new clinical trial opportunity

Sjögren’s disease can be difficult, but going through it alone can be even more challenging. It’s time to be seen.

At the Global Healthy Living Foundation, we are committed to connecting you with opportunities to participate in clinical research that has the potential to improve treatment outcomes for patients like you in the future. The DAFFODIL trial is evaluating an investigational medicine for adults with Sjörgen’s disease. 

YOU MAY QUALIFY FOR THIS TRIAL IF YOU:

Have been diagnosed with Sjögren's disease

Are at least 18 years old

About the DAFFODIL Trial

The DAFFODIL Trial is evaluating the efficacy and safety of an investigational medicine for moderate to severe Sjögren’s disease. 

The trial involves up to 30 visits over the course of up to about 3 years. Visits will take place once a week for the first month and about once a month after that. Participants are randomly assigned to 1 of 2 groups and will receive either the investigational medicine or a placebo, administered as an injection under the skin (subcutaneous). A placebo is a substance that looks like the investigational medicine but contains no active ingredients.

For every 5 participants who enroll, 3 will be assigned to the group receiving the investigational medicine. After the first 48 weeks of the trials, eligible participants can move into a long-term extension period, during which all participants will receive the investigational medicine for 96 weeks. Participants may be able to continue their current Sjögren’s disease-related medications. The trial doctor or staff will provide more information about this.

You can play a role in helping researchers evaluate investigational medications for Sjögren’s’ disease by participating in this trial. Participants may be reimbursed for trial-required travel and expenses.

You may be able to participate in the DAFFODIL Trial if you:

What Are Investigational Trials?

Investigational trials help researchers learn about the safety and efficacy of investigational medicines before they can be approved for public use. These studies play a key role in advancing treatment options.

Diversity in research is important. This trial welcomes participants of all backgrounds affected by Sjögren’s disease, including differences in race, gender, age, location, income, and disability status.

What Is Informed Consent?

Informed consent is an important process that happens before joining a clinical trial. It ensures that you understand the study, including its potential risks and benefits, so you can decide whether to participate.

Before you agree to join, the trial doctor or staff will:

  • Explain the details of the study.
  • Answer any questions you may have.
  • Provide written and verbal information about the trial.

If you choose to participate, you will sign an informed consent form (ICF) to confirm that you:

  • Understand the study.
  • Know your rights as a participant.
  • Are volunteering by choice.

You can always ask more questions—even after signing.

Stay Informed on Upcoming Clinical Trial Opportunities

Even if you’re not ready to be a part of a clinical trial, or you aren’t eligible for this one, you can still stay informed on upcoming clinical trial opportunities by joining our email list. 

Hidden

Next Steps: Sync an Email Add-On

To get the most out of your form, we suggest that you sync this form with an email add-on. To learn more about your email add-on options, visit the following page (https://www.gravityforms.com/the-8-best-email-plugins-for-wordpress-in-2020/). Important: Delete this tip before you publish the form.
Name(Required)
Privacy(Required)
Back To Top