Safety Study of of Intravenous CCL2-LPM in Patients With IgA Nephropathy
A Dose-Escalating Phase I Study to Evaluate the Safety, Pharmacokinetics and Pharmacodynamics of Intravenous OPL-CCL2-LPM in Patients With IgA Nephropathy
Sponsor: Osprey Pharmaceuticals USA, Inc.
Terminated
Study terminated due to resources and slow enrollment; not due to safety
This PHASE1 trial investigates IGA Nephropathy and Proteinuria and is currently terminated or withdrawn. Osprey Pharmaceuticals USA, Inc. leads this study, which shows 5 recorded versions since 2009 — indicating limited longitudinal coverage. The change history captured here reflects the iterative nature of clinical trial conduct.
Status Flow
Change History
5 versions recorded-
Sep 2024 — Present [monthly]
Terminated PHASE1
-
Jul 2024 — Sep 2024 [monthly]
Terminated PHASE1
-
Jan 2021 — Jul 2024 [monthly]
Terminated PHASE1
-
Jun 2018 — Jan 2021 [monthly]
Terminated PHASE1
-
Jan 2017 — Jun 2018 [monthly]
Terminated PHASE1
First recorded
Mar 2009
Trial started
Per CT.gov start date — pre-dates our first snapshot
Eligibility Summary
No eligibility information available.
Contact Information
- Osprey Pharmaceuticals USA, Inc.
For direct contact, visit the study record on ClinicalTrials.gov .