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Compound · clinical trials

Felzartamab

Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 6 trials in our USA, India, China and UK registers that name Felzartamab as an intervention. Synced 24 Sep 2026
6Trials tracked
4Recruiting now
1Lead sponsor
4Country registers
Maintained by Sreepriya Prasannan
MSc Digital Transformation of Life Sciences (Innopharma Education / Griffith College); MSc & BSc Botany HSE Spark Ignite 2026 โ€” Top 14 finalist
Compiled from ClinicalTrials.gov registry records ยท Last verified ยท Editorial standards

Felzartamab is named as a drug or biological intervention in 6 clinical trials in our USA, India, China and UK trial registers, 4 of which are recruiting. The lead sponsor is Biogen. Registered phases: Phase 3 and Phase 2. Conditions studied include Antibody-mediated Rejection; Microvascular Inflammation; Immunoglobulin A Nephropathy (IgAN).

01

Clinical trials of Felzartamab

6 trials
NCT IDStudyPhaseStatusLead sponsorRegister
NCT06935357 A Study to Learn About the Effects of Felzartamab Infusions on Adults With Immunoglobulin A Nephropathy (IgAN) (ClinicalTrials.gov ↗)
Immunoglobulin A Nephropathy (IgAN)
Phase 3 Recruiting Biogen UK, USA, India, China
NCT06962800 A Study to Learn More About the Effects and Safety of Felzartamab Infusions in Adults With Primary Membranous Nephropathy (PMN) (ClinicalTrials.gov ↗)
Primary Membranous Nephropathy
Phase 3 Recruiting Biogen USA, India, China
NCT07219043 A Study to Learn About the Effects of Felzartamab Infusions in Adults With Kidney Transplants Who Have Late Isolated Microvascular Inflammation (ClinicalTrials.gov ↗)
Microvascular Inflammation
Phase 2 Recruiting Biogen USA
NCT07722546 A Study to Learn About The Effects of Felzartamab on Thyroid Function and Its Safety in Adults With Graves' Disease Ages 18 to 75 Years Old (ClinicalTrials.gov ↗)
Graves' Disease
Phase 2 Recruiting Biogen USA
NCT07444489 A Study to Learn More About the Long-Term Safety and Effects of Felzartamab Infusions in Adults With Kidney Transplants Who Have Antibody-Mediated Rejection (AMR) or Microvascular Inflammation (MVI) (TRANSCEND/TRANSPIRE LTE) (ClinicalTrials.gov ↗)
Antibody-mediated Rejection, Microvascular Inflammation
Phase 3 By invitation Biogen USA
NCT06685757 A Study to Learn More About the Effects and Safety of Felzartamab Infusions in Adults With Kidney Transplants Who Have Antibody-Mediated Rejection (AMR) (ClinicalTrials.gov ↗)
Antibody-mediated Rejection
Phase 3 Active, closed Biogen USA

Registers list studies that are recruiting, about to open, active but closed to enrolment, or enrolling by invitation. The UK and USA registers cover industry-sponsored studies only. Trial titles and statuses are copied from the registry as published.

02

Conditions studied

5 conditions
Condition (as registered)Trials
Antibody-mediated Rejection2
Microvascular Inflammation2
Immunoglobulin A Nephropathy (IgAN)1
Primary Membranous Nephropathy1
Graves' Disease1
03

Sponsors

lead sponsor per trial
Lead sponsorTrials
Biogen6
04

Trials by country register

A trial with sites in more than one country appears in each of those registers.

How this page is built

Everything on this page is copied from public ClinicalTrials.gov registry records โ€” it is not written from memory, and nothing here describes how Felzartamab works or whether it is effective. Each trial links to its own record so you can check it yourself.

This page is built automatically: a daily sync job reads the registry records behind our country trial registers, collects every trial that lists Felzartamab (or a registered synonym) as a drug or biological intervention, and tabulates the registry fields directly. Placebos and generic comparators are excluded. There is no AI drafting and no per-compound editorial pass, and the page has not been clinically reviewed. The “last verified” date above is the timestamp of that sync, not a review date. Our general editorial approach is described in our editorial standards and corrections policy. The ClinicalTrials.gov data on this page was last retrieved on 24 Sep 2026.

Please verify before you rely on this. This page is general information for life-science and pharmaceutical professionals. It is not medical advice, and it has not been reviewed by a clinician โ€” our editorial team holds life-science qualifications, not clinical ones. It is not exhaustive and may not reflect the most recent label change. Always check the official prescribing information (US Prescribing Information or EU SmPC) and speak to your doctor or pharmacist before acting on anything here. Drugs in the same class are not automatically interchangeable, and approvals, brand names and indications differ between the US, the EU/Ireland (EMA/HPRA) and other regions. Spotted an error? Tell us โ€” we correct promptly and log it.