Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Neurodoron is an anthroposophic and complementary medicine developed by Weleda AG, indicated for the treatment of neurasthenia (nervous exhaustion) and metabolic weakness. It is a multi-component preparation containing three active ingredients: Aurum metallicum praeparatum (prepared gold), Kalium phosphoricum (potassium phosphate), and Ferrum-Quarz (iron-quartz). Originally launched in 1954 as Kalium phosphoricum comp., it was rebranded as Neurodoron in 2007. The drug is intended to address symptoms such as nervousness, irritability, restlessness, anxiety, and sleep disorders. As an anthroposophic medicine, it does not target a specific biological receptor in the conventional pharmacological sense but is designed to harmonize the human organism according to anthroposophic principles. It has been evaluated in Phase IV clinical trials in Germany to confirm its efficacy and safety in patients with nervous exhaustion.
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 Neurodoron.