Zejula

niraparib · GlaxoSmithKline Trading Services Limited
ORPHAN AUTHORISED IN THE EU

What Zejula is used for

Zejula is indicated: as monotherapy for the maintenance treatment of adult patients with advanced epithelial (FIGO Stages III and IV) high-grade ovarian, fallopian tube or primary peritoneal cancer who are in response (complete or partial) following completion of first-line platinum-based chemotherapy. as monotherapy for the maintenance treatment of adult patients with platinum sensitive relapsed high grade serous epithelial ovarian, fallopian tube, or primary peritoneal cancer who are in response (complete or partial) to platinum based chemotherapy.

Approved use, as published by the European Medicines Agency.

What the labels mean

  • Orphan medicine: for a rare disease (affecting no more than 5 in 10,000 people in the EU).

Key facts

Brand
Zejula
Active substance
niraparib
Disease area
Fallopian Tube Neoplasms; Peritoneal Neoplasms; Ovarian Neoplasms
Medicine group
Antineoplastic agents
ATC code
L01XK02
Marketing authorisation holder
GlaxoSmithKline Trading Services Limited
Authorised in the EU since
2017

Official information

Specialist medicine: started and supervised by a specialist doctor or hospital. This page is a plain-language summary of public official information, not medical advice; follow your doctor and the official product information.

Common questions

What is Zejula used for?

Zejula is indicated: as monotherapy for the maintenance treatment of adult patients with advanced epithelial (FIGO Stages III and IV) high-grade ovarian, fallopian tube or primary peritoneal cancer who are in response (complete or partial) following completion of first-line platinum-based chemotherapy. as monotherapy for the maintenance treatment of adult patients with platinum sensitive relapsed high grade serous epithelial ovarian, fallopian tube, or primary peritoneal cancer who are in response (complete or partial) to platinum based chemotherapy.

What is the active substance in Zejula?

Zejula contains niraparib.

Who makes Zejula?

The EU marketing authorisation holder is GlaxoSmithKline Trading Services Limited.

Is Zejula an orphan medicine?

Yes. Zejula is designated an orphan medicine in the EU, for a rare disease (Fallopian Tube Neoplasms; Peritoneal Neoplasms; Ovarian Neoplasms).

Source: European Medicines Agency medicines data (ema.europa.eu), reproduced with acknowledgement of the source. Page made 5 November 2026 by Satya Babu.

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For information only, not medical advice. This page is a plain-language summary written from standard prescribing information and the public guides linked below. Brands sometimes change their formula, so always check the composition printed on the pack. Doses here are typical adult doses; yours may differ. Do not start, stop or change a medicine without your doctor or pharmacist, and keep all medicines away from children. In an emergency, call 112 (India) or your local emergency number.