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Callisto’s bowel treatment proves effective in mice

Biotech firm Callisto Pharmaceuticals has received positive preliminary results from the company's drug, SP304, which is currently being evaluated pre-clinically for the treatment of inflammatory bowel diseases. Data showed a pronounced reduction of inflammation following treatment with SP304.

The drug was evaluated in a TNBS-induced ulcerative colitis mouse model, which is an animal model widely used to evaluate drug candidates for treatment of human inflammatory bowel diseases (IBD). SP304 demonstrated a significant reduction in histopathological indicators of inflammation.

SP304, an orally deliverable and highly stable peptide, is an analog of the native human peptide uroguanylin, a guanylate cyclase receptor agonist (GCRA) normally produced in the intestinal tract. SP304, unlike the parent peptide uroguanylin, exists in a single active conformer, and is an excellent candidate for drug development.

“The histopathology data demonstrating the anti-inflammatory properties of SP304 are particularly impressive because the peptide was administered once a day at very small doses of 0.01-0.02 mg,” remarked Dr Kunwar Shailubhai, senior vice president of discovery research at Synergy Pharmaceuticals, a wholly owned subsidiary of Callisto Pharmaceuticals.