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Study identifier: NCT01155362 Synced from ClinicalTrials.gov · August 07, 2026
● Study status: Completed

PDA001 for the Treatment of Adults With Moderate-to-Severe Crohn's Disease

Condition: Crohn's Disease  ·  Sponsor: Celularity Incorporated

PhasePhase 2
Planned participants50
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersNo

About this study

This Phase 2a study evaluated the efficacy, safety, and tolerability of intravenous human placenta-derived cells (PDA001) compared with placebo in adults with moderate-to-severe Crohn's disease. Three PDA001 dose levels were evaluated.

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.

Locations (13)

Cedars Sinai Medical CenterLos Angeles, California, United States
University of California, IrvineOrange, California, United States
Yale School of Medicine Digestive DiseasesNew Haven, Connecticut, United States
University of FloridaGainesville, Florida, United States
University of Chicago Medical CenterChicago, Illinois, United States
Indiana UniversityIndianapolis, Indiana, United States
Mt Sinai HospitalNew York, New York, United States
Rochester General HospitalRochester, New York, United States
Stony Brook UniversityStony Brook, New York, United States
Case Western Reserve UniversityCleveland, Ohio, United States
Vanderbilt UniversityNashville, Tennessee, United States
Baylor College of MedicineHouston, Texas, United States

+ 1 more locations — full list on the registry record.

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