Drug

Lisocabtagene maraleucel

As of the edition of 20 October 2026, Lisocabtagene maraleucel is a gene: marketed, first approved in 2021 (US); acts on CD19; US protection ends in 2033.

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

The drug

Status
Marketed; latest approval 2022
Kind
Gene
Brand name
Breyanzi
First approved
5 February 2021 (US)
Approvals on record
3 in 3 regions
Holder of the most recent approval
Bristol Myers Squibb; 2 holders in all
Registered trials
30, 3 stopped early
Disease areas
Blood and lymph; Cancer; Immune system; Heart and blood vessels; Digestive system

US protection

US protection ends in 2033.

US protection ends in 2033, 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 Juno Therapeutics. 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

2 companies on route B because of this drug.

Companies on route B for this drug

In the product

2 companies are on route B because of Lisocabtagene maraleucel.

Target

GeneProteinUniProt
CD19B-lymphocyte antigen CD19P15391

Registered trials

PhaseTrialsCompletedActiveStopped early
Phase not stated6050
Phase 15320
Phase 2174101
Phase 32002
All trials30

Who has held its approvals

CompanyRoleYears
Bristol Myers SquibbApplicant and Lead sponsor of trials2017 to now
Juno TherapeuticsAcquired holder2021 to now