Ironwood’s Phase III Data Could Expand Linzess Market Share
Executive Summary
The company also hopes that positive safety data for pediatric patients could help with discussions with the FDA to make an OTC version of the drug.
You may also be interested in...
Ironwood Phase III Data Emphasizes Likely Linzess Label Expansion
Ironwood presented Phase III data on Linzess (linaclotide) at Digestive Disease Week for the treatment of 6-17 year-olds with functional constipation; US FDA approval is expected in a month.
Teva Pays Out A Further $1m On Intuniv
Teva will pay out more than $1m as part of a settlement deal over Intuniv (guanfacine) involving indirect purchasers, newly-filed court documents reveal. Meanwhile, the firm has also just gained a 2029 entry date for a 72mcg strength of its linaclotide rival to Linzess through a separate settlement.
Ironwood Ends Phase III GERD Program, Will Cut 100 Jobs
The company has no development programs left in its R&D pipeline and will focus entirely on the commercialization of IBS drug Linzess while seeking late-stage assets from external sources.