PDA001 for the Treatment of Adults With Moderate-to-Severe Crohn's Disease
| 대상 질환 | Crohn's Disease |
|---|---|
| 임상 단계 | 2상 |
| 스폰서 | Celularity Incorporated |
| 상태 | 완료 |
| 참여자 수 | 50 명 |
| 중재(약물) | Human Placenta-Derived Cells PDA001 Intravenous Infusion, Vehicle Control |
| 시작일 | 2010년 8월 |
| 완료일 | 2012년 2월 |
| 결과 공개일 | 2026년 7월 7일 |
요약
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.
Percentage of Subjects With Clinical Response Based on Crohn's Disease Activity Index (CDAI) at Both Week 4 and Week 6
| 200 × 10^6 Cells of Human Placenta-Derived Cells PDA001 | 5 Participants |
|---|---|
| 800 × 10^6 Cells of Human Placenta-Derived Cells PDA001 | 5 Participants |
| Vehicle Control | 0 Participants |
| 1.6 × 10^9 Cells of Human Placenta-Derived Cells PDA001 | 2 Participants |
BENITIONS에서 보기 ClinicalTrials.gov 원문 보기
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