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A Phase III, single-arm, multicenter pediatric clinical study evaluating atrasentan in children and adolescents aged 2 to <18 years with primary immunoglobulin A nephropathy (IgAN).

Basic Information

Recruitment status	Pending
Health condition(s) or Problem(s) studied	Immunoglobulin A Nephropathy
Date of first enrollment	03/06/2026
Target sample size	2
Countries of recruitment
Study type	Interventional
Intervention(s)	Cohort 1 (=<40 kg): EXV811 0.75 mg administered orally Cohort 2 (>=30 kg to <40 kg): Dose adjusted based on body weight Cohort 3 (>=20 kg to <30 kg): Dose adjusted based on body weight Cohort 4 (>=10 kg to <20 kg): Dose adjusted based on body weight The doses for Cohorts 2, 3, and 4 will be determined based on the PK data obtained from the preceding cohort.

Outcome(s)

Primary Outcome	Change From Baseline in Proteinuria at Week 36
Secondary Outcome

Key inclusion & exclusion criteria

Age minimum	>= 2age old
Age maximum	< 18age old
Gender	Both
Include criteria	1. Signed informed consent by parent(s)/legal guardian(s) for the pediatric patient must be obtained before any study-specific assessment is performed. A consent or assent may also be required for some participants depending upon their age and local requirement. 2. Male and female participants 2 to < 18 years of age as of Day 1. 3. eGFR >= 30 mL/min/1.73m2 where eGFR is calculated using the modified Schwartz formula at Screening and confirmed during the Run-in Period. 4. Kidney biopsy-proven primary IgAN, with biopsy performed within 3 years of Screening with < 50% tubulointerstitial fibrosis and < 25% crescents. In case a kidney biopsy within 3 years from Screening is not available, a kidney biopsy may be performed if it is part of the planned diagnostic approach and clinical management of the participant. 5. Proteinuria due to primary diagnosis of IgAN as assessed by UPCR >= 1 g/g (113 mg/mmoL) sampled from FMV at Screening on Day -90 and Day -60 as well as during the Run-in Period despite treatment with maximum tolerated dose of ACE inhibitor/ARB for at least 120 days prior to Day 1. Note: UPCR will be assessed based on one FMV sample at Day -90 and based on the geometric mean of 2 FMV samples for the Day -60 visit and during the Run-in Period. 6. All participants must have been on supportive care including stable dose regimen of ACE inhibitor or ARB at either the locally approved maximal daily dose per body weight, or the maximally tolerated dose (per Investigator's judgment for pediatric use), for at least 120 days before first study drug administration. In addition, if participants are taking diuretics, other antihypertensive medication, or other background medication for IgAN (such as SGLT2 inhibitors), the doses should also be stabilized for at least 120 days prior to the first dosing of study treatment. Note: Participants with allergies or intolerance to ACE inhibitors and ARBs are eligible for the study. Participants with allergies or intolerance to RAS inhibitors are eligible but will not exceed ~5% of the total population treated (maximum of 2 participants). 7. The minimum body weight of enrolled pediatric participants is 10 kg at Screening and confirmed on Day 1. 8. Parent(s)/guardian(s) are to be able to communicate well with the investigator and to understand and comply with the study's requirements for their child.
Exclude criteria	1. Participation in any other investigational drug trial or use of other investigational drugs at the time of enrollment, or within 5 elimination half-lives of enrollment, or within 30 days of enrollment, whichever is longer; or longer if required by local regulations. 2. History of hypersensitivity to any of the study drugs or its excipients or to drugs of similar chemical classes. 3. Any secondary IgAN as defined by the investigator. 4. A clinical diagnosis of IgA vasculitis (IgAV or Henoch-Schoenlein purpura) based on typical palpable purpura with or without arthralgia and abdominal pain. 5. Evidence of significant urinary obstruction or difficulty in voiding, any urinary tract disorder causing significant urinary obstruction or difficulty in voiding at Screening and confirmed at Baseline/Day 1. 6. Concurrent diagnosis of CKD other than IgAN at Screening and before first study drug administration. 7. Current acute kidney injury (AKI) defined by Acute Kidney Injury Network (AKIN) criteria within 4 weeks of Screening. 8. Presence of rapidly progressive glomerulonephritis (RPGN) as defined by 50% decline in eGFR within 3 months prior to Screening or during Screening and Run-in periods. 9. Presence of nephrotic syndrome at Screening based on the investigator's judgement. 10. BNP value of >200 pg/mL at Screening. 11. Hemoglobin below 9 g/dL at Screening or prior history of blood transfusion for anemia within 3 months of Screening. 12. Platelet count <80,000/microL at Screening. 13. On Day 1 participants' body weight falls below the lower limit of the cohort in which the participant was initially screened and lower body weight cohort is not open for enrollment. 14. Known history of congenital heart disease, heart failure or clinically significant fluid retention such as pulmonary edema, uncontrolled peripheral edema, pleural effusion, or ascites before treatment. 15. Current use of any homeopathic and/or herbal medications for the treatment of IgAN disease. 16. History of an alcohol or illicit drug-related disorder within the past 3 years at Screening. 17. Confirmed blood pressure >150 mmHg systolic or >95 mmHg diastolic for 12 to <18 years of age; >140 mmHg systolic or >90 mmHg diastolic for 6 to <12 years of age; >120 mmHg systolic or >80 mmHg diastolic for 2 to <6 years of age; based on the mean of 3 measurements obtained at Screening; or clinically significant hypotension at screening. 18. Participants previously treated with immunosuppressive or other immunomodulatory agents. Participants treated with endothelin (receptor) antagonists (including sparsentan) within 120 days prior to first study drug administration. 19. History of organ transplantation (subjects with history of corneal transplant are not excluded) before treatment. 20. Major concurrent comorbidities before treatment. 21. Any medical condition deemed likely to interfere with the subject's participation in the study before treatment. 22. Active systemic bacterial infection within 14 days prior to study drug administration. 23. Presence of fever >= 38 celsius degree (100.4 fahrenheit degree) within 7 days prior to study drug administration. 24. Human immunodeficiency virus (HIV) infection. 25. Liver disease, such as active hepatitis B virus (HBV) or hepatitis C virus (HCV) infection defined as Hepatitis B surface antigen (HBsAg) positive or Hepatitis C virus ribonucleic acid (HCV-RNA) positive at Screening, or liver injury as indicated by abnormal liver function tests at Screening and Baseline as defined below: Any single parameter of ALT, AST, GGT, alkaline phosphatase must not exceed 3X upper limit of normal (ULN) Serum bilirubin must not exceed 2X ULN 26. History of malignancy of any organ system (except for predefined exceptions). 27. Pregnant or nursing (lactating) female participants (of childbearing potential). 28. Subjects taking prohibited therapies before treatment. 29. Women of childbearing potential, defined as all women physiologically capable of becoming pregnant from menarche until becoming post-menopausal, unless they are using highly effective methods of contraception (failure rate < 1% per year) while taking study treatment and for 1 month after stopping study treatment.