Tenovus Scotland
This sponsor has funded 2 studies across 1 countries.
| EU PAS ID | Status | Title | Protocol uploaded | Results uploaded |
|---|---|---|---|---|
| 33586 | Ongoing | Risk of angiotensin converting enzyme inhibitor intolerance in asthma compared to the general population | Yes | No |
| 35083 | Ongoing | Risk of switching to angiotensin-II receptor blocker therapy in people with asthma who initiate ACE inhibitor therapy compared to the general... | Yes | No |
PAS by Risk Management Plan (RMP) requirement
Tenovus Scotland
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
Tenovus Scotland
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
Tenovus Scotland
1 Study countries specified are the following:
- United Kingdom