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临床试验/EUCTR2017-001677-16-DE
EUCTR2017-001677-16-DE进行中(未招募)1 期

A randomized, double-blind, multi-centre, placebo-controlled, parallel-arm phase 2 trial to assess safety, efficacy and pharmacokinetics of CD11301 0.03% and 0.06% gel in the treatment of Cutaneous T-Cell Lymphoma (CTCL), stages IA, IB and IIA - Safety, efficacy and pharmacokinetics of CD11301 gel in early stage CTC

Galderma S.A.0 个研究点目标入组 86 人开始时间: 2017年11月9日最近更新:

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
86

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. Adults = 18 years of age at the screening visit.
  • 2. Have a clinical diagnosis of cutaneous T cell lymphoma (CTCL) stage IA, IB, or IIA including documentation of a skin biopsy within the last twelve (12) months with histological findings consistent with CTCL (Olsen et al, 2007). If the histological documentation is not available, a (non-target lesion) skin biopsy may be performed at the Screening visit for confirmation.
  • 3. For stage IIA, only subjects with a classification of N0 (No clinically abnormal peripheral lymph nodes) or N1 (clinically abnormal lymph node(s) histopathology Dutch grade 1 or NCI LN0-2) can be enrolled.
  • 4. Subjects must be B0 (absence of significant blood involvement: ?5% of peripheral blood lymphocytes or <250/mcL are atypical (Sezary) cells, fewer than 20% Sezary cells or fewer than 250 Sezary cells/µL.
  • One of the following can be substituted for Sezary cells: up to 1,600/µL CD4 cells and lower than 250/µL CD4+/CD26- or CD4+/CD7- cells
  • 5. Subjects may only be included when therapies, according to the S2k – Leitlinie – Kutane Lymphome, Stand 08/2017, are either contraindicated and/or ineffective and/or not well tolerated.
  • 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 42
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 42

排除标准

  • 1. Participation in previous studies with resiquimod.
  • 2. Known or suspected allergies or sensitivities to any component of the resiquimod gel.
  • 3. History of clinically meaningful allergic reactions to imiquimod.
  • 4. History of autoimmune disease including (but not limited to) rheumatoid arthritis, autoimmune hepatitis, autoimmune thyroiditis, Sjögren syndrome, psoriasis, or systemic lupus erythematosus.

研究者

发起方
Galderma S.A.

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