Patient Guide: Safety, Tolerability, and Pharmacokinetics of HRS-3802 Monotherapy in Patients With Malignant Solid Tumors

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 6 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06770569
Status: 🟢 Enrolling Now
Condition: Advanced Solid Tumors
Phase: PHASE1

Where You Can Participate

This study is available at 6 locations across the country.

Top locations include:
  • • Saint Leonards, New South Wales
  • • Sydney, New South Wales
  • • Tugun, Queensland
  • • And 3 more locations

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Safety, Tolerability, and Pharmacokinetics of HRS-3802 Monotherapy in Patients With Malignant Solid Tumors - Join Clinical Trial NCTNCT06770569

How to Join This Clinical Trial - NCTNCT06770569

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
NCTNCT06770569 - 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 6 locations. Find a study site near you:

Clinical Research Site

Saint Leonards, New South Wales 2065 - Australia

Status: NOT_YET_RECRUITING

Clinical Research Site

Sydney, New South Wales 2109 - Australia

Status: NOT_YET_RECRUITING

Clinical Research Site

Tugun, Queensland 4224 - Australia

Status: NOT_YET_RECRUITING

Clinical Research Site

Adelaide, South Australia 5000 - Australia

Status: NOT_YET_RECRUITING

Clinical Research Site

Frankston, Victoria 3199 - Australia

Status: NOT_YET_RECRUITING

Clinical Research Site

Beijing, Beijing 100021 - 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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