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Clinical Trials/NCT01291901
NCT01291901
Completed
Phase 2

A Phase II, Randomized, Double Blind, Placebo-controlled, Multicenter Study to Investigate the Impact of NP2 in Subjects With Intractable Pain Due to Malignancy

Diamyd Inc18 sites in 1 country33 target enrollmentJanuary 2011

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Intractable Pain
Sponsor
Diamyd Inc
Enrollment
33
Locations
18
Primary Endpoint
Pain Measured by the Numerical Rating Scale (NRS)
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

The purpose of this study is to examine the impact of intradermal delivery of NP2 on pain scores and pain medication usage in subjects with intractable pain due to malignant disease. A second purpose is to confirm safety and secondary efficacy measurements.

Detailed Description

Chronic severe pain remains a significant unmet medical need in patients that have progressive cancer. Existing treatments have limited efficacy and also suffer significant side effects. This is a multi-center, randomized, double blind, placebo-controlled clinical trial designed to evaluate the impact of intradermal injection of NP2 in subjects who have intractable pain due to malignant disease. NP2 is a gene transfer vector engineered to express human preproenkephalin, a gene naturally involved in pain control. Delivery of NP2 directly to the site of pain caused by cancer is intended to provide increased Enkephalin peptides, which bind to opioid receptors, that may allow better pain control.

Registry
clinicaltrials.gov
Start Date
January 2011
End Date
November 2013
Last Updated
11 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Diamyd Inc
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Histologically confirmed malignant disease.
  • Intractable pain related to malignancy.
  • Females must be postmenopausal or practicing birth control.
  • Able to provide appropriate written consent.

Exclusion Criteria

  • Positive pregnancy test prior to receiving study treatment.
  • Serious uncontrolled medical condition other than malignancy (e.g. congestive heart failure, coagulopathy, uncontrolled diabetes).
  • Evidence of active Hepatitis B, Hepatitis C, or HIV infection.
  • Evidence of viral, bacterial, or fungal infection in the planned treatment area.

Outcomes

Primary Outcomes

Pain Measured by the Numerical Rating Scale (NRS)

Time Frame: Days -5 to -1 predosing and days 3 to 14 postdosing

• Change from baseline of the average daily NRS pain score (scale of 0 to 10 ) of Placebo compared to Active NP2 cohorts.

Secondary Outcomes

  • Opioid Pain Medication Usage Morphine Equivalent Units (MEU)(Days -5 to -1 predosing and 3 to 14 postdosing)
  • Pain SF-MPQ(Baseline and Week 1, 2 and 4)
  • Quality of Life ECOG(Baseline and Week 1, 2 and 4)
  • Quality of Life SF-12(Baseline and Week 1, 2 and 4)

Study Sites (18)

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