supp.fit

TUDCA

9 benefits mapped to clinical evidence across supplements.

Dose per serving from products

170 products in our catalogue print how much TUDCA a serving holds.

Most common: 1 g to 2.5 g, 28% of 170 products.

Dose per servingProducts
50 mg or less
7
50 mg to 100 mg
8
100 mg to 250 mg
28
250 mg to 500 mg
44
500 mg to 1 g
34
1 g to 2.5 g
48
over 2.5 g
1

Dose per serving from research

12 study groups in 8 studies say how much TUDCA participants took a day.

These are the doses the studies gave. They are not a recommendation.

Most common: 1 g to 2.5 g, 50% of 12 study groups.

Daily doseStudy groups
250 mg to 500 mg
2
500 mg to 1 g
4
1 g to 2.5 g
6

See every study group

Benefit Evidence

Brain health
Moderate

Neuroprotection, less inflammation

ALS decline slowed +0.42/month

Survival +6.5 months

308 people
Cell health
Moderate

Reduced damage/inflammation

Slowed decline,+6.5mo

308 people
Nerve health
Moderate

Slower ALS decline +0.42/mo

Longer survival +6.5 mo

308 people

Liver enzymes down

ALP/symptoms improved

Albumin up

349 people

↓ inflammatory markers

immune shift

197 people

Antioxidant enzymes +

Oxidative stress -

MDA -

171 people

Liver enzymes ↓

Albumin ↑, fibrosis ↔

Bile UDCA ↑

150 people

GBEF +13.3%

Symptoms -3.8

63 people

Immune cells shifted +

Bile acids increased

47 people

Research sources

Brain health (3)
  1. Tauroursodeoxycholic acid in the treatment of patients with amyotrophic lateral sclerosis

    PubMed ID: 25664595

    Phase II ALS RCT: TUDCA slowed functional decline, supporting neuroprotective/brain support effects.

  2. Trial of Sodium Phenylbutyrate-Taurursodiol for Amyotrophic Lateral Sclerosis

    PubMed ID: 32877582

    Taurursodiol combination slowed ALS progression over 24 weeks in humans (functional benefit).

  3. Long-term survival of participants in the CENTAUR trial of sodium phenylbutyrate-taurursodiol in amyotrophic lateral sclerosis

    PubMed ID: 33063909

    Survival analysis: longer median survival with early taurursodiol exposure, supporting clinical neuro benefit.

Cell health (3)
  1. Long-term survival of participants in the CENTAUR trial of sodium phenylbutyrate-taurursodiol in amyotrophic lateral sclerosis

    PubMed ID: 33063909

    Survival analysis: participants on taurursodiol-containing treatment lived longer, supporting neuro/cellular benefit.

  2. Tauroursodeoxycholic acid in the treatment of patients with amyotrophic lateral sclerosis

    PubMed ID: 25664595

    Phase II ALS trial: one‑year TUDCA slowed functional decline, consistent with cellular neuroprotection.

  3. Trial of Sodium Phenylbutyrate-Taurursodiol for Amyotrophic Lateral Sclerosis

    PubMed ID: 32877582

    Taurursodiol combination slowed ALS functional decline over 24 weeks (human RCT).

Nerve health (3)
  1. Trial of Sodium Phenylbutyrate-Taurursodiol for Amyotrophic Lateral Sclerosis

    PubMed ID: 32877582

    Taurursodiol combination slowed ALS progression in a 24‑week RCT (human clinical neuro benefit).

  2. Tauroursodeoxycholic acid in the treatment of patients with amyotrophic lateral sclerosis

    PubMed ID: 25664595

    Phase II ALS RCT: one‑year TUDCA significantly slowed ALS functional decline — strong human evidence for neuronal support.

  3. Long-term survival of participants in the CENTAUR trial of sodium phenylbutyrate-taurursodiol in amyotrophic lateral sclerosis

    PubMed ID: 33063909

    Survival benefit analysis: earlier taurursodiol exposure associated with longer median survival in ALS cohort.

Liver support (2)
  1. A multicenter, randomized, double-blind trial comparing the efficacy and safety of TUDCA and UDCA in Chinese patients with primary biliary cholangitis

    PubMed ID: 27893675

    24‑week non‑inferiority RCT in PBC: TUDCA non‑inferior to UDCA for ALP reduction; some symptomatic improvement.

  2. Tauroursodeoxycholic acid for the treatment of HCV-related chronic hepatitis: a multicenter placebo-controlled study

    PubMed ID: 9840118

    Large multicenter RCT in HCV hepatitis: TUDCA significantly lowered aminotransferases vs placebo.

Inflammation (2)
  1. Bile acid metabolites predict multiple sclerosis progression and supplementation is safe in progressive disease

    PubMed ID: 39447576

    MS trial: immune cell shifts (reduced central memory CD4+ and Th1/17) suggest anti‑inflammatory immunomodulation.

  2. Tauroursodeoxycholic acid for the treatment of HCV-related chronic hepatitis: a multicenter placebo-controlled study

    PubMed ID: 9840118

    HCV RCT: reductions in aminotransferases reflect reduced hepatic inflammation.

Antioxidant (2)
  1. Trial of Sodium Phenylbutyrate-Taurursodiol for Amyotrophic Lateral Sclerosis

    PubMed ID: 32877582

    Taurursodiol combination showed slowed ALS progression, consistent with reduced neuronal cell stress.

  2. Tauroursodeoxycholic acid in the treatment of patients with amyotrophic lateral sclerosis

    PubMed ID: 25664595

    ALS clinical trial effects align with TUDCA's putative ER stress‑relieving, cytoprotective mechanisms.

Detoxification (1)
  1. Tauroursodeoxycholic acid for the treatment of HCV-related chronic hepatitis: a multicenter placebo-controlled study

    PubMed ID: 9840118

    HCV RCT: lowered aminotransferases indicating reduced hepatic injury and improved clearance of toxic bile/metabolites.

Digestive support (1)
  1. Acupoint Catgut Embedding as Adjunctive Therapy for Patients With Gallstones

    PubMed ID: 33471487

    TUDCA improved symptom scores in functional gallbladder patients (though GBEF unchanged without adjunctive ACE).

Immune support (1)
  1. Bile acid metabolites predict multiple sclerosis progression and supplementation is safe in progressive disease

    PubMed ID: 39447576

    Randomized MS trial showed TUDCA raised bile acids and altered immune cell populations vs placebo.

Similar by evidence

Supplements the same benefits carry qualifying findings for — a fact about the evidence graph, not a recommendation to swap.

Products with TUDCA

Search all

262 products whose verified label declares TUDCA — not every bottle that mentions it in a title.