NCT07180420

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
12

participants targeted

Target at below P25 for phase_1

Timeline
Completed

Started Mar 2024

Shorter than P25 for phase_1

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
15 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 8, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 8, 2024

Completed
1.4 years until next milestone

First Submitted

Initial submission to the registry

September 5, 2025

Completed
13 days until next milestone

First Posted

Study publicly available on registry

September 18, 2025

Completed
Last Updated

September 18, 2025

Status Verified

September 1, 2025

Enrollment Period

15 days

First QC Date

September 5, 2025

Last Update Submit

September 11, 2025

Conditions

Keywords

naloxone intramuscular forearm

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)

EXPERIMENTAL

intramuscular (IM) to extensor digitorum communis (EDC)/forearm muscle

Drug: naloxone IM

Interventions

naloxone IM to the EDC/forearm muscle

Naloxone intramuscular (IM)

Eligibility Criteria

Age18 Years - 55 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

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

Study Sites (1)

JCCT

Lenexa, Kansas, 66219, United States

Location

Study Officials

  • Thomas Krol, PharmD

    STAT Therapeutics Inc

    STUDY CHAIR

Study Design

Study Type
interventional
Phase
phase 1
Allocation
NA
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Model Details: The study was an outpatient, open-label, single period, single treatment, single dose proof of concept (PoC) trial in 12 healthy volunteers
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

Locations