US pharma major Pfizer (NYSE: PFE) will stop its late-stage trial of Ibrance (palbociclib) early after hitting its primary endpoint.
The data, as assessed by an independent data monitoring committee, showed that the trial met the target of demonstrating an improvement in progression-free survival in certain patients with metastatic breast cancer. This data marks the “first randomized Phase III trial results” for Ibrance, a CDK 4/6 inhibitor.
The PALOMA-3 study was designed to assess the safety and efficacy of Ibrance in combination with AstraZeneca’s (LSE: AZN) Faslodex (fulvestrant) versus Faslodex versus placebo in patients with hormone receptor-positive, HER2-negative metastatic breast cancer following disease progression during or after endocrine therapy.
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