SBIR-STTR Award

Evaluation of a Novel H3 Antagonist, GT 2016, for ADHD
Award last edited on: 6/1/09

Sponsored Program
SBIR
Awarding Agency
NIH : NINDS
Total Award Amount
$850,029
Award Phase
2
Solicitation Topic Code
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Principal Investigator
Clark E Tedford

Company Information

Gliatech Inc

23420 Commerce Park Road
Cleveland, OH 44122
   (216) 831-3200
   N/A
   N/A
Location: Single
Congr. District: 11
County: Cuyahoga

Phase I

Contract Number: 1R43NS033808-01
Start Date: 00/00/00    Completed: 00/00/00
Phase I year
1995
Phase I Amount
$100,000
The long-term objectives are to develop novel histamine H3 receptor antagonists to increase wakefulness, attention and enhance cognitive abilities. The specific aims of this grant are (1) to test a novel non- thiourea H3 antagonist, GT-2016, for its ability to increase histamine release in various rat brain regions, including the frontal and parietal cortex, hippocampus, corpus striatum and hypothalamus (2) to determine if GT-2016 possesses cognition-enhancing properties in normal juvenile and adult rats (3) to produce an attention deficit disorder (ASS) juvenile rat pup model and evaluate the cognitive impairments in this model (4) to determine if GT-2016 reverses the cognitive deficits in a rat model of ADD. The first aim will provide information on the regional specificity of GT-2016 on histamine turnover. The subsequent aims are to demonstrate the cognition enhancement of GT-2016 in juvenile and young adult normal rats. The third aim will use postnatal intracisternal administration 6-OHDA, five days following birth, to produce a selective loss in dopaminergic neurons. These animals will be tested for hyperactivity and cognitive deficits and reversal of the deficits will then be determined for GT-2016. Data generated from this research could identify the use of H3 antagonists in the treatment of cognitive disorders including ADD. PROPOSED COMMERCIAL APPLICATION: A novel H3 antagonist, GT-2016, will be tested for its effects on brain histamine release and cognitive enhancing properties in normal rats and an animal model of ADD.

Phase II

Contract Number: 2R44NS033808-02A1
Start Date: 00/00/00    Completed: 00/00/00
Phase II year
1997
(last award dollars: 1998)
Phase II Amount
$750,029

The long-term objectives are to develop novel histamine H3 receptor antagonists for attention deficit hyperactive disorders (ADHD) and related cognitive diseases. Specific Aims are (year 1): (1) synthesis of gram quantities of stable GT-2016 salt for expanded in vivo testing. GT- 2016 salt will be compared versus clinically utilized ADHD agents (methylphenidate, d-amphetamine and pemoline) in 3 behavioral models for efficacy. Comparisons of the H3 antagonist in (2) developmentally immature juvenile rat pups (3) a 6-OH DA rat ADHD model and (4) a genetic-based ADHD SNAP(CM) mouse model will provide 3 rodent models with cognitive and/or activity outcomes. Additionally, EEG profiling in (5) normal rats and (6) narcoleptic dogs will provide arousal and vigilant assessments, general behavioral, cardiovascular and respiratory outcomes. Specific Aims for year 2 would involve studies determining the specificity and safety of the drugs' actions. These include: (7) drug abuse potential studies, (8) mutagenesis testing, (9) 14C-GT-2016 distribution studies and metabolite identification, (10) pharmacokinetics, (11) drug metabolism and liver induction profiles, and (12) toxicological testing. This research would be the first to identify the utility of H3 antagonists in the treatment of cognitive disorders including ADHD and provide valuable information towards clinical development.