Study of ARO-DIMERPA in Adult Participants With Mixed Hyperlipidemia - Join Clinical Trial NCTNCT07223658
How to Join This Clinical Trial - NCTNCT07223658
Learn how to participate in this PHASE1, PHASE2 trial studying an investigational therapy for Hyperlipidemia; Mixed. Current status: NOT_YET_RECRUITING.
Am I Eligible for This Clinical Trial?
This clinical research study is looking for participants with Hyperlipidemia; Mixed. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.
- Condition Being Studied
 - Hyperlipidemia; Mixed
 - Treatment Being Tested
 - Investigational treatment
 - Study Phase
 - PHASE1, PHASE2 - Safety and effectiveness study
 - Enrollment Status
 - NOT_YET_RECRUITING
 - Study Identifier
 - NCTNCT07223658 - 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 multiple locations. Find a study site near you:
How to Enroll in This Study
To learn more about participating in this PHASE1, PHASE2 clinical trial for Hyperlipidemia; Mixed:
- Review the eligibility criteria with your healthcare provider
 - Contact the study team for a pre-screening interview
 - Schedule an in-person screening visit if eligible
 - Review and sign the informed consent form
 - Begin participation in the clinical trial
 
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