Condition (MeSH)
Nephritis, Hereditary
ClinicalTrials.gov lists 37 trials for Nephritis, Hereditary or a narrower condition beneath it. Genzyme, a Sanofi Company has the most among industry and government lead sponsors, with 3.
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Trials per phase
37 of the 37 trials are tagged with Nephritis, Hereditary itself; the rest are tagged with a narrower condition beneath it.
When did Nephritis, Hereditary trials start? (15)
Shown in this order: most recent first, 1990 onwards. 2026 is partial: trials registered with a 2026 start date so far, not a full year.
Trials over time, by phase
- Phase 1
- Phase 1/2
- Phase 2
- Phase 2/3
- Phase 3
- Phase 4
- Not applicable
- Observational
Top of scale: 5
Trials registered with a start date in each year, 1990 onward, stacked by phase (complete years only; the current partial year is in the table's notes). The table below lists the same counts, most recent years first.
| Year | Trials started |
|---|---|
| 2026 (partial year) | 2 |
| 2025 | 2 |
| 2024 | 3 |
| 2023 | 4 |
| 2022 | 5 |
| 2021 | 4 |
| 2019 | 2 |
| 2018 | 2 |
| 2017 | 3 |
| 2014 | 1 |
Showing 10 of 15 earlier years.
No forecast is made for this condition: it averages 3.2 trial starts a year over the five years to September, under the 5 a year the method needs.
Recruitment duration, a model prediction: 4 trials still running at the 2026-10-09 snapshot, fewer than the 5 needed for a median. Source: ClinicalTrials.gov / AACT (CTTI), public domain.
What phase are Nephritis, Hereditary trials in? (8)
Shown in this order: phase order.
Show the trials by phase as a table
| Phase | Trials |
|---|---|
| Phase 1 | 1 |
| Phase 1/2 | 1 |
| Phase 2 | 10 |
| Phase 2/3 | 2 |
| Phase 3 | 3 |
| Phase 4 | 2 |
| Not applicable | 2 |
| Observational | 16 |
How many Nephritis, Hereditary trials are recruiting? (6)
Shown in this order: the order a trial moves through, from not yet recruiting to unknown.
| Status | Trials |
|---|---|
| Not yet recruiting | 2 |
| Recruiting | 10 |
| Active, not recruiting | 4 |
| Completed | 16 |
| Terminated | 4 |
Showing 5 of 6 statuses.
Status as registered on ClinicalTrials.gov. Each trial is counted once.
Which lead sponsors run the most Nephritis, Hereditary trials? (8)
Shown in this order: most trials first. Lead sponsors the registry classes as industry, NIH, US federal, other government or network. A hospital or university the registry files as government can appear here. Sponsors it classes as academic or other are shown on the full page, because that class cannot separate an institution from a named investigator.
| Sponsor | Trials |
|---|---|
| Genzyme, a Sanofi Company | 3 |
| Biogen | 2 |
| Eloxx Pharmaceuticals, Inc. | 2 |
| Novartis Pharmaceuticals | 2 |
| Bayer | 1 |
Showing 5 of 8 sponsors.
Which drugs are being tested for Nephritis, Hereditary? (4)
Shown in this order: most trials first. One row per drug, matched to a single molecule under all its names, ranked by number of trials.
| Drug | Trials |
|---|---|
| BMS-512148 | 2 |
| Bardoxolone Methyl | 2 |
| RAMIPRIL | 2 |
| Exaluren | 2 |
Interventions as named in the registry (11)
Shown in this order: most trials first.
| Drug | Trials |
|---|---|
| ACE inhibitor | 1 |
| Benazepril, Valsartan and Fluvastatin | 1 |
| Benazepril hydrochloride 10 milligram (mg) Tab | 1 |
| RG012 | 1 |
| SGLT2 Inhibitor | 1 |
Showing 5 of 11 interventions.
These are the names sponsors entered on ClinicalTrials.gov that we have not matched to a single molecule. Some are drugs under a brand or code name; others are procedures, doses or arm labels.
Which serious adverse events do Nephritis, Hereditary trials report? (10)
Shown in this order: most subjects affected first. Subjects affected summed across trials, a cross-trial signal, not a rate.
| Adverse event | Subjects affected | Trials |
|---|---|---|
| End stage renal disease | 10 | 2 |
| Glomerular Filtration Rate Decreased | 3 | 1 |
| Acute kidney injury | 2 | 2 |
| Asthenia | 2 | 2 |
| Chronic kidney disease | 2 | 1 |
Showing 5 of 10 adverse events.
Which publications cover Nephritis, Hereditary? (25)
Shown in this order: major-topic papers first, then newest, then most linked to trials.
Showing 5 of 25 publications.
Prevalence (4)
Shown in this order: jurisdiction, then disease name. Orphanet observation for the mapped ORPHA concept; the mapping relation column says whether that concept is exactly this condition or broader or narrower.
| Orphanet disease | Type | Class | Geography | Jurisdiction | Mapping relation |
|---|---|---|---|---|---|
| Alport syndrome | Point prevalence | Unknown | Europe | Not stated | Exact |
| Alport syndrome | Point prevalence | Unknown | Europe | Not stated | Exact |
| Alport syndrome | Prevalence at birth | 1-9 / 100 000 | Finland | Not stated | Exact |
| Alport syndrome | Prevalence at birth | 1-9 / 100 000 | Finland | Not stated | Exact |
Rare-disease identity (2)
Shown in this order: exact, broader, narrower, other.
| Orphanet disease | ORPHA code | Relation | Source |
|---|---|---|---|
| Alport syndrome | 63 | Exact | Orphanet Rare Disease Ontology (ORDO) |
| Alport syndrome | 63 | Exact | Orphadata Science knowledge files, Product 1 |
Not on this page
Not measured: delivery record.
Checked, with nothing recorded for this condition: sub-conditions in mesh.