Repositioning Candidate Details

Candidate ID: R0895
Source ID: DB05894
Source Type: investigational
Compound Type: small molecule
Compound Name: GT 389-255
Synonyms: --
Molecular Formula: --
SMILES: --
DrugBank Description: Peptimmune’s lead product GT 389-255, is a novel lipase inhibitor and fat binding hydrogel polymer conjugate for the treatment of obesity which has completed single and multiple ascending dose (SAD and MAD) Phase I trials. It is expected to block fat absorption with fewer side effects than currently marketed lipase inhibitors.
CAS Number: --
Molecular Weight:
DrugBank Indication: Investigated for use/treatment in obesity.
DrugBank Pharmacology: --
DrugBank MoA: GT 389-255 is a novel conjugate of a proprietary pancreatic lipase inhibitor and a fatbinding hydrogel polymer for the treatment of obesity. GT 389-255 is a novel conjugate of a proprietary pancreatic lipase inhibitor and a fat binding hydrogel polymer for the treatment of obesity. It acts within the gastro-intestinal tract to prevent fat digestion and is expected to inhibit > 30% of fat absorption. The novel conjugate is expected to have fewer side-effects than currently marketed therapies. The currently marketed pancreatic lipase inhibitor Orlistat, is associated with oily incontinence, caused by mal-absorbed triglycerides. GT 389-255 is expected to have minimal systemic exposure. Less than 1% of the lipase inhibitor is absorbed and the fat binding polymer is not absorbed.
Targets: --
Inclusion Criteria: Therapeutic strategy associated