Safety and Efficacy of TUDCA as add-on Treatment in Patients Affected by ALS (TUDCA-ALS)

• ClinicalTrials.gov Identifier: NCT03800524
• Recruitment Status: Active, not recruiting
• First Posted: January 11, 2019
• Last Update Posted: July 10, 2023
• Sponsor: Humanitas Mirasole SpA
• Collaborators: University of Ulm; University of Sheffield; University Hospital, Tours; KU Leuven; UMC Utrecht; University of Dublin, Trinity College; Bruschettini S.r.l.; Istituto Superiore di Sanità; Motor Neurone Disease Association; European Commission
• Information provided by (Responsible Party): Humanitas Mirasole SpA

Tracking Information

• First Submitted Date: January 4, 2019
• First Posted Date: January 11, 2019
• Last Update Posted Date: July 10, 2023
• Actual Study Start Date: February 22, 2019
• Estimated Primary Completion Date: December 31, 2023 (Final data collection date for primary outcome measure)

Current Primary Outcome Measures (submitted: January 8, 2019)

Number of responder patients [ Time Frame: 18 months ]

Identification of the responder patients defined as those showing an improvement of at least 20% in the ALSFRS-R slope

• Original Primary Outcome Measures: Same as current

Current Secondary Outcome Measures (submitted: July 7, 2023)

• Survival time [ Time Frame: 18 months ]
  Survival time measured by death or respiratory insufficiency
• ALS disease functional rating scale - revised version (ALSFRS-R) [ Time Frame: 18 months ]
  Difference in change from baseline in ALSFRS-R. Each task of the scale is rated on a five-point scale from 0 = can't do, to 4 = normal ability. Individual item scores are summed to produce a reported score ranging from 0 = worst to 48 = best.
• ALS Assessment Questionnaire-40 (ALSAQ-40) [ Time Frame: 18 months ]
  Difference in change from baseline in ALSAQ-40. The instrument contains 40 statements that measure five dimensions of health state: Physical Mobility (10 statements), Activities of Daily Living and Independence (10 statements), Eating and Drinking (5 statements), Communication (5 statements), Emotional Functioning (10 statements). The patient must indicate how often (Never, Rarely, Sometimes, Often, or Always) the statement have been true. Dimension scores are coded on a likert scale, ranging from 0 (best health as assessed by the scale) to 100 (worse health as assessed by the measure).
• Forced Vital Capacity [ Time Frame: 18 months ]
  Difference in change from baseline in Forced Vital Capacity
• EuroQol 5-Dimension-5 Levels (EQ-5D-5L) scale [ Time Frame: 18 months ]
  Difference in change from baseline in EQ-5D-5L scale. The EQ-5D-5L descriptive system comprises 5 dimensions (mobility, self-care, usual activities, pain/discomfort and anxiety/depression). Each dimension has 5 levels: 1.no problems, 2.slight problems, 3.moderate problems, 4.severe problems, 5.extreme problems. The patient is asked to indicate his/her health state by ticking (or placing a cross) in the box against the most appropriate statement in each of the 5 dimensions. This decision results in a 1-digit number expressing the level selected for that dimension. The digits for 5 dimensions can be combined in a 5-digit number describing the patient health state. Numbers 1-5 have no arithmetic properties and should not be used as a cardinal score.
• Medical Research Council (MRC) scale [ Time Frame: 18 months ]
  Difference in change from baseline in muscle force assessed by the MRC scale. The scale rates muscle strength of 6 muscles (3 at the upper and 3 at the lower limbs), bilaterally. Each muscle is graded from 0 = no movement, to 5 = normal strength, giving a total sum-score that ranges from 0 (total paralysis) to 60 (normal strength).
• Neurofilaments levels [ Time Frame: 18 months ]
  Effect of TUDCA on Neurofilament levels in comparison to placebo
• MMP-9 levels [ Time Frame: 18 months ]
  Effect of TUDCA on MMP-9 expression in comparison to placebo
• Long-term safety and tolerability [ Time Frame: 18 months ]
  assessed through adverse reaction, concomitant treatment, physical examination, vital signs and routine haematology and biochemistry analyses

Original Secondary Outcome Measures (submitted: January 8, 2019)

• Survival time [ Time Frame: 18 months ]
  Survival time measured by death or respiratory insufficiency
• ALS disease functional rating scale - revised version (ALSFRS-R) [ Time Frame: 18 months ]
  Difference in change from baseline in ALSFRS-R. Each task of the scale is rated on a five-point scale from 0 = can't do, to 4 = normal ability. Individual item scores are summed to produce a reported score ranging from 0 = worst to 48 = best.
• ALS Assessment Questionnaire-40 (ALSAQ-40) [ Time Frame: 18 months ]
  Difference in change from baseline in ALSAQ-40. The instrument contains 40 statements that measure five dimensions of health state: Physical Mobility (10 statements), Activities of Daily Living and Independence (10 statements), Eating and Drinking (5 statements), Communication (5 statements), Emotional Functioning (10 statements). The pa-tient must indicate how often (Never, Rarely, Sometimes, Often, or Always) the statement have been true. Dimension scores are coded on a likert scale, ranging from 0 (best health as assessed by the scale) to 100 (worse health as assessed by the measure).
• Forced Vital Capacity [ Time Frame: 18 months ]
  Difference in change from baseline in Forced Vital Capacity
• EuroQol 5-Dimension-5 Levels (EQ-5D-5L) scale [ Time Frame: 18 months ]
  Difference in change from baseline in EQ-5D-5L scale. The EQ-5D-5L descriptive system comprises 5 dimensions (mobility, self-care, usual activi-ties, pain/discomfort and anxiety/depression). Each dimension has 5 levels: 1.no problems, 2.slight problems, 3.moderate problems, 4.severe problems, 5.extreme problems. The patient is asked to indicate his/her health state by ticking (or placing a cross) in the box against the most appropriate statement in each of the 5 dimensions. This decision results in a 1-digit number express-ing the level selected for that dimension. The digits for 5 dimensions can be combined in a 5-digit number describing the patient health state. Numbers 1-5 have no arithmetic properties and should not be used as a cardinal score.
• Medical Research Council (MRC) scale [ Time Frame: 18 months ]
  Difference in change from baseline in muscle force assessed by the MRC scale. The scale rates muscle strength of 6 muscles (3 at the upper and 3 at the lower limbs), bilaterally. Each muscle is graded from 0 = no movement, to 5 = normal strength, giving a total sum-score that ranges from 0 (total paralysis) to 60 (normal strength).
• Neurofilaments levels [ Time Frame: 18 months ]
  Effect of TUDCA on Neurofilament levels in comparison to placebo
• MMP-9 levels [ Time Frame: 18 months ]
  Effect of TUDCA on MMP-9 expression in comparison to placebo

• Current Other Pre-specified Outcome Measures: Not Provided
• Original Other Pre-specified Outcome Measures: Not Provided

Descriptive Information

• Brief Title: Safety and Efficacy of TUDCA as add-on Treatment in Patients Affected by ALS
• Official Title: Safety and Efficacy of Tauroursodeoxycholic (TUDCA) as add-on Treatment in Patients Affected by Amyotrophic Lateral Sclerosis (ALS)
• Brief Summary: This is a Phase III, multi-centre, randomized, double-blind, placebo-controlled, parallel-group study to evaluate Safety and Efficacy of Tauroursodeoxycholic (TUDCA) as add-on Treatment in Patients Affected by Amyotrophic Lateral Sclerosis (ALS).

Detailed Description

Enrolled patients will be randomized to one of two treatment arms: TUDCA or identical placebo by oral route. The randomization will be performed in a ratio one to one for the two arms.

TUDCA will be administered orally at the dose of 1 g twice daily (2 g daily) for 18 months. Patients will be taking also riluzole at the dose of 50 mg twice daily (100 mg daily).

Patient randomization will take place after a screening (lead-in) period of 12 weeks (3 months) with 3 assessments at 6-week intervals. Clinical assessments during the trial phase will be performed every three months. This will allow measuring the progression rate before and after starting treatment (either active or placebo).

• Study Type: Interventional
• Study Phase: Phase 3
• Study Design: Allocation: Randomized; Intervention Model: Parallel Assignment; Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor); Primary Purpose: Treatment
• Condition: Amyotrophic Lateral Sclerosis (ALS)

Intervention

• Drug: Tauroursodeoxycholic Acid
  • Tauroursodeoxycholic acid (TUDCA) 250 mg capsules
  • Doses: 4 capsules (1 g) twice daily 10-15 minutes after a meal
  • Mode of administration: orally
  • Duration: 18 months
  Other Names:

  • TUDCA
  • Tudcabil
  • Taurolite
• Drug: Placebo
  • Placebo 250 mg capsules
  • Doses: 4 capsules (1 g) twice daily 10-15 minutes after a meal
  • Mode of administration: orally
  • Duration: 18 months

Study Arms

• Experimental: Tauroursodeoxycholic acid (TUDCA)
  • Tauroursodeoxycholic acid (TUDCA) 250 mg capsules
  • Doses: 4 capsules (1 g) twice daily 10-15 minutes after a meal
  • Mode of administration: orally
  • Duration: 18 months
  Intervention: Drug: Tauroursodeoxycholic Acid
• Placebo Comparator: Reference therapy
  • Placebo capsules identical to active compound
  • Doses: 4 capsules (1 g) twice daily 10-15 minutes after a meal
  • Mode of administration: orally
  • Duration: 18 months
  Intervention: Drug: Placebo

• Publications *: Albanese A, Ludolph AC, McDermott CJ, Corcia P, Van Damme P, Van den Berg LH, Hardiman O, Rinaldi G, Vanacore N, Dickie B; TUDCA-ALS Study Group. Tauroursodeoxycholic acid in patients with amyotrophic lateral sclerosis: The TUDCA-ALS trial protocol. Front Neurol. 2022 Sep 27;13:1009113. doi: 10.3389/fneur.2022.1009113. eCollection 2022.

Recruitment Information

• Recruitment Status: Active, not recruiting
• Actual Enrollment (submitted: October 17, 2022): 337
• Original Estimated Enrollment (submitted: January 8, 2019): 440
• Estimated Study Completion Date: December 31, 2023
• Estimated Primary Completion Date: December 31, 2023 (Final data collection date for primary outcome measure)

Eligibility Criteria

Inclusion Criteria:

• Probable laboratory-supported, probable, or definite ALS, as defined by El Escorial Revised ALS diagnostic criteria at screening visit (month -3)
• Disease duration ≤ 18 months at screening visit (month -3)
• Able to perform reproducible pulmonary function tests at screening visit (month -3)
• Forced vital capacity or slow vital capacity ≥70% of normal at screening visit (month -3)
• Stable on riluzole treatment for 3 months in the lead-in period
• Signed informed consent at screening visit (month -3)

Exclusion Criteria:

• Treatment with edaravone
• Other causes of neuromuscular weakness
• Presence of other neurodegenerative diseases
• Significant cognitive impairment, clinical dementia or psychiatric illness
• Severe cardiac or pulmonary disease
• Other diseases precluding functional assessments
• Other life-threatening diseases
• Any use of non-invasive ventilation (e.g. continuous positive airway pressure, non-invasive bi-level positive airway pressure or non-invasive volume ventilation) for any portion of the day, or mechanical ventilation via tracheostomy, or on any form of oxygen supplementation
• Gastrointestinal disorder that is likely to impair absorption of study drug from the gastrointestinal tract
• Has taken any investigational study drug within 30 days or five half-lives of the prior agent, whichever is longer, prior to dosing
• Any clinically significant laboratory abnormality
• Other concurrent investigational medications
• Active peptic ulcer
• Previous surgery or infections of small intestine
• Patients unable to easily swallow the treatment pills
• Acute inflammation of the gallbladder or bile ducts
• Occurrence of frequent biliary colic, biliary infections, severe pancreatic abnormalities
• Bile duct obstruction, calcified X-ray opaque gallstones and reduced mobility of the gallbladder
• Subjects who weigh 88 lbs (40 kg) or less
• Aspartate aminotransferase or alanine aminotransferase concentrations more than 3 times the upper limit of normal
• Creatinine clearance 50 ml/min or less
• Any clinically significant neurological, haematological, autoimmune, endocrine, cardiovascular, neoplastic, renal, gastrointestinal, or other disorder that, in the Investigator's opinion, could interfere with the subject's participation in the study, place the subject at increased risk, or confound interpretation of study results
• Consideration by the investigator, for any reason, that the subject is an unsuitable candidate to receive TUDCA or that the subject is unable or unlikely to comply with the dosing schedule or study evaluations
• The patient of reproductive potential is sexually active and is not willing to use highly effective contraception during the study and up to 90 days after the day of last dose
• The patient is pregnant or breast feeding

Sex/Gender

• Sexes Eligible for Study: All

• Ages: 18 Years to 80 Years (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Contacts: Contact information is only displayed when the study is recruiting subjects
• Listed Location Countries: Belgium, France, Germany, Ireland, Italy, Netherlands, United Kingdom

Administrative Information

• NCT Number: NCT03800524
• Other Study ID Numbers: H2020/755094/2017/IT-01; 2018-002722-22 ( EudraCT Number ); 755094 ( Other Grant/Funding Number: European Commission )
• Has Data Monitoring Committee: Yes

U.S. FDA-regulated Product

• Studies a U.S. FDA-regulated Drug Product: No
• Studies a U.S. FDA-regulated Device Product: No

IPD Sharing Statement

• Plan to Share IPD: Yes

Plan Description

Once the dataset has been analysed, a complete, cleaned, anonymized copy of the final data used in conducting the final analyses will be made available to be used in further studies by the research partners or by other research groups and clinicians.

To prevent misuse and misinterpretation, relevant study metadata (such as the study protocol, case report forms, documentation providing information about the methodology and procedures used to collect the data, definition of variables and statistical code) will be shared in a data repository with a stable URL. Patient anonymity and legal compliance will be assured throughout all the steps of data transfer.

• Supporting Materials: Study Protocol
• Supporting Materials: Statistical Analysis Plan (SAP)
• Supporting Materials: Informed Consent Form (ICF)
• Supporting Materials: Clinical Study Report (CSR)
• Supporting Materials: Analytic Code
• Time Frame: Three months after the data-entry process and final data curation
• Access Criteria: Data will be made available only to qualified designated persons (methodologists, biostatisticians) from other academic institutions, on request. User registration will be required in order to access files.

• Current Responsible Party: Humanitas Mirasole SpA
• Original Responsible Party: Same as current
• Current Study Sponsor: Humanitas Mirasole SpA
• Original Study Sponsor: Same as current

Collaborators

• University of Ulm
• University of Sheffield
• University Hospital, Tours
• KU Leuven
• UMC Utrecht
• University of Dublin, Trinity College
• Bruschettini S.r.l.
• Istituto Superiore di Sanità
• Motor Neurone Disease Association
• European Commission

Investigators

• Study Chair: Alberto Albanese, MD; Humanitas Mirasole SpA

• PRS Account: Humanitas Mirasole SpA
• Verification Date: July 2023