PDA001 for the Treatment of Adults With Moderate-to-Severe Crohn's Disease
| 対象疾患 | Crohn's Disease |
|---|---|
| 相 | 第2相 |
| スポンサー | Celularity Incorporated |
| ステータス | 完了 |
| 参加者数 | 50 名 |
| 介入（薬剤） | Human Placenta-Derived Cells PDA001 Intravenous Infusion, Vehicle Control |
| 開始日 | 2010年8月 |
| 完了日 | 2012年2月 |
| 結果公開日 | 2026年7月7日 |
概要
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 |
BENITIONS で見る ClinicalTrials.gov の原文を見る
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