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Atrasentan

Alternative Names: atrasentan, CHK-01, CHK01, CHK 01
Latest Update: 2025-01-14
Latest Update Note: News Article

Product Description

Atrasentan is a highly selective ETAR antagonist with an approximate 1800:1 selectivity for ETAR to ETBR (Sourced from: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3065231/)

Mechanisms of Action: ETa Antagonist,Mineralocorticoid Receptor Antagonist

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: Oral

FDA Designation: Orphan Drug - IgA Nephropathy *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Chinook Therapeutics
Company Location: SEATTLE WA 98102
Company CEO: Eric Dobmeier
Additonal Commercial Interests: AbbVie

Clinical Description

Map of Global Clinical Trials for Atrasentan

Countries in Clinic: Argentina, Australia, Brazil, Canada, China, Colombia, Czech Republic, France, Germany, Hong Kong, India, Italy, Japan, Korea, Malaysia, New Zealand, Poland, Portugal, South Korea, Spain, Taiwan, United Kingdom, United States

Active Clinical Trial Count:

Highest Development Phases

Phase 3: Glomerulonephritis|IgA Nephropathy|Kidney Diseases

Phase 2: Diabetic Nephropathy|Glomerulosclerosis, Focal Segmental|Glomerulosclerosis, Nodular|Nephritis, Hereditary

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

CHK0101

P3

Unknown Status

IgA Nephropathy

2027-06-30

ALIGN

P3

Active, not recruiting

Glomerulonephritis|Kidney Diseases|IgA Nephropathy

2026-12-18

CHK01-03

P2

Unknown Status

IgA Nephropathy

2026-05-25

ASSIST

P2

Recruiting

Kidney Diseases|Glomerulonephritis|IgA Nephropathy

2025-10-22

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