Multiple Sclerosis Clinical Trials in New York

View 26 new treatments for Multiple Sclerosis in New York, NY near me. Every day, Power helps hundreds of Multiple Sclerosis patients connect with leading medical research.
View 27 trials in New York
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Frexalimab for Multiple Sclerosis

Sanofi Clinic, New York + 3 more

The purpose of this randomized, double-blind, placebo-controlled, parallel group study is to determine the efficacy of frexalimab in delaying the disability progression and the safety up to approximately 51 months administration of study intervention compared to placebo in male and female participants with nrSPMS (aged 18 to 60 years at the time of enrollment). People diagnosed with nrSPMS are eligible for enrollment as long as they meet all the inclusion criteria and none of the exclusion criteria. Study details include: This event-driven study will have variable duration ranging from approximately 27 to 51 months. The study intervention duration will vary ranging from approximately 27 to 51 months. The number of scheduled visits will be up to 27 (including 3 follow-up visits) with a visit frequency of every month for the first 6 months and then every 3 months.Show More

Verified

Recruiting
Phase 3
Est. 6 - 12 Weeks
Unregistered Study Lead
Research Team

Ocrelizumab Exposure During Pregnancy for Multiple Sclerosis

Hoffmann-La Roche Clinic, New York + 1 more

This trial will study how a medication for multiple sclerosis transfers from pregnant women to their babies. The focus is on women who took the medication around the time of pregnancy. Researchers will look at how this affects the baby's immune cells and overall health.Show More
Waitlist

No Placebo Trial

Phase 4
Est. 4 - 6 Weeks
Clinical Trials
Study Director

Ocrelizumab for Multiple Sclerosis

Research Clinic, New York + 3 more

This trial is testing if patients with early relapsing multiple sclerosis can stop taking Ocrelizumab after initial treatment without their disease getting worse. Ocrelizumab is a medication given through an IV that helps manage multiple sclerosis by reducing harmful immune cells. The study will monitor patients for new disease activity over several years.Show More
Recruiting
Phase 4
Est. 3 - 6 Weeks
Amit Bar-Or, M.D.
Study Chair

Ofatumumab for Early Relapsing-Remitting Multiple Sclerosis

Novartis Clinic, North Massapequa + 1 more

This study will evaluate the impact of ofatumumab in Relapsing Remitting Multiple Sclerosis (RRMS) participants that are very early in the course of their disease using clinical and magnetic resonance imaging (MRI) outcomes. The study will also assess changes in disease using monitoring techniques including digital biometric device use, biomarker analysis and non-conventional MRI. Select outcomes in the ofatumumab treated group will be compared to a group of Healthy participants to determine if there are similarities between the groups after the patients with MS undergo treatment with ofatumumab.Show More
Waitlist

No Placebo Trial

Phase 4
Est. 6 - 12 Weeks
Unregistered Study Lead
Research Team

High-Dose Ocrelizumab for Multiple Sclerosis

Hoffmann-La Roche Clinic, New York + 2 more

This trial is testing if a higher dose of ocrelizumab given through an IV drip is more effective and safe for patients with Primary Progressive Multiple Sclerosis (PPMS). The drug works by reducing harmful immune cells to potentially slow down the disease. Ocrelizumab is the first drug approved for treating both relapsing and primary progressive forms of multiple sclerosis.Show More
Waitlist

No Placebo Trial

Phase 3
Est. 4 - 6 Weeks
Clinical Trials
Study Director

Ozanimod for Multiple Sclerosis

Celgene Clinic, New York + 6 more

This is a multicenter, longitudinal, single-arm, open-label study to describe the change from baseline in cognitive processing speed, measured by the SDMT, in subjects with RMS treated with ozanimod HCl 1 mg at 3 years. All subjects will receive orally administered ozanimod HCl 1 mg. The primary efficacy endpoint is the proportion of subjects with a clinically meaningful increase in raw score of ≥ 4 points or 10% from baseline (improved). The treatment period is 36 months. For all subjects who finish the subject and for those who discontinue, there will be a 30-day (± 15 days) and a 90-day (± 10 days) Safety Follow-up Visit. There is no planned protocol extension following the end of the study. Approximately 250 subjects with RMS will be recruited for this study. Subjects with RMS will be enrolled in this study if they have received ≤ 1 DMT, have an EDSS ≤ 3.5, and have been diagnosed with RMS within 5 years of study entry. The Investigator will be responsible for the overall conduct of the study at the site, confirmation of subject eligibility, routine study subject clinical management including for MS relapses, and management of AEs.Show More
Waitlist

No Placebo Trial

Phase 3
Est. 6 - 12 Weeks
Bristol-Myers Squibb
Study Director

Ofatumumab for Multiple Sclerosis

Novartis Clinic, Woodmere + 2 more

Open-label study to evaluate the effectiveness of treatment with ofatumumab in subjects transitioning from any fumarate-based RMS approved therapy or fingolimod due to breakthrough disease.Show More
Waitlist

No Placebo Trial

Phase 3
Est. 3 - 6 Weeks
Unregistered Study Lead
Research Team

Ocrelizumab vs Fingolimod for Pediatric Multiple Sclerosis

Hoffmann-La Roche Clinic, New York + 3 more

This double-blind, double-dummy study will evaluate the safety and efficacy of ocrelizumab compared with fingolimod in children and adolescents with RRMS aged between 10 and \< 18 years over a flexible duration. The double-blind period will last until after the last participant randomized has completed 24 weeks.Show More
Waitlist
Phase 3
Est. 6 - 12 Weeks
Clinical Trials
Study Director

Ublituximab for Multiple Sclerosis

TG Clinic, New York + 1 more

The primary purpose of this phase 3b study is to assess the efficacy of a modified regimen of ublituximab as measured by T1 Gadolinium (Gd)-enhancing lesions.
Recruiting

No Placebo Trial

Phase 3
Est. 4 - 6 Weeks
Unregistered Study Lead
Research Team

Tolebrutinib for Primary Progressive Multiple Sclerosis

Sanofi Clinic, Stony Brook + 7 more

Primary Objective: To determine the efficacy of SAR442168 compared to placebo in delaying disability progression in primary progressive multiple sclerosis (PPMS) Secondary Objectives: To evaluate efficacy of SAR442168 compared to placebo on clinical endpoints, magnetic resonance imaging (MRI) lesions, cognitive performance, physical function, and quality of life To evaluate safety and tolerability of SAR442168 To evaluate population pharmacokinetics (PK) of SAR442168 in PPMS and its relationship to efficacy and safety To evaluate pharmacodynamics of SAR442168Show More
Waitlist
Phase 3
Est. 6 - 12 Weeks
Clinical Sciences & Operations
Study Director
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Frequently Asked Questions

How much do multiple sclerosis clinical trials pay?

Each trial will compensate patients a different amount, but $50-100 for each visit is a fairly common range. Further, most trials will cover the costs of an Uber to-and-from the clinic. Factors that can affect compensation include the phase of the trial, the length of the trial, the frequency of visits, and the specific condition being studied.

Do I need to be insured to participate in a medical study?

Clinical trials are almost always free to participants, and so do not require insurance. The only exception here are trials focused on Cancer, because only a small part of the typical treatment plan is actually experimental. For these cancer trials, participants typically need insurance to cover all the non-experimental components.

How do multiple sclerosis clinical trials work?

After a researcher reviews your profile, they may choose to invite you in to a screening appointment, where they'll determine if you meet 100% of the eligibility requirements. If you do, you'll typical be sorted into one of the treatment groups, and will receive your study drug. For some trials, there is a chance you'll receive a placebo. Across multiple sclerosis trials in New York, 42% of clinical trials have a placebo. Typically you'll be required to check-in with the clinic every month or two. The average trial length in this city for multiple sclerosis patients is 6 Months.

What does the "phase" of a clinical trial mean?

The phase of a trial reveals what stage the drug is in getting approval for a specific condition. Phase 3 trials are in the final step before approval. The drug already has data showing both safety and effectiveness. Phase 2 trials are those where the drug has some data showing safety in humans, but where effectiveness has typically only been shown in animals and non-human experiments. Phase 1 trials are the trials where we don't have safety data in humans. As a general rule, phase 3 trials are more promising than phase 2, and phase 2 trials are more promising than phase 1.

Where in New York is research being conducted for multiple sclerosis?

Prominent hospitals in New York conducting multiple sclerosis clinical trials include Columbia University Irving Medical Center and Icahn School of Medicine at Mount Sinai. Approximately 11 trials are ongoing as of 2024, primarily in the northern part of Manhattan.

What promising new drugs are being tested?

In New York, multiple sclerosis research is exploring treatments like Monoclonal Antibodies and Stem Cell Transplants. Notable specific interventions being studied include Ocrelizumab, Autologous Hematopoietic Stem Cell Transplantation, and Fingolimod.