E.1 Medical condition or disease under investigation |
E.1.1 | Medical condition(s) being investigated |
Type II Diabetes Mellitus |
Diabete Millito di tipo 2 |
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E.1.1.1 | Medical condition in easily understood language |
Type 2 Diabetes |
Diabete di tipo 2 |
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E.1.1.2 | Therapeutic area | Diseases [C] - Hormonal diseases [C19] |
MedDRA Classification |
E.1.2 Medical condition or disease under investigation |
E.1.2 | Version | 20.1 |
E.1.2 | Level | LLT |
E.1.2 | Classification code | 10020639 |
E.1.2 | Term | Hyperglycemia |
E.1.2 | System Organ Class | 100000004861 |
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E.1.3 | Condition being studied is a rare disease | No |
E.2 Objective of the trial |
E.2.1 | Main objective of the trial |
To test the hypothesis that LY900014 is noninferior to insulin lispro on glycemic control (NIM = 0.4% for HbA1c) in patients with T2D, when administered as prandial insulin (0 to 2 minutes prior to the meal), in combination with basal insulin glargine or insulin degludec for 26 weeks. |
Verificare l¿ipotesi secondo cui LY900014 ¿ non inferiore all¿insulina lispro per quanto riguarda il controllo glicemico (margine di non inferiorit¿ [NIM] = 0,4% per l¿emoglobina A1c [HbA1c]) in pazienti con diabete di tipo II, quando somministrata come insulina prandiale (da 0 a 2 minuti prima del pasto) in associazione a insulina glargine basale o insulina degludec basale, per un periodo di 26 settimane |
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E.2.2 | Secondary objectives of the trial |
Secondary objectives include testing the hypothesis that LY is superior to insulin lispro in controlling 1 and 2 hour postprandial glucose (PPG) excursions, when administered as prandial insulin. To test the hypothesis that LY is superior to insulin lispro on improving glycemic control (HbA1c) when administered as prandial insulin. |
Verificare l¿ipotesi secondo cui LY900014 ¿ superiore all¿insulina lispro nel controllare le escursioni glicemiche postprandiale (PPG) a 1 ora, quando somministrata come insulina prandiale. Verificare l¿ipotesi secondo cui LY900014 ¿ superiore all¿insulina lispro nel migliorare il controllo glicemico (HbA1c), quando somministrata come insulina prandiale |
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E.2.3 | Trial contains a sub-study | No |
E.3 | Principal inclusion criteria |
You can take part in this study if: · You were diagnosed with type 2 diabetes at least one year ago. · You are 18 years old or older. · You are already being treated with insulin allowed for study participation. · Your blood glucose levels are within allowed limits for study participation.
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• Hanno una diagnosi di diabete di tipo 2 da almeno 1 anno • Hanno almeno 18 anni di età • Sono stati trattati con insulina permessa per la partecipazione allo studio • I livelli glicemici rientrano nei limiti consentiti per la partecipazione allo studio.
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E.4 | Principal exclusion criteria |
You cannot take part in this study if: · You have had emergency treatment for very low blood glucose or poor blood glucose control in the last 6 months. · You are taking certain diabetes medications that are not allowed for study participation. · You have major problems with your heart, kidneys, liver, or you have a blood disorder. You have had or are now being treated for certain types of cancer. |
• Hanno ricevuto un trattamento di emergenza a causa di grave ipoglicemia o insufficiente controllo della glicemia negli ultimi 6 mesi. • Stanno assumendo un certo tipo di farmaci per il diabete che non è permesso per la partecipazione allo studio • Hanno avuto gravi problemi cardiaci, reni, epatici o disordini ematici • Siano stati trattati o siano in trattamento per determinati tipi di tumore.
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E.5 End points |
E.5.1 | Primary end point(s) |
Difference between LY900014 and insulin lispro in change from baseline to Week 26 in HbA1c |
Differenza tra LY900014 e insulina lispro per quanto riguarda la variazione dell’HbA1c dal basale alla settimana 26 |
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E.5.1.1 | Timepoint(s) of evaluation of this end point |
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E.5.2 | Secondary end point(s) |
1. Difference between LY900014 and insulin lispro in the 1-hour or 2- hour PPG excursion (serum glucose measured 1 hour or 2 hours after the start of the meal minus fasting serum glucose) from an MMTT at Week 26 2. Difference between LY900014 and insulin lispro in change from baseline to Week 26 in HbA1c 3. Rate (events/patient/100 years) of severe hypoglycemic events from baseline through Week 26 4. Rate (events/patient/year and/or events/patient/30 days) and incidence (percent of patients with at least 1 event) of documented symptomatic postmeal hypoglycemia within 1 and 2 hours after start of a meal from baseline through Week 26 5. Rate (events/patient/year and/or events/patient/30 days) and incidence (percent of patients with at least 1 event) of documented symptomatic hypoglycemic events from baseline through Week 26 6. Change from baseline 1,5-AG values at Week 26 7. Change from baseline 10-point SMBG values at Week 26 8. Change from baseline in total, basal and prandial insulin dose at Week 26 9. Change from baseline ITSQ regimen inconvenience and lifestyle flexibility domain scores at Week 26 10.The proportion of patients with HbA1c <7% and =6.5% at Week 26
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Differenza tra LY900014 e insulina lispro nell¿escursione del PPG a 1 ora (livelli di glucosio nel siero misurati 1 ora dopo l¿inizio del pasto meno i livelli di glucosio nel siero a digiuno) da un test di tolleranza con pasto misto (MMTT) alla settimana 26 -Differenza tra LY900014 e insulina lispro nell¿escursione del PPG a 2 ore (livelli di glucosio nel siero misurati 2 ore dopo l¿inizio del pasto meno i livelli di glucosio nel siero a digiuno) da un test MMTT alla settimana 26 -Differenza tra LY900014 e insulina lispro per quanto riguarda la variazione dell¿HbA1c dal basale alla settimana 26 -Tasso (eventi/paziente/anno e/o eventi/paziente/30 giorni) e incidenza (percentuale di pazienti con almeno un evento) di ipoglicemie postprandiali sintomatiche documentate a 1 e 2 ore dall¿inizio del pasto dal basale alla settimana 26 -Tasso (eventi/paziente/anno e/o eventi/paziente/30 giorni) e incidenza (percentuale di pazienti con almeno un evento) di ipoglicemie sintomatiche documentate dal basale alla settimana 26 -Tasso (eventi/paziente/100 anni) di eventi ipoglicemici severi dal basale alla settimana 26 8. Variazione dei valori di 1,5-AG dal basale alla settimana 26 9. Variazione dei valori di SMBG a 10 punti dal basale alla settimana 26 10. Variazione delle dosi di insulina totale, basale e prandiale e del rapporto dose di insulina prandiale/totale dal basale alla settimana 26 11. Variazione dei punteggi dei domini del questionario ITSQ per la valutazione dei disagi connessi al regime di trattamento e della flessibilit¿ nello stile di vita dal basale alla settimana 26 12. La percentuale di pazienti con valori di HbA1c <7% e < o=6,5% alla settimana 26
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E.5.2.1 | Timepoint(s) of evaluation of this end point |
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E.6 and E.7 Scope of the trial |
E.6 | Scope of the trial |
E.6.1 | Diagnosis | No |
E.6.2 | Prophylaxis | No |
E.6.3 | Therapy | No |
E.6.4 | Safety | Yes |
E.6.5 | Efficacy | Yes |
E.6.6 | Pharmacokinetic | No |
E.6.7 | Pharmacodynamic | No |
E.6.8 | Bioequivalence | No |
E.6.9 | Dose response | No |
E.6.10 | Pharmacogenetic | No |
E.6.11 | Pharmacogenomic | No |
E.6.12 | Pharmacoeconomic | No |
E.6.13 | Others | No |
E.7 | Trial type and phase |
E.7.1 | Human pharmacology (Phase I) | No |
E.7.1.1 | First administration to humans | No |
E.7.1.2 | Bioequivalence study | No |
E.7.1.3 | Other | No |
E.7.1.3.1 | Other trial type description | |
E.7.2 | Therapeutic exploratory (Phase II) | No |
E.7.3 | Therapeutic confirmatory (Phase III) | Yes |
E.7.4 | Therapeutic use (Phase IV) | No |
E.8 Design of the trial |
E.8.1 | Controlled | Yes |
E.8.1.1 | Randomised | Yes |
E.8.1.2 | Open | No |
E.8.1.3 | Single blind | No |
E.8.1.4 | Double blind | Yes |
E.8.1.5 | Parallel group | Yes |
E.8.1.6 | Cross over | No |
E.8.1.7 | Other | No |
E.8.2 | Comparator of controlled trial |
E.8.2.1 | Other medicinal product(s) | Yes |
E.8.2.2 | Placebo | No |
E.8.2.3 | Other | No |
E.8.2.4 | Number of treatment arms in the trial | 2 |
E.8.3 |
The trial involves single site in the Member State concerned
| No |
E.8.4 | The trial involves multiple sites in the Member State concerned | Yes |
E.8.4.1 | Number of sites anticipated in Member State concerned | 4 |
E.8.5 | The trial involves multiple Member States | Yes |
E.8.5.1 | Number of sites anticipated in the EEA | 33 |
E.8.6 Trial involving sites outside the EEA |
E.8.6.1 | Trial being conducted both within and outside the EEA | Yes |
E.8.6.2 | Trial being conducted completely outside of the EEA | Information not present in EudraCT |
E.8.6.3 | If E.8.6.1 or E.8.6.2 are Yes, specify the regions in which trial sites are planned |
Argentina |
Australia |
India |
Japan |
Korea, Republic of |
Mexico |
Puerto Rico |
Russian Federation |
Taiwan |
United States |
Germany |
Hungary |
Italy |
Slovakia |
Spain |
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E.8.7 | Trial has a data monitoring committee | No |
E.8.8 |
Definition of the end of the trial and justification where it is not the last
visit of the last subject undergoing the trial
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E.8.9 Initial estimate of the duration of the trial |
E.8.9.1 | In the Member State concerned years | 1 |
E.8.9.1 | In the Member State concerned months | 3 |
E.8.9.1 | In the Member State concerned days | 0 |
E.8.9.2 | In all countries concerned by the trial years | 1 |
E.8.9.2 | In all countries concerned by the trial months | 3 |
E.8.9.2 | In all countries concerned by the trial days | 0 |