New biodegradable anal plug to manage Faecal Incontinence
My-qup is developing an anal plug, qup, for the management of faecal incontinence (FI) that will reduce the environmental impact that other solutions like pads, diapers and non degradable anal plugs produce. It will be sold to aut...
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Información proyecto My-qup
Duración del proyecto: 6 meses
Fecha Inicio: 2016-12-01
Fecha Fin: 2017-06-30
Líder del proyecto
MY-QUP MEDICAL SL
No se ha especificado una descripción o un objeto social para esta compañía.
Presupuesto del proyecto
71K€
Fecha límite de participación
Sin fecha límite de participación.
Descripción del proyecto
My-qup is developing an anal plug, qup, for the management of faecal incontinence (FI) that will reduce the environmental impact that other solutions like pads, diapers and non degradable anal plugs produce. It will be sold to autonomous patients to help them recover their Quality of Life (QoL). FI affects most parts of the patient's life, including laboral, social and sex life. qup users will be able to regain control of their defecation, providing enough safety to return to their previous lifestyle. My-qup Medical considers the whole user experience with a holistic design that tackles all the sides of conservative treatment (non-surgical treatment) and management of FI.
The main achievements of the project are the innovation in the material and the design. It will significantly reduce waste and use of resources. The material has been developed to comply with the European Guides of flushability. The next challenges for the product are to prove the usability and efficacy with the users, and to find manufacturers to start a small production to conduct a clinical trial.
The estimated global market of FI is USD 2,000 MM with an estimated prevalence of a 10% of adult population with a growing incidence due to an aging population. There are 93 million potential users in the developed world that will be, in most cases, chronic patients. The potential client of My-qup Medical will be the user of qup: autonomous patients that, if it wasn’t for this condition, could have a normal life. As FI is a global problem, after reaching the developed world it will be necessary to study the entry in developing countries.
SME Instrument Phase I would serve to assess: the feasibility of licensing vs. reaching the market, the usability of the product (including efficacy, comfort, satisfaction and safety) and the patent strategy. The results will be measured in a Business Plan, a usability test and a European patent application.