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Giving Upfront Anti-p40 to Reduce toxicity from Dual Immune Checkpoint Inhibition in Mesothelioma

Key facts

Where
Rotterdam, HollandiaSee the site
Phase
2. fázis

Where in Hollandia

  • Erasmus Universitair Medisch Centrum Rotterdam (Erasmus MC)Rotterdam, HollandiaToborzás még nem indult

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Trial details

Who runs it
Erasmus Universitair Medisch Centrum Rotterdam (Erasmus MC)
Trial code
EU 2026-526036-38-00
Record updated
2026. július 9.
Original description
To evaluate whether co-administration of an anti-p40 antibody reduces the incidence of severe (grade ≥3) irAEs in patients receiving dual ICB with anti–PD-1 and anti–CTLA-4 antibodies.Read full original descriptionShow less

Giving Upfront Anti-p40 to Reduce toxicity from Dual Immune Checkpoint Inhibition in MESOthelioma

To evaluate whether co-administration of an anti-p40 antibody reduces the incidence of severe (grade ≥3) irAEs in patients receiving dual ICB with anti–PD-1 and anti–CTLA-4 antibodies.

Inclusion: A diagnosis of pathologically confirmed irresectable pleural mesothelioma (confirmed by histology or cytology); Age 18 years or older; ECOG performance status of 0 or 1, or a Karnofsky Performance Scale of 70 or higher; Eligible for dual ICB treatment.

Exclusion: Current use of immunomodulatory drugs within 14 days prior to initiation of ICB; Known hypersensitivity to ustekinumab; Active (mycobacterial) infection; Chronic, recurring infections.

EU CTIS 2026-526036-38-00