Skip to main content

The chemotherapy drug patupilone (EPO906) has failed to show a survival advantage over DoxilÒ/CaelyxÒ (pegylated liposomal doxorubicin) in patients with advanced ovarian cancer that is resistant to platinum-based therapy. Novartis reported the results in a press release.1

The Phase III trial was conducted in 168 sites in 22 countries and involved 829 patients with advanced ovarian cancer who were randomized to receive patupilone or Doxil/Caelyx. The primary endpoint of the study was survival.

The drug failed to show a significant survival advantage. Based on these data, Novartis does not plan to seek regulatory approval for the use of patupilone in advanced ovarian cancer. The drug is still being evaluated in trials for other tumor types, including metastatic colorectal cancer, as well as in patients with brain metastases from non–small cell lung cancer and hormone-refractory prostate cancer.

Reference:

Scroll to Continue

Recommended Articles

Image placeholder title

Zenocutuzumab - the first approved systemic therapy for patients with NRG1 fusion–positive NSCLC or pancreatic adenocarcinoma.

Zenocutuzumab targeted therapy approved for treatment of pancreatic ductal adenocarcinoma and non-small cell lung cancer with NRG1 fusions.

small cell lung cancer

Immunotherapy After Chemoradiotherapy Promising in Limited-Stage Small Cell Lung Cancer

Adjuvant therapy with Imfinzi (durvalumab) significantly improved survival outcomes for patients with limited-stage SCLC

Gut microbiome

Breakthrough in Understanding Tamoxifen's Effectiveness in Breast Cancer: Gut Bacteria Play a Crucial Role

Since tamoxifen is taken orally and travels through the digestive system, variations in patient responses may be connected to the gut microbiome—the trillions of bacteria in our intestines that differ significantly from one person to another.

1 Novartis News Release. Novartis phase III trial examining EPO906 (patupilone) for pateitns with advanced ovarian cancer failed to meet primary endpoint. Available at: Accessed May 27, 2010.

Copyright © 2018 CancerConnect. All Rights Reserved.