Drug

Taliglucerase alfa

As of the edition of 20 October 2026, Taliglucerase alfa is an enzyme: marketed, first approved in 2012 (US); US protection ended in 2024.

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

The drug

Status
Marketed; latest approval 2012
Kind
Enzyme
Brand name
Elelyso
First approved
1 May 2012 (US)
Approvals on record
2 in 1 region
Holder of the most recent approval
Pfizer
Registered trials
14, 1 stopped early
Disease areas
Inherited and neonatal; Nervous system; Nutrition and metabolism; Blood and lymph; Digestive system

US protection

US protection ended in 2024.

US protection ended in 2024, 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 Pfizer. 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

1 listing counts towards this date. The exact date and each listing are in the product.

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Registered trials

PhaseTrialsCompletedActiveStopped early
Phase not stated2100
Phase 12200
Phase 22100
Phase 35500
Phase 43201
All trials14

Who has held its approvals

CompanyRoleYears
PfizerOriginator and Lead sponsor of trials2010 to now