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Basaglar ® (insulin glargine injection)
100 units/mLThis information is provided in response to your request. Resources may contain information about doses, uses, formulations and populations different from product labeling. See Prescribing Information above, if applicable.
Clinical Studies - Type 1 and Type 2 Diabetes Mellitus
Adult patients with inadequately controlled T1DM participated in a 24-week, open-label, active-controlled study with a 28-week extension to evaluate the glucose lowering effect of once-daily Basaglar compared with that of once-daily administration of another IG-100 product or a non-US-approved IG-100 product, both in combination with mealtime insulin lispro.1
Adult patients with T2DM participated in a double-blind, active-controlled study to evaluate the glucose lowering effect of once-daily Basaglar plus OAMs compared with that of another IG-100 product or a non-US-approved IG-100 product administered once daily along with OAMs. Patients were
insulin naïve (~60%) and had failed to achieve adequate glycemic control on at least 2 OAMs, or
already on another IG-100 product or a non-US-approved IG-100 product along with at least 2 OAMs with adequate or inadequate glycemic control (~40%).1
Results
At week 24, the percentage of patients who achieved HbA1c levels less than 7% was similar between treatment groups (Table 1. Achievement of HbA1c Levels Less Than 7% at 24 Weeks in Phase 3 Clinical Studies of Basaglar ).1
Table 1. Achievement of HbA1c Levels Less Than 7% at 24 Weeks in Phase 3 Clinical Studies of Basaglar1
|
Basaglar +
Insulin Lispro |
Comparator
IG-100 Productsb
+ Insulin Lispro |
Basaglar +
OAMs |
Comparator
IG-100 Productsb
+ OAMs |
Patient population |
T1DM |
T2DM |
||
Percentage of patients achieving HbA1c <7%d |
34.5 |
32.2 |
48.8 |
52.5 |
Abbreviations: Basaglar = Basaglar® (insulin glargine injection) 100 units/mL; HbA1c = glycated hemoglobin; IG-100 = insulin glargine 100 units/mL; OAM = oral antihyperglycemic medication; T1DM = type 1 diabetes mellitus; T2DM = type 2 diabetes mellitus.
a Includes 1 patient randomized to the Basaglar treatment group who was not included in the full analysis set.
b Another IG-100 product and a non-US-approved IG-100 product.
c A total of 3 patients randomized to the Basaglar treatment group did not receive study drug and were not included in the full analysis set.
d Results were calculated based on the number of patients in the full analysis set using their last observed postbaseline value of HbA1c. Observed HbA1c data at 24 weeks were available from 256 (95.5%) patients in the Basaglar treatment group and 258 (96.6%) patients in the comparator IG-100 treatment group in patients with T1DM and from 331 (88%) patients in the Basaglar treatment group and 329 (87%) patients in the comparator IG-100 treatment group in patients with T2DM.
Enclosed Prescribing Information
BASAGLAR® (insulin glargine injection), for subcutaneous use, Lilly
HUMALOG® (insulin lispro injection), for subcutaneous or intravenous use, Lilly
1. Basaglar [package insert]. Indianapolis, IN: Eli Lilly and Company; 2018.
Glossary
Basaglar = Basaglar® (insulin glargine injection) 100 units/mL
HbA1c = glycated hemoglobin
IG-100 = insulin glargine 100 units/mL
OAM = oral antihyperglycemic medication
T1DM = type 1 diabetes mellitus
T2DM = type 2 diabetes mellitus
Date of Last Review: February 04, 2019
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