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28-day repeated dose toxicity and toxicokinetics study on new melatonergic antidepressant GW117 in beagle dogs
Mei Gao1,2, Kai Chen2, Wei Gu3
1Shandong Provincial Key Laboratory of Animal Resistance Biology, College of Life Sciences, Shandong Normal University, Jinan, 250014, China.
Abstract:
GW117 is new melatonergic antidepressant being developed to show better antidepressant action than agomelatine. The purpose of this study was to evaluate the toxicity and to determine potential target organs after oral (gavage) administration of the test article GW117 for 28 days and to assess the reversibility after a 4-week recovery phase in beagle dogs. Toxicokinetics was also evaluated. Four groups were designed in this study, including the vehicle control group and the GW117 50, 150 and 500 mg/kg/day groups, with 5 dogs/sex/group. Body weight, hematology, clinical chemistry, gross necropsy, organ weight, histopathology, and other indicators were examined. Results showed that animals dosed at ≥150 mg/kg/day showed gastrointestinal reactions (watery feces and dark green/red brown feces), with a dose-response relationship in the incidence and severity grade. Female dogs at 500 mg/kg/day had an increase in organ weight and ratios of the liver at the end of the dosing phase. Histopathology examination showed that some animals at 500 mg/kg/day, especially female animals, had minimal centrilobular hepatocyte hypertrophy in the liver, which reversed after 28-day recovery. With the exception of the above, no GW117-related abnormality was noted. Meanwhile, there were no sexual differences in drug exposure and accumulation after the first and last dosing. The no observed adverse effect dose level (NOAEL) was 150 mg/kg/day, under which mean Cmax and AUC0 → t were 583.5 and 2767.0 ng/ml*h for females and 663.2 and 4046.3 ng/ml*h for males on Day 28.
Insights
The novel melatonergic antidepressant GW117 demonstrated a no observed adverse effect level (NOAEL) of 150 mg/kg/day in beagle dogs. Gastrointestinal effects and reversible liver changes were noted at higher doses.
Area of Science:
- Pharmacology
- Toxicology
- Drug Development
Background:
- GW117 is a novel melatonergic antidepressant candidate.
- It is being developed as a potentially improved alternative to agomelatine.
- Preclinical safety evaluation is crucial for new drug development.
Purpose of the Study:
- To evaluate the 28-day oral toxicity of GW117 in beagle dogs.
- To identify potential target organs for GW117 toxicity.
- To assess the reversibility of any observed effects after a 4-week recovery period.
Main Methods:
- A 28-day oral gavage study in beagle dogs (5 dogs/sex/group).
- Dose groups: vehicle control, GW117 (50, 150, 500 mg/kg/day).
- Evaluated parameters included body weight, hematology, clinical chemistry, gross necropsy, organ weight, histopathology, and toxicokinetics.
Main Results:
- Gastrointestinal reactions (watery, discolored feces) observed at ≥150 mg/kg/day in a dose-dependent manner.
- Minimal, reversible centrilobular hepatocyte hypertrophy in the liver noted at 500 mg/kg/day, primarily in females.
- No significant GW117-related abnormalities, sexual differences in exposure, or accumulation were observed below 500 mg/kg/day.
Conclusions:
- The no observed adverse effect dose level (NOAEL) for GW117 was determined to be 150 mg/kg/day.
- Observed toxicities (gastrointestinal, hepatic) were dose-dependent and reversible.
- GW117 exhibits a generally favorable safety profile in beagle dogs at doses up to 150 mg/kg/day.

