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atrasentan

Generic: ATRASENTAN HYDROCHLORIDE·Brand: VANRAFIA, Vanrafia

atrasentan: sourced relationships with 2 companies · 5 clinical trials tracked · 1 FDA decision.

atrasentan evidence translation

What we can confirm

1 FDA record · 5 tracked trials

What it means

More than one company relationship is source-backed. Until you choose one, AI stays drug-only and does not guess ownership.

What to watch

Watch active trials and any change in FDA or trial status.
BioSniper AIPage evidence connected

Prepared research question

What is verified about atrasentan, and what remains unknown?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence5 indications · 0 study sponsors

Related indications

IgA nephropathy (IgAN) and proteinuric glomerular diseasesAlport SyndromeDiabetic Kidney DiseaseFocal Segmental GlomerulosclerosisIgA Nephropathy

Study sponsors

No additional listed-company sponsor is linked.

Dated Pipeline Records (2)
CompanyDated record stage
CHINOOK THERAPEUTICS, INC. (KDNY)
developer · Reported 2022-03-17 · Current development: unknownSource
IgA nephropathy (IgAN) and proteinuric glomerular diseases
Phase 3
Novartis AG (NVS)
Reported 2025-04-02 · Current development: unknownSource
Approved
Clinical Trial Registry Records (5)

A Phase IIIb, Multi-center, Two-arm, Randomized, Double-blind, Parallel Group Study to Evaluate the Efficacy and Safety of Zigakibart and Atrasentan Versus Zigakibart and Placebo in Patients With Primary IgA Nephropathy

NCT07850752Registry updated 2026-09-30·Phase 3
Not yet recruiting

Primary endpoint: Change in proteinuria from Baseline to Week 36, based on 24 hour urine collection

InterventionalRandomizeddouble340 targetStarted 2026-12Completion 2030-12Novartis Pharmaceuticals

A Multicenter, Single Arm, Open Label, Pilot Study to Assess the Effect of Atrasentan Alongside Supportive Care on Structural and Functional Changes in Kidneys of Adult Patients With IgA Nephropathy (IgAN)

NCT07820995Registry updated 2026-09-21·Phase 4
Not yet recruiting

Primary endpoint: Proportion of participants achieving improvement in at least one component of the composite kidney mpMRI endpoint at Month 6

Interventionalopen20 targetStarted 2026-09Completion 2028-121 site · United StatesUniversity of Illinois at Chicago

A Randomized, Double-blind, Placebo-controlled, Crossover Study of Atrasentan in Subjects With IgA Nephropathy on Sodium-glucose Cotransporter-2 Inhibitors (SGLT2i)

NCT05834738Registry updated 2026-07-20·Phase 2
Completed

Primary endpoint: Percentage Change in Proteinuria (UPCR From a 24-Hour Urine Collection) From Baseline to Week 12

InterventionalRandomizedtriple54 enrolledStarted 2023-07Completion 2025-1030 sites · Australia, Brazil, Malaysia, South Korea…Novartis Pharmaceuticals

A Phase 2, Open-Label, Basket Study of Atrasentan in Patients With Proteinuric Glomerular Diseases

NCT04573920Registry updated 2026-06-01·Phase 2
Active, not recruiting

Primary endpoint: Change in proteinuria for IgAN, FSGS, and Alport syndrome patients receiving 0.75 mg atrasentan QD

Interventionalopen103 targetStarted 2021-03Completion 2026-1033 sites · Australia, Italy, South Korea, Spain…Novartis Pharmaceuticals

A Phase 3, Randomized, Double-blind, Placebo-controlled Study of Atrasentan in Patients With IgA Nephropathy at Risk of Progressive Loss of Renal Function

NCT04573478Registry updated 2026-06-04·Phase 3
Active, not recruiting

Primary endpoint: Double-blind period: Change in proteinuria

InterventionalRandomizeddouble404 targetStarted 2020-12Completion 2028-0450 sites · Argentina, Australia, Brazil, Canada…Novartis Pharmaceuticals
FDA Decisions1 records
Approval(NVS)FDA ↗
NDA219208Type 1 - New Molecular EntityStandardOralTablet

Frequently asked questions

Which companies have sourced relationships with atrasentan?

atrasentan has dated SEC/FDA relationship records for CHINOOK THERAPEUTICS, INC., Novartis AG.

How many clinical trials involve atrasentan?

BioSniper tracks 5 clinical trials involving atrasentan.

What is atrasentan's latest FDA decision?

The most recent tracked FDA decision for atrasentan is Approval, dated April 2, 2025.