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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/ct2/show/NCT01952145




Registration number
NCT01952145
Ethics application status
Date submitted
24/09/2013
Date registered
27/09/2013
Date last updated
3/01/2019

Titles & IDs
Public title
A Trial Comparing the Efficacy and Safety of Insulin Degludec/Liraglutide Versus Insulin Glargine in Subjects With Type 2 Diabetes Mellitus
Scientific title
A Trial Comparing the Efficacy and Safety of Insulin Degludec/Liraglutide Versus Insulin Glargine in Subjects With Type 2 Diabetes Mellitus (DUAL™ V - Basal Insulin Switch)
Secondary ID [1] 0 0
2012-004413-14
Secondary ID [2] 0 0
NN9068-3952
Universal Trial Number (UTN)
Trial acronym
DUAL™ V
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Diabetes 0 0
Diabetes Mellitus, Type 2 0 0
Condition category
Condition code
Metabolic and Endocrine 0 0 0 0
Diabetes

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Treatment: Drugs - insulin degludec/liraglutide
Treatment: Drugs - insulin glargine

Experimental: Insulin degludec/liraglutide OD plus metformin -

Active Comparator: Insulin glargine OD plus metformin -


Treatment: Drugs: insulin degludec/liraglutide
Insulin degludec/liraglutide is injected subcutaneously s.c. (under the skin) once daily (OD). Dose individually adjusted. Subjects should continue their pre-trial treatment with metformin.

Treatment: Drugs: insulin glargine
Insulin glargine is injected subcutaneously s.c. (under the skin) once daily (OD). Dose individually adjusted. Subjects should continue their pre-trial treatment with metformin.
Intervention code [1] 0 0
Treatment: Drugs
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Change From Baseline in HbA1c (Glycosylated Haemoglobin)
Timepoint [1] 0 0
Week 0, week 26
Secondary outcome [1] 0 0
Change From Baseline in Body Weight
Timepoint [1] 0 0
Week 0, week 26
Secondary outcome [2] 0 0
Number of Treatment Emergent Confirmed Hypoglycaemic Episodes
Timepoint [2] 0 0
During 26 weeks of treatment

Eligibility
Key inclusion criteria
- Type 2 diabetes mellitus - HbA1c 7.0-10.0% [53-86 mmol/mol] (both
inclusive) by central laboratory analysis - Current treatment with insulin glargine for at
least 90 days prior to screening - Stable daily dose of insulin glargine between 20 units
and 50 units (both inclusive) for at least 56 days prior to screening. Total daily dose
should be within the range of 20-50 units, both inclusive, on the day of screening, but
individual fluctuations of plus/minus 10 procent within the 56 days prior to screening are
acceptable - Stable daily dose of metformin (above or equal to 1500 mg or max tolerated
dose) for at least 90 days prior to screening - Body mass index (BMI) below or equal to 40
kg/m^2
Minimum age
18 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
- Any use of oral antidiabetic agents (OADs) (except for
metformin) within 90 days prior to Visit 1 (screening) - Current use of any drug (except
metformin and insulin glargine) or anticipated change inconcomitant medication, which in
the investigator's opinion could interfere with the glucose metabolism (e.g. systemic
corticosteroids) - Previous and/or current treatment with any insulin regimen other than
basal insulin, e.g. prandial or pre-mixed insulin (short term treatment due to intercurrent
illness includinggestational diabetes is allowed at the discretion of the investigator) -
Previous and/or current treatment with glucagon-like peptide-1 (GLP-1) receptor agonists
(e.g. exenatide, liraglutide) - Impaired liver function, defined as ALAT (alanine
aminotransferase) above or equal to 2.5 times upper normal range (UNR) - Impaired renal
function defined as serum-creatinine above or equal to 133 micromol/L (above or equal to
1.5 mg/dL) for males and above or equal to 125 micromol/L (1.4 mg/dL) for females, or as
allowed according to local contraindications for metformin - Screening calcitonin above or
equal to 50 ng/L - Personal or family history of medullary thyroid carcinoma (MTC) or
multiple endocrine neoplasia type 2 (MEN2) - History of chronic pancreatitis or idiopathic
acute pancreatitis

Study design
Purpose of the study
Treatment
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Open (masking not used)
Who is / are masked / blinded?



Intervention assignment
Parallel
Other design features
Phase
Phase 3
Type of endpoint/s
Statistical methods / analysis

Recruitment
Recruitment status
Completed
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
20/09/2013
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
4/11/2014
Sample size
Target
Accrual to date
Final
557
Recruitment in Australia
Recruitment state(s)
NSW,QLD,VIC
Recruitment hospital [1] 0 0
Novo Nordisk Investigational Site - Blacktown
Recruitment hospital [2] 0 0
Novo Nordisk Investigational Site - Wollongong
Recruitment hospital [3] 0 0
Novo Nordisk Investigational Site - Herston
Recruitment hospital [4] 0 0
Novo Nordisk Investigational Site - Ipswich
Recruitment hospital [5] 0 0
Novo Nordisk Investigational Site - Robina
Recruitment hospital [6] 0 0
Novo Nordisk Investigational Site - East Ringwood
Recruitment postcode(s) [1] 0 0
2148 - Blacktown
Recruitment postcode(s) [2] 0 0
2500 - Wollongong
Recruitment postcode(s) [3] 0 0
4029 - Herston
Recruitment postcode(s) [4] 0 0
4305 - Ipswich
Recruitment postcode(s) [5] 0 0
4226 - Robina
Recruitment postcode(s) [6] 0 0
3135 - East Ringwood
Recruitment outside Australia
Country [1] 0 0
United States of America
State/province [1] 0 0
California
Country [2] 0 0
United States of America
State/province [2] 0 0
Colorado
Country [3] 0 0
United States of America
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Florida
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United States of America
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Illinois
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United States of America
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Indiana
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United States of America
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Kentucky
Country [7] 0 0
United States of America
State/province [7] 0 0
Louisiana
Country [8] 0 0
United States of America
State/province [8] 0 0
Missouri
Country [9] 0 0
United States of America
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North Carolina
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United States of America
State/province [10] 0 0
Ohio
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United States of America
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Oklahoma
Country [12] 0 0
United States of America
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Pennsylvania
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United States of America
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Tennessee
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United States of America
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Texas
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United States of America
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Utah
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United States of America
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Washington
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Argentina
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Buenos Aires
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Argentina
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Capital Federal
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Argentina
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Corrientes
Country [20] 0 0
Argentina
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Salta
Country [21] 0 0
Argentina
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Zarate
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Greece
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Athens
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Greece
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Ioannina
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Greece
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Larissa
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Greece
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Thessaloniki
Country [26] 0 0
Hungary
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Budapest
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Hungary
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Eger
Country [28] 0 0
Hungary
State/province [28] 0 0
Gyor
Country [29] 0 0
Hungary
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Gyula
Country [30] 0 0
Hungary
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Miskolc
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Mexico
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Hidalgo
Country [32] 0 0
Mexico
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Morelos
Country [33] 0 0
Mexico
State/province [33] 0 0
México, D.F.
Country [34] 0 0
Mexico
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Durango
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Mexico
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Monterrey
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Russian Federation
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Kazan
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Russian Federation
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Kirov
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Russian Federation
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Moscow
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Russian Federation
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Novosibirsk
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Russian Federation
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Saint-Petersburg
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Russian Federation
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St. Petersburg
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Russian Federation
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Tomsk
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Russian Federation
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Volgograd
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Russian Federation
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Vsevolozhsk
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Slovakia
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Bardejov
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Slovakia
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Dolny Kubin
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Slovakia
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Kosice
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Slovakia
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Levice
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Slovakia
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Lubochna
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Slovakia
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Poprad
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Slovakia
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Povazska Bystrica
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Slovakia
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Prievidza
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Slovakia
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Trnava
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Slovakia
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Velky Meder
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South Africa
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Gauteng
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South Africa
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KwaZulu-Natal
Country [57] 0 0
South Africa
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Alberton
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Spain
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Almería
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Spain
State/province [59] 0 0
Granada
Country [60] 0 0
Spain
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Palma de Mallorca
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Spain
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Sevilla
Country [62] 0 0
Spain
State/province [62] 0 0
Valencia

Funding & Sponsors
Primary sponsor type
Commercial sector/Industry
Name
Novo Nordisk A/S
Address
Country

Ethics approval
Ethics application status

Summary
Brief summary
This trial is conducted globally. The aim of the trial is to compare the efficacy and safety
of insulin degludec/liraglutide versus insulin glargine in subjects with type 2 diabetes
mellitus.
Trial website
https://clinicaltrials.gov/ct2/show/NCT01952145
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
Global Clinical Registry (GCR, 1452)
Address 0 0
Novo Nordisk A/S
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for scientific queries



Summary Results

For IPD and results data, please see https://clinicaltrials.gov/ct2/show/NCT01952145