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NCT07146906RecruitingPhase 2

A study to assess the effects of zigakibart on IgA nephropathy.

An open-label, uncontrolled, multicenter study to assess the effect of zigakibart treatment on histologic, circulating, and excreted markers of kidney disease and dysfunction in adult patients with IgA nephropathy

Source: EU CTIS (euclinicaltrials.eu) · Last updated 17 Aug 2026

Brief summary (registry, in English)

Does zigakibart treatment alter the course of disease in adults with IgAN?

Status (registry)
Recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
15 (estimated)
First submitted
5 Nov 2025
Start date
23 Apr 2026
Lead sponsor
Novartis Pharma AG
NCT number
NCT07146906
EU CT number
2024-519699-24-00

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 15
  • 14 sites in 5 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of EU CTIS (euclinicaltrials.eu). It describes the study, not your situation.

Who cannot take part

Copied verbatim from EU CTIS (euclinicaltrials.eu) and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Has not used medications suppressing or affecting the immune system (not including short-term use of corticosteroids) in the past year.

Other illness

  • Does not have urinary problems such as frequent urinary tract infections (UTIs) or trouble emptying the bladder.

Lab values

  • Does not have a weakened immune system or unacceptably low immunoglobulin levels Total IgG (<6.0 g/L).

Other

  • Does not have IgA vasculitis.
  • Does not have high blood pressure that is not well controlled.

Who the study is looking for

  • Male or female adults 18 years of age or older who weigh at least 45 kg with a BMI no greater than 35.0 kg/m2 and were diagnosed with IgAN within the past 5 years.
  • Moderate kidney function (eGFR ≥45 mL/min/1.73 m²).
  • Persistent protein in urine defined as total urine protein ≥0.5 g/day or urine protein-creatinine ratio (UPCR) ≥0.5 g/g despite supportive therapy, or total urine protein >1.5 g/day or UPCR >1.5 g/g at the time of clinical presentation or diagnosis if diagnosed within the past 6 months.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on EU CTIS (euclinicaltrials.eu)

Sites (14)

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

SiteCityCountrySite status
Vseobecna fakultni nemocnice v Praze
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PragueCzechiaNot yet recruiting
Medizinische Hochschule Hannover
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HanoverGermanyRecruiting
Universitaetsmedizin der Johannes Gutenberg-Universitaet Mainz KöR
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MainzGermanyRecruiting
LMU Klinikum Muenchen AöR
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MunichGermanyRecruiting
Hospital Clinic de Barcelona
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BarcelonaSpainRecruiting
Clínica Universidad de navarra
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PamplonaSpainRecruiting
University Hospital Virgen Del Rocio S.L.
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SevillaSpainRecruiting
Hospital Universitario Dr. Peset Aleixandre
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ValenciaSpainRecruiting
Azienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia
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BresciaItalyRecruiting
Istituti Clinici Scientifici Maugeri S.p.A. Societa' Benefit In Forma Abbreviata Istituti Clinici Scientifici Maugeri S.p.A. Sb O Anche Ics Maugeri S.p.A. Sb O Maugeri S.p.A. Sb
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PaviaItalyRecruiting
Istituto Di Ricerche Farmacologiche Mario Negri
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RanicaItalyRecruiting
Samodzielny Publiczny Zaklad Opieki Zdrowotnej Centralny Szpital Kliniczny Uniwersytetu Medycznego W Lodzi
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LodzPolandNot yet recruiting
Uniwersytecki Szpital Kliniczny w Opolu
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OpolePolandNot yet recruiting
Uniwersyteckie Centrum Kliniczne Warszawskiego Uniwersytetu Medycznego
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WarsawPolandNot yet recruiting

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