Surrogate Endpoints in FSGS
Projects
Portfolio:
Drugs
Barrier Type:
Clinical Trial Endpoints
Despite being associated with a relatively rapid decline in kidney function, there are no approved drugs and no accepted endpoints for registration of investigational products for FSGS. The focus of this project was to identify surrogate endpoints for use in clinical trials in FSGS patients, by reviewing published literature and analyzing data from cohorts/completed trials to identify candidate surrogates for endpoints, identifying risk factors for progression, critically assessing the candidate measures, and identifying gaps in the data.
A Kidney Health Initiative working group sought to identify potential short-term and intermediate candidate surrogate outcome measures by performing a critical review of the literature in FSGS, focused on prospective cohort studies and prospective interventional clinical trials; and analyzing data from available FSGS databases.
Publications & Resources
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- Drugs, Education and Resources
- Clinical Trial Endpoints, Drugs
- Clinical Trial Infrastructure, Drugs
- Devices, Patient Preferences
- Devices, Patient Preferences
- Patient and Family Engagement, Patient Preferences
Workgroup
- Laura H. Mariani – Renal Division, University of Michigan, Ann Arbor, Michigan
- Howard Trachtman – Department of Pediatrics/Nephrology, University of Michigan, Ann Arbor, Michigan
- Aliza Thompson – Center for Drug Evaluation and Research, US Food and Drug Administration, Silver Spring, Maryland
- Barbara S. Gillespie – Fortrea, Durham, North Carolina; Kidney Center, University of North Carolina, Chapel Hill, North Carolina
- Michelle Denburg – Children’s Hospital of Philadelphia, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania
- Ulysses Diva – Travere Therapeutics, San Diego, California
- Duvuru Geetha – School of Medicine, Johns Hopkins University, Baltimore, Maryland
- Peter J. Greasley – Research and Early Development, Cardiovascular, Renal and Metabolism, BioPharmaceuticals R&D, AstraZeneca, Gothenburg, Sweden
- Michelle A. Hladunewich – University of Toronto, Toronto, Ontario
- Robert B. Huizinga – Aurinia Pharmaceuticals, Victoria, British Columbia, Canada
- Jula K. Inrig – Travere Therapeutics, San Diego, California
- Radko Komers – Travere Therapeutics, San Diego, California
- Louis-Philippe Laurin – Division of Nephrology, Maisonneuve-Rosemont Hospital, Montreal, Quebec, Canada
- Dustin J. Little – Clinical Development, Late Cardiovascular, Renal and Metabolism, AstraZeneca, Gaithersburg, Maryland
- Patrick H. Nachman – University of Minnesota, Minneapolis, Minnesota
- Kimberly A. Smith – Center for Drug Evaluation and Research, US Food and Drug Administration, Silver Spring, Maryland
- Liron Walsh – Goldfinch Bio, Boston, Massachusetts
- Keisha L. Gibson – Kidney Center, University of North Carolina, Chapel Hill, North Carolina