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CompletedNCT05303480Updated Jan 25, 2023

Deep Phenotyping of Cutaneous T Cell Lymphoma, Type Mycosis Fungoides

An interventional study of Chlormethine in Mycosis Fungoides, sponsored by Centre for Human Drug Research, Netherlands. Completed at 1 site in Netherlands. Open to participants aged 18 Years to 75 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2023-01-25.

Sponsored by Centre for Human Drug Research, Netherlands · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
32
Allocation
Non-randomized
Ages
18 Years to 75 Years
Sex
All
01

Study summary

Mycosis fungoides (MF) is an ultra-orphan disease of which the etiology remains unknown. MF is diagnosed by correlating clinical appearance with histopathological analysis of often multiple invasive skin punch biopsies. To move patient care and the development of novel treatments for MF forward, objective, sensitive and reliable tools that are preferably non-invasive are desired. Therefore, the objective of the current study is to phenotype the early stages of mycosis fungoides in detail and to assess the response of chlormethine (CL) gel monotherapy. With this approach the investigators aim to detect novel biomarkers and to establish methodologies for the (non-)invasive monitoring of MF.

Read the detailed description

In recent years, knowledge about the wide spectrum of cutaneous T-cell lymphomas (CTCL) has broadened. Mycosis fungoides (MF) comprises about 50-70% of all primary cutaneous T-cell lymphomas (Willemze et al, 2019). Many CTCL are misdiagnosed due to clinical and histopathological similarity to other skin conditions (such as psoriasis vulgaris, atopic dermatitis and tinea corpora), low prevalence of disease and a lack of reliable tools for detection of these diseases, resulting in delayed diagnosis with years of discomfort and possibly a worse prognosis. Furthermore, standard treatment has never been proven curative, has many side effects and exacerbations are frequent. To date, the etiology of mycosis fungoides remains unknown and little research has been conducted into the mechanisms underlying its development and its response to treatment.

Mycosis fungoides lesions change over time and differ between patients, consisting of three morphologically different stages: patches (erythematosquamous maculae), plaques (erythematosquamous, elevated and occasionally infiltrated lesions) and tumors (with or without ulceration). Only a relatively small group of patients advances to tumor stage MF during their lifetime. Mycosis fungoides is diagnosed by correlating clinical appearance with histopathological analysis of an invasive skin punch biopsy. Additionally, often multiple biopsies are required after diagnosis, e.g. when a lesion is clinically advancing to a different stage or if lesion origin is ambiguous. Currently no other biomarkers besides skin punch biopsies markers are available for the diagnosis of MF, the evaluation of a MF lesion over time, and the monitoring of a potential treatment effect. To advance MF patient care and the development of novel treatments for MF objective, sensitive and reliable (preferably non-invasive) tools are desired.

Therefore, the objective of the current study is to evaluate disease-related characteristics and biomarkers, the intra- and inter-patient variability of biomarkers, to evaluate biomarkers for disease-monitoring following CL gel treatment and to investigate and monitor skin-related adverse events that might develop after CL gel application in MF patients. With this approach the investigators aim to detect novel biomarkers and to establish methodologies for the (non-)invasive monitoring of MF.

For this purpose, a multi-modal patient profiling approach with in-depth characterization of cutaneous T-cell lymphomas will be performed. A clinical study will be conducted investigating the biology of the disease compared to healthy volunteers (part A) and patients' response to intervention (part B). The former to characterize objectively measured disease characteristics and mechanisms underlying its development, the latter to monitor the biomarker response associated to a MF-CTCL treatment, in this case CL gel. The study focusses on cellular, molecular, biophysical, imaging and microbiome analyses in comparison to healthy controls and between lesional and non-lesional skin of MF patients.

02

Conditions studied

  • Mycosis Fungoides

Keywords

  • Mycosis Fungoides
  • Cutaneous T Cell Lymphoma
  • Biomarker
  • Chlormethine
  • Ledaga
03

In context

Mycoses

539 studies on the registry are indexed under Mycoses; 55 are open to participants now.

This study's enrollment of 32 is below the median of 46 across 358 interventional studies indexed under Mycoses.

Browse Mycoses studies →

Lead sponsor

Centre for Human Drug Research, Netherlands is the lead sponsor of 12 studies on the registry; 3 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Eligibility criteria

Healthy volunteers must meet all of the following inclusion criteria:

  1. Signed informed consent prior to any study-mandated procedure;
  2. Male or female subjects, 18 to 75 years of age, inclusive at screening; in general, stable good health as per judgement of the investigator based upon the results of a medical history, physical examination, vital signs, ECG and laboratory assessments performed at screening. Repeated laboratory testing may be performed at the discretion of the clinical investigators;
  3. Body mass index (BMI) ≥ 18.0 and ≤ 40.0 kg/m2; during COVID-19 pandemic only ≥ 18.0 and ≤ 33.0 kg/m2;
  4. No clinically significant skin disease as judged by the investigator;
  5. No history of hypertrophic scarring or keloid;
  6. Subject is willing to refrain from extensively washing (including bathing, swimming, showering and excessive sweating) the skin 4 hours before every study visit;
  7. Subject is willing and able to washout and withhold any topical treatment (prescription and over the counter products) in the treatment area (if possible matched location to most common location of target lesions of the MF group, and otherwise 100cm2 on the lower back) for 2 weeks prior to Day 1;
  8. Subject is willing to refrain from application of any topical product (e.g. ointments, crème or washing lotions) on the skin 24 hours prior to every study visit day;
  9. Subject is willing and able to washout (topical and oral) antibiotic therapy for 14 days prior to Day 1;
  10. Subject is willing to use effective contraception from screening until EOS if subject is male or women of childbearing potential;
  11. Subject has the ability to communicate well with the investigator in the Dutch language and is willing to comply with the study requirements.

Eligible MF patients must meet all of the following inclusion criteria at screening:

  1. Signed informed consent prior to any study-mandated procedure;
  2. Male or female subjects, 18 to 75 years of age, inclusive at screening; in general, stable good health as per judgement of the investigator based upon the results of a medical history, physical examination, vital signs, ECG and laboratory assessments performed at screening. Repeated laboratory testing may be performed at the discretion of the clinical investigators
  3. Body mass index (BMI) ≥ 18.0 and ≤ 40.0 kg/m2; during COVID-19 pandemic only ≥ 18.0 and ≤ 33.0 kg/m2;
  4. At least one patch and/or plaque lesion present, with at least one dimension with a diameter of ≥ 6cm;
  5. Confirmed MF-diagnosis (stage 1a/1b) by histology (or clinico-histopathological correlation) within the last 10 years;
  6. Willing and able to washout any topical treatment for MF (at least 2 weeks) and any systemic treatment for MF (at least 4 weeks) prior to Day 1, resulting in a washout of 8 weeks for topical treatment and 10 weeks for disease-related systemic treatment prior to the first dosing day (day 43);
  7. No previous use of CL gel (Ledaga) in the past two years;
  8. Subject is willing and able to washout (topical and oral) antibiotic therapy for 14 days prior to Day 1;
  9. Subject is willing to refrain from extensively washing (including bathing, swimming, showering and excessive sweating) the skin 6 hours before every study visit day and up to 2 hours after application of the treatment gel;
  10. Subject is willing to use effective contraception during the study if subject is male or women of child bearing potential, for up to 90 days after the last dose of study treatment;
  11. Male subjects must be willing to withhold from any sperm donation during the study and up to 90 days after the last dose of study treatment.

Eligible healthy volunteers must meet none of the following exclusion criteria at screening:

  1. History of immunological abnormality (e.g., immune suppression) that may interfere with study objectives, in the opinion of the investigator;
  2. The use of systemic antibiotic therapy for >2 months the past 12 months;
  3. The use of any oral/systemic medication (e.g. immunomodulatory, immunosuppressive) within 28 days prior to Day 1, if the investigator judges that it may interfere with the study objectives.
  4. Positive hepatitis B surface antigen (HBsAg), hepatitis C antibody (HCV ab), or human immunodeficiency virus antibody (HIV ab) at screening;
  5. Participation in an investigational drug study within 3 months prior to screening or more than 4 times a year;
  6. Loss or donation of blood over 500mL within three months prior to screening;
  7. History of alcohol consumption exceeding 5 standard drinks per day on average within 3 months of screening. Alcohol consumption will be prohibited from at least 24 hours preceding each study visit;
  8. Positive urine test for drugs or history of abuse at screening or pre-dose. Urine drug test may be repeated at the discretion of the investigator;
  9. Pregnant, a positive pregnancy test, intending to become pregnant, or breastfeeding;

  10. Any other known factor, condition, or disease that might interfere with study conduct or interpretation.

    Eligible MF-patients must meet none of the abovementioned and following exclusion criteria at screening:

  11. Have any current relevant skin infections/disease in the treatment area other than the observational disease (mycosis fungoides), inclusively, but not limited to atopic dermatitis, psoriasis vulgaris, dermatomycosis and other skin malignancies.

  12. Having received treatments for MF or any other disease within the following intervals prior to the start of the study (The use of topical emollients is allowed during the study. For target lesions it is allowed up to 24h before every study visit day):

    1. \< 2 weeks for topical treatment, e.g. corticosteroids, retinoids, vitamin D analogs
    2. \<4 weeks for phototherapy, e.g. UVB, PUVA, PDT
    3. \<4 weeks for non-biologic systemic treatment, e.g. retinoids, methotrexate
    4. \<6 weeks for peginterferon alfa-2a
    5. \<8 weeks for radiotherapy or surgery in the treatment area
    6. \<3 months for any systemic chemotherapeutical treatment
  13. Known hypersensitivity to chlormethine gel or its excipients.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Single group
Masking
None (open label)
Enrollment
32 participants (actual)

Study arms

  • Active comparator
    Chlormethine gel

    Chlormethine gel 0.016% in 60mg tube, topical home administration from day 0 to day 155.

    Drug: Chlormethine

  • No intervention
    Healthy volunteers

    Healthy volunteer cohort (observational)

Interventions

  • DrugChlormethine

    Chlormethine gel 0.016%

    Also known as: Ledaga, Valchlor

06

What researchers measure

Primary outcomes

  1. Composite Assessment of Index Lesions Disease Severity Score (CAILS)

    CAILS is a composite score to quantify lesion severity and consists of scoring erythema, hypo-/hyperpigmentation, plaque elevation, desquamation and lesion size. The CAILS score of a single lesion ranges from 0 (unaffected) to 50 (severely affected).

    Time frame: from day -42 to day 155

  2. Modified Severity Weighted Assessment Tool (mSWAT)

    mSWAT combines the assessment of the severity of lesions and the area affected into a single score ranging from 0 (unaffected) to 400 (severely affected).

    Time frame: from day -42 to day 155

  3. Objective Response Rate (ORR)

    The Objective Response Rate (ORR) measures the lesional response as the change from baseline for the CAILS and mSWAT score. The ORR is the number of patients with complete response (100% clearance) + the number of patients with partial response (50%-99%) divided by the total number of patients.

    Time frame: from day 43 to day 155

  4. SKINDEX-29: Quality of life (QoL)

    The Skindex-29 is a valid 29-item self-report measure that evaluates health-related QoL for patients with dermatological diseases. The score is subdivided in a domain for symptoms, emotions and fuctioning; domain scores range from 0 (no impact) to 100 (severely impacted). Total Skindex-29 score is calculated as a mean of the three domains, ranging from 0 (no impact on QoL) to 100 (QoL severely impacted).

    Time frame: from day 0 to day 155

  5. Treatment Satisfaction Questionnaire for Medication (TSQM)

    TSQM consists of 14 questions and explores the subject satisfaction regarding the effectiveness, the side effects, convenience and global satisfaction of the investigational drug. The TSQM score ranges from 0 (lowest satisfaction) to 100 (highest satisfaction).

    Time frame: from day 43 to day 155

  6. Patient reported outcomes

    Patients will be asked to report on their condition through a Numerical Rating Scale (0 (better)- 100 (worse)) for itch, pain and sleeplessness.

    Time frame: from day 0 to day 155

  7. Erythema measurement of the skin

    Redness of the skin will be determined using a colorimeter

    Time frame: from day 0 to day 155

  8. 3D Multispectral imaging

    The redness and superficial morphology of (non-)lesional skin sites will be determined using a 3D multispectral imaging system.

    Time frame: from day 0 to day 155

  9. Laser Speckle Contrast Imaging (LSCI)

    The cutaneous microcirculation of (non-)lesional skin sites will be monitored over a 40 second timespan with a laser speckle contrast imager.

    Time frame: from day 0 to day 155

  10. Thermography

    Body surface temperature of (non-)lesional skin will be determined using a thermal imaging infrared camera.

    Time frame: from day 0 to day 155

  11. Optical Coherence Tomography (OCT)

    OCT is a non-invasive assessment which visualizes skin morphology in vivo to a depth of 2 mm with the use of infrared light.

    Time frame: from day 0 to day 155

  12. Skin barrier function by Trans-Epidermal Water Loss (TEWL)

    The barrier status by trans epidermal water loss of (non-)lesional skin will be determined using TEWL. (g/m2/h)

    Time frame: from day 0 to day 155

  13. Cutaneous microbiome

    The cutaneous microbiome of (non-)lesional skin is collected by swabbing. The abundance of bacteria is thereafter determined using next-generation sequencing.

    Time frame: from day 0 to day 155

  14. Faecal microbiome

    The bacterial composition of stool samples pre- and post-treatment will be determined using next-generation sequencing.

    Time frame: from day 43 to day 155

  15. Skin surface biomarkers

    Superficial protein biomarkers of (non-)lesional skin will be assessed by a non-invasive transdermal patch by FibroTx. The presence of protein biomarkers will be determined using ELISA. The following biomarkers will be assessed (ng/ul): IL-8, CXCL-2, IL-1A, IL-1RA, CCL-17 and CCL-27 and VEGF.

    Time frame: from day 0 to day 155

  16. Lipidomics of the stratum corneum by liquid chromatography mass spectroscopy

    Tape stripping will be performed on (non-)lesional skin and lipids are subsequently extracted from the tape and analyzed using Liquid Chromatography-Mass Spectrometry (ng/cm2).

    Time frame: from day 0 to day 155

  17. Patient genotyping

    A whole blood sample will be used to scan for common mutations in genes implicated in mycosis fungoides using next-generation sequencing.

    Time frame: day 43

  18. Blister immune cell subsets

    Blisters will be induced on the (non-)lesional skin and the blister exudate aspirated. Blister exudate will be analyzed for the presence of immune cells (e.g. CD4+ and CD8+ T-Cells) using flow cytometry.

    Time frame: day 43

  19. Blister protein biomarkers by high-throughput, multiplex immunoassays of proteins by Proximity Estension Assay (PEA) technology

    Blisters will be induced on the (non-)lesional skin and blister fluid aspirated. Blister fluid will be analyzed for the presence of various chemokines and cytokines using the Olink inflammation and immuno-oncology panel (96 proteins per panel, e.g. PD-L1, IL-4, IL-12, IL-13, ng/ml).

    Time frame: day 43

  20. Immunohistochemistry and Imaging Mass Cytometry/VECTRA of biopsies

    Biopsies will be sectioned and stained for the determination of the cutaneous homeostasis and tumor micro-environment by visualising infiltration of cellular immune subsets (e.g. presence of CD4 and CD8).

    Time frame: from day 43 to day 155

  21. Circulating protein biomarkers by PCR amplification

    Blood will be drawn using a venipuncture during visits and analyzed for the presence of various chemokines and cytokines (e.g. CCL20, CCL17, CXCL8).

    Time frame: from day 0 to day 155

  22. Cells/ml; Circulating immune cell subsets

    Blood will be drawn using a venipuncture during visits and analyzed for the presence of immune cells (e.g. CD4+ and CD8+ T-Cells) using flow cytometry.

    Time frame: from day 0 to day 155

  23. Itch Tracking by Derma Track

    Subjects are requested to wear a smartwatch during the night to register total duration of scratch movements.

    Time frame: from day 0 to day 155

  24. User experience and subjective burden questionnaire

    Measures the user experience and subjective burden of the different imaging modalities used in this study. Scores ranging from 0 (no burden) to 100 (severe burden).

    Time frame: from day 43 to day 155

  25. Blister immune cell subsets during dermatitis reactions

    Blisters will be induced on the lesional skin and the blister exudate aspirated. Blister exudate will be analyzed for the presence of immune cells (e.g. CD4+ and CD8+ T-Cells) using flow cytometry.

    Time frame: from day 43 to day 155

  26. Change from baseline in blister immune cell subsets after 16 weeks of treatment

    Blisters will be induced on the lesional skin and the blister exudate aspirated. Blister exudate will be analyzed for the presence of immune cells (e.g. CD4+ and CD8+ T-Cells) using flow cytometry.

    Time frame: day 43 and day 155

  27. Blister protein biomarkers by high-throughput, multiplex immunoassays of proteins by Proximity Estension Assay (PEA) technology

    Blisters will be induced on the lesional skin and blister fluid aspirated. Blister fluid will be analyzed for the presence of various chemokines and cytokines using the Olink inflammation and immuno-oncology panel (96 proteins per panel, e.g. PD-L1, IL-4, IL-12, IL-13, ng/ml).

    Time frame: from day 43 to day 155

  28. Change from baseline in blister protein biomarkers, by high-throughput, multiplex immunoassays of proteins by Proximity Estension Assay (PEA) technology

    Blisters will be induced on the lesional skin and blister fluid aspirated. Blister fluid will be analyzed for the presence of various chemokines and cytokines using the Olink inflammation and immuno-oncology panel (96 proteins per panel, e.g. PD-L1, IL-4, IL-12, IL-13, ng/ml).

    Time frame: day 43 and day 155

07

Study locations

1 site
  • Centre for Human Drug Research
    Leiden, 2333 CL, Netherlands
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 25, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05303480
Lead sponsor
Centre for Human Drug Research, Netherlands
Collaborators
Recordati Rare Diseases
Responsible party
Sponsor
First posted
Mar 31, 2022
Start date
Dec 7, 2021
Primary completion
Dec 8, 2022
Completion
Dec 8, 2022
Last update
Jan 25, 2023

Study contacts

Robert Rissmann, Prof. Dr.
principal investigator · Centre for Human Drug Research

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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