Today’s news of the licensing of Trodelvy (sacituzumab govitecan) brings little comfort to women with triple negative incurable secondary breast cancer, as the drug’s developer, company Gilead Sciences (Nasdaq: GILD), failed to reach an agreement with NHS England to provide the drug free-of-charge to eligible patients, ahead of a National Institute for Health cand Care Excellence (NICE) decision on routine National Health Service (NHS) access next year, says the charity Breast Cancer Now.
Instead, hundreds of women in England who already face short prognoses and limited treatment options could now face an agonizing wait of up to eight months to access Trodelvy and the chance it brings of precious extra time with loved ones and doing what matters most to them.
Trodelvy’s licensing through the Project Orbis scheme, which the Medicines and Healthcare products Regulatory Agency (MHRA) joined at the start of the year, comes only a day after that of a lung cancer drug, sotorasib, and four months after another drug, both of which were successfully made immediately available to patients following licensing via an interim access scheme agreed by the drug companies Amgen (Nasdaq: AMGN) and AstraZeneca (LSE: AZN) with NHS England.
This article is accessible to registered users, to continue reading please register for free. A free trial will give you access to exclusive features, interviews, round-ups and commentary from the sharpest minds in the pharmaceutical and biotechnology space for a week. If you are already a registered user please login. If your trial has come to an end, you can subscribe here.
Login to your accountTry before you buy
7 day trial access
Become a subscriber
Or £77 per month
The Pharma Letter is an extremely useful and valuable Life Sciences service that brings together a daily update on performance people and products. It’s part of the key information for keeping me informed
Chairman, Sanofi Aventis UK
Copyright © The Pharma Letter 2024 | Headless Content Management with Blaze