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Study identifier: NCT07456800 Synced from ClinicalTrials.gov · August 08, 2026
● Study status: Completed

PK of Deupirfenidone Versus Pirfenidone in Older Healthy Subjects

Condition: Pharmacokinetic Analysis  ·  Sponsor: PureTech

PhasePhase 1
Planned participants116
Who can joinAll sexes, 60 Years to 80 Years
Healthy volunteersYesCheck eligibility criteria ↓
Where3 locations

Sponsor, CRO or site team? See where this study is running → — listed sites, countries and recruiting context. Everything below is written for patients and caregivers.

About this study

A three-part, randomized, double-blind study in healthy older adults to identify a dose of deupirfenidone for further clinical study.

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

Talk to the study team

No contact information is available for this study as per the public registry record.

Always discuss trial participation with your own doctor first.

Full eligibility criteria (exactly as the study team wrote them)

* Male or female between 60 and 80 years old (inclusive) at the time of Screening. * In good general health at Screening, free from clinically significant laboratory values, or clinically significant unstable medical, surgical, or psychiatric illness, as determined by the Investigator. Subjects with mild, chronic, stable disease and on stable medication could be included if deemed medically prudent by the Investigator. * Has a body mass index (BMI) between ≥18.0 and ≤50.0 kg/m2 at Screening.

Reproduced word-for-word from the public registry record — the study team can answer questions about it.

Locations (3)

Collaborative Neuroscience Network, LLC.Long Beach, California, United States
Accel Research SitesLake Mary, Florida, United States
Hassman ResearchBerlin, New Jersey, United States

More studies in these areas

This study lists sites in the areas below. Each link shows other recruiting studies near that city, from the public registry record.

Long BeachLake MaryBerlin

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