GENENTECH NUTROPIN AND LILLY HUMATROPE PHASE IV TURNER's SYNDROME STUDIES SHOULD INCLUDE TREATMENT OPTIMIZATION; NEW hGH INDICATION RECOMMENDED
Lilly and Genentech should conduct post-marketing studies to optimize treatment and assess the long-term safety of their human growth hormone products in Turner's syndrome, FDA's Endocrinologic & Metabolic Drugs Advisory Committee recommended at its Dec. 10 meeting.
You may also be interested in...
Newly released Medicare Part D data sheds light on the sales hit that branded pharmaceutical manufacturers will face when the coverage gap discount program gets under way in 2011
FDA appears headed for a showdown with clinicians and the pharmaceutical industry over the proposed new clinical trial endpoints for acute bacterial skin and skin structure infections, the guidance's approach for justifying a non-inferiority margin and proposed changes in the types of patients that should be enrolled in trials
Specialty drug maker Shire has quietly begun scouting deals with a brand-new $50 million venture fund, the latest of several in-house investment arms to launch with their parent company's pipelines, not profits, as the measure of their worth