Looking to get more out of your MDS treatment?

You may be eligible to participate in a study evaluating a new drug for individuals with higher-risk MDS, which aims to enhance the effectiveness of standard chemotherapy treatment.

See If You May Qualify

Can I Participate?

You may be able to participate in this MDS clinical study if you:

Are 18 years of age or older

Have been diagnosed with higher-risk MDS

Higher-risk includes:

  • Intermediate-
  • High-
  • Very high-risk MDS
Or

Have been diagnosed with MDS and previously treated with a hypomethylating agent such as Azacitidine (Vidaza) or Decitabine (Dacogen or Inqovi)

You do not qualify if you have:

Received a stem cell transplant from a donor to replace your bone marrow in the last six months
Have been informed that you have poor kidney or liver function

What You May Receive

By enrolling in this Phase I/II study, you may receive:

Access to physicians with extensive experience in managing MDS

Study drug at no cost to you

Travel, lodging, and meal reimbursements for study visits

What Is the Purpose of This Study?

The purpose of this MDS study is to evaluate a study drug that may help improve the immune response and overall treatment outcomes for patients with MDS when combined with standard chemotherapy (azacitidine).

Why Join This MDS Study?

By enrolling in this Phase I/II study, you may participate in clinical research looking to determine if the study drug can enhance your immune system’s response to standard chemotherapy (azacitidine) and reduce your cancer.

You will be seen by MDS experts and help advance research about treatment for MDS.  

What To Expect

1

See If You May Qualify

Click here to see if you may qualify for the study. Then, select a date and time for a short phone call with a PatientWing representative. Applying is voluntary and doesn’t require commitment to study participation.

2

Phone Call with PatientWing

If initially eligible, a PatientWing representative will call you to discuss the study, additional eligibility criteria, and answer your questions.  If you are still eligible at the end of this screening call, you’ll be connected to a member of the team at a study site location.

3

Screening at the Study Site

The team at a participating study site will determine if you are eligible to participate in the study by reviewing your medical records. You will have the opportunity to ask questions and make an informed decision about your participation.

4

Study

This study will consist of weekly or biweekly study visits. On average, patients participate in the study for 6-10 months, but you may continue treatment longer based on the opinion of the study doctor.

For Loved Ones

The family, friends, and healthcare teams of those with MDS play an important role in supporting their loved one's health and wellbeing. If  you are a caregiver of someone with MDS, you can  apply  for the study on their behalf by clicking  the button below.

You have the option to either enter the patient's information or your own contact information.  Please speak with the patient prior to entering their information.

Frequently Asked Questions

How do I get started?
Click See If You May Qualify and enter your information to express interest in the study.
Where is the study conducted?
We have sites located throughout the US and will help you identify the best site for you to visit.
Has the study drug been tested before?
Yes, the study drug was tested in over 200 patients with different types of cancer and was shown to be well tolerated.
Is there a chance I will receive a placebo?
No, everyone enrolled in this study will be given the study drug. There is no placebo.
Is there any cost for me to participate?
There is no cost to participate in this clinical study. The study sponsor will pay for the costs of the study drug and any tests or procedures needed. You can talk to the study site staff about travel arrangements and expense related reimbursements.
What type of MDS must I have to participate?
This study is for adults with intermediate- to very high-risk MDS. If you have lower-risk MDS and were previously treated with a hypomethylating agent, such as Azacitidine (Vidaza) or Decitabine (Dacogen or Inqovi), you may still apply.

About Study Team

Faron Pharmaceuticals

Faron Pharmaceuticals is a European clinical-stage biopharmaceutical company based in Finland that is developing novel treatments for cancer. The company is dedicated to developing therapies that make a real difference in patients’ lives, while striving to understand and enhance the entire patient experience.

PatientWing

Our mission to bring better treatments to more people faster starts with you. We help sponsors find patients to participate in their clinical studies. With our focus on rare diseases and expertise in navigating the enrollment process, we're here for you every step of the way.

Have Questions?

Call, email us, or fill out the form. We’re here to help.

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