TUDCA (tauroursodeoxycholic acid) is a bile acid made in the liver; it is ursodeoxycholic acid (ursodiol) bound to the amino acid taurine. It has been used for chronic liver diseases that slow bile flow, and in research it has been studied mainly for ALS (amyotrophic lateral sclerosis).
Also known as: tauroursodeoxycholic acid, tauroursodiol.
A placebo-controlled ALS pilot trial used 1 g twice a day for 54 weeks (Elia 2016). These are study protocols, not a recommendation.
It is sold in the US as a dietary supplement. Under the 1994 dietary supplement law (DSHEA), FDA does not approve dietary supplements before they are marketed, and the maker, not FDA, is responsible for safety and labeling.
How it differs from ursodiol: ursodiol (ursodeoxycholic acid) is an FDA-approved prescription drug for dissolving certain gallbladder stones and for preventing gallstones during rapid weight loss in people with obesity. The ursodiol label says the liver binds absorbed ursodiol to glycine or taurine; TUDCA is the taurine-bound form. TUDCA itself is not an FDA-approved drug.
What studies show: in a pilot trial of 34 people with ALS already taking riluzole, TUDCA (1 g twice a day for 54 weeks) was well tolerated, and more people improved on TUDCA (87%) than on placebo (43%); the authors call these preliminary data (Elia 2016). A larger phase 3 trial (TUDCA-ALS, planned for 320 people) was set up to test this; its protocol was published in 2022, and the company supplying the TUDCA is an industrial partner (Albanese 2022). A different product combining TUDCA with sodium phenylbutyrate was FDA-approved for ALS, but its phase 3 trial (PHOENIX) found no benefit at 48 weeks and the maker moved to withdraw it from the US and Canadian markets (Ketabforoush 2024).
Safety: side effects were no more common than with placebo in the pilot trial (Elia 2016). The sources here do not describe drug interactions.
We could not find a single published half-life or time to peak for TUDCA that applies to a supplement dose, so we do not list one.
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