Ozmosi | YY-162 Drug Profile
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YY-162

Alternative Names: yy-162, yy162, yy 162
Clinical Status: Inactive
Latest Update: 2019-02-25
Latest Update Note: Clinical Trial Update

Product Description

YY162 attenuated the increase in reactive oxygen species (ROS) and decrease in BDNF levels induced by Aroclor1254 in SH-SY5Y neuroblastoma cells. YY162 significantly attenuated Aroclor1254-induced ADHD-like behavior and oxidative stress in ICR mice. Furthermore, YY162 attenuated reductions in p-TrkB, BDNF, dopamine transporter (DAT) and norepinephrine transporter (NET) expression.Ê (Sourced from: https://pubmed.ncbi.nlm.nih.gov/24394491/)

Mechanisms of Action: No Mechanism

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: Oral

FDA Designation: *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Yuyu Pharma
Company Location:
Company CEO:
Additional Commercial Interests: None

Clinical Description

Countries in Clinic:

Active Clinical Trial Count:

Recent & Upcoming Milestones

Highest Development Phases

Phase 3: Psychotic Disorders|Attention Deficit Disorder with Hyperactivity

Trial ID

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

NCT01536210

ADHD

P3

Completed

Attention Deficit Disorder with Hyperactivity|Psychotic Disorders

2012-08-01

2019-03-19

Treatments

NCT01201187

yuyu

P3

Completed

Psychotic Disorders|Attention Deficit Disorder with Hyperactivity

2010-04-01

2019-03-19

Treatments

Recent News Events

Date

Type

Title