Phase II Pharmacokinetic and Pharmacodynamic Study of DEX in Subjects Aged 12 Months Through <24 Months

Pain Clinical Trial

Official title:

A Phase II, Randomized, Open-Label, Single Center, Pharmacokinetic and Pharmacodynamic Study of Dexmedetomidine in Pediatric Subjects Aged 12 Months Through <24 Months

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01378988
• Other study ID #: DEX-11-01
• Status: Completed
• Phase: Phase 2
• First received: June 20, 2011
• Last updated: June 29, 2015
• Start date: June 2011
• Est. completion date: August 2011

Study information

• Verified date: June 2015
• Source: Hospira, Inc.
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to investigate the pharmacokinetic, pharmacodynamic, and safety of dexmedetomidine at 2 different dose levels in pediatric subjects, aged 12 months through <24 months, administered as an intravenous loading dose followed by continuous infusion for a minimum of 6 hours and up to 24 hours in an intensive care setting.

Description:

Phase II, randomized, open-label, single-center, study evaluating the pharmacokinetics and pharmacodynamics of dexmedetomidine in pediatric subjects across two dose levels (Dose Level 1 consists of a 0.7 mcg/kg loading dose immediately followed by a 0.5 mcg/kg/hr maintenance infusion; Dose Level 2 consists of a 1.0 mcg/kg loading dose immediately followed by a 0.75 mcg/kg/hr maintenance infusion). The study population will consist of intubated and mechanically ventilated pediatric subjects who require sedation in an intensive care setting for a minimum of 6 hours but not to exceed 24 hours. Subjects eligible for enrollment are 12 months to <24 months of age.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 5
• Est. completion date: August 2011
• Est. primary completion date: August 2011
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 12 Months to 23 Months

Eligibility

Inclusion Criteria:

1. Subject is 12 months to <24 months of age at screening.

2. Subject is intubated and mechanically ventilated in an intensive care setting and is anticipated to require a minimum of 6 hours of continuous IV sedation.

3. Subject has adequate renal function, defined as: Serum creatinine =1.0 mg/dL.

4. The subject's parent(s) or legal guardian(s) must voluntarily sign and date the informed consent document approved by the Institutional Review Board.

Exclusion Criteria:

1. Pediatric subjects with neurological conditions that prohibit an evaluation of sedation such as:

• Diminished consciousness from increased intracranial pressure

• Extensive brain surgery (surgery requiring intracranial pressure monitor)

• Diminished cognitive function per Principal Investigator (PI) discretion

• Subjects with immobility from neuromuscular disease or continuous infusion of neuromuscular blocking agents.

2. Subjects with second degree or third degree heart block unless subject has a permanent pacemaker or pacing wires are in situ.

3. Subjects who have hepatic impairment as defined by a serum glutamic-pyruvic transaminase/alanine aminotransferase (SGPT/ALT) >90 U/L at the time of screening.

4. Subjects who have hypotension, based on repeat assessments within 15 minutes preceding the start of study drug, defined as: Systolic blood pressure (SBP) <70 mmHg.

5. Pre-existing bradycardia based on repeated assessments within 15 minutes preceding the start of study drug, defined as: Heart rate (HR) <70 bpm.

6. Subject who have acute thermal burns involving more than 15 percent total body surface area.

7. Subjects who have a known allergy to dexmedetomidine, midazolam or fentanyl.

8. Subject who has received dexmedetomidine within 15 hours prior to the start of study drug.

9. Subjects with a life expectancy that is <72 hours.

10. Subjects that are expected to have hemodialysis (continuous hemofiltration), peritoneal dialysis or extracorporeal membrane oxygenation (ECMO) treatments within 48 hours prior to the start of study drug or during the duration of the study.

11. Subjects who have been treated with a-2 agonists/antagonists within 2 weeks.

12. Subjects with a spinal cord injury above T5 (5th Thoracic Vertebra).

13. Subjects who have received another investigational drug as part of an investigational drug study within the past 30 days.

14. Subjects who, in the opinion of the investigator, may not be able to comply with the safety monitoring requirements of this clinical study.

Study Design

Allocation: Randomized, Endpoint Classification: Pharmacokinetics/Dynamics Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Pain
• Sedation

Intervention

Drug:
• Dexmedetomidine
For sedation according to protocol

Locations

Country	Name	City	State
United States	Children's Hospital of Pittusburgh of UPMC	Pittsburgh	Pennsylvania

Sponsors (1)

Lead Sponsor	Collaborator
Hospira, Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Area Under the Plasma Concentration-time Curve (AUC0-8)	Area under the plasma concentration-time curve of dexmedetomidine at 0 to Infinity hours	30 minutes prior to loading dose (LD); 5 minutes before finishing LD; 0.5, 1, 2 and 4-6 hours during maintenance infusion (MI); 30 minutes prior (within 24 hours of start of MI) and 10 minutes, 0.5, 1, 2, 4 and 10 hours end of MI	No
Primary	Observed Peak Plasma Concentration (Cmax)	Maximum observed concentration of dexmedetomidine in plasma	30 minutes prior to loading dose (LD); 5 minutes before finishing LD; 0.5, 1, 2 and 4-6 hours during maintenance infusion (MI); 30 minutes prior (within 24 hours of start of MI) and 10 minutes, 0.5, 1, 2, 4 and 10 hours end of MI	No
Primary	Steady State Concentration (Css)	Concentration of dexmedetomidine at steady state in plasma	30 minutes prior to loading dose (LD); 5 minutes before finishing LD; 0.5, 1, 2 and 4-6 hours during maintenance infusion (MI); 30 minutes prior (within 24 hours of start of MI) and 10 minutes, 0.5, 1, 2, 4 and 10 hours end of MI	No
Primary	Terminal Elimination Half-life (t1/2)	Terminal elimination half-life of dexmedetomidine. Half-life is the time required for plasma concentration of the drug to decrease by 50%.	30 minutes prior to loading dose (LD); 5 minutes before finishing LD; 0.5, 1, 2 and 4-6 hours during maintenance infusion (MI); 30 minutes prior (within 24 hours of start of MI) and 10 minutes, 0.5, 1, 2, 4 and 10 hours end of MI	No
Primary	Time to Reach Maximum Plasma Concentration (Tmax)	Observed time to reach maximum plasma concentration of dexmedetomidine, expressed in hours	30 minutes prior to loading dose (LD); 5 minutes before finishing LD; 0.5, 1, 2 and 4-6 hours during maintenance infusion (MI); 30 minutes prior (within 24 hours of start of MI) and 10 minutes, 0.5, 1, 2, 4 and 10 hours end of MI	No
Primary	Weight-Adjusted Plasma Clearance (CLw)	Weight-Adjusted Plasma Clearance of dexmedetomidine after intravenous administration.	30 minutes prior to loading dose (LD); 5 minutes before finishing LD; 0.5, 1, 2 and 4-6 hours during maintenance infusion (MI); 30 minutes prior (within 24 hours of start of MI) and 10 minutes, 0.5, 1, 2, 4 and 10 hours end of MI	No
Primary	Plasma Clearance (CL)	Clearance of dexmedetomidine after intravenous administration. Clearance is the rate at which the drug is removed from the plasma after the dose.	30 minutes prior to loading dose (LD); 5 minutes before finishing LD; 0.5, 1, 2 and 4-6 hours during maintenance infusion (MI); 30 minutes prior (within 24 hours of start of MI) and 10 minutes, 0.5, 1, 2, 4 and 10 hours end of MI	No
Primary	Volume of Distribution (Vd)	Volume of distribution of dexmedetomidine after intravenous administration. Volume of distribution measures how much the drug spreads through the body after the dose.	30 minutes prior to loading dose (LD); 5 minutes before finishing LD; 0.5, 1, 2 and 4-6 hours during maintenance infusion (MI); 30 minutes prior (within 24 hours of start of MI) and 10 minutes, 0.5, 1, 2, 4 and 10 hours end of MI	No
Primary	Weight-Adjusted Volume of Distribution (Vdw)	Weight-Adjusted Volume of distribution of dexmedetomidine after intravenous administration.	30 minutes prior to loading dose (LD); 5 minutes before finishing LD; 0.5, 1, 2 and 4-6 hours during maintenance infusion (MI); 30 minutes prior (within 24 hours of start of MI) and 10 minutes, 0.5, 1, 2, 4 and 10 hours end of MI	No
Primary	Average Total Faces, Legs, Activity, Cry, and Consolability (FLACC) Score	FLACC scale is a 5 category observational measure to assess pediatric pain on face, legs, activity, cry and consolability. Responses in each category are scored between 0 to 2 (0 = normal, relaxed to 2 = upset, rigid), for a maximum total score of 10.	Prior to loading dose and every hour during the maintenance infusion; within 5 minutes after any fentanyl administration during DEX infusion or every 4 hours in case of continuous fentanyl infusion; within 5 minutes prior and after titration of fentanyl	Yes
Primary	Absolute Time That Subject is in UMSS Range 2-4 During Treatment Period	The level of sedation will be assessed using the University of Michigan Sedation Scale (UMSS).; Score 0 (awake/alert); Score 1 (sleepy/responds appropriately); Score 2 (somnolent/arouses to light stimuli); Score 3 (deep sleep/arouses to deeper physical stimuli); Score 4 (unarousable).; The UMSS scores obtained just prior the loading dose (LD) and 5 and 10 minutes during LD; 0, 5, 10, 15, 30, and 60 minutes and thereafter every 4 hours of the maintenance infusion; within 5 minutes of obtaining each pharmacokinetic sample; within 5 minutes prior and after any midazolam rescue during dexmedetomidine infusion period.	During the treatment (6 to 24 hours)	Yes
Primary	Number of Subjects Who Received Rescue Medication for Sedation and Analgesic	Participants who received rescue medication midazolam for sedation and/or fentanyl for analgesic during study drug Infusion	During the treatment (6 to 24 hours)	Yes