proportion of patients who achieved a 33% reduction in pain intensity

Full Information

First Posted
May 15, 2007
Last Updated
August 13, 2010
Sponsor
DARA Therapeutics
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1. Study Identification

Unique Protocol Identification Number
NCT00474916
Brief Title
Neuropathic Pain in Patients With Cancer
Official Title
A Phase 2 Double-Blind Dose Escalation Study of KRN5500 for Neuropathic Pain in Patients With Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
August 2010
Overall Recruitment Status
Completed
Study Start Date
June 2006 (undefined)
Primary Completion Date
March 2009 (Actual)
Study Completion Date
April 2009 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
DARA Therapeutics

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to collect beginning information on whether intravenous (IV) administration of KRN5500 is safe and effective for treatment of neuropathic pain in patients with cancer.
Detailed Description
Neuropathic pain is a type of pain that results from nerve damage and is characterized by an abnormal hypersensitivity to harmless as well as harmful stimuli. This type of pain is extremely difficult to manage, fails to respond to standard analgesic medications or interventions, and often gets worse instead of better over time. Current approved therapeutic agents often have intolerable side effects and limited efficacy. Thus, there is an urgent need to develop safe and effective drugs to treat neuropathic pain. Study DTCL100 will be conducted at multiple centers and will enroll patients that have advanced cancer AND neuropathic pain that has not responded well to previous treatment. Eighteen patients will be randomly assigned to receive up to 8 doses of active drug (KRN5500) or placebo. A maximum of 8 doses will be administered weekly over a 10 week period. Patients are encouraged to complete at least 4 treatment visits before a decision is made to complete the full 10 weeks of treatment and the 1 month followup period.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Neuropathic Pain
Keywords
Neuropathic pain, Cancer

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
19 (Actual)

8. Arms, Groups, and Interventions

Arm Title
KRN5500
Arm Type
Experimental
Arm Description
KRN5500 escalating dose of .6, 1.2, 1.8, or 2.2 mg/m2 in IV infusion of normal saline
Arm Title
Normal Saline
Arm Type
Placebo Comparator
Arm Description
Placebo consists of IV infusion of normal saline
Intervention Type
Drug
Intervention Name(s)
KRN5500
Intervention Description
Patients are seen weekly and dosed for pain with IV medication of active drug/KRN5500 or placebo . The dose can be escalated, from .6 mg/m2, to 1.2, 1.8, and 2.2 mg/m2.
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Normal Saline given as dose escalation for placebo
Primary Outcome Measure Information:
Title
Average pain intensity over the previous 24 hours as measured by a numeric rating scale (NRS) ranging from 0 to 10 where 0 represents "no pain" and 10 represents the "worst possible pain."
Time Frame
Weekly for 10 weeks plus 30 day followup
Secondary Outcome Measure Information:
Title
Physical Examination, Vital signs and body weight, Electrocardiogram, Laboratory parameters, Adverse events, Clinical Opiate Withdrawal Scale, rescue medication, Proportion of patients who achieved a 33% reduction in pain intensity
Time Frame
Weekly for 10 weeks plus 30 day followup

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 18 years or older Diagnosis of advanced or recurrent cancer No options for curative chemotherapy, but palliative chemotherapy allowed under certain conditions Refractory neuropathic pain rated 4 or greater on 0-10 scale and failure to respond to 2 commonly used treatments If taking opioids for pain, stable regimen over past week before enrolling Karnofsky performance status of 40 or more Females must be sterile or post-menopausal Exclusion Criteria: Radiation to site of neuropathic pain for past 4 weeks Major surgery within past 2 weeks Liver function and other key labs outside normal parameters ECG showing significant abnormality Myocardial Infarction (heart attack) within past 6 months History of interstitial lung disease History of severe allergic reaction to drugs containing polysorbate 80 Other investigational drug within 2 weeks or 5 half-lives (whichever is longer
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Richard Penson, MD, MRCP
Organizational Affiliation
Massachusetts General Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Cancer Institute Medical Group
City
Los Angeles
State/Province
California
ZIP/Postal Code
90025
Country
United States
Facility Name
Ghassan Al-Jazayrly, M.D., Inc.
City
Los Angeles
State/Province
California
ZIP/Postal Code
90027
Country
United States
Facility Name
University of California / Irvine Chao Family Comprehensive Cancer Center
City
Orange
State/Province
California
ZIP/Postal Code
92868
Country
United States
Facility Name
Keog Pharma, Inc.
City
Jupiter
State/Province
Florida
ZIP/Postal Code
33477
Country
United States
Facility Name
Hematology and Oncology Specialists, LLC
City
Covington
State/Province
Louisiana
ZIP/Postal Code
70433
Country
United States
Facility Name
St. Agnes Healthcare, Inc
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21229
Country
United States
Facility Name
Massachusetts General Hospital
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02114
Country
United States
Facility Name
East Orange VA Medical Center
City
East Orange
State/Province
New Jersey
ZIP/Postal Code
07018
Country
United States
Facility Name
Duke University Medical Center
City
Durham
State/Province
North Carolina
ZIP/Postal Code
27710
Country
United States
Facility Name
Carolina Pain Institute, PA
City
Winston-Salem
State/Province
North Carolina
ZIP/Postal Code
27103
Country
United States
Facility Name
Huntsman Cancer Institute
City
Salt Lake City
State/Province
Utah
ZIP/Postal Code
84112
Country
United States
Facility Name
Dr. Rivera-Colon
City
Rio Piedras
ZIP/Postal Code
00921
Country
Puerto Rico

12. IPD Sharing Statement

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Neuropathic Pain in Patients With Cancer

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