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Planned

DemeRx DMX-1001: Planned Oral Noribogaine Development in Alcohol Use Disorder

Sponsor: DemeRx, Inc.

Study record at a glance

Design, population, outcomes, and follow-up
Study IDdmx-1001-aud
DesignPlanned clinical development: the company describes an alcohol-interaction study supporting a planned Phase 2 trial in alcohol use disorder
Condition / topicAlcohol use disorder
PopulationPeople with alcohol use disorder are the intended Phase 2 population described in the company announcement
Sample sizeNot stated for the planned alcohol use disorder trial in the cited announcement
ComparatorNot stated for the planned alcohol use disorder trial in the cited announcement
Follow-upNot stated for the planned alcohol use disorder trial in the cited announcement
Outcome focusClinical development of DMX-1001, an oral noribogaine candidate, for alcohol use disorder; no registered outcome set is cited in the announcement

What it suggests

DemeRx announced FDA acceptance of its Investigational New Drug application in April 2026, permitting the described development program to proceed toward further study

What it cannot establish

IND acceptance is not evidence of efficacy or approval. The announcement cannot establish the final trial design, comparative benefit, long-term safety, or whether the planned study will begin as anticipated

Recruitment relevance

Enrollment has not opened in the current editorial evidence. An accepted IND does not mean that a trial is recruiting; check a future registry record or sponsor instructions before seeking participation

Do not travel, discontinue medication, or change care based on this summary. The sponsor and the current primary source govern participation decisions.

How this summary was framed

This record reports the design and registered or officially announced research question before interpretation. Unknown sample, comparator, follow-up, and outcome details remain marked as unknown. The Atlas does not infer results from recruitment status, regulatory acceptance, funding, or study completion.

UC Irvine MIND-OUD

Changes in reward-circuit functional connectivity, drug-cue BOLD activation, regional glutamate and glutamine, EEG alpha power, opioid withdrawal, and craving

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Stanford MISTIC

Change in WHODAS 2.0 disability and functioning scores; the broader editorial record also describes clinical and neuroimaging assessments

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Texas IMPACT

Program-level development of controlled ibogaine research; no study-specific registered outcome set is identified in the cited program source

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ICEERS Spanish trial

Rate of methadone dose decrease, adverse events at different doses, and electrocardiogram measures including QT interval and ST wave

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The Evidence Atlas is an educational editorial index, not medical advice or a recruitment service. Eligibility and openings must be confirmed with the study sponsor. MindScape Retreat is not a site for these studies.