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Doxycycline and tauroursodeoxycholic acid

Fondazione IRCCS Policlinico San Matteo di Pavia · Phase 3 active Small molecule

Doxycycline and tauroursodeoxycholic acid combination works by reducing inflammation and oxidative stress while promoting bile acid signaling to protect mitochondrial function and reduce hepatocellular injury.

Doxycycline and tauroursodeoxycholic acid combination works by reducing inflammation and oxidative stress while promoting bile acid signaling to protect mitochondrial function and reduce hepatocellular injury. Used for Primary biliary cholangitis (PBC), Non-alcoholic fatty liver disease (NAFLD) / Non-alcoholic steatohepatitis (NASH).

At a glance

Generic nameDoxycycline and tauroursodeoxycholic acid
Also known asStandard of care therpay
SponsorFondazione IRCCS Policlinico San Matteo di Pavia
Drug classCombination therapy (antibiotic + bile acid derivative)
TargetMatrix metalloproteinases, FXR (farnesoid X receptor), TGR5 (G-protein coupled bile acid receptor 1)
ModalitySmall molecule
Therapeutic areaHepatology / Gastroenterology
PhasePhase 3

Mechanism of action

Doxycycline is a tetracycline antibiotic with anti-inflammatory and anti-fibrotic properties that inhibit matrix metalloproteinases and reduce inflammatory cytokine production. Tauroursodeoxycholic acid (TUDCA) is a bile acid that activates farnesoid X receptor (FXR) and G-protein coupled bile acid receptor 1 (TGR5), enhancing mitochondrial function and reducing endoplasmic reticulum stress. Together, they target multiple pathways involved in liver disease progression.

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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