Cutaneous T-Cell Lymphoma/Mycosis Fungoides

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Review clinical trials related to Cutaneous T-Cell Lymphoma/Mycosis Fungoides. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Systemic Therapies in the Treatment of Cutaneous T-cell Lymphoma

The study is designed to describe the different approaches of systemic therapies for the treatment of Cutaneous T-cell Lymphoma in real world setting.

Participants needed: 400
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Fondazione Italiana Linfomi - ETSUpdated: Dec 2, 2025Locations: 18
Eligibility criteria

Confirmed diagnosis of CTCL according to the EORTC 2017 update criteria1. [+4]

Patients not meeting the above-mentioned inclusion criteria. [+1]

Status: Not yet recruiting

Long-term Assessment of Chlormethine Gel in Mycosis Fungoides

The study aims to provide comprehensive insights into the long-term therapeutic outcomes, potential adverse effects, and overall patient experience with chlormethine gel, thereby informing clinical practice and guiding future treatment strategies for mycosis fungoides.

Participants needed: 190
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Fondazione Italiana Linfomi - ETSUpdated: Jul 4, 2025Locations: 20
Eligibility criteria

Patients age ≥ 18 [+6]

Patients for whom retrospective data or information on the type of therapy, dura... [+2]

Status: Recruiting

A Study of Molecular Subtyping-based Therapeutic Strategies for Cutaneous T-cell Lymphoma

Cutaneous T-cell lymphoma (CTCL) is a group of diseases resulting from clonal hyperplasia of memory T cells in the skin. The increasing incidence and high treatment costs have posed significant challenges to public health and the economy. Current treatment guidelines only provide partial control, leading to varying remission times and recurrence rates. This study aims to use molecular subtyping and immunohistochemistry to guide treatment selection for CTCL patients, aiming to prolong clinical benefit, improve treatment safety, and reduce economic burden.

Participants needed: 100
Trial details
Age: 18-75Biological sex: AllType: ObservationalSponsor: Peking University First HospitalUpdated: May 31, 2024Locations: 3Duration: 2 Years
Eligibility criteria

Signed informed consent; [+3]

Received other anti-tumor therapy other than skin-targeted therapy (phototherapy... [+15]