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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
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

Full criteria on ClinicalTrials.gov

Sites (8)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Research Site
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ClaytonAustraliaRecruiting
John Hunter Hospital
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NewcastleAustraliaRecruiting
Nepean Hospital
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PenrithAustraliaRecruiting
Royal Perth Hospital
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PerthAustraliaNot yet recruiting
Research Site
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Saint AlbansAustraliaRecruiting
Concord Hospital
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SydneyAustraliaRecruiting
Prince of Wales Hospital
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SydneyAustraliaNot yet recruiting
Research Site
Coordinator of this site? Confirm its status
WoolloongabbaAustraliaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.