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临床试验/NCT05863104
NCT05863104已完成2 期

An Open-label, Uncontrolled, Multicenter Study to Evaluate the Safety, Local Tolerability, Systemic Exposure, and Efficacy of 1% Glycopyrronium Bromide (GPB) Cream in Adolescents With Severe Primary Axillary Hyperhidrosis

Dr. August Wolff GmbH & Co. KG Arzneimittel1 个研究点 分布在 1 个国家目标入组 44 人开始时间: 2023年3月7日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
44
试验地点
1
主要终点
Number of patients with Adverse Drug Reaction during treatment

研究概览

简要总结

The aim of this study is to evaluate the safety, tolerability and systemic exposure (in a subset of patients) of topical administration of 1% GPB in adolescents with severe primary axillary hyperhidrosis.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
12 Years 至 17 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Medical diagnosis of severe primary axillary hyperhidrosis with a PRHS score of ≥5 with symptoms for at least 3 months before Screening
  • At least 50 mg of sweat production in each axilla measured gravimetrically over a period of 5 minutes at room temperature along with a humidity consistent with the normal climate in that area (patients have to acclimatize to that room for at least 30 minutes before the measurement)
  • Adolescents of both sexes aged 12 to 17 years (until study completion) with a body mass index percentile ≥10 and ≤90 (according to Kromeyer-Hauschild et al 2001)
  • Local tolerability assessment (skin reaction) score = 0

排除标准

  • Secondary hyperhidrosis, ie, hyperhidrosis that is secondary to other underlying diseases such as (but not limited to) hyperthyroidism, lymphoma, and malaria
  • Previous surgical treatment of hyperhidrosis including sympathectomy, surgical debulking of the sweat glands, subcutaneous tissue curettage, ultrasonic surgery, microwave treatment (miraDry), or laser treatment
  • Botulinum toxin treatment for the treatment of axillary hyperhidrosis in the previous 4 months
  • Hypersensitivity to glycopyrrolate, or to any of the excipients of the investigational medicinal product (IMP)

研究组 & 干预措施

Glycopyrronium Bromide (GPB) Cream

Experimental

Formulation containing Glycopyrronium Bromide (GPB) for topical application

干预措施: Glycopyrronium Bromide (GPB) Cream (Drug)

结局指标

主要结局

Number of patients with Adverse Drug Reaction during treatment

时间窗: Baseline to Day 57

Number of patients with a local tolerability assessment (skin reaction score) >0 during treatment

时间窗: Baseline to Day 57

Αbsolute change in GP plasma concentration from Baseline to Day 15

时间窗: Baseline to Day 15

次要结局

  • Absolute change in logarithmic values of total sweat production assessed by GM from Baseline to Day 29(Baseline to Day 29)
  • Absolute change in the Children's dermatology life quality index (CDLQI) score from Day 29 to Day 57(Day 29 to Day 57)
  • Relative change in total sweat production assessed by GM from Day 29 to Day 57(Day 29 to Day 57)
  • Proportion of responders assessed by GM at Day 29 and Day 57(Day 29 and Day 57)
  • Absolute change in patient-rated hyperhidrosis severity (PRHS) score from Baseline to Day 29 and Day 57(Baseline to Day 29 and Day 57)
  • Absolute change in patient-rated hyperhidrosis severity (PRHS) score from Day 29 to Day 57(Day 29 to Day 57)
  • Absolute change in the Children's dermatology life quality index (CDLQI) score from Baseline to Day 29 and Day 57(Baseline to Day 29 and Day 57)
  • Absolute change in GP plasma concentration from Baseline to Day 8(Baseline to Day 8)
  • Absolute change in GP plasma concentration from Day 8 to Day 15(Day 8 to Day 15)
  • Frequency, severity, and relation of ADRs, SAEs, TEAEs, SUSARs, and discontinuations due to TEAEs(Screening to 14 Days after End of Treatment)
  • Local tolerability based on the skin reaction score(Day 1, Day 29, Day 57/End of Treatment and 14 Days after Day 57/End of Treatment)
  • Neurological assessment of anticholinergic effects by a 4-point scale(7 to 4 Days before Baseline, Day 15, Day 29, Day 43, Day 57/End of Treatment)
  • Absolute change in logarithmic values of total sweat production assessed by GM from Baseline to Day 57(Baseline to Day 57)
  • Absolute change in logarithmic values of total sweat production assessed by GM from Day 29 to Day 57(Day 29 to Day 57)
  • Relative change in total sweat production assessed by GM from Baseline to Day 29 and Day 57(Baseline to Day 29 and Day 57)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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