Last reviewed · How we verify
NCT05441826
Efficacy and Safety of VB119 in Subjects With Minimal Change Disease (MCD) and Focal Segmental Glomerulosclerosis (FSGS)
Phase 2 trial testing VB119 in Minimal Change Disease in 1 participant. Terminated before completion.
3 May 2023
Quick facts
| Lead sponsor | Tenet Medicines |
|---|---|
| Phase | Phase 2 |
| Status | Terminated |
| Study type | INTERVENTIONAL |
| Allocation | na |
| Design | single group |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 1 |
| Start date | 3 May 2022 |
| Primary completion | 3 May 2023 |
| Estimated completion | 12 October 2023 |
| Sites | 1 location across United States |
Drugs / interventions tested
- VB119 — full drug profile →
Conditions studied
- Minimal Change Disease — all drugs for Minimal Change Disease →
- Focal Segmental Glomerulosclerosis — all drugs for Focal Segmental Glomerulosclerosis →
Sponsor
Tenet Medicines — full company profile →
Who can join
18 and older, any sex, with Minimal Change Disease or Focal Segmental Glomerulosclerosis. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Phase 2, multi-center, proof-of-concept study to evaluate the safety and efficacy of VB119 on the maintenance of remission and duration of response in adults with primary MCD or primary FSGS who previously responded to steroid therapy.
Publications & conference data
3 peer-reviewed publications reference this trial (live from Europe PMC):
-
Management of adult patients with podocytopathies: an update from the ERA Immunonephrology Working Group.
Mirioglu S, Daniel-Fischer L, Berke I, Ahmad SH, et al · · 2024 · cited 23× · PMID 38341276 · DOI 10.1093/ndt/gfae025 -
Novel Treatment Paradigms: Focal Segmental Glomerulosclerosis.
de Cos M, Meliambro K, Campbell KN. · · 2023 · cited 22× · PMID 36644367 · DOI 10.1016/j.ekir.2022.10.004 -
Advances in Focal Segmental Glomerulosclerosis Treatment From the Perspective of the Newest Mechanisms of Podocyte Injury.
Zhu Y, Xu G. · · 2025 · cited 2× · PMID 39935575 · DOI 10.2147/dddt.s498457
Verify or expand the search:
- PubMed search for NCT05441826
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other trials of VB119
Trials testing the same drug.
- NCT04652570 — Efficacy and Safety of VB119 in Subjects With Membranous Nephropathy · Phase 1, PHASE2 · terminated
Other recruiting trials for Minimal Change Disease
Currently open trials in the same condition.
- NCT05588063 — taVNS for FRNS in Children · NA · recruiting
- NCT05583942 — A Pilot Trial of taVNS for SRNS in Children (kidNEY-VNS) · NA · recruiting
- NCT04571658 — NEPTUNE Match Study · NA · recruiting
- NCT05505500 — Interview Study of Adult and Child Patients and Parents of Children With Swelling Due to Nephrotic Syndrome. · recruiting
- NCT05003986 — Study of Sparsentan Treatment in Pediatrics With Proteinuric Glomerular Diseases · Phase 2 · recruiting
Other Tenet Medicines trials
Trials by the same sponsor.
- NCT04652570 — Efficacy and Safety of VB119 in Subjects With Membranous Nephropathy · Phase 1, PHASE2 · terminated
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT05441826 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 9 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Tenet Medicines
- Last refreshed: 22 April 2024
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05441826.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing