Pharmacokinetics (PK) and Safety of Multiple Doses of Intranasal Naloxone in Healthy Adults

Opioid Overdose Clinical Trial

Official title:

A Phase 1, Open Label, Randomized Study to Investigate the Pharmacokinetics and Safety of Multiple Doses of Intranasal Naloxone in Healthy Adult Participants

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05377255
• Other study ID #: EBS-NAR-001
• Status: Completed
• Phase: Phase 1
• Start date: March 28, 2022
• Est. completion date: May 10, 2022

Study information

• Verified date: March 2024
• Source: Emergent BioSolutions
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study will be a Phase 1, single-center, open-label, randomized cross-over study to evaluate the PK of a new AP003 device which delivers two sprays of 4 mg naloxone hydrochloride intranasally.

Description:

Based on the intended AP003 product presentation there will be two devices in each carton allowing for administration of a total of 16 mg. This study is designed for subjects to receive naloxone therapy either through the AP003 device or through the currently approved NARCAN® nasal spray (4 mg) device (per label), reference therapy. After administration of the therapy patients will be followed by a 48-hour washout period before treatment crossover. Key study parameters include safety and PK. Safety evaluations will include but not limited to complete and system directed physical examinations (including signs of nasal irritation such as erythema, edema, and erosion), administration of a Brief Smell Identification Test (B-SIT), assessments of vital signs, 12 lead electrocardiogram (ECG), continuous cardiac telemetry monitoring (CCT) , clinical laboratory tests (e.g., hematology, chemistry, urinalysis, pregnancy test), and evaluation of adverse events.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 24
• Est. completion date: May 10, 2022
• Est. primary completion date: May 10, 2022
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 55 Years

Eligibility

Inclusion Criteria:

• Are able to consent and freely provide informed consent.
• Females and males 18-55 years of age, inclusive.
• Have a body mass index (BMI) less than or equal to 34.0 kg/m2.
• Generally healthy, in the opinion of the Investigator, based on medical history, physical examination, vital signs, screening laboratory assessments and 12-lead ECG evaluation.
• If female:

1. Have a negative pregnancy test at Screening (serum pregnancy test) and before dosing at Day -1 (urine pregnancy test)

2. Female subjects of non-childbearing potential must be:

• Post-menopausal (spontaneous amenorrhea for at least 12 months prior to dosing) with confirmation by documented FSH levels =40 mIU/mL; or
• Surgically sterile (bilateral oophorectomy, bilateral salpingectomy, hysterectomy, or tubal ligation) at least 3 months prior to dosing.

3. Women of childbearing potential who are not planning to be pregnant during the study period and who are using one of the following effective methods of contraception during the study period and for at least 30 days after last study

visit:

• Simultaneous use of hormonal contraceptive (e.g. oral, patch, depot injection, implant, vaginal ring, intrauterine device) or non-hormonal intrauterine device for at least 4 weeks prior to dosing (must agree to use the same contraceptive throughout the study) and condom for the male partner.
• Simultaneous use of diaphragm or cervical cap with spermicide and condom for the male partner, started at least 21 days prior to dosing.

Exclusion Criteria:

• Subjects planning to become pregnant during the study or currently breastfeeding.
• Any acute condition, in the opinion of the Investigator, that is not fully resolved at least 4 weeks prior to baseline.
• Subject has a deviated septum, previous rhinoplasty, abnormal nasal anatomy, other nasal symptoms (i.e., blocked and/or runny nose), or other nasal surgeries (i.e., polyp removal) within 1 year, or needs to use another nasal spray product during study.
• Subject with current upper respiratory infection (URI) or has had URI within 7 days prior to screening.
• Subject has had an episode of epistaxis within 30 days prior screening or has experienced recurrent episodes of epistaxis within 1 year prior to screening.
• Subject has used any prescription or nonprescription drugs/supplements with increased risk of bleeding within 28 days or 5 half-lives (whichever is longer) or complementary and alternative medicines within 28 days before the first dose of study drug with exception of oral contraceptives. All other prescription medications, over-the-counter, and natural health products within 14 days or 5 half-lives prior to the first dosing.
• Subject is currently participating in another clinical study of an investigational drug or has been dosed with any investigational drug within 30 days or 5 half-lives (whichever is longer) of the compound.

Related Conditions & MeSH terms

• Drug Overdose
• Opiate Overdose
• Opioid Overdose

Intervention

Combination Product:
• 16 mg naloxone AP003
4 doses of 4 mg each (total: 16 mg) of naloxone through the AP003 device
• 8 mg naloxone NARCAN Nasal Spray
2 doses of 4 mg each (total: 8 mg) of the naloxone through the NARCAN Nasal Spray device

Locations

Country	Name	City	State
United States	Syneos Health Clinical Research Services	Miami	Florida

Sponsors (1)

Lead Sponsor	Collaborator
Emergent BioSolutions

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Mean naloxone plasma concentration AP003 dosing periods.	The mean naloxone plasma concentration during the two AP003 dosing periods.	PK samples taken at various timepoints over the course of Pre-dose and post-dose for 12 hours.
Primary	Mean naloxone plasma concentration Narcan dosing periods	The mean naloxone plasma concentration during the two Narcan dosing periods.	PK samples taken at various timepoints over the course of Pre-dose and post-dose for 12 hours.
Primary	Incidence of treatment emergent adverse events (TEAEs), serious adverse events (SAE)	Incidence of treatment emergent adverse events (TEAEs), serious adverse events (SAE) by treatment thru End of Study Visit (within 7 days after 2nd dose).	Through end of study visit (within 7 days after second dose)
Primary	Incidence of abnormal vital signs	Incidence of abnormal vital signs (heart rate, blood pressure, and respiration rate) by treatment thru End of Study Visit (within 7 days after 2nd dose).	Through end of study visit (within 7 days after second dose)
Primary	Incidence of clinically significant ECG	Incidence of clinically significant ECG by treatment thru End of Study Visit (within 7 days after 2nd dose).	Through end of study visit (within 7 days after second dose)
Primary	Incidence of clinical laboratory changes	Incidence of clinical laboratory changes by treatment thru End of Study Visit (within 7 days after 2nd dose).	Through end of study visit (within 7 days after second dose)
Primary	Incidence of adverse events of special interest (AESI) indicating of nasal irritation	Incidence of adverse events of special interest (AESI) indicating of nasal irritation (erythema, edema, and erosion) by treatment thru End of Study Visit (within 7 days after 2nd dose).	Through end of study visit (within 7 days after second dose)
Primary	Incidence of changes in B-SIT assessment	Incidence of changes in B-SIT assessment within an AP003 period thru End of Study Visit (within 7 days after 2nd dose).	Through end of study visit (within 7 days after second dose)