Patient Guide: An Open-Label Extension Study to Evaluate the Safety and Tolerability of SPT-300 (GlyphAllo) in Participants With Major Depressive Disorder, With or Without Anxious Distress (BUOY-1 OLE Study)

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 10 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT07161700
Status: ENROLLING_BY_INVITATION
Condition: Major Depressive Disorder (MDD), Major Depressive Disorder With Anxious Distress
Phase: PHASE2

Where You Can Participate

This study is available at 10 locations across the country.

Top locations include:
  • • Chino, California
  • • Glendale, California
  • • Atlanta, Georgia
  • • And 7 more locations

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An Open-Label Extension Study to Evaluate the Safety and Tolerability of SPT-300 (GlyphAllo) in Participants With Major Depressive Disorder, With or Without Anxious Distress (BUOY-1 OLE Study) - Join Clinical Trial NCTNCT07161700

How to Join This Clinical Trial - NCTNCT07161700

Learn how to participate in this PHASE2 trial studying an investigational therapy for Major Depressive Disorder (MDD), Major Depressive Disorder With Anxious Distress. Current status: ENROLLING_BY_INVITATION.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Major Depressive Disorder (MDD), Major Depressive Disorder With Anxious Distress. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Major Depressive Disorder (MDD), Major Depressive Disorder With Anxious Distress
Treatment Being Tested
Investigational treatment
Study Phase
PHASE2 - Safety and effectiveness study
Enrollment Status
ENROLLING_BY_INVITATION
Study Identifier
NCTNCT07161700 - 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 10 locations. Find a study site near you:

Clinical Research Site

Chino, California 91710 - United States

Status: Contact for availability

Clinical Research Site

Glendale, California 91206 - United States

Status: Contact for availability

Clinical Research Site

Atlanta, Georgia 30328 - United States

Status: Contact for availability

Clinical Research Site

Decatur, Georgia 30030 - United States

Status: Contact for availability

Clinical Research Site

Boston, Massachusetts 02116 - United States

Status: Contact for availability

Clinical Research Site

St Louis, Missouri 63141 - United States

Status: Contact for availability

Clinical Research Site

Brooklyn, New York 11235 - United States

Status: Contact for availability

Clinical Research Site

Staten Island, New York 10314 - United States

Status: Contact for availability

Clinical Research Site

North Canton, Ohio 44720 - United States

Status: Contact for availability

Clinical Research Site

Irving, Texas 75062 - United States

Status: Contact for availability

How to Enroll in This Study

To learn more about participating in this PHASE2 clinical trial for Major Depressive Disorder (MDD), Major Depressive Disorder With Anxious Distress:

  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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