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Clinical Trials/EUCTR2016-000685-39-NL
EUCTR2016-000685-39-NL
Active, not recruiting
Phase 1

Investigation of efficacy and safety of three dose levels of subcutaneous semaglutide once daily versus placebo in subjects with non-alcoholic steatohepatitis.A 72-week randomised, double-blind, placebo-controlled, six-armed parallel group, multi-centre, multinational trial

ovo Nordisk A/S0 sites288 target enrollmentSeptember 13, 2016

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
on-alcoholic steatohepatitis
Sponsor
ovo Nordisk A/S
Enrollment
288
Status
Active, not recruiting
Last Updated
5 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
September 13, 2016
End Date
TBD
Last Updated
5 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • 1\. Informed consent obtained before any trial\-related activities. Trial\-related activities are any procedures that are carried out as part of the trial, including activities to determine suitability for the trial, except for protocol described pre\-screening activities which require a separate informed consent.
  • 2\. Male or female, aged 18\-75 years (both inclusive) (for Japan: male or female aged 20\-75 years (both inclusive) at the time of signing informed consent.
  • 3\. Histologic evidence of NASH based on central pathologist evaluation of a liver biopsy obtained up to 21 weeks before screening.
  • 4\. A histological NAS \> \= 4 with a score of 1 or more in each sub\-component of the score based on central pathologist evaluation.
  • 5\. NASH fibrosis stage 1, 2 or 3 according to the NASH CRN fibrosis staging system based on central pathologist evaluation.
  • 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 245
  • F.1\.3 Elderly (\>\=65 years) yes

Exclusion Criteria

  • 1\. Known or suspected abuse of alcohol (\> 20 g/day for women or \> 30 g/day for men), alcohol dependence\* or narcotics. (\* \= assessed by the Alcohol Use Disorders Identification Test (AUDIT questionnaire)).
  • 2\. Diagnosis of type 1 diabetes according to medical records.
  • 3\. HbA1c \> 10% at screening.
  • 4\. History or presence of pancreatitis (acute or chronic).
  • 5\. Calcitonin \= 50 ng/L at screening.
  • 6\. Family or personal history of multiple endocrine neoplasia type 2 or medullary thyroid carcinoma. Family is defined as a first degree relative.
  • 7\. Body Mass Index (BMI) \= 25\.0 kg/sqm at the screening visit (visit 1\).
  • 8\. Female who is pregnant, breast\-feeding or intends to become pregnant or is of childbearing potential and not using an adequate contraceptive method (adequate contraceptive measures as required by local regulation or practice).

Outcomes

Primary Outcomes

Not specified

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