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Not yet recruitingPriority 4 · Lower priorityNCT07477769

Lymphocyte Phenotype of Autosomal Recessive Congenital Ichthyoses Mutated NIPAL4 (Nipal4-nEDD)

ClinicalTrials.gov

Plain-language summary

This study is studying blood sampling for people with cutaneous T-cell lymphoma (skin lymphoma). The study measures how well this treatment works and monitors for side effects. This trial does not currently list US sites.

Who can join (key eligibility)

  • Age 18 Years or older
  • See full trial listing for complete eligibility

Final eligibility is determined by the trial team. This list is a starting point only.

What's being tested

blood sampling (OTHER): Supplementary blood collection performed during routine venipuncture

Drugs / treatments
blood sampling
Treatment length
Ask the trial team for details
Visit frequency
Ask the trial team for details

At a glance

Phase
Not applicable
Status
Not yet recruiting
Design
Non-randomized, blind
Enrollment target
10 patients
Primary endpoint
Proportion of blood lymphocyte phenotype
Ages
18 Years to —
Start date
2026-04-01
Est. completion
2027-10-01

Locations

0 US sites · 0 total

No US sites currently listed.

Contact

Sponsor
Assistance Publique - Hôpitaux de Paris (OTHER)
Contact
Emmanuelle Bourrat, MD | emmanuelle.bourrat@aphp.fr | 01 42 49 90 90

Tags

CTCLany
TrialCompass — Clinical Trial Summary

Lymphocyte Phenotype of Autosomal Recessive Congenital Ichthyoses Mutated NIPAL4 (Nipal4-nEDD)

NCT07477769

Status: Not yet recruiting | Priority: Lower

Plain-language summary

This study is studying blood sampling for people with cutaneous T-cell lymphoma (skin lymphoma). The study measures how well this treatment works and monitors for side effects. This trial does not currently list US sites.

Who can join

  • Age 18 Years or older
  • See full trial listing for complete eligibility

What's being tested

blood sampling (OTHER): Supplementary blood collection performed during routine venipuncture

Drugs / treatments: blood sampling

Treatment length: Ask the trial team for details

Visit frequency: Ask the trial team for details

Trial design

Non-randomized, blind

Enrollment target: 10 patients

Primary endpoint: Proportion of blood lymphocyte phenotype

Ages: 18 Years to —

Start date: 2026-04-01 | Est. completion: 2027-10-01

Locations

0 US sites · 0 total

Contact

Emmanuelle Bourrat, MD | emmanuelle.bourrat@aphp.fr | 01 42 49 90 90

Sponsor: Assistance Publique - Hôpitaux de Paris (OTHER)

Tags

CTCL · any

View on ClinicalTrials.gov

https://clinicaltrials.gov/study/NCT07477769

Prepared using TrialCompass (trialcompass.com) on July 4, 2026. For informational purposes only. Always discuss with your healthcare team.
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Data sourced from ClinicalTrials.gov.

For informational purposes only. Not medical advice — always consult your healthcare team.

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Data last updated: June 2026

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