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Study identifier: NCT04851015 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Low Dose Trimethoprim-Sulfamethoxazole for the Treatment of Pneumocystis Jirovecii Pneumonia

Condition: Pneumocystis · Pneumocystis Pneumonia · Pneumocystis Jirovecii Infection  ·  Sponsor: Todd C. Lee MD MPH FIDSA

PhasePhase 3
Planned participants416
Who can joinAll sexes, 18 Years to 100 Years
Healthy volunteersNo

About this study

Pneumocystis jirovecii pneumonia (PCP) is an opportunistic fungal infection of immunocompromised hosts which causes in significant morbidity and mortality. The current standard of care, trimethoprim-sulfamethoxazole (TMP-SMX) at a dose of 15-20 mg/kg/day of TMP, is associated with serious adverse events, including hypersensitivity reactions, drug-induced liver injury, cytopenia, and renal failure occurring among 20-60% of patients. The frequency of adverse events increases in a dose dependent manner and commonly limits the use of TMP-SMX. Reduced treatment doses of TMP-SMX for PCP reduced ADEs without mortality differences in a recent meta-analysis of observational studies. We therefore propose a Phase III randomized, placebo-controlled trial to directly compare the efficacy and safety of low dose (10 mg/kg/day of TMP) compared to the standard-of-care (15 mg/kg/day) among patients with PCP for the primary outcome of Win Ratio hierarchical composite of death, ECMO, invasive ventilation, grade 4 toxicity, non-invasive ventilation, change of therapy and length of stay.

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

Talk to the study team

Babykumari Chitramuthu, PhD  ·  514-934-1934  ·  babykumari.chitramuthu@muhc.mcgill.ca

Always discuss trial participation with your own doctor first.

Locations (1)

McGill University Health Centre (Royal Victoria Hospital and Montreal General Hospital)Montreal, Quebec, CanadaRecruiting

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Source record: clinicaltrials.gov/study/NCT04851015