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Study identifier: NCT05700565 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Treatment of Immune-related Adverse Events Refractory to Standard Therapy and Associated Changes in Immunophenotype

Condition: Immune-related Adverse Event  ·  Sponsor: Lucie Heinzerling

PhaseN/A
Planned participants50
Who can joinAll sexes, N/A to no upper limit
Healthy volunteersNo

About this study

This study is an open, monocentric study. It includes patients with irAE refractory to standard therapy or patients where corticosteroids cannot be tapered. Patients will either be treated with ECP or second line immunosuppressive therapy according to investigator's choice. Patients will be followed for 24 weeks after first treatment.

This description comes directly from the study's public registry record.

Talk to the study team

Lucie Heinzerling  ·  +49 89 4400 56326  ·  lucie.heinzerling@med.uni-muenchen.de

Dirk Tomsitz  ·  +49 89 4400 56326  ·  dirk.tomsitz@med.uni-muenchen.de

Always discuss trial participation with your own doctor first.

Locations (1)

LMU Klinikum HauttumorzentrumMunich, GermanyRecruiting

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Source record: clinicaltrials.gov/study/NCT05700565