Study of felzartamab compared to placebo in adults with IgA nephropathy

3 1 1

What is this study about?

This study focuses on IgA Nephropathy, a kidney disease where abnormal antibodies build up in the kidneys. The main treatment being tested is Felzartamab, which is given through intravenous administration. The study will compare this medication against a placebo to see how well it works in reducing protein in the urine of adult patients with this condition.

Several supportive medications may be used during the study, including Desloratadine, Diphenhydramine, Cetirizine, Fexofenadine, Paracetamol, Methylprednisolone, Levocetirizine, Loratadine, and Famotidine. These medications are used to manage potential side effects or symptoms that participants might experience during the treatment. A Saline solution will also be used as part of the treatment process.

The purpose of this research is to evaluate how effective Felzartamab is compared to placebo in reducing the amount of protein in the urine of people with IgA Nephropathy. The study will last several years, during which participants will receive regular infusions of either Felzartamab or placebo, and their kidney function will be monitored through various tests.

1 Initial Treatment Phase

You will receive either felzartamab or placebo through intravenous administration (into a vein).

During treatment, you must continue taking your current kidney medications at stable doses, including ACE inhibitors or ARB medications.

Your protein levels in urine and kidney function will be regularly monitored through urine and blood tests.

2 Pre-medication Protocol

Before each felzartamab infusion, you will receive medications to prevent possible reactions:

Antihistamines (such as diphenhydramine, cetirizine, or desloratadine)

Paracetamol

Methylprednisolone

3 Monitoring Phase

Regular checks will measure:

– Changes in protein levels in your urine

– Kidney function through blood tests

– Physical examination and vital signs

– Heart activity through ECG testing

– Presence of antibodies against the study medication

4 Long-term Follow-up

The study continues until June 2029

Your kidney function will be monitored for signs of improvement or decline

Any side effects or health changes will be documented and assessed

Who Can Join the Study?

  • Must have IgA nephropathy confirmed by kidney biopsy within the last 10 years. For patients with type 2 diabetes, the biopsy must be from the last 24 months
  • Must have adequate kidney function measured by eGFR (a blood test that shows how well your kidneys are working):
    – At least 30 mL/min/1.73m² for most patients
    – Between 20-30 mL/min/1.73m² may be accepted for specific study groups
  • Must be on a stable dose of blood pressure medications (ACE inhibitors or ARBs) for at least 12 weeks, or have documented intolerance to these medications
  • May be taking other medications for kidney disease (SGLT2 inhibitors, endothelin receptor blockers, or mineralocorticoid receptor blockers) if the dose has been stable for at least 12 weeks
  • Must have significant protein in urine, shown by either:
    – At least 1.0 gram of protein in a 24-hour urine collection, or
    – A urine protein-to-creatinine ratio of at least 0.8 grams per gram
  • Both men and women can participate
  • Must be an adult (18 years or older)
  • If taking a medication called sparsentan, cannot be taking ACE inhibitors or ARBs at the same time

Who Cannot Join the Study?

  • History of organ transplant or current plans for kidney transplant
  • Active hepatitis B or C infection (viral infections affecting the liver)
  • Known HIV infection
  • Current diagnosis of cancer or cancer treatment in the past 5 years
  • Other types of kidney diseases besides IgA nephropathy
  • History of severe allergic reactions to medications
  • Pregnancy or breastfeeding
  • Participation in other clinical trials within the past 30 days
  • Severe heart disease or uncontrolled high blood pressure
  • Serious infections requiring hospitalization within the past 3 months
  • Use of certain medications that affect the immune system
  • Alcohol or drug abuse within the past year
  • Any condition that, in the opinion of the study doctor, would make participation unsafe

Where you can join this trial?

Verified and Recommended Sites

No sites found in this category

Verified Sites

Other Sites

Site Name City Country Status
Azienda Ospedaliero Universitaria Di Modena Modena Italy
Hospital Del Mar Barcelona Spain
Hospital Universitari De Girona Doctor Josep Trueta Girona Spain
University Multiprofile Hospital For Active Treatment St. Ivan Rilski EAD Sofia Bulgaria
Fundacio Puigvert Barcelona Spain
Azienda Universitaria Ospedaliera Consorziale Policlinico Bari Bari Italy
Hopital Beaujon Clichy France
Clfizjibo Uboclkjsbzwjzk Srmhgnggt Woluwe-Saint-Lambert Belgium
Hnffarxuysas Hekqwpnx Athens Greece
Cfxorp Hzvcbyabxpl Dcjubqbgtzktp Vhyctt La Roche sur Yon France
Llpix Gbvtbnz Hllbjtxg Ob Aawkgr Athens Greece
Ulmxndelnq Gdvqpka Huhnuugg Oq Tbwrthxucqew Aofyh Thessaloniki Greece
Mbuimcp Cwsiwi Hlly Eokz Sofia Bulgaria
Uvsjtytxkv Gievurx Huswncqv Ox Ipbihcgt Ioannina Greece
Hhulnefm Vtkc drdngzfu Barcelona Spain
Hhtikkuh Uqshjjlwueqae dx A Clwegy A Coruna Galicia Spain
Alhc Gdahfz Oumaatfy Maadwamkjjcej Nyxvkfay Milan Italy
Cakyuat Uabpkpbjhymokrljrvjv Bfrsha Kef Berlin Germany
Hybktkgg Ukhpaooowdinm Fbiuuznfm Jlpufta Djiu Madrid Spain
Cqpbzy Hkbnirvxhd E Uttrhhloeuioa Do Czrdzlg Ejnvqw Coimbra Portugal
Gglddzx Ulmftlayrk Hzkepzdm Oc Pomaeu Patras Greece
Uzjrtvhmozlwcnceoxgvl Hmeibajyie Aaw Heidelberg Germany
Sqbpwqmroe Bxvitoe Mtbjeq Rijeka Croatia
Uixivgjrbhtt Lughxoz Leipzig Germany
Uoklfufpwurxnh Cbimbsk Koykbjulv Gdansk Poland
Cghvab Hpjrosvkgle Ulnsympzatmvr Dp Nqvgo Nimes France
Ipqiojrqn Fvm Ckszwgty Agi Errveydcsxqn Myyzuggk Prague Czechia
Hymhmsfg Uiusalmakhrsr 1f Dd Ogfudhg Madrid Spain
Uqsxryrfwb Dfiyu Suwlt Di Bbgllqa Brescia Italy
Gdloze Nplhaalaqx Thasastxrxdhv Gykdmo Pswmogsllezv Thessaloniki Greece
Amdtbsqp Zumcqlxnur Guzzgtmfj Kortrijk Belgium
Ceie Clfakl Cukkgcf Awsdaxwbf Bdjhy Aigreqdzsl Braga Portugal
Uchqngjcto Gzgakcz Hrsxidsn Oc Hbuiytmci Heraklion Greece
Mvijwkk Cwreaz Miemevdtew Pvfntt Obk Pleven Bulgaria
Higkfrpr Ufjchfzwhitwfg Sfhyeglxcq &mfuqbh Hbskpxe dd Hkrpbazuqgl STRASBOURG, Alsace France
Usncvrtxsz Gvnzbek Hptancay Afzhpyg Gsdrymo Hbrtoglc Ou Wigt Astiam H Avod Vxcyelh Chaidari Greece
Acazstz Sxucobqvm Uvlackysvpnbs Gjqdvqnf Isuhnfbv Trieste Italy
Gmmauyg Hhtcorlo Ou Azhs Arta Greece
Sge Sai z onme Cracow Poland
Kiisjjdl blaqxypu cuzmlb Rotyzi (ptrqvdkb Hvmuiqed Cencvl Rhsjmjp Rijeka Croatia
Dmncrmfpfp Ceergovyuyjq Cdgale (vzbc &boldjviujod Aqdddhivqpp Emsu Sofia Bulgaria
Anodqky Sdwptxidc Lscldv di Srsqnrq Eboli Italy
Curctk Hmiozqzklcj Udatqnfezxbyx dfohfpqug Orléans France
Bioheemp Uonebgcucs Hvmmgnxa Cqqfyi Besançon France
Onsbtldz Skk Gyfzlfjb Bkqrq Turin Italy
Jlu Yfvonot Zcvdhnwdes Ieper Belgium
Gqoxvf Ucaztqgqwj Famglhkfd Frankfurt Germany
Cppvwz Hzxomodjkq Dn Bmvpc Vxtja Enbmbv (pnrh Ekjntvw Aveiro Portugal
Cqqomj Htrnlapilx ds Sranlip Eacypr Setubal Portugal
Gojvdi Hsuvvnvjovy Dp Ll Rftigq Du Mduyazgm Ez Swl Aaebdq Mulhouse France
Zcyhlvobfc Ouus Lnfhnni Genk Belgium
Imzxuxjs Do Rsrxergh Ffhsqnuptmjysp Mbwvf Naabf Ranica Italy
Allclop Okbrzjimnhj Upvmshayvjape Pgejy Parma Italy
Creujp Hizzyvdtxfs Ulfgbtmouctfs Rgrjr Reims France
Hmelqzzo Fbbm Suresnes France
Ahirvgx Uekbb Smnlpxcah Lgvxck Dg Pcjxmvfz Piacenza Italy
Upujxhb Lpnlk Dp Saapr Ds Gionpsckkbdy Ecjehu Vila Nova De Gaia Portugal
Hbflejxm Sad Plzfm Da Abwimwzxx Caceres Spain
Hpptfbed Ujhfxxrmihhlt Dx Gstvob Getafe Spain
Tpykx Pbtznavktxl Sqneghjyavnp Crsgmnn Mfmvgorm Stl z ojyp Szczecin Poland
Pftufv Mol Kizweb Cracow Poland
Nmaduzvhwiihudt Zspqpfx Vixbntrdmaxfivrodzsqvr Gan Villingen-Schwenningen Germany
Ulwsobunzeybk Sqwbblt Khtdromhd No 2 Ptk w Stfsiljbde Szczecin Poland
Vmgpqrhhq Fsytnnra Nzpkxatlx V Pngkm Prague Czechia
Cndzyt Hxbnjldhens Uyuxvutcajeuj Anygkw Poobwxcc Amiens France
Umgasnydwigwtzzxtmtwu Dobbnftdbka Akg Duesseldorf Germany
Ufqidyuaas Mjbrhrs Cxvyoh Hgpwrjldvkivyxnku Hamburg Germany
Rpogek Bhbxb Gylebxrabami fgyu majaxiromnsq Fgiohbizy mzb Stuttgart Germany
Sbegiephhemh Ktozauhr Blcgvmrnskls gsohg Brunswick Germany

Want to learn more about this study or check if you can participate? Contact us.

Trial status

Country Status Recruitment Start
Belgium Belgium
Recruiting
30.08.2025
Bulgaria Bulgaria
Recruiting
30.08.2025
Croatia Croatia
Recruiting
30.08.2025
Czechia Czechia
Recruiting
30.08.2025
France France
Recruiting
30.08.2025
Germany Germany
Recruiting
30.08.2025
Greece Greece
Recruiting
30.08.2025
Italy Italy
Recruiting
30.08.2025
Poland Poland
Recruiting
30.08.2025
Portugal Portugal
Recruiting
30.08.2025
Spain Spain
Recruiting
30.08.2025

Trial locations

Felzartamab is an investigational medication being studied for the treatment of IgA nephropathy, which is a kidney disease. It works by targeting and reducing specific antibodies in the body that contribute to kidney inflammation and damage. This medication is given to patients alongside their standard treatments to help reduce the amount of protein in their urine, which is a sign of kidney disease severity.

Placebo is an inactive substance that contains no medication. It is used as a comparison to help determine if felzartamab is effective in treating IgA nephropathy.

IgA Nephropathy – A kidney disease where an antibody called immunoglobulin A (IgA) builds up in the kidneys. The disease occurs when IgA deposits in the kidneys, causing inflammation that can interfere with the kidneys’ ability to filter waste from blood. It develops gradually over many years and primarily affects the kidney’s filtering units called glomeruli. The condition often starts during the teenage years or early adulthood. Over time, it can cause protein and blood to leak into the urine, leading to changes in urination patterns and visible blood in urine. The disease progresses differently in each person, with some experiencing very slow progression while others notice more rapid changes in kidney function.

Trial ID:
2024-519345-30-00
Protocol code:
299IG301
NCT ID:
NCT06935357
Trial Phase:
Therapeutic confirmatory (Phase III)

Other Trials to Consider

  • Study of Mezagitamab in Adults with Primary IgA Nephropathy (Berger’s Disease) to Reduce Protein in Urine

    Recruiting

    3 1
    Austria Czechia France Germany Hungary Italy +6
  • Study of Atacicept Treatment for Patients with Multiple Autoimmune Glomerular Diseases

    Recruiting

    2 1 1
    Investigated Drugs:
    Belgium France Germany Italy Poland Spain