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临床试验/NL-OMON48691
NL-OMON48691已完成2 期

A phase 2, randomized, double blind, vehicle controlled, parallel group study to explore the efficacy, pharmacodynamics and safety of topical ionic contra-viral therapy (ICVT), comprised of digoxin and furosemide in actinic keratosis - Topical ionic contra-viral therapy in actinic keratosis

Maruho Co., Ltd.0 个研究点目标入组 32 人开始时间: 待定最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
入组人数
32

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 99(—)

入选标准

  • For enrollment of subjects the following criteria must be met:
  • 1. Male and female subjects *18 years with a condition of general good health
  • (with the exception of AK). The health status is verified by absence of
  • evidence of any clinical significant active or uncontrolled chronic disease
  • other than AK following a detailed medical history, a complete physical
  • examination including vital signs, 12-lead ECG, hematology, blood chemistry,
  • virology and urinalysis;
  • 2. Confirmed clinical AK diagnosis by dermatologist (biopsy proven after end of
  • study, in untreated part of the AK field)
  • 3. At least 2 facial fields of at least 25 cm2 (but preferably >35 cm2) present
  • at screening and baseline visit where at least 2 AK lesions are visible in each
  • field (preferably the forehead, temple or cheek)
  • 4. Able to participate and willing to give written informed consent and to
  • comply with the study restrictions.
  • 5. Ability to communicate well with the investigator in Dutch.
  • 6. Willing to refrain from using other topical products in the treatment area,
  • or prohibited medications for the duration of the study.
  • 7. Willing to limit sun exposure of the involved skin to the extent
  • vocationally possible.
  • 8. Subjects and their partners of childbearing potential must use effective
  • contraception, for the duration of the study and for 3 months after the last

排除标准

  • Eligible subjects must meet none of the following exclusion criteria:
  • 1. Have used or received any treatment for AK in the treatment area within 28
  • days prior to enrollment (including topical medications, immunosuppressive or
  • immunomodulating agents, phototherapy, oral retinoids, or other therapies for
  • 2. Have any current pathologically relevant skin conditions in the field area
  • other than AK (e.g. squamous cell carcinoma or basal cell carcinoma).
  • 3. Have a known hypersensitivity to any of the investigational product
  • ingredients, including digoxin and furosemide.
  • 4. Current use of systemic digoxin or furosemide.
  • 5. Participation in an investigational drug or device study within 3 months
  • prior to screening or more than 4 times a year
  • 6. Loss or donation of blood over 500 mL within three months (males) or four
  • months (females) prior to screening or intention to donate blood or blood
  • products during the study.
  • 7. If a woman of childbearing potential, pregnant, or breast-feeding, or
  • planning to become pregnant during the study.

研究者

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