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The SVM Center continues to work on ways to support the scleroderma community by increasing access to care and providing resources to connect. Learn more
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Fall 2022: New Programs and Research
The SVM center continues to work on ways to support our patient community by increasing access to care and providing resources to connect with other members of the scleroderma community.
Fast Track Appointments
Fast Track decreases the time a newly diagnosed person needs to wait for an appointment with a scleroderma specialist.  To get care quickly, complete our fast track form. If you are already under care, but would like to make a new appointment with a specialist, book online here.
The Buddy Program
The SVM Center introduced the Buddy program in late March. Since then we have received many inquiries on how to participate in the program. This program aims to connect those who struggle with scleroderma, vasculitis or myositis with those who can provide support, which can be particularly helpful for those recently diagnosed.
We hope to facilitate opportunities where participants can share their lived experiences, challenges, share coping strategies and insights regarding self-help strategies. Presently we are only inviting patients seen by HSS physicians to participate in the buddy program. If you wish to participate, please fill out a volunteer consent (to provide support), or if you're looking for support, fill out a support consent form.
Highlighted Studies
A Randomized, Double-Blind, Placebo-Controlled Study of Belimumab and Rituximab Combination Therapy for the Treatment of Diffuse Cutaneous Systemic Sclerosis: “BRISSc”
HSS is the sponsor for this single center, this double blinded, randomized, placebo-controlled trial assessing this anti-B-cell strategy in patients with early diffuse systemic sclerosis. Patients will be randomized in a 2-to-1 fashion to treatment with Rituximab 1000 mg every other week for two infusions followed by weekly belimumab (200 mg subcutaneously) or placebo infusions followed by weekly subcutaneous placebo injections. All patients in the trial will be treated with background mycophenolate meaning that both groups will be receiving active therapy with a very standard option for this disease. The duration of therapy in the trial will be one year. Additionally, patients will have the option to enroll into a one-year open label phase upon completion of the double blind trial. In this open label extension, participants will get weekly belimumab injections for a year.
Enrolling now! Contact: Liza Morales, 212.774.2561

A Randomized Double-Blind, Placebo Controlled Trial of Abatacept (CTLA4-Ig) in Giant Cell Arteritis (ABAGART)
This study is looking at the efficacy of abatacept, a medication for treating rheumatoid arthritis, in treating GCA. Patients will be randomized in a 1:1 ratio to receive either 125mg subcutaneous abatacept or placebo. All patients will receive glucocorticoids that will be tapered and discontinued by week 26. Patients who achieve and stay in remission will be treated with abatacept/placebo for 12 months. Patients who relapse during the study or do not achieve remission by month 3 will have the option to receive open label treatment with abatacept.
Enrolling now! Contact Aliza Bloostein, 212-774-2123
Please see the HSS Scleroderma, Vasculitis and Myositis Center site for our research, education and outreach efforts. For questions, email Elizabeth Soto-Cardona, MPH, Center Manager at sotoe@hss.edu.
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