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Study identifier: NCT06860542 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Inhaled Budesonide for REcurrence Prevention and Adjuvant THerapy in Checkpoint Inhibitor Pneumonitis

Condition: Pneumonitis · Immune-related Adverse Event  ·  Sponsor: AHS Cancer Control Alberta

PhasePhase 2
Planned participants94
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The introduction of immune checkpoint inhibitors (immunotherapy) that stimulate our immune system to recognize and attack cancer cells has been one of the most exciting advances in oncology over the last decade. These medications are now employed across almost half of cancer types and settings, however they come with a cost. In some patients, instead of attacking cancer cells alone, the stimulated immune system damages healthy tissues (immune related adverse events), with one of the most severe and potentially deadly such complications being immune attack on the lungs, or checkpoint inhibitor pneumonitis (CIP). When treated promptly with oral or intravenous steroids, acute CIP improves in many cases, however for approximately one-fifth of patients the lung inflammation is difficult to control, resulting in recurrent shortness of breath, the need for extended courses of oral or intravenous steroids, impacting quality of life and cancer therapy decisions. The goal of the trial is to assess whether use of inhaled steroids, a type of medication commonly used in asthma patients, for one year after a first diagnosis of CIP may help the lung inflammation resolve and not return, without the repeated use of oral or intravenous medications that carry more side effects.

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

Talk to the study team

Alexander Watson, MD  ·  587-231-5098  ·  alexander.watson@cancercarealberta.ca

Amy Abel

Always discuss trial participation with your own doctor first.

Locations (1)

Arthur J.E. Child Comprehensive Cancer CentreCalgary, Alberta, CanadaRecruiting

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Source record: clinicaltrials.gov/study/NCT06860542