Technological Offers
ALCORE: Integrative Therapy for Alcohol Use Disorder (AUD)
Description
A novel family of lipid sulfamide derivatives (led by N-oleyl sulfamide, NOS) active via both oral and parenteral routes.
Innovative mechanism of action based on the dual modulation of the metabolic receptor PPARα and the sensory target VR1 (TRPV1).
Demonstrated synergistic effect when combined with opioid antagonists (nalmefene/naltrexone) and compatibility with GLP-1 receptor agonists.
Medical need
Currently approved treatments (naltrexone, acamprosate) exhibit clinical efficacy rates below 50% and high treatment dropout rates.
High rate of clinical relapse triggered by prior abstinence periods, stress, or contextual/environmental cues.
Lack of targeted oral therapies capable of reducing compulsive alcohol seeking without altering overall caloric intake.
Results
- Significant reduction in self-administration and voluntary alcohol consumption in vivo (Wistar rats). in vivo (ratas Wistar).
- Substantial inhibition of compulsive consumption and effective prevention of both abstinence-induced and context-induced relapse.
- Target validation via specific receptor blockade with capsazepine (VR1 antagonist) and proven synergy with nalmefene.
Prevalence
Worldwide: >100M people affected; >3M annual deaths.
In Spain: 3.6% of adult population (6.47% in males); 32% high-risk consumption among youth.
Market
~$1.5B Mercado global AUD; ~$2.5B Mercado global ASH; >$25B Mercado NASH/Hígado graso
Another fact
Harmful alcohol use accounts for 5.1% of the global disease burden and generates socioeconomic costs exceeding 2% of GDP in developed countries.
Therapy
IBIMA Plataforma BIONAND inventors
FERNANDO RODRÍGUEZ DE FONSECA
Research group of IBIMA involved: C-06
ANTONIA MARÍA SERRANO CRIADO
Research group of IBIMA involved: C-06
FRANCISCO JAVIER PAVÓN MORÓN
Research group of IBIMA involved: A-03
JUAN MANUEL DECARA DEL OLMO
Research group of IBIMA involved: C-06