Helsinn to present two posters at the San Antonio Breast Cancer Symposium (SABCS) 2020 evaluating high CINV recurrence in breast cancer patients and CINV duration as its predictor
Lugano, Switzerland, December 7, 2020 – Helsinn, a Swiss pharmaceutical group focused on building quality cancer care and rare disease products, today announces that two scientific posters reviewing chemotherapy-induced nausea and vomiting (CINV) recurrence and an assessment of recurrence in later chemotherapy cycles, will be presented at the San Antonio Breast Cancer Symposium (SABCS). The symposium is taking place online from 8-11 December 2020.
Dr Rudolph M. Navari, of the World Health Organization, and lead investigator of both studies: “The first abstract reports that success in cycle 1 prophylaxis led to high success across subsequent cycles, while conversely cycle 1 failure led to high repeat failure for aprepitant, and to a lesser degree for NEPA. One possible explanation for the differential risks seen after the first cycle may be in the duration of CINV treatment failure, as shown in our second study presented at this conference.
In clinical practice, we see considerable heterogeneity in the duration of CINV. Our second abstract demonstrated that CINV duration (short vs extended) in cycle 1 strongly predicted CINV recurrence in subsequent cycles. This suggests a simple yet important new step for oncology practices: clinicians should monitor breakthrough CINV duration and follow guideline recommendations to change antiemetic prophylaxis when extended CINV does occur.”
William L. Bailey, Helsinn Therapeutics (U.S.) Vice President of Medical & Scientific Affairs: “Helsinn is committed to preventing CINV and reducing the burden of extended CINV events in all cycles of chemotherapy. These data in breast cancer patients presented at the SABCS 2020 highlight the need for close CINV monitoring and demonstrate our strong commitment to improving the lives of people with cancer.”
Presentation Details
Abstract 1 Title: Chemotherapy-induced nausea and vomiting (CINV) risk after prior breakthrough CINV: unmasking the false average
Date: December 9, 2020
Session Name: Poster Session 13 Poster 13-09
Time, Location: The full abstract can be viewed now on the SABCS website: https://www.sabcs.org/
Abstract 2 Title: Duration of chemotherapy-induced nausea and vomiting (CINV) as a predictor of later-cycle CINV
Date: December 9, 2020
Session Name: Poster Session 13 Poster 13-27
Time, Location: The full abstract can be viewed now on the SABCS website: https://www.sabcs.org/
About NEPA (AKYNZEO®)
AKYNZEO® is the first and only 5-HT3 and NK1 receptor antagonists fixed combination approved for the prevention of chemotherapy-induced acute and delayed nausea and vomiting. A single dose of AKYNZEO® given with dexamethasone has been shown to prevent chemotherapy-induced nausea and vomiting for 5 full days.
INDICATION
AKYNZEO® (netupitant 300mg/palonosetron 0.5mg) capsules was approved in October 2014 in the United States and is indicated in combination with dexamethasone in adults for the prevention of acute and delayed nausea and vomiting associated with initial and repeat courses of cancer chemotherapy, including, but not limited to, highly emetogenic chemotherapy.
AKYNZEO® (fosnetupitant 235mg/palonosetron 0.25) for injection was approved in April 2018 and AKYNZEO® injection was approved in May 2020 in the United States. Each is indicated in combination with dexamethasone in adults for the prevention of acute and delayed nausea and vomiting associated with initial and repeat courses of highly emetogenic cancer chemotherapy.
Limitations of Use
AKYNZEO® is a combination of palonosetron, a serotonin-3 (5-HT3) receptor antagonist, and netupitant or fosnetupitant, substance P/neurokinin-1 (NK-1) receptor antagonists: palonosetron prevents nausea and vomiting mainly during the acute phase and netupitant/fosnetupitant prevents nausea and vomiting during both the acute and delayed phase after cancer chemotherapy.
IMPORTANT SAFETY INFORMATION
Warnings and Precautions
Adverse Reactions
Drug-drug Interactions
Use in Specific Populations
For more information about AKYNZEO® please see the full US Prescribing Information
About the Helsinn Group
Helsinn is a privately-owned Swiss Pharma Company which, since 1976, has been improving the lives of patients, guided by core family values of respect, integrity and quality. The Group has an extensive portfolio of marketed innovative cancer and rare disease therapies, a robust drug development pipeline and ambitions to further accelerate its growth through in-licensing and acquisition to address unmet medical needs. Helsinn operates a unique integrated licensing business model, achieving success with over 80 long-standing partners in 190 countries, who share our values. The Group’s pharmaceutical business, (Helsinn Healthcare) is headquartered in Lugano, Switzerland with operating subsidiaries in the U.S. (Helsinn Therapeutics US) and China (Helsinn Pharmaceuticals China) which market the Group’s products directly in these countries. The Group has additional operating subsidiaries in Switzerland (Helsinn Advanced Synthesis, an active pharmaceutical ingredient manufacturer) and Ireland (Helsinn Birex Pharmaceuticals, a drug product manufacturer). Helsinn Investment Fund was created to enhance the future of healthcare by providing funding and strategic support to innovative companies.
Helsinn Group plays an active and central role in promoting social transformation in favor of people and the environment. Corporate social responsibility is at the heart of everything we do which is reinforced in the company’s strategic plan by a commitment to sustainable growth.
To learn more about Helsinn Group please visit www.helsinn.com
For more information:
Helsinn Group Media Contact:
Paola Bonvicini
Group Head of Communication
Lugano, Switzerland
Tel: +41 (0) 91 985 21 21
Email: Info-hhc@helsinn.com
For more information, please visit www.helsinn.com and follow us on Twitter, LinkedIn and Vimeo
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