Chronic kidney disease due to glomerulonephritis
Glomerulonephritis-related CKD: treatable, not curable, progression can slow.AI-generated
Milestones
dot size = significance- 1958Chlorothiazide approved (FDA)
- 1959Hydrochlorothiazide approved (FDA)
- 1960Chlorthalidone approved (FDA)
- 1976Somatropin approved (FDA)
- 1978Calcitriol approved (FDA)
- 1980Calcifediol anhydrous approved (FDA)
- 1982Calcium acetate approved (FDA)
- 1982Folic acid approved (FDA)
- 1982Ferric oxyhydroxide approved (FDA)
- 1982Pyridoxine approved (FDA)
What's being tested now
Trials started per year, stacked by phase (darker = later phase). Source: ClinicalTrials.gov via Clin2, which tracks studies recruiting in recent years — early years undercount.
See all 1099 active Chronic kidney disease trials on Clin2 →Where we are
AI-generatedChronic kidney disease due to glomerulonephritis is at the disease-modifying stage: no cure exists once CKD is established, but ACE inhibitors/ARBs and immunosuppression for active inflammatory subtypes can slow decline and reduce events. Some early or specific forms are reversible. Over decades, outlook has improved gradually; progression is often slower with modern therapy, though many still advance to kidney failure. A key milestone was FDA approval of chlorothiazide in 1958, which made blood-pressure control more practical. The pipeline is active: 1,063 trials started in the last five years, including 91 phase-3 studies, with 1,099 currently active.
- Can chronic kidney disease from glomerulonephritis be reversed?
- Once CKD is established, damage is generally irreversible. Some early or specific inflammatory forms may improve with immunosuppression. Treatment focuses on slowing further decline and managing complications.
- How does this condition usually progress over time?
- Progression varies. Without treatment, kidney function often declines steadily over years. With blood-pressure control and appropriately used immunosuppression, the decline can slow, but many people eventually reach advanced kidney failure.
- What treatments have changed the outlook?
- The 1958 approval of chlorothiazide was a turning point, making blood-pressure control easier and slowing kidney damage. Later ACE inhibitors, ARBs, and immunosuppressives improved kidney survival. Ongoing trials continue testing new approaches.
- Are there new treatments being studied?
- Yes. More than 1,063 trials have started in the last five years, including 91 phase-3 studies, and 1,099 are currently active. Research focuses on slowing progression and better targeting inflammation.