Take Control: A Randomized Trial Evaluating the Efficacy and Safety of Self- Versus Physician-Managed Titration of Insulin Glargine 300 U/mL (Gla-300) in Patients with Uncontrolled Type 2 Diabetes
posted on 2019-04-17, 12:58authored byD Russell-Jones, A Dauchy, E Delgado, G Dimitriadis, HA Frandsen, L Popescu, B Schultes, K Strojek, M Bonnemaire, AR de Climens, M Davies
Aim
To compare the efficacy and safety of self‐ vs physician‐managed titration of insulin glargine 300 U/mL (Gla‐300), in patients with inadequately controlled type 2 diabetes.
Methods
Take Control (EudraCT number: 2015‐001626‐42) was a 24‐week, multinational, open‐label, controlled, 2‐arm, parallel‐group study in insulin‐naïve and pre‐treated patients, randomized 1:1 to a self‐ or physician‐managed titration of Gla‐300. The fasting self‐monitored plasma glucose (SMPG) target was 4.4–7.2 mmol/L. The primary outcome was non‐inferiority of HbA1c change from baseline to week 24. Secondary outcomes included SMPG target achievement without hypoglycaemia, hypoglycaemia incidence, adverse events and patient‐reported outcomes (PROs).
Results
At week 24, the least squares (LS) mean HbA1c reduction was 0.97 % and 0.84 % in the self‐ and physician‐managed groups, respectively, with an LS mean difference of −0.13 % [95% CI: −0.2619 to −0.0004] demonstrating non‐inferiority (p<0.0001) and superiority (p=0.0247) of self‐ versus physician‐managed titration. Significantly more of the self‐ than physician‐managed group achieved SMPG target without hypoglycaemia (67% vs 58%, p=0.0187). Overall, hypoglycaemia incidence was similar in each group. No safety concerns were reported. In both groups, similar PRO improvements were observed for distress related to diabetes disease burden and for confidence in diabetes self‐management, with even more individuals achieving a clinically relevant reduction in emotional burden and fewer individuals with high emotional burden in the self‐managed group.
Conclusions
Self‐managed titration of Gla‐300 was superior to physician‐managed titration in terms of HbA1c reduction, accompanied by similar total PRO scores, with a clinically‐relevant reduction in emotional burden, and similar hypoglycaemia frequency.
Funding
This work was supported by Sanofi, Paris, France. Editorial assistance was provided by
Arthur Holland, PhD, of Fishawack Communications, and was funded by Sanofi.
History
Citation
Diabetes, Obesity and Metabolism, 2019
Author affiliation
/Organisation/COLLEGE OF LIFE SCIENCES/School of Medicine/Diabetes Research Centre
Qualified researchers may request access to patient level data and related study documents
including the clinical study report, study protocol with any amendments, blank case report
form, statistical analysis plan, and dataset specifications. Patient level data will be
anonymized and study documents will be redacted to protect the privacy of trial
participants. Further details on Sanofi’s data sharing criteria, eligible studies, and process for
requesting access can be found at: https://www.clinicalstudydatarequest.com.;The file associated with this record is under embargo until 12 months after publication, in accordance with the publisher's self-archiving policy. The full text may be available through the publisher links provided above.