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Generated: December 15, 2018

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CLINICAL TRIALS PROFILE FOR MENTHOL; METHYL SALICYLATE

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Clinical Trials for Menthol; Methyl Salicylate

Trial ID Title Status Sponsor Phase Summary
NCT00916942 Study of NGX-4010 With the Use of Open Label Lidocaine (2.5%)/Prilocaine (2.5%) Cream for the Treatment of Postherpetic Neuralgia (PHN) Completed NeurogesX Phase 2 This study is an open-label multi-center to evaluate the tolerability of treatment with NGX-4010 use with pre-patch topical application of a topical anesthetic cream. This is an open-label study. No hypothesis testing will be performed. Eligible subjects will have PHN and a level of pain at an intensity level deemed appropriate for open-label treatment with NGX-4010, as judged by the Investigator. Painful areas of up to a maximum of 1000 cm2 will be pre-treated with lidocaine (2.5%)/prilocaine (2.5%) cream for 60 minutes followed by a single, 60-minute application of NGX-4010. Subjects may be on chronic pain medication regimens, but currently will not be using any topical pain medications on the affected areas, such as non-steroidal anti-inflammatory drugs, menthol, methyl salicylate, local anesthetics including Lidoderm® (lidocaine patch 5%), steroids or capsaicin.
NCT02017197 Therapeutic Equivalence Between Branded and Generic WARFArin Tablets in Brazil Completed Fundação de Amparo à Pesquisa do Estado de São Paulo Phase 4 The purpose of this study is to assess whether the switch from branded to generic warfarin or between different generic warfarin tablets may cause fluctuation in the results of coagulation tests (International Normalized Rate, acronym INR) in patients, thus predisposing them to unnecessary risks.
NCT02017197 Therapeutic Equivalence Between Branded and Generic WARFArin Tablets in Brazil Completed Federal University of São Paulo Phase 4 The purpose of this study is to assess whether the switch from branded to generic warfarin or between different generic warfarin tablets may cause fluctuation in the results of coagulation tests (International Normalized Rate, acronym INR) in patients, thus predisposing them to unnecessary risks.
NCT02400320 Local Skin Safety Study of a Topical Pain Relief Spray Containing a Combination of Diclofenac, Methyl Salicylate, and Menthol Withdrawn GlaxoSmithKline Phase 4 The purpose of this study is to determine local skin safety of a topical analgesic spray containing a combination of diclofenac, methyl salicylate, menthol and compare it with a topical analgesic gel containing a combination of diclofenac, methyl salicylate, and menthol.
NCT02666846 Assess the Efficacy and Safety in Volunteers of DCF100, TIB200 and SPR300 vs. Placebo and Control(s) in a UV Pain Model Completed Parexel Phase 1 This is a randomised, double blind, cross over clinical study in healthy human volunteers (including pharmacokinetic [PK] sampling and laser Doppler assessment of local blood flow in a subset of up to 6 subjects per cohort of 20) to assess the efficacy and safety of three different topical analgesics (DCF100, TIB200 and SPR300) versus placebo and active control(s) in a model of UV-induced inflammatory pain.
NCT02666846 Assess the Efficacy and Safety in Volunteers of DCF100, TIB200 and SPR300 vs. Placebo and Control(s) in a UV Pain Model Completed Futura Medical Developments Ltd. Phase 1 This is a randomised, double blind, cross over clinical study in healthy human volunteers (including pharmacokinetic [PK] sampling and laser Doppler assessment of local blood flow in a subset of up to 6 subjects per cohort of 20) to assess the efficacy and safety of three different topical analgesics (DCF100, TIB200 and SPR300) versus placebo and active control(s) in a model of UV-induced inflammatory pain.
NCT02874963 FM-SRP and Tooth Extraction Improve Type 2 Diabetes Mellitus in Periodontitis Recruiting University of Ljubljana, Faculty of Medicine N/A This intervention study is designed to evaluate the effects of non-surgical procedure in addition to surgical procedure on systemic inflammation and glycemic control in with type 2 diabetes mellitus patients with periodontitis in comparison with non-diabetic periodontic patients.
Trial ID Title Status Sponsor Phase Summary

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Clinical Trial Conditions for Menthol; Methyl Salicylate

Condition Name

Condition Name for Menthol; Methyl Salicylate
Intervention Trials
Periodontitis 2
Oral Biofilm 1
Dental Plaque 1
Type 2 Diabetes Mellitus 1
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Condition MeSH

Condition MeSH for Menthol; Methyl Salicylate
Intervention Trials
Periodontitis 2
Diabetes Mellitus 1
Atrial Fibrillation 1
Neuralgia, Postherpetic 1
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Clinical Trial Locations for Menthol; Methyl Salicylate

Trials by Country

Trials by Country for Menthol; Methyl Salicylate
Location Trials
United States 5
Brazil 1
Spain 1
Kosovo 1
United Kingdom 1
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Trials by US State

Trials by US State for Menthol; Methyl Salicylate
Location Trials
Utah 1
North Carolina 1
Missouri 1
Georgia 1
Florida 1
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Clinical Trial Progress for Menthol; Methyl Salicylate

Clinical Trial Phase

Clinical Trial Phase for Menthol; Methyl Salicylate
Clinical Trial Phase Trials
Phase 4 3
Phase 2 1
Phase 1 1
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Clinical Trial Status

Clinical Trial Status for Menthol; Methyl Salicylate
Clinical Trial Phase Trials
Completed 3
Recruiting 2
Withdrawn 1
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Clinical Trial Sponsors for Menthol; Methyl Salicylate

Sponsor Name

Sponsor Name for Menthol; Methyl Salicylate
Sponsor Trials
GlaxoSmithKline 1
Federal University of São Paulo 1
University of Santiago de Compostela 1
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Sponsor Type

Sponsor Type for Menthol; Methyl Salicylate
Sponsor Trials
Other 5
Industry 4
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Serving hundreds of leading biopharmaceutical companies globally:

Moodys
Federal Trade Commission
McKinsey
Cipla
Teva
Fuji
Fish and Richardson
Merck
Deloitte

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