Patient Guide: Rhu-pGSN for Acute Respiratory Distress Syndrome (ARDS)

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 61 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT05947955
Status: 🟢 Enrolling Now
Condition: Infections, Respiratory Distress Syndrome, Respiratory Distress Syndrome, Newborn, Acute Lung Injury, Syndrome
Phase: PHASE2

Where You Can Participate

This study is available at 61 locations across the country.

Top locations include:
  • • Irvine, California
  • • Augusta, Georgia
  • • Chicago, Illinois
  • • And 58 more locations

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Rhu-pGSN for Acute Respiratory Distress Syndrome (ARDS) - Join Clinical Trial NCTNCT05947955

How to Join This Clinical Trial - NCTNCT05947955

Learn how to participate in this PHASE2 trial studying an investigational therapy for Infections, Respiratory Distress Syndrome, Respiratory Distress Syndrome, Newborn, Acute Lung Injury, Syndrome. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Infections, Respiratory Distress Syndrome, Respiratory Distress Syndrome, Newborn, Acute Lung Injury, Syndrome. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Infections, Respiratory Distress Syndrome, Respiratory Distress Syndrome, Newborn, Acute Lung Injury, Syndrome
Treatment Being Tested
Investigational treatment
Study Phase
PHASE2 - Safety and effectiveness study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT05947955 - ClinicalTrials.gov Identifier
Sponsored By
Study sponsor

What to Expect as a Participant

Participating in this clinical trial involves:

  • Initial screening to determine eligibility
  • Regular study visits and health assessments
  • Receiving the study treatment or placebo
  • Medical monitoring and follow-up care
  • Contributing to medical research that may help others
  • Potential access to new treatments before they're widely available

Clinical Trial Benefits and Compensation

Participants in this clinical research study may receive:

  • Close medical monitoring by healthcare professionals
  • Access to potential new treatments
  • Compensation for time and travel (varies by study)
  • No-cost study-related medical care
  • The opportunity to help advance medical knowledge

Where Is This Clinical Trial Located?

This study is enrolling participants at 61 locations. Find a study site near you:

Clinical Research Site

Irvine, California 92868 - United States

Status: RECRUITING

Clinical Research Site

Augusta, Georgia 30912 - United States

Status: RECRUITING

Clinical Research Site

Chicago, Illinois 60611 - United States

Status: RECRUITING

Clinical Research Site

Louisville, Kentucky 40202 - United States

Status: RECRUITING

Clinical Research Site

Louisville, Kentucky 40202 - United States

Status: RECRUITING

Clinical Research Site

Rochester, Minnesota 55905 - United States

Status: RECRUITING

Clinical Research Site

Hannibal, Missouri 63401 - United States

Status: RECRUITING

Clinical Research Site

Lincoln, Nebraska 68506 - United States

Status: RECRUITING

Clinical Research Site

Houston, Texas 77030 - United States

Status: RECRUITING

Clinical Research Site

Temple, Texas 76508 - United States

Status: RECRUITING

And 51 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE2 clinical trial for Infections, Respiratory Distress Syndrome, Respiratory Distress Syndrome, Newborn, Acute Lung Injury, Syndrome:

  1. Review the eligibility criteria with your healthcare provider
  2. Contact the study team for a pre-screening interview
  3. Schedule an in-person screening visit if eligible
  4. Review and sign the informed consent form
  5. Begin participation in the clinical trial

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