Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
TAH9922 is an oral liquid formulation of atomoxetine, a selective norepinephrine transporter (NET) inhibitor, developed by Taihe Pharmaceutical (Taho Pharma). It is specifically designed for the treatment of Attention Deficit Hyperactivity Disorder (ADHD) in pediatric patients who may have difficulty swallowing capsules. By selectively inhibiting the presynaptic norepinephrine transporter, the drug increases the concentration of norepinephrine in the synaptic cleft, particularly in the prefrontal cortex, which is associated with improved attention and impulse control. TAH9922 is being developed via the 505(b)(2) regulatory pathway in the United States, and its US commercial rights have been licensed to a partner for NDA filing.
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 atomoxetine (Taihe Pharmaceutical).