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Philadelphia、PAにおける間質性肺疾患の臨床試験

Philadelphiaとその周辺地域(約30マイル以内)の拠点で、間質性肺疾患に関する16件の研究が参加者を募集しています。研究を開いて、参加資格と連絡方法を確認してください。

公式研究テキスト(英語)

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FIBRONEER-ACT: A Study to Test Whether Nerandomilast Helps People With Fibrosing Interstitial Lung Disease at Risk for Disease Progression

被験者募集中第3相
  • University of Pennsylvania, Philadelphia
  • Temple University, Philadelphia
18歳以上 · 全性別 · 2026/10/01更新 · NCT07540988

A Study to Test Whether Nerandomilast Can Help Slow Down Changes in the Lung in People With a Family History of Pulmonary Fibrosis

被験者募集中第3相
  • University of Pennsylvania, Philadelphia
40歳以上 · 全性別 · 2026/09/30更新 · NCT07201922

LAM-001 for the Treatment of Pulmonary Hypertension Associated With Interstitial Lung Disease (PH-ILD)

被験者募集中第2相
  • Thomas Jefferson University, Philadelphia
  • Temple Lung Center, Temple University, Philadelphia
18歳〜80歳 · 全性別 · 2026/09/29更新 · NCT05798923

A Study to Investigate the Long-term Safety and Efficacy of Belimumab in Adults With Interstitial Lung Disease (ILD) Associated With Systemic Sclerosis (SSc) and Other Connective Tissue Diseases (CTD) (BLISSconneCTD-OLE)

被験者募集中第3相
  • GSK Investigational Site, Philadelphia
  • GSK Investigational Site, Philadelphia
18歳以上 · 全性別 · 2026/09/09更新 · NCT06716606

A Study of the Efficacy and Safety of Belimumab in Adults With Interstitial Lung Disease Associated With Connective Tissue Disease

被験者募集中第3相
  • GSK Investigational Site, Philadelphia
18歳以上 · 全性別 · 2026/09/08更新 · NCT06572384

A Study of the Efficacy and Safety of Belimumab in Adults With Systemic Sclerosis Associated Interstitial Lung Disease

被験者募集中第2/3相
  • GSK Investigational Site, Philadelphia
  • GSK Investigational Site, Philadelphia
18歳以上 · 全性別 · 2026/09/08更新 · NCT05878717

Multi-site Study of the Clinical Impact of an AI-assisted Approach to Referring Patients With Interstitial Lung Disease for Diagnostic Evaluation of Pulmonary Hypertension

被験者募集中
  • Thomas Jefferson University, Philadelphia
  • Temple University of The Commonwealth System of Higher Education, Philadelphia
18歳以上 · 全性別 · 2026/09/02更新 · NCT06911632

DeciPHer-ILD: A Real-world Patient Registry in Group 3 Pulmonary Hypertension Associated With Interstitial Lung Disease (PH-ILD)

被験者募集中観察研究
  • University of Pennsylvania, Philadelphia
  • Thomas Jefferson University - Sidney Kimmel Medical College, Philadelphia
  • Temple Lung Center, Philadelphia
  • 他1件
18歳以上 · 全性別 · 2026/08/26更新 · NCT06388421

Platform Clinical Study for Conquering Scleroderma

被験者募集中第2相
  • University of Pennsylvania, Philadelphia
  • Thomas Jefferson University Hospital, Philadelphia
18歳以上 · 全性別 · 2026/08/18更新 · NCT06195072

Idiopathic Pulmonary Fibrosis and Interstitial Lung Disease Prospective Outcomes Registry

被験者募集中観察研究
  • Temple University, Philadelphia
  • Thomas Jefferson University, Philadelphia
21歳以上 · 全性別 · 2026/08/12更新 · NCT01915511

A Study of ROC-101 in Patients With Pulmonary Arterial Hypertension (PAH) and Pulmonary Hypertension Associated With Interstitial Lung Disease (ILD-PH) (ROCSTAR STUDY)

被験者募集中第2相
  • Temple University, Philadelphia
18歳〜80歳 · 全性別 · 2026/08/10更新 · NCT07175038

Study of the Efficacy and Safety of Inhaled Treprostinil in Subjects With Progressive Pulmonary Fibrosis (TETON-PPF)

被験者募集中第3相
  • Hospital of the University of Pennsylvania, Philadelphia
  • Jefferson Honickman Center, Philadelphia
  • Temple University Hospital, Philadelphia
18歳以上 · 全性別 · 2026/07/13更新 · NCT05943535

TRANSPIRE: Lung Injury in a Longitudinal Cohort of Pediatric HSCT Patients

被験者募集中観察研究
  • Children's Hospital of Philadelphia, Philadelphia
24歳以下 · 全性別 · 2026/06/22更新 · NCT04098445

Feasibility of Semaglutide in Advanced Lung Disease

被験者募集中第1/2相
  • University of Pennsylvania Perelman School of Medicine, Philadelphia
18歳〜80歳 · 全性別 · 2026/04/21更新 · NCT05746039

Study Evaluating INS018_055 Administered Orally to Subjects With Idiopathic Pulmonary Fibrosis

被験者募集中第2相
  • Temple University Hospital-Temple Lung Center, Philadelphia
40歳以上 · 全性別 · 2025/11/12更新 · NCT05975983

他の都市における間質性肺疾患の試験

Philadelphiaにおける他の研究

ClinicalTrials.govより、2026/10/06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。