Trial Outcomes & Findings for A Study of Cephalexin Liquid for Pediatrics in Healthy Adults Participants (NCT NCT02123472)
NCT ID: NCT02123472
Last Updated: 2015-06-25
Results Overview
Recruitment status
COMPLETED
Study phase
PHASE1
Target enrollment
28 participants
Primary outcome timeframe
Pre-dose, 0.25, 0.5, 0.75, 1.0, 1.25, 1.5, 1.75, 2.0, 2.5, 3.0, 3.5, 4.0, 5.0, 6.0, and 7.0 hours in each period
Results posted on
2015-06-25
Participant Flow
Participant milestones
| Measure |
Cephalexin Dosing Sequence AB
Each participant was administered Cephalexin A formulation (Treatment A, Reference - 1 occasion) and Cephalexin B formulation (Treatment B, Test - 1 occasion).There was an interval of 1 day between doses.
|
Cephalexin Dosing Sequence BA
Each participant was administered Cephalexin B formulation (Treatment B, Test - 1 occasion) and Cephalexin A formulation (Treatment A, Reference - 1 occasion).There was an interval of 1 day between doses.
|
|---|---|---|
|
Period 1 (7 Days)
STARTED
|
14
|
14
|
|
Period 1 (7 Days)
COMPLETED
|
14
|
14
|
|
Period 1 (7 Days)
NOT COMPLETED
|
0
|
0
|
|
Washout Period (1 Day)
STARTED
|
14
|
14
|
|
Washout Period (1 Day)
COMPLETED
|
14
|
14
|
|
Washout Period (1 Day)
NOT COMPLETED
|
0
|
0
|
|
Period 2 (7 Days)
STARTED
|
14
|
14
|
|
Period 2 (7 Days)
COMPLETED
|
14
|
13
|
|
Period 2 (7 Days)
NOT COMPLETED
|
0
|
1
|
Reasons for withdrawal
| Measure |
Cephalexin Dosing Sequence AB
Each participant was administered Cephalexin A formulation (Treatment A, Reference - 1 occasion) and Cephalexin B formulation (Treatment B, Test - 1 occasion).There was an interval of 1 day between doses.
|
Cephalexin Dosing Sequence BA
Each participant was administered Cephalexin B formulation (Treatment B, Test - 1 occasion) and Cephalexin A formulation (Treatment A, Reference - 1 occasion).There was an interval of 1 day between doses.
|
|---|---|---|
|
Period 2 (7 Days)
Withdrawal by Subject
|
0
|
1
|
Baseline Characteristics
A Study of Cephalexin Liquid for Pediatrics in Healthy Adults Participants
Baseline characteristics by cohort
| Measure |
Overall Study
n=28 Participants
Each participant was administered Cephalexin A formulation (Treatment A, Reference - 1 occasion) and Cephalexin B formulation (Treatment B, Test - 1 occasion)
|
|---|---|
|
Age, Continuous
|
28.3 Years
STANDARD_DEVIATION 5.11 • n=5 Participants
|
|
Sex: Female, Male
Female
|
10 Participants
n=5 Participants
|
|
Sex: Female, Male
Male
|
18 Participants
n=5 Participants
|
|
Ethnicity (NIH/OMB)
Hispanic or Latino
|
28 Participants
n=5 Participants
|
|
Ethnicity (NIH/OMB)
Not Hispanic or Latino
|
0 Participants
n=5 Participants
|
|
Ethnicity (NIH/OMB)
Unknown or Not Reported
|
0 Participants
n=5 Participants
|
|
Region of Enrollment
Mexico
|
28 participants
n=5 Participants
|
PRIMARY outcome
Timeframe: Pre-dose, 0.25, 0.5, 0.75, 1.0, 1.25, 1.5, 1.75, 2.0, 2.5, 3.0, 3.5, 4.0, 5.0, 6.0, and 7.0 hours in each periodPopulation: All participants who had at least one study treatment and had evaluable pharmacokinetic (PK) data.
Outcome measures
| Measure |
Cephalexin (Test)
n=26 Participants
Cephalexin (Treatment B) manufactured in Italy by Facta administered once orally in one of two study periods.
|
Cephalexin (Reference)
n=26 Participants
Cephalexin (Treatment A) manufactured in Mexico by Eli Lilly administered once orally in one of two study periods.
|
|---|---|---|
|
Pharmacokinetics: Area Under the Concentration Versus Time Curve From Time Zero to Infinity [AUC(0-∞)] of Cephalexin Following a Single Dose
|
36.256 hour*microgram per milliliter (h*µg/mL)
Geometric Coefficient of Variation 15.513
|
38.198 hour*microgram per milliliter (h*µg/mL)
Geometric Coefficient of Variation 14.385
|
SECONDARY outcome
Timeframe: Pre-dose, 0.25, 0.5, 0.75, 1.0, 1.25, 1.5, 1.75, 2.0, 2.5, 3.0, 3.5, 4.0, 5.0, 6.0, and 7.0 hours in each periodPopulation: All participants who had at least one study treatment and had evaluable pharmacokinetic (PK) data.
Outcome measures
| Measure |
Cephalexin (Test)
n=26 Participants
Cephalexin (Treatment B) manufactured in Italy by Facta administered once orally in one of two study periods.
|
Cephalexin (Reference)
n=26 Participants
Cephalexin (Treatment A) manufactured in Mexico by Eli Lilly administered once orally in one of two study periods.
|
|---|---|---|
|
Pharmacokinetics: Time to Reach Maximum Observed Concentration (Tmax) of Cephalexin Following a Single Dose Maximum
|
0.750 Hours
Standard Deviation 0.197
|
0.750 Hours
Standard Deviation 0.154
|
SECONDARY outcome
Timeframe: Pre-dose, 0.25, 0.5, 0.75, 1.0, 1.25, 1.5, 1.75, 2.0, 2.5, 3.0, 3.5, 4.0, 5.0, 6.0, and 7.0 hours in each periodPopulation: All participants who had at least one study treatment and had evaluable pharmacokinetic (PK) data.
Outcome measures
| Measure |
Cephalexin (Test)
n=26 Participants
Cephalexin (Treatment B) manufactured in Italy by Facta administered once orally in one of two study periods.
|
Cephalexin (Reference)
n=26 Participants
Cephalexin (Treatment A) manufactured in Mexico by Eli Lilly administered once orally in one of two study periods.
|
|---|---|---|
|
Pharmacokinetics: Maximum Concentration (Cmax) of Cephalexin
|
24.608 Microgram per milliliter(μg/mL)
Geometric Coefficient of Variation 20.712
|
26.410 Microgram per milliliter(μg/mL)
Geometric Coefficient of Variation 22.140
|
Adverse Events
Cephalexin (Test)
Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths
Cephalexin (Reference)
Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths
Serious adverse events
Adverse event data not reported
Other adverse events
Adverse event data not reported
Additional Information
Chief Medical Officer
Eli Lilly and Company
Phone: 800-545-5979
Results disclosure agreements
- Principal investigator is a sponsor employee
- Publication restrictions are in place
Restriction type: GT60