Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Methydur is a **sustained-release oral formulation of methylphenidate**, developed using DURECT's proprietary ORADUR technology. It combines both immediate-release and extended-release mechanisms to provide rapid onset (within 2 hours) and prolonged therapeutic effect (8–12 hours) for once-daily dosing. Methydur is indicated for the treatment of **attention deficit hyperactivity disorder (ADHD)** in children and adults, aiming to reduce in-school dosing and risk of social stigma. The ORADUR technology confers abuse-deterrent properties, making extraction of the active ingredient for misuse more difficult. The drug is designed to improve medication adherence, consistency, and avoid impact on nighttime sleep. It was first launched in Taiwan in September 2020 by Orient Pharma, which also oversees manufacturing and regional commercialization efforts. DURECT originated the formulation and licensed global rights to Orient Pharma[1][2][5][7][8].
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 methydur.