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Educational Videos/Journal Articles

We have created a range of expert lead video content/journal articles and downloadable resources to support you and your advanced ovarian cancer patients who have been prescribed ZEJULA.

Journal Articles

Videos Content

GyncancerXchange

Ovarian Cancer Experts explore the implications of the latest data supporting first-line maintenance treatment with PARPi in patients with advanced ovarian cancer.

ZEJULA Summary of Product Characteristics.

Speaker: Dr Antonio González-Martín, MD, PhD ; Prof lain McNeish,MD, PhD, FRCP ; Prof Michael Friedlander, AM, FRACP, PhD

While treatment outcomes for patients with gynaecological cancers have improved, clinical challenges and unmet needs remain. This video from global experts in the field of gynaecological cancers is a patient-centric event which aims to address key topics in first-line maintenance therapy for advanced ovarian cancer. This programme will feature discussions and insights to support treatment decision making centering on efficacy and quality of life in advanced ovarian cancer

Agenda & Objectives

Chapter 1 of 4

PARPi Monotherapy

Chapter 2 of 4

Understanding Key Drivers

Chapter 3 of 4

Patient Case

Chapter 4 of 4

Adverse events should be reported directly to the Health Products Regulatory Authority (HPRA) on their website: www.hpra.ie. Adverse events should also be reported to GlaxoSmithKline on 1800 244 255.

PM-IE-NRP-WCNT-240002 | Date of Preparation: July 2024

ZEJULA is indicated1

  • 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 platinumsensitive relapsed high grade serous epithelial ovarian, fallopian tube, or primary peritoneal cancer who are in response (complete or partial) to platinum-based chemotherapy.

Footnotes

HCP, healthcare professional; MoA, mechanism of action; QoL, quality of life.

Adverse events should be reported directly to the Health Products Regulatory Authority (HPRA) on their website: www.hpra.ie.
Adverse events should also be reported to GlaxoSmithKline on 1800 244 255 or via online form https://gsk.public.reportum.com/.

Zejula is a registered trademark of the GlaxoSmithKline group of companies.

November 2025 PM-IE-NRP-WCNT-240001