Drug

Ramucirumab

As of the edition of 20 October 2026, Ramucirumab is an antibody: marketed, first approved in 2014 (US); acts on KDR; US protection ended in 2026.

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

The drug

Status
Marketed; latest approval 2015
Kind
Antibody
Brand name
Cyramza
First approved
21 April 2014 (US)
Approvals on record
10 in 4 regions
Holder of the most recent approval
Eli Lilly; 2 holders in all
Registered trials
158, 17 stopped early
Disease areas
Cancer; Digestive system; Lungs and airways; Urinary and reproductive; Pregnancy and women's health; Skin and connective tissue

US protection

US protection ended in 2026.

The orphan exclusivity ended in 2026 (it covers one use only). The application that gives this date is held by Eli Lilly.

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 Ramucirumab.

Target

GeneProteinUniProt
KDRVascular endothelial growth factor receptor 2P35968

Registered trials

PhaseTrialsCompletedActiveStopped early
Phase not stated6210
Phase 1342273
Phase 296482713
Phase 3221461
All trials158

Who has held its approvals

CompanyRoleYears
Eli LillyApplicant and Lead sponsor of trials2014 to now