At its inaugural R&D meeting for analysts on February 22 (see alsoMarketletter February 26), GlaxoSmithKline's chief executive, Jean-Pierre Garnier, gave details of the strategy which the company will adopt as it copes with a near-term gap in the pipeline and the R&D productivity and patent expiry problems facing the entire pharmaceutical industry.
Dr Garner, who described the GSK pipeline on several occasions as "awesome," said that the company would nevertheless still need to pursue an aggressive in-licensing strategy to support its anticipated growth in the future. The cost of in-licensing drugs is going up, but GSK is trying to reduce this cost burden by partnering projects which are not in late-stage development. The nine projects in-licensed by the firm in the last year (see table 1), which compares favorably with other firms which often only license two or three a year, illustrate this strategy.
This sentiment was echoed by GSK's chairman for R&D, Tachi Yamada, who noted that with 117 drugs in clinical trials and 161 in development, "there will be considerable culling" of projects in order to focus the company's R&D resources.
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 2025 | Headless Content Management with Blaze