30 Participants NeededMy employer runs this trial

BICX104 + Bupropion for Opiate Dependence

SR
Overseen ByStudy Recruitment Inquiries, Segal Trials
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial tests a new method of delivering naltrexone, a medication for opioid addiction, through a small implant under the skin (BICX104 naltrexone implantable pellet). Researchers aim to determine if this implant is as effective as the existing monthly injection (Vivitrol, a naltrexone depot injection) and whether combining it with bupropion (a medication often used for depression and smoking cessation) enhances results. Ideal candidates for the trial are those who have recently been opioid-free, are generally healthy, and do not have a history of substance abuse or specific medical conditions like epilepsy or certain heart problems. As a Phase 1 trial, the research focuses on understanding how the treatment works in people, offering participants a chance to be among the first to receive this innovative treatment.

Do I need to stop my current medications to join the trial?

Yes, you may need to stop certain medications. The trial excludes participants who are currently taking antidepressants, certain stimulants, or medications that could interact with the study drugs. It's best to discuss your current medications with the study team to see if they are allowed.

Is there any evidence suggesting that this trial's treatments are likely to be safe?

Research has shown that naltrexone, the main ingredient in the BICX104 implant, has been safely used to treat addiction for a long time. It is available in forms like pills and monthly injections, which patients have tolerated well. The BICX104 implant is designed to release naltrexone steadily over about three months. Previous studies on similar naltrexone implants found no major safety issues and demonstrated effectiveness in reducing opioid use.

Bupropion, also part of the trial, has been used with naltrexone in other treatments, mainly for weight loss, and has a good safety record. Some people might experience mild side effects like nausea or headaches, but these are usually not severe.

This trial is in its early stages, focusing mainly on safety. Researchers typically administer the treatment to a small group of healthy volunteers to check for any adverse reactions. So far, naltrexone and bupropion have been safe in other settings, suggesting a promising safety profile for this combination in the trial.12345

Why are researchers excited about this trial's treatments?

Researchers are excited about the treatments involving BICX104 and bupropion for opiate dependence because they offer innovative delivery methods and combinations. BICX104 is a naltrexone implantable pellet, which provides a long-term, consistent release of medication, potentially improving adherence compared to the standard monthly Vivitrol injections. Additionally, the combination of BICX104 with bupropion, an extended-release oral medication, could enhance effectiveness by addressing both opiate cravings and withdrawal symptoms. These approaches aim to simplify treatment regimens and improve outcomes for individuals struggling with opiate dependence.

What evidence suggests that this trial's treatments could be effective for opiate dependence?

Research has shown that naltrexone implants, such as BICX104, can aid individuals with opioid addiction by gradually releasing medication. This method has proven effective in helping people remain in treatment longer and reducing relapse risk. Studies have found that naltrexone implants can lower death rates among those addicted to opioids. In this trial, some participants will receive BICX104 alone, while others will receive BICX104 combined with bupropion. Bupropion, a medication also used for depression and smoking cessation, has shown promise in treating other addictions, such as methamphetamine addiction. While the specific combination of BICX104 and bupropion for opioid addiction is still under investigation, both have individually demonstrated effectiveness in related conditions. Additionally, another group in this trial will receive Vivitrol, a naltrexone depot injection, as a comparator.26789

Are You a Good Fit for This Trial?

This trial is for healthy adults aged 18-65, with a BMI between 18.5 and 30, who are opioid-free (confirmed by drug tests), able to understand English or Spanish, willing to use birth control if needed, and can commit to all study visits.

Inclusion Criteria

Must agree to comply with all study requirements and be willing to complete entire study
Willing and able to provide informed consent and to read and understand study documents in English or Spanish
Meet subjective and objective measures of being opioid-free prior to study treatment initiation, including negative urine drug screen results at screening and enrollment
See 4 more

Exclusion Criteria

History of angle-closure glaucoma
I need to take opioid pain medications during the study.
History of any psychiatric disorder OR suicidal ideation, behavior, or risk of self-harm as evidenced by endorsement of items 2, 3, 4, or 5 on the C-SSRS
See 13 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

3 weeks
1 visit (in-person)

Treatment

Participants receive BICX104 implantable pellets with or without bupropion, or Vivitrol injections

12 weeks
12 visits (in-person)

Follow-up

Participants are monitored for safety and effectiveness after treatment

12 weeks
4 visits (in-person)

Safety Follow-up

Final safety assessments including PK sampling and adverse event monitoring

4 weeks
1 visit (in-person)

What Are the Treatments Tested in This Trial?

Interventions

  • BICX104 naltrexone implantable pellet
  • Bupropion XL
  • Vivitrol (Naltrexone depot injection)

Trial Overview

The study compares an implantable naltrexone pellet (BICX104) alone or with bupropion pills against monthly Vivitrol injections. Participants are randomly assigned to different groups and monitored over about six months for safety and how the drugs move through the body.

How Is the Trial Designed?

4

Treatment groups

Experimental Treatment

Active Control

Group I: BICX104 (2 Pellets) + bupropion XL 450 mg QDExperimental Treatment2 Interventions
Group II: BICX104 (1 Pellet) + bupropion XL 450 mg QDExperimental Treatment2 Interventions
Group III: BICX104 (1 Pellet)Experimental Treatment1 Intervention
Group IV: Vivitrol q 28 daysActive Control1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

BioCorRx Pharmaceuticals Inc

Lead Sponsor

National Institute on Drug Abuse (NIDA)

Collaborator

Trials
2,658
Recruited
3,409,000+

Citations

Naltrexone Implant for Opioid Use Disorder - PMC - NIH

The approval of oral naltrexone initially showed much promise, as the drug was observed to be highly potent in antagonizing the effects of opioids while ...

BioCorRx, Inc. Announces Initiation of Clinical Study by ...

BICX104 is designed to provide sustained plasma concentrations of naltrexone for approximately three months following a minimally invasive ...

Naltrexone Implant Versus Daily Pill

The current study showed that an extended-release naltrexone implant may provide an evidence-based strategy to increase treatment retention and reduce relapse.

Naltrexone implants for addiction to opiates

The NLM published a study, which found naltrexone implants to be effective at lowering deaths for people who are addicted to opioids.

5.

pubmed.ncbi.nlm.nih.gov

pubmed.ncbi.nlm.nih.gov/30880163/

Slow-release naltrexone implant versus oral ... - PubMed

Untreated opioid addiction in people with HIV is associated with poor HIV treatment outcomes. Slow-release, long-acting, implantable naltrexone might improve ...

Naltrexone Depot Formulations for Opioid and Alcohol ... - PMC

This article systematically reviews the literature on naltrexone depot or implant treatment for alcohol and opioid dependence. Apart from treatment effect ...

NCT04828694 | Pharmacokinetic and Safety Study of ...

BICX104 is an eroding implantable pellet that contains 1 g naltrexone and 11 mg magnesium stearate that will be inserted subcutaneously. It will be administered ...

Naltrexone Implant Versus Daily Pill

A new abdominal implant containing 1000 mg of naltrexone, approved for use in Russia, has the potential to block the effects of opioids for 2 months. To test ...

Naltrexone Implants - Medical Clinical Policy Bulletins

Secondary outcomes were opioid craving, recreational use of substances other than opioids, mental health, quality of life (QOL) as well as criminal activity.