Bimzelx

Bimekizumab · UCB, Inc.
PRESCRIPTION ONLY (USA)

Bimzelx ingredients

Active ingredientStrength
Bimekizumab160 mg/mL, 320 mg/2mL

What Bimzelx is used for

The FDA lists the approved uses on the official label (below). In the EU, bimekizumab is approved as Bimzelx for:

Plaque psoriasis Bimzelx is indicated for the treatment of moderate to severe plaque psoriasis in adults who are candidates for systemic therapy. Psoriatic arthritis Bimzelx, alone or in combination with methotrexate, is indicated for the treatment of active psoriatic arthritis in adults who have had an inadequate response or who have been intolerant to one or more disease-modifying antirheumatic drugs (DMARDs). Axial spondyloarthritis Non-radiographic axial spondyloarthritis (nr-axSpA) Bimzelx is indicated for the treatment of adults with active non-radiographic axial spondyloarthritis with objective signs of inflammation as indicated by elevated C-reactive protein (CRP) and/or magnetic resonance imaging (MRI) who have responded inadequately or are intolerant to non-steroidal anti-inflammatory drugs (NSAIDs). Ankylosing spondylitis (AS, radiographic axial spondyloarthritis) Bimzelx is i…

EU wording from the European Medicines Agency; US approved uses can differ.

Key facts

Brand
Bimzelx
Generic name
Bimekizumab
Made by
UCB, Inc.
Forms
Injection, Solution
Given
Subcutaneous
FDA approval
Biologic licence (BLA) BLA761151
On the US market since
2023

Official information

Specialist medicine: started and supervised by a specialist doctor or hospital. This page is a plain-language summary of public official information, not medical advice; follow your doctor and the official product information.

Common questions

What is Bimzelx?

Bimzelx (Bimekizumab) is a specialist medicine made by UCB, Inc., approved by the US FDA.

What are the ingredients of Bimzelx?

Bimzelx contains Bimekizumab (160 mg/mL, 320 mg/2mL).

Is Bimzelx approved in Europe?

The same active substance is approved in the EU as Bimzelx.

From the FDA National Drug Code directory (open.fda.gov, public domain) and the European Medicines Agency medicines list. Page made 5 November 2026 by Satya Babu.

← All specialty medicines, USA

For information only, not medical advice. This page is a plain-language summary written from standard prescribing information and the public guides linked below. Brands sometimes change their formula, so always check the composition printed on the pack. Doses here are typical adult doses; yours may differ. Do not start, stop or change a medicine without your doctor or pharmacist, and keep all medicines away from children. In an emergency, call 112 (India) or your local emergency number.