Study to Evaluate the Safety and Analgesic Activity of ATx08-001 in Subjects With Postherpetic Neuralgia

Completed · Phase 2 · Has a placebo group

Conditions studied: Postherpetic Neuralgia

In brief

This is a Phase 2 randomized, double-blind, placebo-controlled, multiple-dose, multicenter, parallel-group study to evaluate the analgesic activity of ATx08-001, a novel selective peroxisome proliferator-activated receptor modulator (SPPARM), in subjects with moderate-to-severe postherpetic neuralgia pain. Eligible subjects will be randomized to receive either placebo or Atx08-001. Study drug will be administered orally twice a day for 7 days. Subjects will be evaluated for neuropathic pain intensity at regular intervals over a 6 hour period on Day 1 following the first dose of study drug. They will then be discharged from the clinic and will complete diary assessments of pain severity twice a day at home. Subjects will be asked to return to the clinic on Day 8 to complete their last set of pain evaluations.

Key facts

Study ID: NCT01318226
Run by: Aestus Therapeutics
People needed: 61
Starts: 2011-03-01
Expected to finish: 2011-07-01
Last updated by the study team: 2011-08-23

Who can join

Age: 18 and older, up to 85. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

Is able to provide written informed consent prior to study entry
Is male or female, 18 - 85 years of age
Has a diagnosis of postherpetic neuralgia that has been present for at least 3 months since the resolution of the skin rash (shingles), and has been associated with at least moderate pain
Has a body mass index (BMI) between 17 and 36, inclusive
Has on average postherpetic neuralgia pain severity of at least "4" on the 11-point NPRS-12 scale over three days prior to the Treatment Visit.
At the Treatment Visit, entry into the study for dosing will require a baseline score of 4 or greater on the following 'Numerical Pain Rating Scale' (NPRS-NOW): "How would you rate your pain RIGHT NOW using a zero to ten scale, where zero equals no pain and ten is the worst pain you can imagine." If the subject fails to qualify for the Treatment Visit because of a baseline pain score below 4, he or she may return on any day within a fourteen day period to attempt to qualify again. A subject will be allowed a maximum of two reassessments to qualify on the basis of the NPRS-NOW scale.
Female subjects must be of non childbearing potential (defined as postmenopausal for at least 1 year or surgically sterile [bilateral tubal ligation, bilateral oophorectomy or hysterectomy]) or must be using adequate contraception (practicing one of the following methods of birth control):
Total abstinence from sexual intercourse (minimum of one complete menstrual cycle before study entry),
A partner who is physically unable to impregnate the subject (e.g., vasectomized)
Contraceptives (oral, parenteral, or transdermal) for 3 consecutive months prior to study drug administration,
Intrauterine device (IUD), or
Double barrier method (condoms, sponge, diaphragm, or vaginal ring with spermicidal jellies or cream)
If female of childbearing potential, subject must have a negative serum pregnancy test at screening
Able to communicate meaningfully with the study observer and staff
No known allergies to study medication

You may not qualify if…

Has another source of moderate-to-severe pain apart from the postherpetic neuralgia that might be confused with the PHN pain
Is actively abusing alcohol or drugs
Is unable to refrain from alcohol for a period beginning 24 hours prior to the treatment visit until the end of the study
Is scheduled to undergo any surgical procedures during the period of study duration
Has a history of any active serious medical conditions including cancer (with the exception of benign uterine dysplasia or removed skin carcinomas), cardiovascular, respiratory, renal, hepatic, gastrointestinal, endocrine, immunologic, hematologic, neurologic or psychiatric disease that would contraindicate study participation
Has moderate to severe (New York Heart Association [NYHA] Class 3 or 4) heart failure defined as heart failure which significantly limits physical activity by provoking fatigue, palpitations or dyspnea.
Has a history of either type 1 or type 2 diabetes mellitus
Has taken a fixed scheduled opioid regimen within 3 days prior to the Treatment Visit. A fixed scheduled regimen of another type of analgesic, e.g., nonsteroidal antiinflammatory drug (NSAID) or an adjuvant analgesic will be allowed as long as the dose and schedule of administration were not changed for at least 2 weeks prior to dosing.
Has used a short-acting "as needed" opioid less than 12 hours prior to dosing or an "as needed" NSAID dose less than 24 hours prior to dosing
Has used extended duration oral analgesics up to 48 hours prior to the Treatment Visit
Has applied lidocaine patches or dermal analgesics within 7 days prior to the Treatment Visit
Has received an anesthetic block within two weeks of the Screening Visit
Has received any prior neurolytic nerve block in the area of the PHN pain
Is taking tricyclic, selective serotonin reuptake inhibitor (SSRI) or serotonin and noradrenaline reuptake inhibitor (SNRI) antidepressants for PHN (or for indications other than pain) and the dosage has been changed within 14 days of the Treatment Visit. Only subjects on stable doses from at least 14 days prior to the Treatment Visit through the duration of the study will be eligible to participate
Is taking gabapentin (Neurontin), pregabalin (Lyrica), or duloxetine (Cymbalta) and the dosage has been changed within 14 days of the Treatment Visit. Only subjects receiving stable doses for at least 14 days prior to the Treatment Visit and are willing to continue taking the same doses for the duration of the study will be eligible to participate
Has taken any medication that is a substrate of the cytochrome P450 enzyme CYP2C9 within 4 days of dosing with study drug or is unwilling to refrain from such medications through the course of study drug treatment
Has taken any prescription or over-the-counter medication within three days prior to the Treatment Visit, or herbal agents or other nutraceutical products within 14 days prior to the Treatment Visit, that in the opinion of the Investigator would be expected to confound the analgesic response
Has documented liver failure or a serum ALT, AST, alkaline phosphatase, or GGT greater than 2.5 times the upper limit of normal, or total bilirubin greater than 1.5 times the upper limit of normal without a known, not clinically significant explanation
Has a Brain Natriuretic Peptide (BNP) level > 150 pg/mL
Has a history of poorly controlled hyperthyroidism or hypothyroidism or Thyroid Stimulating Hormone (TSH) levels that are < 0.3 or > 5.5 µlU/mL
Has moderate or severe renal failure defined as a calculated creatinine clearance of < 60mL/min from the Cockcroft \& Gault formula
Has a clinically significant abnormality on 12-lead electrocardiogram
Has a known history of a positive Human Immunodeficiency Virus (HIV) antibody test or known HIV infection
Has a history of a positive Hepatitis B core antibody, or anti-HCV antibody test
Has previously been admitted to this study

Where it is running

Radiant Research — Chandler, Arizona, United States
Premier Research Center — Peoria, Arizona, United States
Homestead Clinical Research — Cutler Bay (Miami), Florida, United States
San Marcus Research Clinic — Miami, Florida, United States
Boston Clinical Trials — Boston, Massachusetts, United States
Quest Research Institute — Bingham Farms, Michigan, United States
Affiliated Clinical Research — Las Vegas, Nevada, United States
Radiant Research — Las Vegas, Nevada, United States
Radiant Research — Dallas, Texas, United States

Full record on ClinicalTrials.gov

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