For Patients

Clinical Trials Are
About You.

Every clinical trial we support exists to help patients like you access potentially life-changing therapies. We are committed to making the trial experience safe, supportive, and transparent.

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Understanding Clinical Trials

What Is a Clinical Trial?

A clinical trial is a research study conducted with human volunteers to evaluate the safety and effectiveness of new medical treatments, devices, or interventions. Clinical trials are the primary way that researchers determine whether new treatments are safe and effective for patients.

Before any new treatment reaches patients, it must go through a series of carefully designed clinical trials. These trials are conducted under strict ethical and regulatory oversight to protect participants and ensure the integrity of the data collected.

Participating in a clinical trial can give you access to new treatments before they are widely available, contribute to medical knowledge that benefits future patients, and receive close medical monitoring throughout the study.

Patient care

Trial Phases

Understanding Trial Phases

Clinical trials are conducted in phases, each with a specific purpose and number of participants.

Phase I

Safety Testing

First-in-human studies with a small group (20–100 participants) to evaluate safety, dosage, and side effects.

Phase II

Efficacy Testing

Larger studies (100–300 participants) to evaluate whether the treatment works and to further assess safety.

Phase III

Confirmatory Testing

Large-scale studies (1,000–3,000+ participants) comparing the new treatment to existing standard of care.

Phase IV

Post-Market Surveillance

Studies conducted after approval to monitor long-term safety and effectiveness in the general population.

Patient Rights

Your Rights as a Trial Participant

Participation in a clinical trial is always voluntary. You have important rights that are protected by law and ethical guidelines.

Informed Consent: You have the right to receive complete information about the trial, including its purpose, procedures, risks, and benefits, before deciding to participate.
Voluntary Participation: You can withdraw from a trial at any time without penalty or loss of benefits to which you are otherwise entitled.
Privacy Protection: Your personal and medical information is kept strictly confidential and protected under applicable data protection laws.
Access to Information: You have the right to ask questions about the trial at any time and to receive answers in a language you understand.
Continued Medical Care: Withdrawing from a trial will not affect your access to standard medical care from your regular healthcare provider.

FAQ

Patient FAQ

Each trial has specific eligibility criteria (inclusion and exclusion criteria) based on factors such as age, medical history, current health status, and prior treatments. The best way to determine your eligibility is to speak with your doctor or contact the research site directly. We can help connect you with the appropriate site for any of our open trials.
Many trials use a randomized design where participants are assigned to either the treatment group or a control group (which may receive a placebo or standard of care). You will be informed about the trial design before you consent to participate. In some trials, all participants receive the experimental treatment.
In most cases, the investigational treatment and study-related procedures are provided at no cost to participants. Some trials also provide compensation for travel and time. Specific details about costs and compensation will be clearly explained during the informed consent process.
You can browse our current open trials on the Open Trials page. You can also speak with your doctor, who may be aware of trials appropriate for your condition. Additionally, public registries like ClinicalTrials.gov list trials worldwide.

Ready to Explore Your Options?

Browse our open trials or contact us to learn more about how you can participate in advancing medical research.

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