Drug

Inebilizumab

As of the edition of 20 October 2026, Inebilizumab is an antibody: marketed, first approved in 2020 (US); acts on CD19; US protection ends in 2032.

Sources: FDA Orange Book and Purple Book, other approval registers, ClinicalTrials.gov, ChEMBL.

The drug

Status
Marketed; latest approval 2024
Kind
Antibody
Brand name
Uplizna
First approved
11 June 2020 (US)
Approvals on record
7 in 5 regions
Holder of the most recent approval
Amgen; 5 holders in all
Registered trials
27, 2 stopped early
Disease areas
Immune system; Nervous system; Cancer; Eye; Blood and lymph; Skin and connective tissue

US protection

US protection ends in 2032.

US protection ends in 2032, computed as 12 years from the first US licence because FDA publishes no date for this product. The application that gives this date is held by Amgen. The date is computed, not published.

This is the US only, and it is not the date generics or biosimilars can enter.

The exact date and the listings behind it

In the product

2 listings count towards this date. The exact date and each listing are in the product.

See the exact date and the 2 listings behind itRequest access. Nothing is shown until you do.

Companies that need a new molecule because of this drug

1 company on route B because of this drug.

Companies on route B for this drug

In the product

1 company is on route B because of Inebilizumab.

Target

GeneProteinUniProt
CD19B-lymphocyte antigen CD19P15391

Registered trials

PhaseTrialsCompletedActiveStopped early
Phase not stated5020
Phase 14400
Phase 210442
Phase 35140
Phase 43020
All trials27

Who has held its approvals

CompanyRoleYears
AmgenOriginator, Applicant and Lead sponsor of trials2020 to now
Mitsubishi Tanabe PharmaApplicant2021 to now
Tanabe PharmaLater holder and Lead sponsor of trials2022 to now