A Clinical Trial to Assess Pharmacokinetic Profiles, Safety and Tolerability of IVL3004 and IVL4002 in Healthy Male Subjects.

A PHASE 1, OPEN-LABEL, EXPLORATORY, FIXED-SEQUENCE, PHARMACOKINETIC SINGLE ASCENDING DOSE STUDY OF IVL3004 VERSUS VIVITROL® (NALTREXONE) LONG-ACTING INJECTABLE (LAI) AND IVL4002 IN HEALTHY SUBJECTS

A Clinical Trial to Assess Pharmacokinetic Profiles, Safety and Tolerability of IVL3004 and IVL4002 in Healthy Male Subjects.

Study Overview

• Status: Recruiting
• Conditions: Alcohol Dependence; Multiple Sclerosis; Opioid Dependence
• Intervention / Treatment: Drug: Vivitrol Injectable Product; Drug: IVL3004; Drug: IVL4002

Detailed Description

A Phase 1, Open-Label, Exploratory, Fixed-Sequence, Pharmacokinetic Single Acending Dose Study of IVL3004 Versus Vivitrol® (Naltrexone) Long-Acting Injectable(LAI) and IVL4002 in Healthy Subjects

• Study Type: Interventional
• Enrollment (Estimated): 40
• Phase: Phase 1

Contacts and Locations

• Study Contact: Name: HyeRyeon Kim; Phone Number: 5134 82-31-608-0514; Email: hr.kim@inventagelab.com
• Study Contact Backup: Name: Heesun Kim; Phone Number: 5134 82-31-608-0514; Email: flower@inventagelab.com

Study Locations

• Australia
  • Queensland
    • Herston, Queensland, Australia, 4006
      • Recruiting
      • Nucleus Network
      • Contact: Michael Wong, Dr.; Phone Number: +61 7 3707 2790; Email: m.wong@nucleusnetwork.com.au

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 14 years to 51 years (Adult)
• Accepts Healthy Volunteers: Yes

Description

Inclusion Criteria:

1. Healthy adult male, ≥18 and ≤55 years of age, non-smokers or occasional smokers (defined as smoking less than 10 cigarettes or nicotine equivalent per week, and willing to abstain from smoking during confinement at the clinical site).
2. BMI ≥18.0 and ≤32.0 kg/m2 and body weight ≥55.0 kg.

3. Healthy as defined by:

   1. The absence of clinically significant illness, infection, or medical/surgical procedure within 4 weeks prior to dosing or planned inpatient surgery (including dental surgery) or hospitalization during the study period.
   2. The absence of clinically significant history of neurological, endocrine, cardiovascular, respiratory, hematological, immunological (including autoimmune), psychiatric, gastrointestinal, renal, hepatic, and metabolic disease.

4. Subjects who are not vasectomized for at least 3 months prior to dosing, and who are sexually active with a female partner of childbearing potential must be willing to use one of the following acceptable contraceptive methods from dosing and for 90 days after dosing:

   a. Simultaneous use of a male condom and, for the female partner, hormonal contraceptives used for at least 4 weeks or intrauterine device placed for at least 4 weeks prior to dosing.

5. Subjects who have had a vasectomy must be willing to use a condom until study exit.
6. Subjects who practice abstinence from sexual intercourse as a usual and preferred lifestyle.
7. Subjects must be willing not to donate sperm for 90 days after dosing.
8. Willing to undergo SC abdominal injection or IM ventral gluteal injection to allow for investigational drug administration.
9. Willing and able to provide written informed consent after the nature of the study has been explained and prior to the commencement of any protocol- specific study procedures.

Exclusion Criteria:

1. Any clinically significant abnormal finding at physical examination at screening or Day -1.
2. Clinically significant abnormal laboratory test results at screening or Day -1, or positive serology test results for human immunodeficiency virus (HIV), hepatitis B or hepatitis C virus at screening.
3. Is prone to skin rashes, irritation, or has a skin condition such as recurrent eczema that is likely to impact the injection site area or demonstrates any abnormal skin tissue in the proposed injection area, as determined by the Investigator.
4. Any history of malignancy or neoplastic disease.
5. History of significant allergic reactions (e.g., drug reaction, anaphylactic reaction, hypersensitivity, angioedema) to any drug, or to any excipient present in the formulations.
6. ALT, AST, or total bilirubin >1.5x upper limit of normal (ULN) at screening or Day -1.
7. Estimated glomerular filtration rate (eGFR) <60 mL/min/1.73m2 as calculated by the 2021 Chronic Kidney Disease-Epidemiology (CKD-EPI) equation at screening or Day -1.
8. Clinically significant ECG abnormalities (QTc >450 ms or PR interval >220 ms) or vital sign abnormalities (systolic blood pressure <90 or >140 mmHg, diastolic blood pressure <40 or >90 mmHg, or heart rate <40 or >100 bpm) at screening or Day -1.
9. History of alcohol abuse within 1 year prior to screening or regular use of alcohol within 6 months prior to screening that exceeds 14 units of alcohol per week (1 unit = 375 mL of beer 3.5%, 100 mL of wine 13.5%, or 30 mL of spirit 40%), or positive alcohol test at screening or Day -1.
10. History of drug abuse within 1 year prior to screening or positive test for drugs of abuse (e.g., phencyclidine, opiates, benzodiazepines, barbiturates, amphetamines, methamphetamines, cocaine, and tetrahydrocannabinol) at screening or Day -1.
11. Presence of any underlying physical or psychological (e.g., depression) medical condition that, in the opinion of the Investigator, would make it unlikely that the participant will comply with the protocol or complete the study per protocol. Mild depression and anxiety that has been resolved at least 6 months prior to screening is accepted.

12. Use of medications for the timeframes specified below, with the exception of hormonal contraceptives and medications exempted by the Investigator on a case-by-case basis because they are judged unlikely to affect the PK profile of the study drug or subject safety:

    1. Depot injection or implant within 3 months prior to dosing;
    2. Strong CYP inhibitors or inducers within 30 days prior to dosing;
    3. Prescription medications within 14 days prior to dosing;
    4. Any vaccine, including COVID-19 vaccine, within 7 days prior to dosing;
    5. OTC medications (including topical and nasal formulations with active pharmaceutical ingredients) within 7 days prior to dosing, except for occasional use of acetaminophen/paracetamol (up to 2 g/day);
    6. Natural health products (including herbal remedies, homeopathic and traditional medicines, probiotics, food supplements such as vitamins, minerals, amino acids, essential fatty acids, and protein supplements used in sports) within 7 days prior to dosing;
    7. Anesthetic agents within 24 hours prior to dosing.
    8. Anticoagulant medications from 15 days prior to dosing to 6 weeks post- dose.
13. Participation in a clinical research study involving the administration of an investigational or marketed drug or device within 30 days prior to dosing, administration of a biological product in the context of a clinical research study within 90 days prior to dosing, or concomitant participation in an investigational study involving no drug or device administration.
14. Donation of plasma within 7 days prior to dosing or donation or loss of 500 mL or more of whole blood within 30 days prior to dosing.
15. Any reason which, in the opinion of the Investigator, would prevent the subject from participating in the study.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Non-Randomized
• Interventional Model: Sequential Assignment
• Masking: None (Open Label)

Number of Arms

4

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Active Comparator: Part A Group 1 (Vivitrol Injection); Vivitrol, Single Dose, IM injection	Drug: Vivitrol Injectable Product; Naltrexone Long-Acting Injection
Experimental: Part A Group 2 (IVL3004 A mg); IM, Single Dose	Drug: IVL3004; Naltrexone Long-Acting Injection
Experimental: Part A Group 3 IVL3004 B mg); IM, Single Dose	Drug: IVL3004; Naltrexone Long-Acting Injection
Experimental: Part B Group 1 (IVL4002 Cmg); SC, Single Dose	Drug: IVL4002; Naltrexone Long-Acting Injection

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Cmax	The maximal observed concentration	Pre-dose, up to Day 57
AUC0-240	Area under the concentration-time curve from time zero to 240hrs	Pre-dose, up to Day 57
AUC240-672	Area under the concentration-time curve from time 240 to 672hrs	Pre-dose, up to Day 57
AUC0-672	Area under the concentration-time curve from time zero to 672hrs	Pre-dose, up to Day 57
AUC0-inf	Area under the concentration-time curve from time zero to infinity	Pre-dose, up to Day 57

Collaborators and Investigators

• Sponsor: Inventage Lab., Inc.

Study record dates

Study Major Dates

• Study Start (Actual): September 11, 2024
• Primary Completion (Estimated): December 30, 2025
• Study Completion (Estimated): December 30, 2025

Study Registration Dates

• First Submitted: November 10, 2022
• First Submitted That Met QC Criteria: November 10, 2022
• First Posted (Actual): November 17, 2022

Study Record Updates

• Last Update Posted (Estimated): September 15, 2025
• Last Update Submitted That Met QC Criteria: September 9, 2025
• Last Verified: September 1, 2025

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Narcotic-Related Disorders; Nervous System Diseases; Mental Disorders; Autoimmune Diseases; Immune System Diseases; Demyelinating Autoimmune Diseases, CNS; Autoimmune Diseases of the Nervous System; Demyelinating Diseases; Substance-Related Disorders; Chemically-Induced Disorders; Alcohol-Related Disorders; Multiple Sclerosis; Opioid-Related Disorders; Alcoholism; Physiological Effects of Drugs; Peripheral Nervous System Agents; Sensory System Agents; Narcotic Antagonists; Alcohol Deterrents; Naltrexone
• Other Study ID Numbers: IVL3004-001

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No
• product manufactured in and exported from the U.S.: No