Ace Therapeutics provides comprehensive preclinical development services for attention deficit hyperactivity disorder (ADHD), covering the entire process from target validation, lead compound screening and optimization, to pharmacodynamic and safety assessments. With advanced platform technologies and animal models, we accurately assess the impact of drugs on ADHD-related neurobiological pathways while ensuring their safety and efficacy. Our one-stop customized solutions can help clients accelerate the development of ADHD therapeutics and drive innovative therapies to market quickly.
Medications can help children manage their ADHD symptoms in their daily lives.
Note: Medications can affect children differently and may have side effects such as decreased appetite or sleep problems. A child may respond well to one medication but not to another.
Ace Therapeutics assists clients in gaining a deeper understanding of the pathophysiologic mechanisms of attention deficit disorder (ADHD), including neurotransmitter systems, brain region function, and genetic factors. Our platform technologies and animal models enable us to elucidate the pathogenesis of ADHD, providing a scientific basis for ADHD diagnosis and innovative therapy development.
The pathophysiology of ADHD research services we offer focus on neuromodulation and neurochemistry.
We offer a full range of preclinical screening and evaluation services for attention deficit disorder (ADHD) drugs, covering the entire process from target validation and compound screening to pharmacodynamic and safety evaluations. Our capabilities in drug screening and evaluation include:
Ace Therapeutics is committed to conducting research and scientific evaluations from multiple perspectives to accelerate your efforts in the development of drugs for ADHD. If you are interested in our services, please contact us to learn how we can support you in your project.
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