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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/NCT01233622




Registration number
NCT01233622
Ethics application status
Date submitted
1/11/2010
Date registered
3/11/2010
Date last updated
23/02/2017

Titles & IDs
Public title
Safety and Efficacy of Galvus as add-on Therapy to Metformin Plus Glimepiride
Scientific title
A Multi-center, Randomized, Double-blind Placebo Controlled Study to Evaluate the Efficacy and Safety of 24 Weeks Treatment With Vildagliptin 50 mg Bid as add-on Therapy to Metformin Plus Glimepiride in Patients With Type 2 Diabetes
Secondary ID [1] 0 0
EudraCT 2010-021097-11
Secondary ID [2] 0 0
CLAF237A23152
Universal Trial Number (UTN)
Trial acronym
Vildagliptin
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Type 2 Diabetes Mellitus 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 - Vildagliptin
Treatment: Drugs - Placebo

Experimental: Vildagliptin (metformin + glimepiride) -

Placebo Comparator: Placebo (metformin + glimepiride) -


Treatment: Drugs: Vildagliptin


Treatment: Drugs: Placebo


Intervention code [1] 0 0
Treatment: Drugs
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
HbA1c Reduction
Timepoint [1] 0 0
24 weeks
Secondary outcome [1] 0 0
FPG reduction
Timepoint [1] 0 0
24 weeks
Secondary outcome [2] 0 0
Safety and tolerability-frequency of treatment emergent adverse events (incl. overall Aes, SAEs, death, Aes leading ot study discontinuation or study drug interruption, pre-specified potential AEs)
Timepoint [2] 0 0
24 weeks
Secondary outcome [3] 0 0
Responder Rate
Timepoint [3] 0 0
24 weeks

Eligibility
Key inclusion criteria
Inclusion criteria

- Confirmed diagnosis of T2DM by standard criteria.

- Treatment with oral anti-diabetic therapy, on stable dose for at least 12 weeks prior
to the screening visit. Acceptable background anti-diabetic therapy includes:
metformin (= 1500 mg) as monotherapy or in combination with SU, TZDs, or glinides

- Age: =18 to = 80 years

- HbA1c of = 7.5 and = 11.0%

- Body Mass Index (BMI) =22 to =45 kg/m2
Minimum age
18 Years
Maximum age
80 Years
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
Exclusion criteria:

- FPG = 270 mg/dL (= 15.0 mmol/L)

- Acute metabolic diabetes complications such as ketoacidosis or hyperosmolar state
(coma) within the past 6 months

- Any of following within past 6 months: Myocardial infarction, TIA or stroke, coronary
artery bypass surgery or percutaneous coronary intervention

- History of hypersensitivity to any of the study drugs or to drugs of similar chemical
classes

- Acute infections which may affect blood glucose control within 4 weeks prior to
screening Other protocol-defined inclusion/exclusion criteria may apply

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
Blinded (masking used)
Who is / are masked / blinded?
The people receiving the treatment/s


The people analysing the results/data
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
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
Sample size
Target
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
Recruitment hospital [1] 0 0
Novartis Investigative Site - Box Hill
Recruitment hospital [2] 0 0
Novartis Investigative Site - Heidelberg
Recruitment hospital [3] 0 0
Novartis Investigative Site - Parkville
Recruitment hospital [4] 0 0
Novartis Investigative Site - St. Leonards
Recruitment postcode(s) [1] 0 0
- Box Hill
Recruitment postcode(s) [2] 0 0
- Heidelberg
Recruitment postcode(s) [3] 0 0
- Parkville
Recruitment postcode(s) [4] 0 0
- St. Leonards
Recruitment outside Australia
Country [1] 0 0
Germany
State/province [1] 0 0
Anderbeck
Country [2] 0 0
Germany
State/province [2] 0 0
Berlin
Country [3] 0 0
Germany
State/province [3] 0 0
Hamburg
Country [4] 0 0
Germany
State/province [4] 0 0
Hildesheim
Country [5] 0 0
Germany
State/province [5] 0 0
Sangerhausen
Country [6] 0 0
Hungary
State/province [6] 0 0
Budapest
Country [7] 0 0
Hungary
State/province [7] 0 0
Erd
Country [8] 0 0
Hungary
State/province [8] 0 0
Torokbalint
Country [9] 0 0
Italy
State/province [9] 0 0
Bergamo
Country [10] 0 0
Italy
State/province [10] 0 0
Cosenza
Country [11] 0 0
Italy
State/province [11] 0 0
Milano
Country [12] 0 0
Italy
State/province [12] 0 0
Padova
Country [13] 0 0
Italy
State/province [13] 0 0
Pisa
Country [14] 0 0
Italy
State/province [14] 0 0
Roma
Country [15] 0 0
Italy
State/province [15] 0 0
Torino
Country [16] 0 0
Korea, Republic of
State/province [16] 0 0
Bundang
Country [17] 0 0
Korea, Republic of
State/province [17] 0 0
Seoul
Country [18] 0 0
Korea, Republic of
State/province [18] 0 0
Suwon
Country [19] 0 0
Mexico
State/province [19] 0 0
Aguascalientes
Country [20] 0 0
Mexico
State/province [20] 0 0
Durango
Country [21] 0 0
Mexico
State/province [21] 0 0
Guadalajara
Country [22] 0 0
Mexico
State/province [22] 0 0
Mexico
Country [23] 0 0
Mexico
State/province [23] 0 0
Pachuca
Country [24] 0 0
Philippines
State/province [24] 0 0
Manila
Country [25] 0 0
Philippines
State/province [25] 0 0
Quezon City
Country [26] 0 0
Romania
State/province [26] 0 0
Alba-Iulia
Country [27] 0 0
Romania
State/province [27] 0 0
Bucharest
Country [28] 0 0
Romania
State/province [28] 0 0
Oradea
Country [29] 0 0
Romania
State/province [29] 0 0
Targu-Mures
Country [30] 0 0
Taiwan
State/province [30] 0 0
Changhua
Country [31] 0 0
Taiwan
State/province [31] 0 0
Taichung
Country [32] 0 0
Taiwan
State/province [32] 0 0
Taipei
Country [33] 0 0
Taiwan
State/province [33] 0 0
Yongkang

Funding & Sponsors
Primary sponsor type
Commercial sector/Industry
Name
Novartis
Address
Country

Ethics approval
Ethics application status

Summary
Brief summary
This study will evaluate the efficacy and safety of vildagliptin 50 mg bid as add-on therapy
to metformin plus glimepiride in patients with Type 2 Diabetes (T2D).
Trial website
https://clinicaltrials.gov/ct2/show/NCT01233622
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
Novartis Pharmaceuticals
Address 0 0
Novartis Pharmaceuticals
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/NCT01233622