Primary Objective: To compare exposure and activity of SAR341402 to NovoRapid® and NovoLog®. Secondary Objective: To assess the safety and tolerability of SAR341402.
The total study duration for a screened subject will be about 3 - 8 weeks (excluding screening of 2 to 28 days), treatment period of 2 days for each 3 periods (1 overnight stay), a washout period of 5-18 days (preferentially 7 days between consecutive dosing), and an end-of-study visit of 1 day between Days 5 and 14 after the last administration of the investigational product.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
30
Pharmaceutical form: solution Route of administration: subcutaneous
Pharmaceutical form: solution Route of administration: subcutaneous
Pharmaceutical form: solution Route of administration: subcutaneous
Investigational Site 276001
Neuss, Germany
Assessment of PK parameters: maximum plasma concentration (Cmax)
Maximum plasma concentration (Cmax) of SAR341402, NovoRapid and NovoLog within 12 hours
Time frame: 12 hours
Assessment of PK parameters: Area under the concentration versus time curve (AUC)
INS-AUC of SAR341402, NovoRapid, and NovoLog from 0 to 12 hours
Time frame: 12 hours
Assessment of PK parameter: AUC from dosing to last concentration (AUClast)
INS-AUClast is AUC from the time of dosing to the last measurable concentration of SAR341402, NovoRapid, and NovoLog from 0 to 12 hours
Time frame: 12 hours
Assessment of PD parameters: Area under the body weight standardized glucose infusion rate (GIR)
Area under the body weight standardized glucose infusion rate (GIR) versus time curve from 0 to 12 hours post administration (GIR-AUC0-12)
Time frame: 12 hours
Assessment of PK: Fractional area under the concentration versus time curve
INS-AUC0-2 and INS-AUC4-tlast
Time frame: 12 hours
Assessment of PK: Time to 20 % of INS-AUC
Time to 20% of AUC (t20%-INS-AUC) within 12 hours
Time frame: 12 hours
Assessment of PK: time to reach INS-Cmax (INS-tmax)
INS-tmax within 12 hours
Time frame: 12 hours
Assessment of PK: time to reach INS-t1/2z (INS-t1/2z)
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INS-t1/2z within 12 hours
Time frame: 12 hours
Assessment of PD: Fractional area under the body weight standardized GIR versus time curve
GIR-AUC0-2 and GIR-AUC4-12
Time frame: 12 hours
Assessment of PD: Time to 20 % of total GIR-AUC0-12h
Time to 20% of total GIR-AUC0-12h (t20%-GIR-AUC0-12h) within 12 hours
Time frame: 12 hours
Assessment of PD: Maximum smoothed body weight standardized GIR (GIRmax)
Maximum smoothed body weight standardized GIR (GIRmax) within 12 hours
Time frame: 12 hours
Assessment of PD: Time to GIRmax (GIR-tmax)
Time to GIRmax (GIR-tmax) within 12 hours
Time frame: 12 hours
Number of adverse events (AEs)
Number of patients with treatment emergent AEs and serious adverse events (SAEs)
Time frame: 8 weeks