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Deciding to participate in a clinical research study is a decision that takes careful thought and consideration. Your healthcare provider (HCP) can be an important partner as you ask questions, explore your options, and decide whether a clinical research study may be right for you.
If you are considering a clinical research study, your healthcare provider can help you understand how a clinical research study may fit into your overall care plan and personal health goals.
Your healthcare provider can help determine if a clinical research study is a good fit for you. They may be able to help you find a clinical research study based on your diagnosis.
They can explain the benefits and risks of participation, based on your own personal health needs.
They can help you understand clinical research study eligibility criteria.
They can offer advice about good questions to ask the clinical research study team.
Your healthcare provider also reviews your medical history and eligibility for a particular research study and may refer you to clinical research sites or specialists.
Your healthcare provider can also work alongside the clinical research study team to help support your ongoing care throughout the study.
It’s okay to bring questions, concerns, or even uncertainty into the conversation. When preparing to speak with your healthcare provider about participating in a clinical research study, it’s important that you feel informed, supported, and comfortable asking questions.
Clinical research studies can bring questions and uncertainty. Having an honest conversation with your healthcare team can help you better understand your options, what participation may involve, and whether a clinical research study may be right for your individual situation.
You and your caregiver should feel comfortable asking for information in simple, easy-to-understand language. Don’t hesitate to ask your healthcare provider to explain unfamiliar terms or provide additional educational resources.
Caregivers can play an important role by attending appointments, taking notes, helping ask questions, and providing emotional and practical support as decisions are made.
Understanding what participation involves—what to expect, timelines, what will be asked of you, and the possible outcomes associated with a clinical research study can help both patients and caregivers make informed decisions together.
Participation in a clinical research study is a personal choice and is always your decision. Your healthcare team can help determine whether a study is the right fit for your individual needs, goals, and treatment journey.
If you’re looking for guidance on the clinical research study process, your healthcare provider is a great place to start. They can help you understand your options, find clinical research studies that match your condition, and walk you through the process.
Caregivers and loved ones can play an important role in helping someone explore and navigate clinical research study options. Often, the support of a caregiver is what can make participation possible. If you are a caregiver, here are some ways you can be actively involved:
It is natural to have lots of questions when you or a loved one are considering a clinical research study. Taking time to learn about clinical research studies and speak openly with your healthcare provider can help you feel more informed and supported as you explore your options.
Those who do choose to participate become part of something larger than any single study: a collective effort to better understand diseases and open up new possibilities for treating them.
We sponsor clinical trials researching investigational therapies for people living with severe autoimmune diseases. Explore currently recruiting studies and learn more about clinical trial participation, eligibility requirements, and study locations
At argenx, every piece of the innovation story connects. See where it leads next.
Discover argenx-sponsored clinical trials currently underway.
Read about the criteria for submitting a pre-approval access request.
Read about the criteria for submitting a post-trial access request