Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
[18F]FEMPA (BAY1006578) is a radiolabeled small molecule developed as a positron emission tomography (PET) imaging agent. It was investigated for its diagnostic potential in distinguishing probable Alzheimer's disease patients from healthy volunteers by visualizing specific brain targets using PET imaging. The compound is used as a tracer to assess pathological changes associated with Alzheimer's disease, aiding in the evaluation of neurodegenerative processes. The developer of this agent is Bayer. Its primary indication has been for diagnostic imaging in Alzheimer’s disease research, and it has undergone phase 1 clinical trials for this purpose.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on [18F]FEMPA.