Proof of Concept (PoC) Evaluation of Naloxone Unique Intramuscular (IM) Injection
1 other identifier
interventional
12
1 country
1
Brief Summary
WHAT IS THE PURPOSE OF THIS RESEARCH STUDY This research study is designed to demonstrate that intramuscular (IM) Injection of FDA Approved Naloxone Hydrochloride (HCI) given in the forearm muscle is approximately the same as given the injection in the buttocks muscle. STAT Therapeutics Inc. is sponsoring this research study. BACKGOUND AND PURPOSE FOR THIS STUDY You are being asked to participate in this research study because you are between the ages of 18 and 55 and appear to be in stable health. Naloxone HCI is FDA approved and has been used to treat symptoms of opioid overdose for over 40 years. This research study is designed to demonstrate that intramuscular (IM) Injection of FDA Approved Naloxone Hydrochloride (HCI) given in the forearm is approximately the same as given the injection in the buttocks. This is the first time Naloxone Hydrochloride (HCI) is given in the forearm muscle. This is an open-label study. This means that you, the Doctor, study staff, and the Sponsor will know the study drug and the dose that you are given.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for phase_1
Started Mar 2024
Shorter than P25 for phase_1
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 24, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 8, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
April 8, 2024
CompletedFirst Submitted
Initial submission to the registry
September 5, 2025
CompletedFirst Posted
Study publicly available on registry
September 18, 2025
CompletedSeptember 18, 2025
September 1, 2025
15 days
September 5, 2025
September 11, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Pharmacokinetic Profile (area under the curve AUC)
Area under the Curve (AUC)
1 day
Secondary Outcomes (1)
PK Profile (Cmax, Tmax, T/2- half-life)
1 day
Study Arms (1)
Naloxone intramuscular (IM)
EXPERIMENTALintramuscular (IM) to extensor digitorum communis (EDC)/forearm muscle
Interventions
Eligibility Criteria
You may qualify if:
- to 55 years of age
- Body mass index (BMI) 18 to 30 kg/m2
- Subjects who do not take prescribed or OTC medications on a regular basis. In the case of recent sporadic use for minor illness, the subject may be enrolled if the investigator deems the use insignificant to study.
- Nonsmokers and subjects who smoked 10 or fewer cigarettes per day.
- Be willing to spend at least 12 hours in the study facility.
You may not qualify if:
- Abnormal wrist or forearm anatomy (or history of prior wrist/forearm surgery).
- Difficult venous access for blood draws
- Active infection in including respiratory tract infection
- Used opioid analgesics for pain relief within the previous 14 days, or, in the judgment of the investigator, had significant acute or chronic medical conditions.
- Known previous or concomitant serious illness or medical condition such as malignancy, HIV, significant gastrointestinal or hepatic disease or cardiovascular event or hepatitis that in the opinion of the investigator may interfere with participation in the study
- Previous Substance Use Disorder (SUD) with injectable drugs.
- Compromised cardiovascular system (history of myocardial infarction- MI, angina, etc., at discretion of principal investigator- PI).
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- STAT Therapeutics Inclead
- Johnson County ClinTrialscollaborator
Study Sites (1)
JCCT
Lenexa, Kansas, 66219, United States
Study Officials
- STUDY CHAIR
Thomas Krol, PharmD
STAT Therapeutics Inc
Study Design
- Study Type
- interventional
- Phase
- phase 1
- Allocation
- NA
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
September 5, 2025
First Posted
September 18, 2025
Study Start
March 24, 2024
Primary Completion
April 8, 2024
Study Completion
April 8, 2024
Last Updated
September 18, 2025
Record last verified: 2025-09