Naloxone Nasal Spray Pharmacokinetic Study
Primary Purpose
Opioid Overdose
Status
Unknown status
Phase
Phase 1
Locations
Jordan
Study Type
Interventional
Intervention
MVP005
MVP005
Naloxone hydrochloride solution for injection with mucosal atomization device
Sponsored by
About this trial
This is an interventional treatment trial for Opioid Overdose focused on measuring Intranasal, nasal spray, opioid, overdose
Eligibility Criteria
Inclusion Criteria:
- Male or female
- 18-60 50 years of age
- Provide written informed consent prior to completing any study specific procedure.
- Body Mass Index (BMI) range 18.5-30 kg/m2
- Clinically acceptable medical history, clinical laboratory evaluations, complete physical examination, vital signs and 12 lead ECG
- Using reliable contraception
Exclusion Criteria:
- Intranasal problems
- Taking prescribed or over the counter medications
- Intake of alcohol, methyl-xanthines or grapefruit or strenuous exercise concurrent with treatment.
Sites / Locations
- International Pharmaceutical Research Center (IPRC)
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Experimental
Active Comparator
Arm Label
Test Product Dose 1
Test Product Dose 2
Comparator Product
Arm Description
Outcomes
Primary Outcome Measures
Pharmacokinetics
Plasma concentration time profiles and area under the curve (AUC), maximum concentation (Cmax), Time to maximum concentration (Tmax), elimination rate constant (Kel) and terminal half life (t1/2)
Secondary Outcome Measures
Number of subjects with adverse events
Continuous adverse event monitoring during the study with prompted assessments in the 12 hours post-dose
Physical Examination
Complete physical examination at screening and final follow-up and specific nasal examination post-dose
Vital signs
Vital signs at screening, final follow-up and pre- and post-dose
ECGs
ECGs at screening and final follow-up
Safety Laboratory Tests
Haematology, biochemistry and urinalysis at screening and final follow-up
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01622504
Brief Title
Naloxone Nasal Spray Pharmacokinetic Study
Official Title
A Phase I Single Dose, Open Label, Randomized, Three Period Crossover Pilot Study to Compare the Pharmacokinetics, Safety and Tolerability of MVP005 Intranasal Spray With Intranasal Administration of Naloxone Solution for Injection in Healthy Adult Subjects
Study Type
Interventional
2. Study Status
Record Verification Date
June 2012
Overall Recruitment Status
Unknown status
Study Start Date
June 2012 (undefined)
Primary Completion Date
July 2012 (Anticipated)
Study Completion Date
August 2012 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Mitovie Pharma Ltd
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
This study aims to compare the pharmacokinetics of naloxone when administered as the Mitovie nasal spray (Test Product) and as a solution for injection (Comparator Product) administered intranasally using a mucosal atomization device (MAD).
Detailed Description
Naloxone hydrochloride is currently only recommended and licensed for intravenous, intramuscular and subcutaneous administration. It has also been used by intranasal administration (off-label use) when the intravenous route is not suitable by administering the Solution for Injection using a mucosal atomization device (MAD). However, due to the volume of naloxone solution administered this way, some of it may be inadvertently swallowed and not absorbed into the nasal mucosa and the product requires administration by medically trained personnel. The study aims to investigate intranasal administration of naloxone using a more concentrated solution and a nasal delivery device.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Opioid Overdose
Keywords
Intranasal, nasal spray, opioid, overdose
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
6 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Test Product Dose 1
Arm Type
Experimental
Arm Title
Test Product Dose 2
Arm Type
Experimental
Arm Title
Comparator Product
Arm Type
Active Comparator
Intervention Type
Drug
Intervention Name(s)
MVP005
Intervention Description
2 mg single dose administered intranasally
Intervention Type
Drug
Intervention Name(s)
MVP005
Intervention Description
4 mg single dose administered intranasally
Intervention Type
Drug
Intervention Name(s)
Naloxone hydrochloride solution for injection with mucosal atomization device
Intervention Description
2 mg single dose administered intranasally
Primary Outcome Measure Information:
Title
Pharmacokinetics
Description
Plasma concentration time profiles and area under the curve (AUC), maximum concentation (Cmax), Time to maximum concentration (Tmax), elimination rate constant (Kel) and terminal half life (t1/2)
Time Frame
0, 5, 10, 15, 20, 30 and 45 minutes and 1.00, 1.50, 2.00, 3.00, 4.00, 6.00, 8.00 and 12.00 hours for each arm
Secondary Outcome Measure Information:
Title
Number of subjects with adverse events
Description
Continuous adverse event monitoring during the study with prompted assessments in the 12 hours post-dose
Time Frame
14 days
Title
Physical Examination
Description
Complete physical examination at screening and final follow-up and specific nasal examination post-dose
Time Frame
14 days
Title
Vital signs
Description
Vital signs at screening, final follow-up and pre- and post-dose
Time Frame
14 days
Title
ECGs
Description
ECGs at screening and final follow-up
Time Frame
14 days
Title
Safety Laboratory Tests
Description
Haematology, biochemistry and urinalysis at screening and final follow-up
Time Frame
14 days
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Male or female
18-60 50 years of age
Provide written informed consent prior to completing any study specific procedure.
Body Mass Index (BMI) range 18.5-30 kg/m2
Clinically acceptable medical history, clinical laboratory evaluations, complete physical examination, vital signs and 12 lead ECG
Using reliable contraception
Exclusion Criteria:
Intranasal problems
Taking prescribed or over the counter medications
Intake of alcohol, methyl-xanthines or grapefruit or strenuous exercise concurrent with treatment.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Rana Hassan, MSc
Phone
+96265627651
Email
r.hassan@iprc.com.jo
First Name & Middle Initial & Last Name or Official Title & Degree
Halah Zqqout, BSc
Phone
+96265627651
Email
h.zqqout@iprc.com.jo
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Abdullah Hiyari, MD
Organizational Affiliation
IPRC, Jordan
Official's Role
Principal Investigator
Facility Information:
Facility Name
International Pharmaceutical Research Center (IPRC)
City
Amman
Country
Jordan
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Rana Hassan, MSc
Phone
+96265627651
Email
r.hassan@iprc.com.jo
First Name & Middle Initial & Last Name & Degree
Halah Zqqout, BSc
Phone
+96265627651
Email
h.zqqout@iprc.com.jo
First Name & Middle Initial & Last Name & Degree
Abdullah Hiyari, MD
12. IPD Sharing Statement
Learn more about this trial
Naloxone Nasal Spray Pharmacokinetic Study
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