A Study to Learn About the Effects of Felzartamab Infusions in Adults With Kidney Transplants Who Have Late Isolated Microvascular Inflammation

NCT ID: NCT07219043

Last Updated: 2026-01-20

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: PHASE2
• Total Enrollment: 81 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2026-01-05
• Study Completion Date: 2028-02-10

Brief Summary

In this study, researchers will learn more about a drug called felzartamab in people who have received a kidney transplant and later developed a condition called microvascular inflammation (MVI). MVI is a type of injury to small blood vessels in the transplanted kidney and may be a sign of rejection by the body. It can lead to serious kidney problems over time.

The main goal of the study is to learn about the effect felzartamab has on inflammation in the transplanted kidney. The main question researchers want to answer is:

• How many participants have no signs of active inflammation in the transplanted kidney after 24 weeks of treatment with felzartamab?

Researchers will also study how felzartamab affects kidney function, immune activity, and overall health. They will monitor safety through kidney biopsies, lab tests, and by recording adverse events throughout the study.

Adverse events are unwanted health problems that may or may not be caused by the study drug.

The study will be done in 2 parts as follows:

• Participants will be randomly assigned to receive either felzartamab or a placebo. A placebo looks like the study drug but contains no real medicine.
• In Part A, participants will receive their assigned drug for 24 weeks. Neither the researchers nor the participants will know who is receiving felzartamab or placebo.
• Part B will last another 28 weeks. All participants will receive felzartamab and both participants and researchers will know this.
• All treatments will be given by intravenous (IV) infusion at the study site.
• Participants will have kidney biopsies at the start of the study, at week 24, and at week 52 to help measure changes in inflammation.
• Participants will stay in the study for about 1 year.

Detailed Description

The primary objective of the study is to evaluate the efficacy of felzartamab compared to placebo in kidney transplant recipients diagnosed with complement activation (C4d)-positive or C4d-negative donor-specific antibody (DSA)-negative MVI (Part A). The secondary objectives of the study are to evaluate the efficacy of felzartamab compared to placebo through additional clinical endpoints (Part A), summarize safety and efficacy of felzartamab up to Week 52 in kidney transplant recipients diagnosed with C4d-positive or C4d-negative DSA negative MVI (Part B) and to assess the pharmacokinetic (PK) profile and immunogenicity of felzartamab (Parts A and B).

Conditions

Microvascular Inflammation

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

Felzartamab

Participants will receive multiple IV doses of felzartamab.

Group Type: EXPERIMENTAL

Felzartamab

Intervention Type: DRUG

Administered IV

Placebo and Felzartamab

Participants will receive multiple IV doses of placebo followed by multiple doses of IV felzartamab.

Group Type: PLACEBO_COMPARATOR

Felzartamab

Intervention Type: DRUG

Administered IV

Placebo

Intervention Type: DRUG

Administered IV

Interventions

Felzartamab

Administered IV

Intervention Type: DRUG

Placebo

Administered IV

Intervention Type: DRUG

Other Intervention Names

MOR202, MOR03087, TJ202, HIB202, BIIB148

Eligibility Criteria

Inclusion Criteria

• C4d-positive or C4d-negative DSA-negative MVI (biopsy-confirmed) without T cell-mediated rejection (TCMR) per central reading, as defined by the Banff 2022 criteria.
• Biopsy must be within 3 months (preferably within 1 month) prior to randomization.

a. For participants who received any prior treatment for antibody-mediated rejection (AMR), MVI, or TCMR as outlined in Exclusion Criterion 5, the biopsy must be performed at least 6 weeks after completing (or stopping) prior treatment.

• Kidney transplant at least 6 months prior to Screening visit (recipients of either living or deceased donors).
• DSA: Human leukocyte antigen (HLA) Class I and II antigen-specific DSA-negative (preformed and de novo DSA) as determined by the local laboratory's definition of positivity using single-antigen bead-based assays within 3 months prior to randomization.

Exclusion Criteria

• Transplant: Blood type (ABO)-incompatible transplant.
• History of multiple organ transplants including en bloc and dual kidney transplants.
• Presence of HLA donor-specific antibodies.
• Acute, rapid decline in renal function, defined as a participant likely to require renal replacement therapy within the next 30 days as determined by the Investigator.
• Prior AMR or TCMR treatment (with the exception of corticosteroids) within 3 months prior to randomization is excluded as listed below. Participants who received any of these treatments between 3 and 6 months prior to randomization must have both a renal biopsy (IC3) and DSA testing at least 6 weeks after completing (or stopping) treatment in order to confirm continuing DSA-negative MVI and to determine eligibility:

1. Intravenous or subcutaneous immunoglobulin (IVIg or subcutaneous immunoglobulin [SCIg]) or PLEX.

2. Complement system inhibitors (e.g., eculizumab).

3. Proteasome inhibitors (e.g., bortezomib).

4. Tocilizumab.

5. Any other investigational agent within 3 months or 5 half-lives (whichever is longer) of randomization.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 74 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Biogen

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Medical Director

Role: STUDY_DIRECTOR

Biogen

Locations

Cooperman Barnabas Medical Center

West Orange, New Jersey, United States

Site Status: RECRUITING

Medical College of Wisconsin

Milwaukee, Wisconsin, United States

Site Status: RECRUITING

Countries

United States

Central Contacts

US Biogen Clinical Trial Center

Role: CONTACT

clinicaltrials@biogen.com

866-633-4636

Global Biogen Clinical Trial Center

Role: CONTACT

clinicaltrials@biogen.com

Facility Contacts

Role: primary

973-322-2146

Role: primary

414-805-6060

Other Identifiers

2025-521742-15

Identifier Type: OTHER

Identifier Source: secondary_id

299AR201

Identifier Type: -

Identifier Source: org_study_id