Midomafetamine for Healthy Adults

RP
Overseen ByResilient Pharmaceuticals
Age: 18 - 65
Sex: Any
Trial Phase: Phase 1
Sponsor: Resilient Pharmaceuticals
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 aims to test the safety of midomafetamine in healthy adults by examining how the body processes the drug and its effects on the heart. Participants will receive either a regular or higher dose, with heart and health assessments conducted before and after administration. This trial suits healthy adults without heart, brain, or mental health issues who are willing to adhere to the study procedures. As a Phase 1 trial, participants will be among the first to help researchers understand how this new treatment works in people.

Do I have to stop taking my current medications for the trial?

The trial information does not specify whether you need to stop taking your current medications. However, since the study is for healthy adults and involves assessing the drug's effects, it's possible that you may need to pause certain medications. Please consult with the study team for specific guidance.

Is there any evidence suggesting that midomafetamine is likely to be safe for humans?

Research has shown that midomafetamine is generally safe under controlled conditions. Studies on similar substances, such as MDMA, indicate they are well-tolerated by healthy individuals. However, some safety concerns should be considered. For example, potential heart risks necessitate heart monitoring in this study using electrocardiograms, which check the heart's electrical activity.

In earlier studies, the main side effects involved the heart and blood pressure, but these were manageable. No serious issues, such as potential for abuse or heart rhythm problems (QT prolongation), were found. These findings suggest midomafetamine is mostly safe, but monitoring during use is important to detect any potential problems early.12345

Why do researchers think this study treatment might be promising?

Midomafetamine is unique because it introduces a novel active ingredient that researchers believe could offer new benefits for patients. Unlike existing treatments that might rely on traditional mechanisms, midomafetamine is administered in sequential dose cohorts, including a targeted therapeutic dose and a supratherapeutic dose, both delivered in a split manner. This innovative approach could potentially enhance efficacy and safety, providing a fresh alternative to current options. Researchers are particularly excited about the potential for midomafetamine to offer benefits that standard treatments may not, making it a promising candidate for future therapeutic strategies.

What evidence suggests that midomafetamine could be effective?

Research has shown that midomafetamine may help treat posttraumatic stress disorder (PTSD). In one study, 86.5% of people who received therapy with midomafetamine noticed improvement. Another study found that 87% of participants responded well to the treatment, compared to 66% who took a placebo (a pill with no active medicine). These results suggest that midomafetamine could be beneficial, especially for those with long-lasting and difficult-to-treat PTSD. While information on its effectiveness for other conditions remains limited, several studies support its positive impact on PTSD. Participants in this trial will receive midomafetamine in sequential dose cohorts to further evaluate its effects.15678

Are You a Good Fit for This Trial?

This trial is for healthy adults aged 18 to 55 who have no significant medical issues, as confirmed by exams and lab tests. Participants must be able and willing to follow all study procedures.

Inclusion Criteria

I am a healthy adult between 18 and 55 years old.
I am medically healthy based on recent exams and tests.
I am able and willing to follow all study procedures.

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

1-2 weeks

Treatment

Participants receive midomafetamine in a split dose administration, with clinical assessments, laboratory testing, and electrocardiographic monitoring

3 days
Daily visits for dosing and assessments

Follow-up

Participants are monitored for safety and adverse events after treatment

4 weeks
End of Study visit on Day 30 +/- 2 Days

What Are the Treatments Tested in This Trial?

Interventions

  • Midomafetamine

Trial Overview

The study is testing the safety of midomafetamine at two different dose levels in healthy adults. It will also look at how the drug moves through the body and its effects on heart function using ECGs.

How Is the Trial Designed?

1

Treatment groups

Experimental Treatment

Group I: ExperimentalExperimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Resilient Pharmaceuticals

Lead Sponsor

Dr. Vince Clinical Research

Collaborator

Trials
3
Recruited
80+

Citations

The effectiveness and value of midomafetamine-assisted ...

Safety data on cardiovascular events were limited; patients treated with MDMA-AP had higher rates of elevated blood pressure (68% vs 22%) and ...

Cost-effectiveness of midomafetamine-assisted therapy ...

These data suggest MDMA-AT may be a cost-effective treatment compared to PT for patients with chronic PTSD of moderate or higher severity.

Midomafetamine-Assisted Psychotherapy for Post- ...

A large majority of the panel voted that the evidence is not adequate to demonstrate that the net health benefit of MDMA-AP is superior to that ...

NDA 215455

Do the available data show that the drug is effective in patients with posttraumatic stress disorder? Do the benefits of midomafetamine with ...

MDMA-Assisted Therapy Receives a Complete Response ...

Exploratory outcomes revealed 45 out of 52 participants (86.5%) who received MDMA-AT exhibited a clinically meaningful improvement—defined as a ...

NCT07584720 | Study of Midomafetamine in Healthy Adults

Safety assessments include monitoring of adverse events, clinical laboratory tests, vital signs, and electrocardiographic measurements.

Study of Midomafetamine in Healthy Adults

Safety assessments include monitoring of adverse events, clinical laboratory tests, vital signs, and electrocardiographic measurements.

Midomafetamine for Healthy Adults

This Phase 1 study is designed to evaluate the safety and tolerability of midomafetamine in healthy adult participants.