Clinical Trials
Visit clinicaltrials.gov, a database of privately and publicly funded clinical studies conducted around the world. Before participating in a study, talk to your health care provider and learn about the risks and potential benefits.
Current Opportunities:
The 4WARD Study: A CN Study is Now Enrolling
A global clinical research study called the 4WARD Study is now enrolling people living with chronic neutropenia (CN).
The 4WARD Study is a Phase 3 study, or clinical trial. The goal of the 4WARD Study is to learn more about the oral investigative study medicine, mavorixafor. The study will evaluate if mavorixafor may increase neutrophil cell counts, may decrease the chance of getting infections and is safe and well tolerated.
You may be eligible to join the study if you:
- Are age 12 and over
- Are diagnosed with chronic neutropenia (including congenital, acquired primary autoimmune, and idiopathic chronic neutropenia)
- Are taking or not taking any treatment for your chronic neutropenia, including granulocyte colony-stimulating factor (G-CSF)
- Meet other study requirements. Talk to your doctor to find out if this study is an option for you.
Chronic neutropenia is a disease with few treatment options. More treatment options are needed. By volunteering to join a study, you can help researchers learn more about chronic neutropenia. Visit 4WARDStudy.com to learn more.
Testimonial
Patient Stories & Experiences
“My first NNN conference was 2018. I spent years before that almost in denial of my condition, feeling very lonely. I always thought the NNN conference was just for families with children not adults with neutropenia. As I grew older I felt I needed to have more of a connection to neutropenia and wanted to meet others with it and doctors that actually KNEW about what I had! That’s exactly what I got!
- Vanessa
“Having a rare disease has been a challenging and rewarding experience that has giving me the opportunity to meet some amazing people. It has taught me to never stop learning! I have an amazing team of doctors that have worked hard to help me life the safest best life possible.”
- Jacqueline
“My first NNN conference was 2018. I spent years before that almost in denial of my condition, feeling very lonely. I always thought the NNN conference was just for families with children not adults with neutropenia. As I grew older I felt I needed to have more of a connection to neutropenia and wanted to meet others with it and doctors that actually KNEW about what I had! That’s exactly what I got!
- Vanessa
“Having a rare disease has been a challenging and rewarding experience that has giving me the opportunity to meet some amazing people. It has taught me to never stop learning! I have an amazing team of doctors that have worked hard to help me life the safest best life possible.”