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临床试验/NL-OMON48978
NL-OMON48978已完成2 期

An International, Multicenter, Open-label, Long Term Extension Study Evaluating the Safety of Diacerein 1% Ointment Topical Formulation in Subjects with Epidermolysis Bullosa Simplex (EBS) - CCP-020-302

Medpace0 个研究点目标入组 3 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
发起方
Medpace
入组人数
3

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
2 至 99(—)

入选标准

  • 1. In the opinion of the Investigator, the subject is capable of understanding
  • and complying with protocol requirements., 2. The subject or, when applicable,
  • the subject's legally acceptable representative signs and dates a written,
  • informed consent/assent form and any required privacy authorization prior to
  • the initiation of any study procedures., 3. Subject has a documented genetic
  • mutation consistent with EBS. , 4. Subjects who participated in the
  • CCP-020-301 or the CCP-020-101 study are eligible to be rolled into the
  • CCP-020-302 open label extension study, regardless of their completion status
  • on the feeder study. , 5. Subject/caregiver agrees to report use of any topical
  • therapies applied to EBS lesions (e.g. medicated cleansers, bleach cleansers,
  • bleach baths, topical antiseptics, topical disinfectants, etc.)., 6. If the
  • subject is a woman of childbearing potential, she has a negative urine
  • pregnancy test and agrees to use an approved effective method of birth control,
  • as defined by this protocol, for the duration of the study., 7. Subject is
  • non-lactating and is not planning for pregnancy during the study period., 8.
  • Subject is willing and able to follow all study instructions and to attend all
  • study visits.

排除标准

  • 1. Subject has EBS lesions to be treated that are infected (i.e., EBS lesions
  • that require topical antibiotic therapy to treat an infection)., 2. Subject has
  • evidence of a systemic infection or has used systemic antibiotics within 7 days
  • prior to Baseline., 3. The subject was discontinued from the feeder study due
  • to an adverse event judged to be related or possibly related to the study
  • medication., 4. Subject has experienced a change in clinical status from the
  • feeder study that, in the investigator's opinion, puts the subject at undue
  • risk to participate.

研究者

发起方
Medpace

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