Patient Guide: A Phase 1/Phase 2 Open-label Study to Evaluate the Safety, Tolerability, and Efficacy of a Single Intravenous Administration of SAR444836 in Adult Participants With Phenylketonuria

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: NCTNCT05972629
Status: ACTIVE_NOT_RECRUITING
Condition: Phenylketonuria
Phase: PHASE1, PHASE2

Where You Can Participate

This study is available at 11 locations across the country.

Top locations include:
  • • San Francisco, California
  • • Aurora, Colorado
  • • Gainesville, Florida
  • • And 8 more locations

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A Phase 1/Phase 2 Open-label Study to Evaluate the Safety, Tolerability, and Efficacy of a Single Intravenous Administration of SAR444836 in Adult Participants With Phenylketonuria - Join Clinical Trial NCTNCT05972629

How to Join This Clinical Trial - NCTNCT05972629

Learn how to participate in this PHASE1, PHASE2 trial studying an investigational therapy for Phenylketonuria. Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Phenylketonuria
Treatment Being Tested
Investigational treatment
Study Phase
PHASE1, PHASE2 - Safety and effectiveness study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT05972629 - 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

San Francisco, California 94143 - United States

Status: Contact for availability

Clinical Research Site

Aurora, Colorado 80045 - United States

Status: Contact for availability

Clinical Research Site

Gainesville, Florida 32610 - United States

Status: Contact for availability

Clinical Research Site

Cleveland, Ohio 44106 - United States

Status: Contact for availability

Clinical Research Site

Pittsburgh, Pennsylvania 15224-1334 - United States

Status: Contact for availability

Clinical Research Site

Charleston, South Carolina 29425 - United States

Status: Contact for availability

Clinical Research Site

Houston, Texas 77030 - United States

Status: Contact for availability

Clinical Research Site

Ciudad Autonoma Buenos Aires, Buenos Aires 1199 - Argentina

Status: Contact for availability

Clinical Research Site

Porto Alegre, Rio Grande do Sul 90035903 - Brazil

Status: Contact for availability

Clinical Research Site

Tel Litwinsky, 52621 - Israel

Status: Contact for availability

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 PHASE1, PHASE2 clinical trial for Phenylketonuria:

  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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