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ペンシルベニアにおける脊髄性筋萎縮症の臨床試験

ペンシルベニア内の拠点で、脊髄性筋萎縮症に関する8件の研究が参加者を募集しています。

ペンシルベニア内の都市

公式研究テキスト(英語)

A Study Evaluating the Effectiveness and Safety of Risdiplam Administered as an Early Intervention in Pediatric Participants With Spinal Muscular Atrophy After Gene Therapy

  • Children'S Hospital of Philadelphia, Philadelphia
被験者募集中第4相
3 Months – 24 Months · 全性別 · 2026/10/02更新 · NCT05861986

A Study to Evaluate How Apitegromab Works in Subjects Who Are Less Than 2 Years Old and Have Spinal Muscular Atrophy

  • The Children's Hospital of Philadelphia, Philadelphia
被験者募集中第2相
2歳以下 · 全性別 · 2026/10/02更新 · NCT07047144

A Study Evaluating the Effectiveness and Safety of Risdiplam Administered in Pediatric Patients With Spinal Muscular Atrophy Who Experienced a Plateau or Decline in Function After Gene Therapy

  • Children'S Hospital of Philadelphia, Philadelphia
被験者募集中第4相
3 Months – 24 Months · 全性別 · 2026/09/10更新 · NCT05861999

A Study to Find Out How Nusinersen is Processed in the Body When Given Through the ThecaFlex DRx™ System in Adult and Pediatric Participants With Spinal Muscular Atrophy (PIERRE-PK)

  • Milton S. Hershey Medical Center | Pennsylvania State University_Hershey, Hershey
  • Children's Hospital of Philadelphia, Philadelphia
被験者募集中第1相
3歳以上 · 全性別 · 2026/09/03更新 · NCT06555419

Study of an Intrathecal Port and Catheter System for Subjects With Spinal Muscular Atrophy

  • Penn State Milton S. Hershey Medical Center, Hershey
  • Children's Hospital Philadelphia, Philadelphia
被験者募集中
3歳以上 · 全性別 · 2026/08/19更新 · NCT05866419

ALS/MND Natural History Study Data Repository

  • Thomas Jefferson University, Philadelphia
  • Temple University Lewis Katz School of Medicine, Philadelphia
  • University of Pittsburgh, Pittsburgh
被験者募集中観察研究
18歳〜90歳 · 全性別 · 2026/05/20更新 · NCT05966038

Registry of Patients With a Diagnosis of Spinal Muscular Atrophy (SMA)

  • Penn State Hershey, Hershey
  • University of Pittsburgh Medical Center, Pittsburgh
被験者募集中観察研究
全年齢 · 全性別 · 2025/01/31更新 · NCT04174157

ClinicalTrials.govより、2026/10/05時点のデータを取得。各研究には独自の参加資格があり、参加可否は研究チームが決定します。