Condition: Immunoglobulin A (IgA) Nephropathy · Sponsor: Purespring Therapeutics Limited
The purpose of the study is to evaluate safety, tolerability, and preliminary effectiveness following administration of PS-002 in adults with primary Immunoglobulin A (IgA) nephropathy. This will be a first-in-human study and will include participants at high risk of disease progression despite receiving current standard-of-care treatment. Participants will be monitored for up to one year after receiving PS-002 and invited to take part in a long-term follow-up study (total follow-up: 5 years).
This description comes directly from the study's public registry record.
Clinical Operations · +44 (0)20 3855 6324 · contact@purespringtx.com
Always discuss trial participation with your own doctor first.
| University of Miami Hospital | Miami, Florida, United States | Recruiting |
| The Johns Hopkins Hospital | Baltimore, Maryland, United States | Recruiting |
| Manchester University NHS Foundation Trust | Manchester, Greater Manchester, United Kingdom | Recruiting |
| Salford Royal Hospital, Northern Care Alliance NHS Foundation Trust | Manchester, Greater Manchester, United Kingdom | Recruiting |
| Leicester General Hospital | Leicester, Leicestershire, United Kingdom | Not Yet Recruiting |
| Nottingham University Hospitals NHS Trust | Nottingham, Nottinghamshire, United Kingdom | Recruiting |
| Southmead Hospital | Bristol, United Kingdom | Recruiting |
| Cardiff and Vale University Health Board | Cardiff, United Kingdom | Not Yet Recruiting |
| Royal Infirmary of Edinburgh Clinical Research Facility | Edinburgh, United Kingdom | Recruiting |
| The Royal London Hospital | London, United Kingdom | Recruiting |
Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.
We email about this public record only. Unsubscribe anytime with one click. Never medical advice.
This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.
Source record: clinicaltrials.gov/study/NCT07182227