Clinical Research at Pars Medicine
Advancing medical care through rigorous, ethical research. Explore our 200+ active clinical trials and discover how you can contribute to breakthrough treatments that benefit patients worldwide.
Active Clinical Trials
We conduct over 200 active clinical trials spanning all phases (Phase I-IV) across multiple therapeutic areas. Here are some of our featured studies:
Advanced Breast Cancer Immunotherapy
Evaluating a novel combination of checkpoint inhibitors with targeted therapy for HER2-positive metastatic breast cancer.
Eligibility: Adults 18+ with confirmed HER2+ breast cancer
Heart Failure Gene Therapy
Testing an innovative gene therapy approach to restore cardiac function in patients with chronic heart failure.
Eligibility: Adults 40-75 with NYHA Class II-III heart failure
Early Alzheimer's Disease Treatment
Investigating a disease-modifying antibody therapy targeting amyloid plaques in early-stage Alzheimer's disease.
Eligibility: Adults 55-85 with mild cognitive impairment
Type 2 Diabetes Novel Therapy
Studying a new dual-action medication that improves both insulin sensitivity and beta cell function.
Eligibility: Adults 18+ with Type 2 diabetes, A1C 7.5-10%
Rheumatoid Arthritis Biologic
Evaluating a next-generation JAK inhibitor for patients with moderate-to-severe RA who have not responded to standard biologics.
Eligibility: Adults 18+ with active RA despite prior treatment
Severe Asthma Biologic Therapy
Testing a new biologic targeting multiple inflammatory pathways in patients with uncontrolled severe asthma.
Eligibility: Adults 18-65 with severe eosinophilic asthma
How to Participate
Participating in a clinical trial may provide access to promising new treatments while contributing to medical research. Follow these steps to get started:
Search for Trials
Use our Clinical Trials Search Tool or browse ClinicalTrials.gov for studies matching your condition.
Contact Research Team
Each trial listing includes contact information. Reach out to learn more about the study and express your interest.
Screening & Eligibility
Our team reviews your medical history to determine if you meet the specific inclusion criteria for the trial.
Informed Consent
Review detailed study information including purpose, procedures, risks, and benefits. Take time to ask questions.
Enrollment
If you choose to enroll, you'll undergo baseline evaluations and begin the study with regular monitoring visits.
Patient Safety & Protections
Your safety and wellbeing are our highest priorities. All clinical trials include comprehensive safeguards:
IRB Oversight
Every trial is reviewed and approved by our independent Institutional Review Board, including physicians, scientists, ethicists, and community members who ensure studies are ethical and scientifically sound.
Informed Consent
You'll receive detailed information about the study and provide voluntary written consent. Consent is ongoing - ask questions or withdraw at any time.
Safety Monitoring
Research teams closely monitor for adverse events. Independent Data Safety Monitoring Boards review safety data with authority to modify or stop studies if needed.
Your Rights
Understand all procedures, ask questions anytime, decline without affecting care, withdraw at any time, and have your information kept confidential.
Potential Benefits
- Access to new treatments not yet widely available
- Close monitoring by expert research teams
- Contribute to medical knowledge for future patients
- No cost for study-related care and treatments
- Possible compensation for time and travel
Potential Risks
- Unknown side effects from investigational treatments
- New treatment may not be effective
- Additional time commitment for study visits
- May require extra tests or procedures
- Possible randomization to standard treatment
Contact Our Research Team
Ready to learn more? Our clinical trials team is here to help you find the right study and answer your questions.
Patient Inquiries
Call: 555-0225
Physician Referrals
Call: 555-0250
We are committed to diversity, equity, and inclusion in clinical research. We actively recruit participants from diverse backgrounds and provide language assistance, transportation support, and flexible scheduling to reduce barriers to participation.