Patient Guide: Evaluating the Safety, Tolerability, Pharmacokinetics, Pharmacokinetics, and Preliminary Efficacy of FS-8002

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: NCTNCT06832982
Status: 🟢 Enrolling Now
Condition: Advanced Solid Tumors
Phase: PHASE1

Where You Can Participate

This study is available at 10 locations across the country.

Top locations include:
  • • Beijing, Beijing
  • • Fujian, Fuzhou
  • • Zhejiang, Hangzhou
  • • And 7 more locations

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Evaluating the Safety, Tolerability, Pharmacokinetics, Pharmacokinetics, and Preliminary Efficacy of FS-8002 - Join Clinical Trial NCTNCT06832982

How to Join This Clinical Trial - NCTNCT06832982

Learn how to participate in this PHASE1 trial studying an investigational therapy for Advanced Solid Tumors. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Advanced Solid Tumors
Treatment Being Tested
Investigational treatment
Study Phase
PHASE1 - Early safety study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT06832982 - 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

Beijing, Beijing 100142 - China

Status: RECRUITING

Clinical Research Site

Fujian, Fuzhou 350013 - China

Status: RECRUITING

Clinical Research Site

Zhejiang, Hangzhou 310003 - China

Status: NOT_YET_RECRUITING

Clinical Research Site

Heilongjiang, Harbin 150081 - China

Status: RECRUITING

Clinical Research Site

Shandong, Jinan 250117 - China

Status: RECRUITING

Clinical Research Site

Guangdong, Meizhou 514031 - China

Status: RECRUITING

Clinical Research Site

Shenyang, Shenyang 110001 - China

Status: RECRUITING

Clinical Research Site

Hebei, Shijiazhuang 050010 - China

Status: RECRUITING

Clinical Research Site

Hubei, Wuhan 430022 - China

Status: RECRUITING

Clinical Research Site

Hubei, Wuhan 430079 - China

Status: RECRUITING

How to Enroll in This Study

To learn more about participating in this PHASE1 clinical trial for Advanced Solid Tumors:

  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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