Patient Guide: A Study to Learn How Nusinersen (Spinraza) Affects Participants With Spinal Muscular Atrophy (SMA) Who Took it Before or During Pregnancy And About The Health of Their Babies

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 11 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT05789758
Status: 🟢 Enrolling Now
Condition: Muscular Atrophy, Spinal
Phase: Not Specified

Where You Can Participate

This study is available at 11 locations across the country.

Top locations include:
  • • Palo Alto, California
  • • Cambridge, Massachusetts
  • • London, Greater London
  • • And 8 more locations

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A Study to Learn How Nusinersen (Spinraza) Affects Participants With Spinal Muscular Atrophy (SMA) Who Took it Before or During Pregnancy And About The Health of Their Babies - Join Clinical Trial NCTNCT05789758

How to Join This Clinical Trial - NCTNCT05789758

Learn how to participate in this Not Specified trial studying an investigational therapy for Muscular Atrophy, Spinal. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Muscular Atrophy, Spinal. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Muscular Atrophy, Spinal
Treatment Being Tested
Investigational treatment
Study Phase
Not Specified - Research study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT05789758 - 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 11 locations. Find a study site near you:

Clinical Research Site

Palo Alto, California 94304 - United States

Status: RECRUITING

Clinical Research Site

Cambridge, Massachusetts 02142 - United States

Status: ACTIVE_NOT_RECRUITING

Clinical Research Site

London, Greater London SW17 0QT - United Kingdom

Status: RECRUITING

Clinical Research Site

Salford, Greater Manchester M6 8HD - United Kingdom

Status: RECRUITING

Clinical Research Site

Southampton, Hampshire SO16 6YD - United Kingdom

Status: RECRUITING

Clinical Research Site

Nottingham, Nottinghamshire NG5 1PB - United Kingdom

Status: RECRUITING

Clinical Research Site

Oswestry, Shropshire SY10 7AG - United Kingdom

Status: RECRUITING

Clinical Research Site

Sheffield, South Yorkshire S10 2SB - United Kingdom

Status: RECRUITING

Clinical Research Site

Newcastle upon Tyne, Tyne and Wear NE7 7ND - United Kingdom

Status: RECRUITING

Clinical Research Site

Birmingham, West Midlands B15 2GW - United Kingdom

Status: RECRUITING

And 1 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this Not Specified clinical trial for Muscular Atrophy, Spinal:

  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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