Efficacy, Safety and Preference Study of a Insulin Pen PDS290 vs. a Novo Nordisk Marketed Insulin Pen in Diabetics

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Novo Nordisk A/S
ClinicalTrials.gov Identifier:
NCT00773279
First received: October 14, 2008
Last updated: October 14, 2013
Last verified: October 2013

October 14, 2008
October 14, 2013
September 2008
June 2009   (final data collection date for primary outcome measure)
HbA1c (glycosylated haemoglobin) for participants treated with PDS290 and FlexPen® [ Time Frame: Week 12 of each treatment sequence ] [ Designated as safety issue: No ]
HbA1c [ Time Frame: After 12 weeks' treatment ] [ Designated as safety issue: No ]
Complete list of historical versions of study NCT00773279 on ClinicalTrials.gov Archive Site
  • Percentage of subject having preference for PDS290 versus FlexPen® in terms of convenience and ease of use [ Time Frame: Week 24 ] [ Designated as safety issue: No ]
  • Summary score for treatment satisfaction [ Time Frame: Week 24 ] [ Designated as safety issue: No ]
  • Score for treatment impact measure for diabetes [ Time Frame: Week 24 ] [ Designated as safety issue: No ]
  • Clinical technical complaints (events/week) [ Time Frame: Week 0 to Week 24 (whole trial period) ] [ Designated as safety issue: No ]
  • Number of hypoglycaemic episodes [ Time Frame: Week 24 ] [ Designated as safety issue: No ]
  • Number of adverse device effects [ Time Frame: From randomisation (week 0) and until 7 days after Week 24 (Visit 16) ] [ Designated as safety issue: No ]
  • Hypoglycaemic episodes, number of events per subject day [ Time Frame: Week 24 ] [ Designated as safety issue: No ]
  • Clinical technical complains [ Time Frame: After 12 weeks' treatment ] [ Designated as safety issue: No ]
  • Compare the effectiveness of PDS290 vs a NovoNordisk marketed insulin pen using questionnaires [ Time Frame: After 12 weeks' treatment ] [ Designated as safety issue: No ]
  • Hypoglycaemic episodes [ Time Frame: After 12 weeks' treatment ] [ Designated as safety issue: Yes ]
  • Adverse events and adverse device effects [ Time Frame: After 12 weeks' treatment ] [ Designated as safety issue: Yes ]
Not Provided
Not Provided
 
Efficacy, Safety and Preference Study of a Insulin Pen PDS290 vs. a Novo Nordisk Marketed Insulin Pen in Diabetics
A Multi-centre, Randomised, Open-label, Cross-over Study to Explore Effectiveness, Safety, and Preference of a New Disposable Pen PDS290 Versus FlexPen® in Subjects With Type 1 or Type 2 Diabetes

This trial is conducted in the United States of America (USA). The aim of this clinical trial is to assess and compare the effect on blood sugar control of insulin detemir and insulin aspart or insulin detemir alone administered by a insulin pen PDS290 (FlexTouch®) versus a Novo Nordisk marketed insulin pen (FlexPen®) in subjects with type 1 or type 2 diabetes mellitus. Furthermore, the subject's preference of the devices will be investigated by the use of questionnaires.

Not Provided
Interventional
Phase 3
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Crossover Assignment
Masking: Open Label
Primary Purpose: Treatment
  • Diabetes
  • Diabetes Mellitus, Type 1
  • Diabetes Mellitus, Type 2
  • Delivery Systems
  • Device: FlexTouch®
    All subjects to receive insulin detemir treatment (and if relevant insulin aspart) with either a insulin pen PDS290 (FlexTouch®) or a Novo Nordisk marketed insulin pen (FlexPen®) for 12 weeks. After 12 weeks, all subjects will continue their insulin treatment with the other injection device.
  • Device: FlexPen®
    All subjects to receive insulin detemir treatment (and if relevant insulin aspart) with either a insulin pen PDS290 (FlexTouch®) or a Novo Nordisk marketed insulin pen (FlexPen®) for 12 weeks. After 12 weeks, all subjects will continue their insulin treatment with the other injection device.
  • Experimental: PDS290
    Interventions:
    • Device: FlexTouch®
    • Device: FlexPen®
  • Active Comparator: FlexPen®
    Interventions:
    • Device: FlexTouch®
    • Device: FlexPen®
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
242
June 2009
June 2009   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Informed consent obtained before any trial-related activities
  • Subjects diagnosed with type 1 or type 2 diabetes. If type 2 diabetics, treatment with or without oral anti diabetic medication is allowed
  • Current users of vial/syringe (pen naïve) treated with short-acting insulin (insulin aspart, glulisine or lispro) and once daily long-acting insulin (detemir or glargine) or once daily long-acting insulin (detemir or glargine) alone
  • Treatment with insulin (i.e. aspart, glulisine, lispro, detemir or glargine) for at least 6 months
  • Body Mass Index (BMI) less than 45.0 kg/m^2
  • HbA1c less than or equal to 9.0% at screening visit based on analysis from central laboratory
  • Able and willing to adhere to the trial-specific insulin regimen for the entire trial period

Exclusion Criteria:

  • Females of childbearing potential who are pregnant, breast-feeding or intend to become pregnant or inadequate contraceptive techniques during the trial period (adequate contraceptive measures are considered as intrauterine device, oral contraceptives and barrier methods)
  • Previous participation in this trial (screening visit)
  • Systemic drugs that may influence glycaemic control (e.g., corticosteroids)
  • Known or suspected allergy to trial product(s) or related products
  • Known or suspected abuse of alcohol or drug abuse
  • Mental incapacity, unwillingness or language barriers precluding adequate understanding or cooperation
  • Previous treatment with sitagliptin
  • Clinically significant, active (or over the past 12 months) disease of the gastrointestinal, neurological, genitourinary, or haematological systems
  • Cardiac disease defined as: Decompensated heart failure (New York Heart class III or IV, unstable angina pectoris within the past 6 months of study enrolment, myocardial infarction within the past 12 months and a clinically significant history of arrhythmias or conduction delays on electrocardiogram (ECG) over the past 12 months
  • Any other severe acute or chronic illness as judged by the Investigator
  • Recurrent major hypoglycaemia (defined as severe central nervous system dysfunction associated with hypoglycaemia, requiring the assistance of another person) or hypoglycaemia unawareness (defined as a condition in which subjects no longer experience the usual warning signs of hypoglycaemia; the symptoms of hypoglycaemia may be different, less pronounced or even absent) or hospitalisation for diabetic ketoacidosis during the previous six months
  • Any other conditions that the Investigator judges would interfere with trial participation or evaluation of results (i.e. planned any diagnostic or therapeutic medical intervention such as surgery)
  • Participated in another clinical trial and received an investigational drug within the last 4 weeks
Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00773279
PDS290-1971
No
Novo Nordisk A/S
Novo Nordisk A/S
Not Provided
Study Director: Gitte S. Fuchs Novo Nordisk A/S
Novo Nordisk A/S
October 2013

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP