EUSA Pharma
This sponsor has funded 2 studies across 8 countries.
| EU PAS ID | Status | Title | Protocol uploaded | Results uploaded |
|---|---|---|---|---|
| 14776 | Finalised | ACCELERATE: AN INTERNATIONAL, OBSERVATIONAL REGISTRY FOR PATIENTS WITH CASTLEMAN DISEASE | Yes | Yes |
| 31973 | Ongoing | A Post-Authorisation Safety Study Patient Registry of patients with high-risk neuroblastoma being treated with the monoclonal antibody dinutuximab... | No | No |
PAS by Risk Management Plan (RMP) requirement
EUSA Pharma
The RMP for a medical product outlines strategies to identify, assess, and mitigate risks, including PAS for further evaluation.
Category 1 studies are imposed as condition of marketing authorisation.
Category 2 studies are imposed as specific obligation of marketing authorisation.
Category 3 studies are required under other circumstances.
PAS by study status
EUSA Pharma
The study status is defined according to the timeline dates specified.
Planned studies have not collected any data yet.
Ongoing studies collect data and should publish protocols as soon as possible.
Finalised studies should publish results in the first two weeks after finalisation.
Countries
EUSA Pharma
8 Study countries specified are the following:
- Austria
- France
- Germany
- Italy
- Norway
- Poland
- Spain
- United Kingdom