A post-trial access (PTA) study of SHP647
Latest Information Update: 02 Jun 2020
Price :
$35 *
At a glance
- Drugs Ontamalimab (Primary)
- Indications Crohn's disease; Inflammatory bowel diseases; Ulcerative colitis
- Focus Therapeutic Use
- 02 Jun 2020 New trial record
- 28 May 2020 According to an Takeda media release, the parameters for this PTA study will be determined in collaboration with the SHP647 program's steering committee and relevant regulatory authorities, and subsequently launched, subject to applicable local regulations and ethical considerations. Treatment will be made available to patients enrolled in this PTA study to meet their individual treatment needs.
- 28 May 2020 According to an Takeda media release, on May 28, the European Commission has released Takeda from the obligation to divest the pipeline compound SHP647 and certain associated rights. Takeda will discontinue the current SHP647 clinical trial program, and it will be providing all eligible trial participants with the opportunity to have continued access to SHP647 in a post-trial access (PTA) study.