None listed
Conditions
Brief summary
The primary purpose of this study is to evaluate the clinical efficacy and safety of topical lidocaine spray in reducing neuropathic pain in patients with Postherpetic Neuralglia (PHN) compared with those on a placebo spray.
Interventions
Lidocaine spray 5% solution
Applied topically to intact skin twice a day, Each application up to 18 sprays (approximately 2.5 mL) is to be applied to the specified area(s) of up to 420cm2. For a treatment of 21 days.
Compliance will be monitored by the return and weighing of the investigation product and interviewing the subject of the usage during study visits
Sponsors
Andros Pharmaceuticals Pty Ltd
Study design
Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used)
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1. Female of non-childbearing potential (ie, 12 months or more of spontaneous amenorrhea, bilateral oophorectomy at least 6 months prior to randomisation, hysterectomy with bilateral oophorectomy at least 6 months prior to randomisation, or for females over 50 years of age, hysterectomy without bilateral oophorectomy at least 6 months prior to randomisation). 2. Females of childbearing potential must be confirmed to be not pregnant at screening. 3. Males with sexual partners or females of childbearing potential must agree to use an effective contraceptive method (abstinence, birth control pills, rings or patches, diaphragm, intrauterine device, condom, surgical sterilization, vasectomy, or progestin implant or injection) from screening to the end of study, and for 1 month after exiting the study. 4. Persistent pain for more than 3 months from the appearance of herpes zoster rash that is not located on the face, above the scalp hairline, or in proximity to mucous membranes. 5. Diagnosis of PHN based on medical history as judged by investigator. 6. Persistent neuropathic pain that involves at least 1 dermatome and covering no more than 420 cm2 7. If the subject has been on stable dose(s) of oral analgesic medication for at least 30 days prior to the screening visit, they need to be willing to maintain the respective dose(s) and medication throughout the study. 8. Pain intensity score in the target area of >=4 at both screening and the randomisation visit. The pain intensity score for a subject may be reevaluated if it is not >=4 at the randomisation visit. 9. Skin is intact over the painful area to be treated.
Exclusion criteria
1. Subject has systemic disease that would put him/her at an additional risk or limit his/her ability to participate in the study as judged by the investigator. 2. Subject has a history of human immunodeficiency virus, hepatitis C, or hepatitis B. 3. Subject has a history of malignancy other than basal cell carcinoma and carcinoma in situ within the past 2 years. 4. Subject has a history of mental illness or psychiatric illness such as dementia, depression, or schizophrenia, that can limit his/her ability to comply with study procedures as judged by the investigator. 5. Subject is unable to apply, or have a caregiver apply, study spray to the most painful skin segments twice a day as directed. 6. Subject has known sensitivity to lidocaine containing products. 7. Subject has active herpes zoster lesions or dermatitis. 8. Subject has other condition(s) that cause severe or chronic pain that may impair the self-assessment of the pain due to PHN as judged by the investigator. 9. Subject was treated in the area of PHN with a local anaesthetic within 14 days of Baseline or had a nerve block within 30 days of Baseline 10. Subject is receiving any prohibited medication or therapy and is unable to washout these medications or therapies for the duration of the study. 11. Subject has used capsaicin patches within 90 days of Baseline or has used other capsaicin preparations on a daily basis in the 90 days prior Baseline. 12. Pregnant or lactating females. 13. Subject has an active history of alcohol or drug abuse. 14. Subject has participated in any other investigational study within 30 days prior to screening. 15. Subject or subject’s direct family is employed by the sponsor or study staff. 16. Subject has any condition that would make him/her unsuitable for the study in the opinion of the investigator or sponsor.
Outcome results
None listed