跳至主要内容
临床试验/EUCTR2007-004649-14-FI
EUCTR2007-004649-14-FI进行中(未招募)不适用

Safety of ASF 1057 cream 0.5% under long term use in the treatment of seborrhoeic dermatitis: A 12 month open label extension multi-centre phase III trial

Astion Pharma A/S0 个研究点目标入组 300 人开始时间: 2007年12月4日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
300

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • 1. Signed and dated informed consent,
  • 2. Completion of Trial ASF 1057 301 as documented on the End of Trial status page in the case report form (CRF).
  • 3. Sexually active females of childbearing potential must be either surgically sterile (hysterectomy or tubal ligation) or use a medically accepted contraceptive method (and agree to use it during the trial) such as:
  • ­- Systemic contraceptive (oral, implant, injection),
  • ­- Diaphragm or cervical cap with intravaginal spermicide,
  • ­- Intrauterine device, or
  • ­- Condom with intravaginal spermicide.
  • In Denmark and Germany, the patients must agree to continue their contraception during the trial and for 1 month after the end of the trial.
  • 4. Willingness and ability to comply with the trial procedures.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • 1. Female patients who are pregnant or breast-feeding,
  • 2. Known allergy to any of the constituents of the product being tested,
  • 3. Known immunosuppressive (e.g., AIDS/HIV) or neurological diseases (e.g., Parkinson or MS),
  • 4. Presence of an other serious or progressive disease which, according to the Investigator may interfere with treatment outcome,
  • 5. Active skin disease such as psoriasis, atopic dermatitis, rosacea, lupus erythematosus, or other inflammatory or infectious skin disease which, according to the Investigator may interfere with treatment outcome,
  • 6. Intention to use topical medical treatment in the area to be treated within the next 12 months, e.g., anti inflammatory (e.g., corticosteroids, non-steroidal anti inflammatory drugs [NSAIDs]), coal tar preparations, anti-seborrhoeic preparations, antihistamines, antibiotics, or antifungal medications,
  • 7. Intention to use of other topical pharmaceutical products on the area to be treated during treatment period.

研究者

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