Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
QuilliChew ER is a central nervous system (CNS) stimulant formulated as an extended-release, cherry-flavored chewable tablet containing methylphenidate hydrochloride. It is indicated for the treatment of Attention Deficit Hyperactivity Disorder (ADHD). The drug works primarily by inhibiting the reuptake of dopamine and norepinephrine in the brain, thereby increasing their synaptic concentrations and enhancing neurotransmission in areas involved in attention and behavior regulation. Methylphenidate-containing medications are classified as Schedule II controlled substances due to their potential for abuse and dependence. QuilliChew ER was approved by the FDA in 2015 as a unique formulation designed for once-daily oral administration[1][2][3][4][5].
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 methylphenidate hydrochloride extended-release chewable tablet.