NCT07606352RecruitingPhase 2
Safety and Efficacy of STL303 In Patients With Primary Immunoglobulin A (IgA) Nephropathy
A Multicenter, Randomised, Double-Blinded, Placebo-Controlled Study to Evaluate the Safety and Efficacy of STL303 In Patients With Primary Immunoglobulin A (IgA) Nephropathy
Source: ClinicalTrials.gov · Last updated 17 Sept 2026
Brief summary (registry, in English)
This is a multicenter, randomized, double-blind, placebo controlled Phase IIb study to explore the efficacy and safety of STL303 capsules in IgAN patients. About 15 patients dignosed with primary IgAN will be enrolled and randomized to three cohorts and take different dosage of STL303 or placebo capsules orally according to protocol.
- Status (registry)
- Recruiting
- Phase (registry)
- Phase 2
- Study type
- Interventional
- Enrollment
- 15 (estimated)
- First submitted
- 7 May 2026
- Start date
- 4 Aug 2026
- Primary completion date
- 31 Jul 2027
- Lead sponsor
- Sitala Bio LTD
- Diseases
- IgA nephropathy
- NCT number
- NCT07606352
What you commit to
- Study type: Interventional · Phase 2
- Planned participants: 15
- From 4 Aug 2026 to the primary completion date, 31 Jul 2027
- 8 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Any organ transplant recipients except corneal.
- Use of immunosuppressive drugs within 90 days or 5 half-lives.
- Prior oral budesonide (Nefecon/Tarpeyo/Kinpeygo) within 6 months.
- Prior complement inhibitors within 30 days, 5 half-lives, or residual effect period.
Other illness
- Other systemic diseases causing proteinuria/CKD or severe urinary obstruction.
- Major systemic diseases preventing participation (e.g., NYHA IV, severe pulmonary disease).
- History of malignancy within 5 years (exceptions apply).
- History of meningococcal, pneumococcal, or Hib infection.
- Chronic/recurrent infections in past year (e.g., liver abscess, pyelonephritis).
- Active systemic infections within 2 weeks or fever greater than 38°C within 7 days.
Lab values
- Rapidly progressive IgAN (eGFR decline greater than or equal to 50% in 3 months, or less than 50% but at high risk).
- Significantly abnormal liver function (greater than 3× ULN enzymes or greater than 2× ULN bilirubin).
Other
- Secondary IgAN or unclear exclusion of secondary causes.
- Known or suspected immunodeficiency or hereditary complement deficiency.
- Poorly controlled blood pressure (SBP greater than 150 or DBP great than 90).
- QTcF greater than 500 ms.
Who the study is looking for
- Male and female patients aged 18 years and older, with primary IgAN confirmed by renal biopsy:
- 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.
- UPCR greater than or equal to 0.75 g/g at screening and after completion of run-in.
- Vaccinated against Neisseria meningitidis and Streptococcus pneumoniae before the first dose.
- 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.
- 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.
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (8)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Research Site Coordinator of this site? Confirm its status | Clayton | Australia | Recruiting |
| John Hunter Hospital Coordinator of this site? Confirm its status | Newcastle | Australia | Recruiting |
| Nepean Hospital Coordinator of this site? Confirm its status | Penrith | Australia | Recruiting |
| Royal Perth Hospital Coordinator of this site? Confirm its status | Perth | Australia | Not yet recruiting |
| Research Site Coordinator of this site? Confirm its status | Saint Albans | Australia | Recruiting |
| Concord Hospital Coordinator of this site? Confirm its status | Sydney | Australia | Recruiting |
| Prince of Wales Hospital Coordinator of this site? Confirm its status | Sydney | Australia | Not yet recruiting |
| Research Site Coordinator of this site? Confirm its status | Woolloongabba | Australia | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.