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Chronic Kidney Disease

Renal 6 original drugs
6
Novel Drugs
17
Reformulations
159
Active Trials
16
Drug Targets

Phase 3 Readouts Pro

12 active Phase 3 trials with confidence-graded completion dates.

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Q2 2026
BCD-131 (pegdarbepoetin beta)
Biocad
Estimated · aging NCT07119372
Q2 2026
Ziltivekimab B
Novo Nordisk
Estimated · fresh NCT05021835
Q2 2026
AP301
Alebund Pharmaceuticals
Estimated · fresh NCT06933472
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Anchored on CT.gov primary completion date. Topline announcements typically precede this by 3–9 months. Confidence labels combine date type (ACTUAL/ESTIMATED) with last-update freshness.

Treatments by Mechanism

Top 12 mechanisms across 54 industry trials with a known mechanism of action.

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SGLT2
5 trials 1 active 3 sponsors
Sodium-Glucose Cotransporter 2 Inhibitor
5 trials 1 active 2 sponsors
CaSR
4 trials 1 active 1 sponsor
Parenteral Iron Replacement
3 trials 1 active 1 sponsor
Glucose-dependent Insulinotropic Polypeptide Receptor Agonist
2 trials 1 active 1 sponsor
Hypoxia-inducible Factor Prolyl Hydroxylase Inhibitor
14 trials 1 sponsor
Vitamin D2 Analog
6 trials 3 sponsors
Erythropoiesis-stimulating Agent
5 trials 2 sponsors
ferric reductase/phosphate
4 trials 2 sponsors
Erythropoietin Receptor
2 trials 2 sponsors
GLP-1 Receptor Agonist
2 trials 2 sponsors
Kinase Inhibitor
2 trials 1 sponsor

MoA derived from FDA pharmClassEpc when intervention matches an approved drug. Codenamed clinical-stage assets without an approved counterpart show "—" and aren't grouped here — they're still in the phase tables below.

Clinical Pipeline by Phase

531 industry-sponsored trials across 179 sponsors

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Reformulations (17 drugs) Click to expand
Generic Drugs (5 ANDA approved) Click to expand

Generic drugs contain the same active ingredient as the brand-name drug and are approved via ANDA (Abbreviated New Drug Application).

Related Indications

Other Renal indications

Drug Categories:

  • Novel Drugs: NDA Type 1/2 (new molecular entity) or original BLA
  • Reformulations: NDA Type 3/5 (new dosage form of existing molecule)
  • Biosimilars: BLA-approved biologics highly similar to reference products
  • Generics: ANDA-approved copies of small molecule drugs

View data sources and methodology