Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
FD-202 is a full-spectrum medicinal cannabis oil developed by Medibis, an Australian pharmaceutical company specializing in cannabinoid-based therapies. The formulation is characterized by a high concentration of cannabidiol (CBD), typically 200 mg/mL, and a low concentration of delta-9-tetrahydrocannabinol (THC), generally less than 2 mg/mL. As a full-spectrum extract, it contains a variety of minor cannabinoids, terpenes, and flavonoids derived from the *Cannabis sativa* plant, which are thought to contribute to its therapeutic profile via the entourage effect. FD-202 is currently being evaluated in clinical research, notably in an open-label feasibility study conducted by Southern Cross University's National Centre for Naturopathic Medicine (NCNM), to assess its safety and efficacy in managing anxiety and improving quality of life in adults with Autism Spectrum Disorder (ASD).
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 FD-202.