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BDD with UDCA

Ewha Womans University Mokdong Hospital · Phase 3 active Small molecule

BDD (a bile acid derivative) combined with UDCA (ursodeoxycholic acid) enhances bile acid signaling and reduces hepatic inflammation and cholestasis.

BDD (a bile acid derivative) combined with UDCA (ursodeoxycholic acid) enhances bile acid signaling and reduces hepatic inflammation and cholestasis. Used for Primary biliary cholangitis (PBC), Primary sclerosing cholangitis (PSC) or other cholestatic liver disease.

At a glance

Generic nameBDD with UDCA
Also known asUDEX
SponsorEwha Womans University Mokdong Hospital
Drug classBile acid derivative combination
TargetFXR (farnesoid X receptor) / TGR5 (likely)
ModalitySmall molecule
Therapeutic areaHepatology / Gastroenterology
PhasePhase 3

Mechanism of action

UDCA is a hydrophilic bile acid that reduces the hydrophobicity of the bile acid pool and protects hepatocytes from cytotoxic bile acids. BDD likely acts as a farnesoid X receptor (FXR) agonist or bile acid receptor modulator to enhance cytoprotective signaling. Together, they reduce cholestasis, hepatic inflammation, and fibrosis progression in cholestatic liver diseases.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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