Is NCT07190196 recruiting in Fayetteville, GA?

Yes, NCT07190196 is currently recruiting participants at its Fayetteville, GA location. This immunoglobulin g4 related disease clinical trial is actively enrolling qualified participants.

Is participation in this Fayetteville clinical trial free?

Yes, all study-related care is provided at no cost to qualified participants. Many studies also offer compensation for time and travel expenses.

Immunoglobulin G4 Related Disease Clinical Trial in Fayetteville, GA

Q: How do I join the immunoglobulin g4 related disease clinical trial in Fayetteville?

To join this clinical trial in Fayetteville, complete the eligibility form on this page. A study coordinator will contact you to discuss next steps and determine if you qualify.

About This Immunoglobulin G4 Related Disease Study in Fayetteville

This is a Phase 3, parallel group, 2-arm, randomized, double blind, placebo-controlled, 52-week treatment study to assess the efficacy and safety of rilzabrutinib as a treatment for adult patients with active IgG4-RD. The purpose of this study is to measure time to IgG4-RD clinical disease flare, and other relevant efficacy endpoints including flare-free rate, control of IgG4-RD disease activity, use of GC rescue and safety parameters such as treatment-emergent adverse events, clinical laboratory values and electrocardiograms (ECG) in participants aged 18 years and above, diagnosed with IgG4-RD and treated with rilzabrutinib tablets over a 52-week placebo-controlled period. Study details include: The study duration will be up to 60 weeks, including a 4 to 6-week screening period, a 52-week double blind treatment period, and 2 weeks of follow up (plus an optional OLE of 108 weeks). The number of visits will be 16 (plus an optional 9 visits during the OLE).

Sponsor: Sanofi

Who Can Participate

Inclusion Criteria

Participants must have an adjudicated clinical diagnosis of IgG4-RD

Participants meeting Step 1 Entry criteria of 2019 ACR/EULAR classification criteria for IgG4-RD and Total inclusion points are ≥20

Participants with active disease at screening in at least one organ system, excluding lymph nodes, as an IgG4-RD Responder Index total activity score ≥ 2

Participants with history or current involvement of at least 1 organ/site (excluding lymph nodes) affected with IgG4-RD.

Participants with active IgG4-RD controlled for at least 2 weeks while on a stable dose of GC.

Participants willing to taper off GC after starting IMP.

Participants willing and able to participate in repeated study protocol mandated or clinically indicated imaging procedures to assess IgG4-RD such as computed tomography (CT), magnetic resonance imaging (MRI), positron emission tomography (PET), or ultrasound.

Participants who have an up-to-date vaccination status as per local guidelines. The last dose of live vaccines should be received at least 30 days before Day 1.

Contraceptive use by men and women should be consistent with local regulations regarding the methods of contraception for those participating in clinical studies.

Exclusion Criteria

Meet any Step 2 Exclusion criteria from the 2019 ACR/EULAR classification criteria for IgG4-RD.

History of retroperitoneal fibrosis, sclerosing mesenteritis, fibrosing mediastinitis, or other overwhelmingly fibrotic expression of IgG4-RD that is the sole disease manifestation.

Active malignancy or history of malignancy within 5 years before Day 1, except completely treated in situ carcinoma of the cervix, completely treated, and resolved nonmetastatic squamous or basal cell carcinoma of the skin.

Known or suspected immunodeficiency, including history of invasive opportunistic infections (eg, histoplasmosis, listeriosis, coccidioidomycosis, pneumocystosis, and aspergillosis) despite infection resolution, or otherwise recurrent infections of abnormal frequency or prolonged duration suggesting an immune compromised status, as judged by the Investigator.

History of serious infections with the potential for recurrence (as judged by the Investigator), with less than 4 weeks interval between resolution of serious infection and first dose of study drug, or currently active moderate to severe infection at Screening (Grade 2 or higher).

Current or chronic history of liver disease unrelated to IgG4-RD.

Refractory nausea and vomiting, malabsorption, external biliary shunt, bariatric surgery, or significant bowel resection that would preclude adequate rilzabrutinib/placebo absorption.

History of solid organ transplant.

Planned major surgical procedure during the participation in this study.

History of drug abuse within the previous 12 months.

Alcoholism or excessive alcohol use, defined as regular consumption of more than approximately 3 standard drinks per day.

Prior participation in any rilzabrutinib studies or other BTK inhibitor studies.

History of treatment with an investigational drug within 6 months or 5 half-lives of the investigational drug, whichever is longer.

Laboratory abnormalities at the screening visit identified by the central laboratory The above information is not intended to contain all considerations relevant to a participant's potential participation in a clinical trial.

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Fayetteville?

Yes, this clinical trial (NCT07190196) has an active research site in Fayetteville, GA that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Immunoglobulin G4 Related Disease Treatment Options in Fayetteville, GA

If you're searching for immunoglobulin g4 related disease treatment options in Fayetteville, GA, this clinical trial (NCT07190196) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Fayetteville research site is actively enrolling participants for this clinical trial. You'll receive care from experienced immunoglobulin g4 related disease specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all immunoglobulin g4 related disease clinical trials near you to find additional studies recruiting in your area.

Immunoglobulin G4 Related Disease Clinical Trial in Fayetteville, GA

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