Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Adhansia XR is a once-daily, extended-release oral capsule formulation of methylphenidate hydrochloride, a central nervous system (CNS) stimulant. It is indicated for the treatment of Attention Deficit Hyperactivity Disorder (ADHD) in patients aged 6 years and older. The medication utilizes a multi-layer bead technology with both immediate- and controlled-release components to provide rapid onset (within one hour) and sustained effect for up to 16 hours post-dose. Methylphenidate acts primarily by blocking the reuptake of norepinephrine and dopamine into presynaptic neurons in the brain, thereby increasing their availability in the synaptic cleft. This mechanism enhances attention and reduces impulsivity and hyperactivity associated with ADHD. Adhansia XR carries a boxed warning for abuse potential and dependence due to its stimulant properties[1][2][3].
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 Adhansia XR.