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New drug for the treatment of rheumatoid arthritis

Descrizione del progetto

Un nuovo farmaco contro l’artrite reumatoide

L’artrite reumatoide è una condizione autoimmune associata a dolore e rigidità delle articolazioni provocati dall’infiammazione. L’obiettivo del progetto RheumArth, finanziato dall’UE, è introdurre il nuovo farmaco AP1189 per la convalida clinica. AP1189 è un agonista contro i recettori della melanocortina che oltre a regolare la pigmentazione cutanea sembra anche inibire l’infiammazione. L’idea è di utilizzare AP1189 per favorire la risoluzione dell’infiammazione legata all’artrite reumatoide. I promettenti dati clinici preliminari relativi alla sicurezza hanno gettato le basi per la convalida dell’efficacia clinica del farmaco AP1189 nei pazienti affetti da questa condizione.

Obiettivo

Rheumatoid arthritis (RA) is a chronic autoimmune disorder causing inflammation and permanent damage in joints and surrounding tissues - leading to severe disability, decreased quality of life, and reduced life expectancy. The disease affects more than 6 million people with annual costs amounting to €45billion in the Europe (EU) alone. There is a wide range of drug therapies for RA, mobilizing a variety of anti-inflammatory and immune modulating effects. However, a significant proportion (30%) of the patients do not respond to current treatments, efficacy is often reduced over time and the incidence of side effects is high and can be severe and life threatening.
AP1189 is new chemically-synthesized small molecule drug for the treatment of Rheumatoid arthritis (RA). Through specific activation of the patients’ self-anti-inflammatory mechanisms, our first drug candidate renders unprecedent combination of safety, effectiveness and patient compliance, without the side effects associated with current therapies. The clinical validation of our drug for RA - 1st indication (foreseen for the Innovation Project) - will not only open a large market within this therapeutic area, as it will allow Synact to set a market foothold in the chronic inflammatory disease market, supporting the company´s medium term strategic positioning as an unique provider of a new generation of anti-inflammatory drugs.
AP1189 clinical validation is on-going with current Phase I clinical trials showing promising preliminary results – safety and tolerance was proved in healthy human volunteers. Next step in the development will be a Phase IIa Proof-Of-Concept (POC) trail to validate our drug´s efficacy profile in RA patients. In this context, the present Phase 1 will be of utmost importance to validate AP1189´s market position and potential in RA and prepare the large clinical validation aimed for in the ensuing SME Instrument Phase II project.

Invito a presentare proposte

H2020-EIC-SMEInst-2018-2020

Vedi altri progetti per questo bando

Bando secondario

H2020-SMEInst-2018-2020-1

Meccanismo di finanziamento

SME-1 - SME instrument phase 1

Coordinatore

SYNACT PHARMA APS
Contribution nette de l'UE
€ 50 000,00
Indirizzo
DRONNINGGARDS ALLE 136
2840 HOLTE
Danimarca

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PMI

L’organizzazione si è definita una PMI (piccola e media impresa) al momento della firma dell’accordo di sovvenzione.

Regione
Danmark Hovedstaden Nordsjælland
Tipo di attività
Private for-profit entities (excluding Higher or Secondary Education Establishments)
Collegamenti
Costo totale
€ 71 429,00