Food Intervention to Reduce Immunotherapy ToXicity
Recruiting
N/A
Interventional Study
Immune-related Adverse Event
Dietary Habits
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Prevention
- Participants needed
- 60 (estimated)
- Sponsor
- Universitair Ziekenhuis Brussel · Other
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About This Trial
The FORX (Food intervention to Reduce immunotherapy toXicity) trial will assess whether supplementing dietary fiber intake by providing weekly boxes containing 30 different plants to patients with solid tumors starting immune checkpoint inhibitor therapy affects the incidence of immune related adverse events.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* solid tumor starting anti-programmed cell death protein 1 (anti-PD1) and/or anti-cytotoxic T-lymphocyte-associated antigen 4 (anti-CTLA4) antibodies as part of standard of care.
* able to sign informed consent.
Exclusion Criteria:
* no oral intake possible.
* probiotic use a…
Contacts