Patient Guide: Non-immunogenic Recombinant Staphylokinase vs Placebo in Patients With Intermediate High-risk Pulmonary Embolism

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 19 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06362746
Status: 🟢 Enrolling Now
Condition: Pulmonary Embolism, Embolism
Phase: PHASE3

Where You Can Participate

This study is available at 19 locations across the country.

Top locations include:
  • • Barnaul, Altai Region
  • • Vyselki, Krasnodar Region
  • • Asino, Tomsk Region
  • • And 16 more locations

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Non-immunogenic Recombinant Staphylokinase vs Placebo in Patients With Intermediate High-risk Pulmonary Embolism - Join Clinical Trial NCTNCT06362746

How to Join This Clinical Trial - NCTNCT06362746

Learn how to participate in this PHASE3 trial studying an investigational therapy for Pulmonary Embolism, Embolism. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Pulmonary Embolism, Embolism
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT06362746 - 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 19 locations. Find a study site near you:

Clinical Research Site

Barnaul, Altai Region 656038 - Russian Federation

Status: RECRUITING

Clinical Research Site

Vyselki, Krasnodar Region 353100 - Russian Federation

Status: RECRUITING

Clinical Research Site

Asino, Tomsk Region 636840 - Russian Federation

Status: RECRUITING

Clinical Research Site

Belgorod, 308007 - Russian Federation

Status: RECRUITING

Clinical Research Site

Kemerovo, 650002 - Russian Federation

Status: RECRUITING

Clinical Research Site

Kirov, 610035 - Russian Federation

Status: RECRUITING

Clinical Research Site

Krasnodar, 350012 - Russian Federation

Status: RECRUITING

Clinical Research Site

Moscow, 105187 - Russian Federation

Status: RECRUITING

Clinical Research Site

Moscow, 108814 - Russian Federation

Status: RECRUITING

Clinical Research Site

Moscow, 115446 - Russian Federation

Status: RECRUITING

And 9 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE3 clinical trial for Pulmonary Embolism, Embolism:

  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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