Overview
Study to Evaluate Efficacy, Safety, Tolerability and Pharmacokinetics of AZD1386 in Patients With Peripheral Neuropathic Pain
Status:
Terminated
Terminated
Trial end date:
2010-02-01
2010-02-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
The primary aim of this study is to investigate if AZD1386 is efficacious as an analgesic in patients with peripheral neuropathic pain. This will be done by comparing the effect of AZD1386 to placebo ("inactive substance") on pain.Phase:
Phase 2Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
AstraZeneca
Criteria
Inclusion Criteria:- Patients with painful symptoms due to neuropathic pain
- Provision of signed informed consent
- Non pregnant females
Exclusion Criteria:
- Other pain conditions that may confound assessment of neuropathic pain, as judged by
the investigator
- History, and/or presence of somatic disease, which may interfere with the objectives
of the study as judged by the investigator