New pill aims to slow kidney disease in IgA nephropathy patients
NCT ID NCT07606352
First seen Jun 27, 2026 · Last updated Sep 18, 2026 · Updated 3 times
Summary
This study tests an experimental drug called STL303 for people with IgA nephropathy, a kidney disease. About 15 adults will receive either STL303 or a placebo to see if the drug is safe and can reduce protein in the urine, a sign of kidney damage. Possible side effects include nausea, dizziness, and tiredness.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
-
About 15 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
Aug 2026
- Expected to finish
-
Sep 2027
An estimate. End dates often move.
- Lead sponsor
-
A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Male and female patients aged 18 years and older, with primary IgAN confirmed by renal biopsy: 2. eGFR (Chronic Kidney Disease Epidemiology Collaboration \[CKD-EPI\] formula) greater than or equal to 30 mL/min/1.73 m2 at screening and after completion of run-in. 3. UPCR greater than or equal to 0.75 g/g at screening and after completion of run-in. 4. Vaccinated against Neisseria meningitidis and Streptococcus pneumoniae before the first dose. 5. Have received stable treatment with RASis (ACEi or ARB) at the maximum recommended dose or MTD for at least 90 days prior to the first dose. 6. If the patient has been treated with SGLT2i, diuretics, other antihypertensive treatments, ERA, and/or hydroxychloroquine for IgAN prior to the first dose, the drug should also be used stably for at least 90 days. Exclusion Criteria: 1. Secondary IgAN or unclear exclusion of secondary causes. 2. Rapidly progressive IgAN (eGFR decline greater than or equal to 50% in 3 months, or less than 50% but at high risk). 3. Other systemic diseases causing proteinuria/CKD or severe urinary obstruction. 4. Known or suspected immunodeficiency or hereditary complement deficiency. 5. Any organ transplant recipients except corneal. 6. Poorly controlled blood pressure (SBP greater than 150 or DBP great than 90). 7. Use of immunosuppressive drugs within 90 days or 5 half-lives. 8. Prior oral budesonide (Nefecon/Tarpeyo/Kinpeygo) within 6 months. 9. Prior complement inhibitors within 30 days, 5 half-lives, or residual effect period. 10. Major systemic diseases preventing participation (e.g., NYHA IV, severe pulmonary disease). 11. Significantly abnormal liver function (greater than 3× ULN enzymes or greater than 2× ULN bilirubin). 12. QTcF greater than 500 ms. 13. History of malignancy within 5 years (exceptions apply). 14. History of meningococcal, pneumococcal, or Hib infection. 15. Chronic/recurrent infections in past year (e.g., liver abscess, pyelonephritis). 16. Active systemic infections within 2 weeks or fever greater than 38°C within 7 days.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for IGAN are added.
Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
-
The study's own enquiry address
This study publishes an address for enquiries. See it below .
-
The places running it
8 sites. The list below names each one and where it is.
-
The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
-
A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Show contact details
Enter your email to view the contact information for this study.
Genom att skicka in godkänner du våra Användarvillkor
Study contacts
-
Contact
Email: •••••@•••••
Locations
-
Concord Hospital
RECRUITINGSydney, New South Wales, 2139, Australia
-
John Hunter Hospital
RECRUITINGNewcastle, New South Wales, 2305, Australia
-
Nepean Hospital
RECRUITINGPenrith, New South Wales, 2747, Australia
-
Prince of Wales Hospital
NOT_YET_RECRUITINGSydney, New South Wales, 2031, Australia
-
Research Site
RECRUITINGWoolloongabba, Queensland, 4102, Australia
-
Research Site
RECRUITINGClayton, Victoria, 3168, Australia
-
Research Site
RECRUITINGSaint Albans, Victoria, 3021, Australia
-
Royal Perth Hospital
NOT_YET_RECRUITINGPerth, Western Australia, 6000, Australia
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can a new pill slow kidney damage in IgA nephropathy?
- Can a gut metabolite shield the kidneys in IgA nephropathy?
- Can a new pill protect kidneys from IgA nephropathy?
- New pill aims to tame kidney disease in Long-Term trial
- New drug aims to protect kidneys in IgA nephropathy patients
- New drug shows promise for kidney disease in phase 2 trial