Alicia Gerke, MD, MBA, assistant professor of Pulmonary, Critical Care, and Occupational Medicine, has been awarded a two-year, $300,000 grant from the Food and Drug Administration. Gerke will continue her research into sarcoidosis, a multi-system inflammatory disease with significant morbidity, including organ dysfunction and even death. Though it is relatively rare–affecting fewer than 185,000 people nationally each year–its natural history is unclear and has no known curative treatment. Randomized clinical trials of drugs have not resulted in proven efficacy most likely in part because half of patients with sarcoidosis resolve naturally, and because the currently used primary outcome measures may not be the best indicator of drug efficacy.
Under this grant, Gerke intends to establish a large, inclusive, retrospective cohort of sarcoidosis patients and define the natural history of sarcoidosis in this population, including their health care use and a longitudinal analysis of their clinical outcomes. Being able to separate the cohort further—into worsening, chronic, or improving categories—should provide important markers for predicting earlier which patients will worsen and thus possess the capacity to show the largest effect of an intervention. Identifying the most appropriate candidates and sample sizes for clinical drug trials should produce more reliable results in future studies. This information should also modify the current treatment guidelines, and ultimately, lesson disease severity and protect organ function.
Is there a way to be part of this study?
Hi, Sarah, thank you for the question and your interest. Though the results of Dr. Gerke’s study may aid future drug trials, this particular study will not enroll subjects.
I was going to ask the same question. I am very eager for treatment and a cure. This illness defiantly has caused many issues in my day to day life.
How s she going to identify patients to have a large cohort to work with?
Hi, Marlene, thank you for your question. Dr. Gerke informs us that this particular study will use a cohort from the Kaiser Permanente database, which includes about 1000 people.
She is also the director of the FSR-SARC national registry through the Sarcoidosis Foundation ( https://www.stopsarcoidosis.org/research/fsr-sarc/ ), and she has been building a web-based registry for people with sarcoidosis, hosted here at the University of Iowa. (For more information about that study, go here: https://www.sarcoidstudy.org/Sarcoidosis/index.html)
Hi. I was wondering if I would be a candidate as I am currently in remission from Neuro Sarcoidosis.
Are you interested in patients in remission?
Hi, Lori, that is terrific news about your remission. We would invite you to explore both of the national registry options linked in our response above. Thank you!
[…] a leader in the effort to build a digital registry of individuals with sarcoidosis, recently received an R01 from the FDA to better categorize individuals with this disease, planting seeds for future research studies. I […]