Understanding the Signals that Guide our Treatment

Aardvark is developing compounds that target Bitter Taste Receptors (TAS2Rs) to address hunger-associated conditions. Our lead program, ARD-101, is designed to target receptors expressed on enteroendocrine cells in the gut lumen, which play a key role in gut-brain signaling. This innovative approach sets us apart from existing treatments and therapies in development.

Role of TAS2Rs in the Gut-Brain Axis:

When activated, TAS2Rs expressed on enteroendocrine cells trigger the local release of gut peptides such as cholecystokinin (CCK) and glucagon-like peptide-1 (GLP-1). These peptides bind to receptors on the vagus nerve, triggering signals to the brain to regulate satiety and food intake.
Role of TAS2Rs in the Gut-Brain Axis:

When activated, TAS2Rs expressed on enteroendocrine cells trigger the local release of gut peptides such as cholecystokinin (CCK) and glucagon-like peptide-1 (GLP-1). These peptides bind to receptors on the vagus nerve, triggering signals to the brain to regulate satiety and food intake.

CCK, a Neuropeptide, Plays an Established Role in Metabolic Regulation

Neuropeptides are natural regulators of metabolism, hunger, weight, and inflammation.

Hunger

Weight

Inflammation

Harnessing a Promising Obesity Target

The gut hormone CCK, which is known to play a key role in regulating satiety, has long been considered a promising pharmaceutical target. However, challenges with systemic exposure of CCK analogues have led to toxicity, raising safety concerns and causing adverse effects.

Favorable Safety Profile of ARD-101

In our preclinical studies and clinical trials to date, ARD-101 has been shown to be restricted to the gut with minimal systemic exposure (~1%). By being limited to the gut, ARD-101 has the potential to regulate hunger and metabolism through gut-brain signaling while potentially minimizing the risk of toxic effects on other tissues of the body.