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<h1>FDA-NIH Rare Disease Day</h1>
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Each year, we support this event to raise awareness about rare diseases, the people they affect, and partnerships that promote research and advance knowledge of new treatments.
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<h2 class="section-heading">FDA-NIH Rare Disease Day 2025</h2>
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--><div class="alert alert-info alert-dismissable d-inline-block" style="text-align:center;width:100%;">After much consideration, we are postponing FDA-NIH Rare Disease Day 2025 and will reschedule it to occur in the coming months. Rare Disease Day is important to all of us, and we want to make sure we can fully focus on the event to make it the best that it can be. We appreciate your understanding and thank you for your continued work raising awareness, developing cures and treatments, and offering resources that give hope to the millions of people in this country affected by rare diseases.</div><div class="contact-box"><h4>Contact</h4><p><a href="mailto:meera.shah@nih.gov"><strong>Meera Shah, M.P.H.</strong></a></p><hr><p><a href="/news-events/events/past-events?keys=%22Rare%20Disease%20Day%22"><strong>See past Rare Disease Day at NIH events</strong></a>.</p></div><p><a href="https://www.rarediseaseday.org/"><strong>Rare Disease Day®</strong></a> takes place worldwide, typically on or near the last day of February each year, to raise awareness among policymakers and the public about rare diseases and their impact on patients’ lives. This year, NCATS and the U.S. Food and Drug Administration (FDA), both agencies within the Department of Health and Human Services, will sponsor a shared Rare Disease Day event as part of this global observance. FDA-NIH Rare Disease Day aims to provide the rare disease community — patients, caregivers, families, patient advocate groups, researchers, clinicians, health care providers, and trainees/students — with information relevant to their lived experiences, including activities by FDA and NIH that promote research and product development for this population with unmet health needs.</p><p>The goals of FDA-NIH Rare Disease Day are to:</p><ul><li>Demonstrate the NIH and FDA commitment to advancing research and regulatory support for people affected by rare diseases.</li><li>Highlight NIH and FDA supported rare diseases research and the development of diagnostics and treatments.</li><li>Initiate a mutually beneficial dialogue among the rare diseases community.</li><li>Exchange the latest rare diseases information with stakeholders to advance research and therapeutic efforts.</li><li>Shine a spotlight on stories told by patients living with a rare disease, their caregivers, and their communities.</li></ul><p>FDA-NIH Rare Disease Day seeks to bring together a broad audience including patients, patient advocates, caregivers, health care providers, researchers, trainees, students, industry representatives, and government staff. </p><h2><!--<button class="buttons btn-1 mt-4" style="cursor:default;" tabindex="-1">
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</button>-->Event Details</h2><p>After much consideration, we are postponing FDA-NIH Rare Disease Day 2025, originally scheduled for Feb. 27-28. We will reschedule it to occur in the coming months. </p><h3>Partners in Planning</h3><p>Planning committee members include representatives from the following organizations:</p><ul><li>NIH: NCATS, Clinical Center, National Cancer Institute (NCI), National Eye Institute (NEI), National Institute on Alcohol Abuse and Alcoholism (NIAAA), National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS), National Institute of Neurological Disorders and Stroke (NINDS), Office of Autoimmune Disease Research (OADR-ORWH)</li><li>FDA: Office of Orphan Products Development (OOPD), Office of the Commissioner (OC), Center for Biologics Evaluation and Research (CBER), Center for Devices and Radiological Health (CDRH), Center for Drug Evaluation and Research (CDER), Oncology Center for Excellence (OCE)</li><li>Rare Diseases Clinical Research Network’s Coalition of Patient Advocacy Groups (RDCRN-CPAG)</li><li>The Children’s Inn at NIH</li><li>EveryLife Foundation for Rare Diseases</li><li>National Organization for Rare Disorders (NORD)</li><li>argenx</li></ul><h2>NCATS and Rare Diseases Research </h2><p>Progress in data science and an increased understanding of disease genetics lead experts to agree that more than an estimated 10,000 rare diseases are affecting millions of people in the United States. Rare diseases often are difficult to diagnose — it can take years. Even after an accurate diagnosis, treatment often is not available because approximately 5% of rare diseases have FDA-approved treatments. Research led by NCATS <a href="/news-events/news/nih-study-suggests-people-with-rare-diseases-face-significantly-higher-health-care-costs">suggests that nationwide medical costs</a> for individuals with rare diseases are likely as high as those faced by people with common diseases, such as cancer and heart failure.</p><p>NCATS is committed to using research to address the <a href="https://directorsblog.nih.gov/2023/01/24/a-rare-public-health-challenge/">public health crisis</a> presented by rare diseases. NCATS Director Joni Rutter recently <a href="/about/director/november-2024">wrote about using translational science</a> to make progress in rare diseases research, including in understanding rare disease biology and therapeutic targets and in building platform approaches that advance drug discovery and development.</p><p>All <a href="/about/divisions-and-offices">NCATS offices and divisions</a> advance the development of and access to more treatments, particularly for diseases with unmet needs. Our Division of Rare Diseases Research Innovation (DRDRI) facilitates and coordinates NIH-wide research activities, including the <a href="/research/research-activities/rdcrn">Rare Diseases Clinical Research Network</a>, the <a href="/research/research-activities/BGTC">Bespoke Gene Therapy Consortium</a>, and the NIH Common Fund’s <a href="https://commonfund.nih.gov/editing">Somatic Cell Genome Editing initiative</a>. DRDRI also works closely with NCATS’ Division of Preclinical Innovation (DPI) on programs and projects with potentially wide-ranging impacts in the rare disease space, including the <a href="https://pave-gt.ncats.nih.gov/">Platform Vector Gene Therapy</a> pilot project. In addition, DPI leads the <a href="/research/research-activities/TRND">NCATS Therapeutics for Rare and Neglected Diseases</a> program, which has enabled more than 40 promising rare disease treatments to enter into clinical trials. DPI is also co-leading a new partnership with other NIH institutes and centers to develop a <a href="/news-events/news/new-path-for-a-gene-therapy-trial-at-NIH-for-a-rare-metabolic-disease">proposed clinical trial for a rare metabolic disease</a>.</p><p>Learn more about NCATS’ <a href="/research/research-activities?research_topics%5b%5d=7">rare diseases research programs</a> and our <a href="/research/our-impact/our-impact-rare-diseases">impact on rare diseases</a>.</p>
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