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

Recruiting Observational Study
Immune-related Adverse Event
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Sex
Any
Study type
Observational
Participants needed
50 (estimated)
Sponsor
Lucie Heinzerling · Other
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About This Trial

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.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. Subjects must we willing and able to comply with scheduled visits and must have given written informed consent. 2. irAE after immune checkpoint inhibitor therapy (PD-1/PD-L1 or PD-1 + CTLA4 blockade) 3. irAE refractory to therapy with corticosteroids or inability to taper cor…
Contacts

Lucie Heinzerling

+49 89 4400 56326

lucie.heinzerling@med.uni-muenchen.de

CONTACT

Dirk Tomsitz

+49 89 4400 56326

dirk.tomsitz@med.uni-muenchen.de

CONTACT