Phase 3
Completed N=143
Switching From Insulin Glargine to Insulin Degludec in Subjects With Type 2 Diabetes Mellitus (BEGIN™)
Source: ClinicalTrials.gov NCT01135992 ↗Enrolled (actual)
143
Serious AEs
2.1%
Results posted
Jan 2016
Primary outcomePrimary: HbA1c (Glycosylated Haemoglobin) — 7.4; 7.2 percentage of glycosylated haemoglobin
Summary
This trial is conducted in the United States of America (USA). The aim of this clinical trial is to assess the implications of switching from insulin glargine (IGlar) to insulin degludec (IDeg) in subjects with type 2 diabetes mellitus.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY HbA1c (Glycosylated Haemoglobin) |
7.4; 7.2 | — |
| SECONDARY Fasting Plasma Glucose (FPG) |
7.0; 6.3 | — |
| SECONDARY Change in Body Weight |
0.1; 0.6 | — |
| SECONDARY Rate of Treatment Emergent Adverse Events (AEs) |
370; 9; 19; 102; 250; 0 | — |
| SECONDARY Rate of Confirmed Hypoglycaemic Episodes |
453; 424 | — |
| SECONDARY Rate of Nocturnal Confirmed Hypoglycaemic Episodes |
111; 83 | — |
Eligibility Criteria
Inclusion Criteria
- Type 2 diabetes mellitus (diagnosed clinically) for at least 6 months
- HbA1c maximum 10 % by central laboratory analysis
- Current treatment with basal-oral therapy (BOT) (no prandial insulin ever) consisting of: at least three months with insulin glargine once daily (average prescribed dose must have been unchanged (within plus/minus 10%) for four weeks prior to Visit 1 as confirmed by patient records or verbal confirmation by the subject) in combination with stable (unchanged doses for at least 3 months prior to Visit 1) OAD (metformin, insulin secretagogues, pioglitazone, sitagliptin or alpha-glucosidase-inhibitor) treatment in any approved (according to label) dose or combination
Exclusion Criteria
- Use within the last three months prior to Visit 1 of: Exenatide, Liraglutide or Thiazoledinediones (TZDs) other than Pioglitazone
- Cardiovascular disease (CVD) defined as: stroke; decompensated heart failure New York Heart Association (NYHA) class III or IV; myocardial infarction; unstable angina pectoris; or coronary arterial bypass graft or angioplasty within the last six months prior to Visit 1
- Recurrent severe hypoglycaemia (more than one severe hypoglycaemic episode during the last 12 months), or hypoglycaemic unawareness as judged by the Investigator, or hospitalisation for diabetic ketoacidosis during the previous six months
- Pregnancy, breast-feeding, the intention of becoming pregnant or not using adequate contraceptive measures according to local requirements
- Previous participation in this trial. Participation is defined as started on trial medication. Rescreening of screening failures is allowed only once within the limits of the recruitment period
- Known or suspected hypersensitivity to trial products or related products
Data sourced from ClinicalTrials.gov (NCT01135992). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.