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Efficacy and Safety of TRK-700 in Patient With Post-Herpetic Neuralgia

TRK-700 An Early Phase II Study in Patients With Post-Herpetic Neuralgia -Double Blind Comparison With Placebo-

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02701374
Enrollment
184
Registered
2016-03-08
Start date
2016-03-31
Completion date
2017-07-31
Last updated
2017-10-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Post-Herpetic Neuralgia

Keywords

TRK-700, Post-Herpetic Neuralgia

Brief summary

In Post-Herpetic Neuralgia(PHN) patients: * To conduct an explorative investigation of the efficacy and safety of repeated oral doses of TRK-700 via a randomized double blind comparative study * To measure the plasma concentration of TRK-700 and its metabolites

Interventions

DRUGPlacebo

Sponsors

Toray Industries, Inc
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
20 Years to 84 Years
Healthy volunteers
No

Inclusion criteria

* Patients with pain persisting for at least 3 months after the onset of herpes zoster * Patients whose average pain score on the Numerical Rating Scale (NRS) over the past 24 hours at preliminary enrollment is at least 4

Exclusion criteria

* Patients with another skin disease that may affect the evaluation of the pain at the site of PHN * Patients with pain other than PHN that may affect the evaluation of pain * Patients with pain that is suspected to be mainly psychogenic * Patients who have received neurolytic or neurosurgical therapy for PHN

Design outcomes

Primary

MeasureTime frameDescription
Change in average Numerical Rating Scale (NRS)baseline to week 8Change in average NRS collected by Pain Diary from baseline to week 8 in subjects receiving TRK-700 versus Placebo

Countries

Japan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026