Drug

Garetosmab

As of the edition of 20 October 2026, Garetosmab is an antibody: marketed, first approved in 2026 (US); acts on INHBA; US protection ends in 2038.

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

The drug

Status
Marketed; latest approval 2026
Kind
Antibody
Brand name
Pasatru
First approved
19 August 2026 (US)
Approvals on record
1 in 1 region
Holder of the most recent approval
Regeneron
Registered trials
10, 3 stopped early
Disease areas
Bones, joints and muscles; Nutrition and metabolism; Nervous system

US protection

US protection ends in 2038.

US protection ends in 2038, 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 Regeneron. 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.

See the exact date and the 1 listing 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 Garetosmab.

Target

GeneProteinUniProt
INHBAInhibin beta A chainP08476

Registered trials

PhaseTrialsCompletedActiveStopped early
Phase not stated1000
Phase 13201
Phase 23111
Phase 33021
All trials10

Who has held its approvals

CompanyRoleYears
RegeneronOriginator and Lead sponsor of trials2026 to now