Status and phase
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About
The purpose of this study is to assess the painkilling efficacy of ASP8477 relative to mock (placebo) in patients that have been diagnosed with painful diabetic peripheral neuropathy or postherpetic neuralgia determined by the change in the average daily pain intensity in patients that initially respond favorably to treatment with ASP8477.
Full description
The study will consist of a Screening Period, Single-Blind Treatment Period, Double-Blind Randomized Withdrawal Period and Follow-up Period.
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
PDPN subject must have:
PHN subject must have pain present ≥ 6 months after healing of the herpes zoster rash.
Exclusion criteria
Primary purpose
Allocation
Interventional model
Masking
132 participants in 2 patient groups, including a placebo group
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Data sourced from clinicaltrials.gov
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