Predictive and Prognostic Biomarkers in Patients With Mycosis Fungoides and S zary Syndrome.

  • STATUS
    Recruiting
  • End date
    Apr 3, 2027
  • participants needed
    120
  • sponsor
    Lund University Hospital
Updated on 3 June 2021
lymphoma
mycosis

Summary

A translational study for identification of prognostic and treatment-predictive biomarkers in Mycosis fungoides and Szary syndrome.

Details
Condition Sézary Syndrome, Lymphoproliferative disorders, Cutaneous T-Cell Lymphoma, Sezary Syndrome, cutaneous T-cell lymphoma, Lymphoproliferative Disorder, Mycosis Fungoides
Treatment Blood tests and testing of analysis of the lymphoma microenvironment in skin, skin barrier and skin microbiology profile.
Clinical Study IdentifierNCT04904146
SponsorLund University Hospital
Last Modified on3 June 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Age 18-100 years
Histologically confirmed (according to the World Health Organization (WHO)/EORTC classification) MF/SS stages I-IV
WHO performance status 0 -3
Absence of psychiatric illness or condition which could interfere with the subjects' ability to understand the requirements of the study
Written informed consent according to International Conference on Harmonization (ICH)/(Good Clinical Practice (GCP), and Swedish regulations
No minimum or maximum required routine laboratory data

Exclusion Criteria

Not applicable. No exclusion criteria are specified
Clear my responses

How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer  to help accelerate the development of new treatments and to get notified about similar trials.

You are contacting

Investigator Avatar

Primary Contact

site

Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

Learn more

If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

Learn more

Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

Learn more

Similar trials to consider

Loading...

Browse trials for

Not finding what you're looking for?

Every year hundreds of thousands of volunteers step forward to participate in research. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.

Sign up as volunteer

user name

Added by • 

 • 

Private

Reply by • Private
Loading...

Lorem ipsum dolor sit amet consectetur, adipisicing elit. Ipsa vel nobis alias. Quae eveniet velit voluptate quo doloribus maxime et dicta in sequi, corporis quod. Ea, dolor eius? Dolore, vel!

  The passcode will expire in None.
Loading...

No annotations made yet

Add a private note
  • abc Select a piece of text from the left.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.
Add a private note