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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: EUCTR
Last refreshed on: 30 June 2019
Main ID:  EUCTR2016-004599-23-ES
Date of registration: 04/07/2017
Prospective Registration: Yes
Primary sponsor: Genkyotex SA
Public title: A study assessing the efficacy and safety of GKT137831 in Patients with Primary Biliary Cholangitis Receiving Ursodeoxycholic Acid and with Persistently Elevated Alkaline Phosphatase
Scientific title: A Double-Blind, Randomized, Placebo-Controlled Clinical Trial to Assess the Efficacy and Safety of Oral GKT137831 in Patients with Primary Biliary Cholangitis Receiving Ursodeoxycholic Acid and with Persistently Elevated Alkaline Phosphatase
Date of first enrolment: 26/07/2017
Target sample size: 102
Recruitment status: Not Recruiting
URL:  https://www.clinicaltrialsregister.eu/ctr-search/search?query=eudract_number:2016-004599-23
Study type:  Interventional clinical trial of medicinal product
Study design:  Controlled: yes
Randomised: yes
Open: no
Single blind: no
Double blind: yes
Parallel group: no
Cross over: no
Other: no
If controlled, specify comparator, Other Medicinial Product: no
Placebo: yes
Other: no
Number of treatment arms in the trial: 3
 
Phase:  Human pharmacology (Phase I): no Therapeutic exploratory (Phase II): yes Therapeutic confirmatory - (Phase III): no Therapeutic use (Phase IV): no
Countries of recruitment
Belgium Canada Germany Greece Israel Italy Spain United Kingdom
United States
Contacts
Name: Isabelle Aelbrecht   
Address:  516, rue Pierre et Marie Curie 31670 Labège France
Telephone: +34932275753
Email: isabelle.aelbrecht@genkyotex.com
Affiliation:  Genkyotex Innovation SA
Name: Isabelle Aelbrecht   
Address:  516, rue Pierre et Marie Curie 31670 Labège France
Telephone: +34932275753
Email: isabelle.aelbrecht@genkyotex.com
Affiliation:  Genkyotex Innovation SA
Key inclusion & exclusion criteria
Inclusion criteria:
Inclusion Criteria:
1. Male or female aged 18 to 80 years, inclusive.
2. Willing and able to give written informed consent and to comply with the requirements of the study.
3. PBC diagnosis as demonstrated by the presence of > or = 2 of the following 3 diagnostic factors:
-History of elevated ALP levels (> ULN) for at least 6 months
-Positive anti-mitochondrial antibody (AMA) titer or if AMA negative or in low titer (< 1:80) PBC-specific antibodies (anti-GP210 and/or anti-SP100 and/or antibodies against the major M2 components [PDC-E2, 2-oxo-glutaric acid dehydrogenase complex])
-Liver biopsy consistent with PBC (based on historic liver biopsy), including non-suppurative, destructive cholangitis affecting mainly the interlobular and septal bile ducts.
4. Serum ALP > or = 1.5 x ULN.
5. Serum GGT > or = 1.5 x ULN.
6. UDCA treatment for at least 6 months and stable dose for at least 3 months prior to Visit 1.
7. Subjects being treated for pruritus with colestyramine must be on a stable dose of colestyramine for at least 8 weeks prior to baseline/Day 1 (Visit 2). Subjects must be willing and able to take colestyramine at least 2 hours before or after study medication.
8. Female subjects of childbearing potential must use a highly effective method of contraception to prevent pregnancy for 4 weeks before randomization and must agree to continue strict contraception for 90 days after last administration of investigational medicinal product (IMP). Male participants with female partners of childbearing potential must be willing to use a condom and require their partner to use an additional form of adequate contraception as approved by the Investigator. This requirement begins at the time of informed consent and ends 90 days after the last administration of IMP. Male study participants must also not donate sperm from baseline until 90 days after the last administration of IMP.
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range 95
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range 7

Exclusion criteria:
1. A positive pregnancy test or breast-feeding for female subjects.
2. Any hepatic decompensation, defined as a past or current history of hepatic encephalopathy, gastrointestinal tract bleeding due to esophageal varices, or ascites
3. International normalized ratio (INR) > 1.2 unless subject is on anticoagulant therapy.
4. ALT > 3 x ULN.
5. Total bilirubin > 1 x ULN.
6. Planned or current plasmapheresis or other extra-corporeal treatments (e.g., molecular adsorbent recirculation system (MARS)) for treatment-refractory pruritus.
7. History of liver transplantation, current placement on a liver transplant list or current Model for End Stage Liver Disease (MELD) score > or = 15.
8. Cirrhosis with complications, including history or presence of: spontaneous bacterial peritonitis, hepatocellular carcinoma.
9. Hepatorenal syndrome (type I or II) or Screening serum creatinine > ULN
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7. Subjects being treated for pruritus with colestyramine must be on a
stable dose of colestyramine for at least 8 weeks prior to baseline/Day 1
(Visit 2). Subjects must be willing and able to take colestyramine at
least 2 hours before or after study medication.
8. Female subjects of childbearing potential must use a highly effective
method of contraception to prevent pregnancy for 4 weeks before
randomization and must agree to continue strict contraception for up to
90 days after last administration of investigational medicinal product
(IMP). Male participants with female partners of childbearing potential
must be willing to use a condom and require their partner to use an
additional form of adequate contraception as approved by the
Investigator. This requirement begins at the time of informed consent
and ends 90 days after the last administration of IMP. Male study
participants must also not donate sperm from baseline until 90 days
after the last administration of IMP.

E.4 PRINCIPAL EXCLUSION CRITERIA (list the most important)
English 1. A positive pregnancy test or breast-feeding for female subjects.
2. Any hepatic decompensation, defined as a past or current history of
hepatic encephalopathy, gastrointestinal tract bleeding due to
esophageal varices, or ascites
3. International normalized ratio (INR) > 1.2 unless subject is on
anticoagulant therapy.
4. ALT > 3 x ULN.
5. Total bilirubin > 1 x ULN.
6. Planned or current plasmapheresis or other extra-corporeal
treatments (e.g., molecular adsorbent recirculation system (MARS)) for
treatment-refractory pruritus.
7. History of liver transplantation, current placement on a liver
transplant list or current Model for End Stage Liver Disease (MELD) score
= 15.
8. Cirrhosis with complications, including history or presence of:
spontaneous bacterial peritonitis, hepatocellular carcinoma.
9. Hepatorenal syndrome (type I or II) or Screening serum creatinine >
ULN.
10. Competing etiology for liver disease (e.g., hepatitis C, active
hepatitis B, non-alcoholic steatohepatitis (NASH), alcoholic liver disease
(ALD), autoimmune hepatitis, primary sclerosing cholangitis, Gilbert's
Syndrome).
11. Subjects receiving prohibited medications within 3 months of
Screening (Visit 1) according to the list (a, b and c) provided in Section
6.6.2.
12. Treatment with any investigational agent within 4 weeks of Visit 1 or
5 half-lives of the investigational medicinal product (whichever is
longer).
13. A history of long QT syndrome.
14. Evidenc


Age minimum:
Age maximum:
Gender:
Female: yes
Male: yes
Health Condition(s) or Problem(s) studied
Primary Biliary Cholangitis
MedDRA version: 20.0 Level: LLT Classification code 10036680 Term: Primary biliary cirrhosis System Organ Class: 100000023866
Therapeutic area: Diseases [C] - Immune System Diseases [C20]
Intervention(s)

Product Code: GKT137831
Pharmaceutical Form: Capsule
INN or Proposed INN: GKT137831
CAS Number: 1218942-37-0
Other descriptive name: GKT137831
Concentration unit: mg milligram(s)
Concentration type: equal
Concentration number: 100-
Pharmaceutical form of the placebo: Capsule
Route of administration of the placebo: Oral use

Primary Outcome(s)
Main Objective: To evaluate the efficacy of oral GKT137831 in comparison with placebo, in subjects with PBC receiving UDCA and with persistently elevated Alkaline Phosphatase (ALP).
Primary end point(s): Primary:
- the percent change from baseline to Week 24 (Visit 7) in serum GGT.
Secondary Objective: - To evaluate the safety of oral GKT137831 in comparison with placebo, in subjects with PBC.
- To estimate the population pharmacokinetics (PK) of GKT137831 and explore any potential Pharmacokinetics-Pharmacodynamics (PK-PD) relationships in this subject population.
- To explore any relationship between genetic parameters and therapeutic responses in a subset of subjects.
Timepoint(s) of evaluation of this end point: The percent change from baseline to Week 24 (Visit 7) in serum GGT.
Serum GGT will be assessed during every treatment visit. (visit's 2-7)
Secondary Outcome(s)
Secondary end point(s): - Absolute and percent change in serum GGT from baseline to each assessment.

- Absolute change in Enhanced Liver Fibrosis (ELF) score from baseline to Weeks 12 and 24.

- Absolute and percent change in serum levels of highsensitivity C-reactive protein (hsCRP) and fibrinogen from baseline to each
assessment.

- Absolute and percent change in serum Alanine Aminotransferase (ALT), Aspartate Aminotransferase (AST) and conjugated and total bilirubin, from baseline to each assessment.

- Absolute and percent change in serum Alanine Aminotransferase (ALT), Aspartate Aminotransferase (AST), conjugated and total bilirubin, and Cytokeratin-18 (CK-18), from baseline to each assessment.

- Absolute and percent change in the Fibrosis-4 (FIB-4) and AST to Platelet Ratio Index (APRI) scores, from baseline to each assessment (FIB-4: age (years) x AST (IU/L)/(platelet count (109/L) x (ALT (IU/L)1/2, APRI: AST (IU/L)/ upper normal limit AST)x100/platelet count (10E9/L).

- Absolute and percent change in liver stiffness as assessed by transient elastography (FibroScan or similar technology), from baseline to Week 24, in patients with values at baseline and Week 24.

- Absolute and percent change in serum levels of collagen fragments indicative of collagen formation and degradation from baseline to Weeks 12 and 24.

-Absolute and percent change in total bile acids from baseline to Week 12 and 24.
Timepoint(s) of evaluation of this end point: Timepoints of the secondary endpoints are included within the secondary objective endpoints section E.5.2 (above)

Most secondary assessments will be assessed from baseline to each visit however the ELF score and collagen fragments will be assessed from baseline to week 12 and week 24.
The change in liver stiffness (FibroScan or similar technology) will be assessed from baseline to week 24.
Secondary ID(s)
2016-004599-23-BE
GSN000300
Source(s) of Monetary Support
Genkyotex Innovation SA
Secondary Sponsor(s)
Ethics review
Status: Approved
Approval date:
Contact:
Results
Results available:
Date Posted:
Date Completed:
URL:
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