← Eichor
Study identifier: NCT05540288 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

NAlmefene Versus Placebo in Addition to Treatment as Usual on Craving in Behavioural Addictions

Condition: Behavioural Addiction  ·  Sponsor: Nantes University Hospital

PhasePhase 3
Planned participants266
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Behavioural addictions (BAs) \[gambling disorder (GD), food addiction (FA), sexual addiction (SA)\] may lead to disastrous consequences. They are often associated with other addictive or psychiatric disorders, and high rates of suicide attempts. Epidemiological studies report prevalence reaching 2.7% for GD, 5% for SA, and up to 7.9% for FA. Many similarities have been highlighted between BAs, as well as with substance use disorders. One core clinical similarity between those disorders is craving (uncontrollable urge to engage in rewarding behaviours), which has been consistently associated with diminished control over the behaviour and relapse. At present, no pharmacological treatment has been approved for BAs, but several medications have been tested. Among them, two opioid receptor antagonists - naltrexone and nalmefene - appear the most promising. By decreasing dopamine neurotransmission in the reward circuitry, they reduce both excitement for rewarding behaviours and craving. Compared to naltrexone, nalmefene seems to have a better safety. To date, no study investigated the efficacy of nalmefene as a pan-addiction treatment for BAs. Two clinical trials have demonstrated its efficacy for the treatment of GD, but no clinical trial was conducted for FA and SA. The investigators hypothesise that nalmefene (36 mg/d), compared to a placebo, can have a therapeutic effect as an add-on to usual treatment for decreasing craving in several BAs.

This description comes directly from the study's public registry record.

Talk to the study team

Marie GRALL-BRONNEC  ·  +33240847620  ·  marie.bronnec@chu-nantes.fr

Always discuss trial participation with your own doctor first.

Locations (13)

CHU de BesançonBesançon, FranceNot Yet Recruiting
CHU de BordeauxBordeaux, FranceRecruiting
CHRU de BrestBrest, FranceRecruiting
CHU de Clermont FerrandClermont-Ferrand, FranceRecruiting
CHU de DijonDijon, FranceNot Yet Recruiting
CH de La RochelleLa Rochelle, FranceRecruiting
Hospices Civils de LyonLyon, FranceRecruiting
CHU de MontpellierMontpellier, FranceNot Yet Recruiting
CHU de NantesNantes, FranceRecruiting
CHU de NîmesNîmes, FranceRecruiting
Hôpitaux Universitaires de StrasbourgStrasbourg, FranceRecruiting
CHRU de ToursTours, FranceRecruiting

+ 1 more locations — full list on the registry record.

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT05540288