FAQs

PRX RESEARCH

Frequently Asked Questions

Have questions about clinical trials? We have answers. Learn more about the process and how you can contribute to medical research.

Participating in a clinical trial offers numerous benefits:

  • Access to innovative treatments and cutting-edge therapies.
  • Personalized care from top healthcare providers.
  • Contributing to medical advancements that benefit everyone.
  • Potential for improved health outcomes.
  • Opportunity to learn more about your condition and its management.

Yes, your participation in our clinical trials is strictly confidential. All information gathered during the study, including your medical history and personal details, is protected by state and federal regulations. We will not disclose any of your information without your explicit consent.

In most of our clinical trials, you will receive compensation for your time, travel expenses, and any other study-related costs. The specific reimbursement amount varies depending on the study and will be discussed in detail during the informed consent process.

Your safety is our top priority. We have several safeguards in place to protect you during your participation in a clinical trial:

  • Thorough review of preclinical data to ensure safety and efficacy.
  • Strict adherence to study protocols and guidelines.
  • Comprehensive informed consent process to ensure you understand the risks and benefits.
  • Continuous monitoring of your health throughout the study.
  • Access to our research team for any questions or concerns.

Our research team will carefully assess your eligibility to ensure the trial is suitable for you. Researchers use specific criteria to determine eligibility for clinical trials. These criteria include:

  • Inclusion criteria: Characteristics that all participants must have to join the trial (e.g., specific diagnosis, age range). 
  • Exclusion criteria: Characteristics that may disqualify someone from participating (e.g., certain medical conditions, medications).

The duration of a clinical trial varies depending on the research objectives and the specific treatment being studied. You will receive detailed information about the study timeline during the informed consent process.

Our experienced medical doctors provide all medical assessments, diagnoses, and advice during your participation in a clinical trial. Our clinical trial team is available to answer any questions you may have, but only our doctors can provide medical guidance.

You can expect the following from our clinical trial team:

  • A comprehensive explanation of the study and its procedures.
  • Clear and informative informed consent process.
  • Thorough evaluation of your health and condition.
  • Ongoing support and communication throughout the study.
  • Access to the study doctor for questions or concerns.
Many clinical trials use a randomized approach to determine which treatment or intervention you receive. This ensures fairness and unbiased results. In some cases, you may receive a placebo, which is an inactive substance that looks like the study medication. The specific intervention you receive will be determined through the randomization process.
Some trials compare drugs or doses to learn which is most effective. The study participants are randomly assigned to one drug and do not know which medication they are taking.
Participation in our clinical trials is typically free of charge. All medical care, tests, and medications related to the study are provided at no cost to you. In many cases, you may also be eligible for reimbursement for your time, travel, and other expenses.
All medical care, including tests and medications related to the clinical trials, is provided at no charge.

You have the right to leave a clinical trial at any time, for any reason, without penalty. Your participation is entirely voluntary. If you decide to withdraw from a study, we encourage you to inform the research team so they can provide any necessary follow-up care.