Technological Offer
Since its formal constitution as a Biomedical Reseach Institute in 2010, INCLIVA has achieved notable achievements because of its research activity. It is worth highlighting the more than 20 patents and 4 registered software programmes, as well as 4 spin-off companies that have been created because of research carried out within INCLIVA.
OPTIMIZATION DEVICE FOR INTRAURETHRAL LUBRICATION IN PEDIATRIC PATIENTS
Grupo: Urología
Tipo: Modelo de utilidad
Novel treatment with PPAR modulators for metabolic diseases
Grupo: Química Médica
Tipo: Patente
Moxifloxacino para uso en el tratamiento de la atrofia muscular espinal
Grupo: Genómica Traslacional Humana
Tipo: Patente
Cathlab Sim: SOFTWARE FOR THE SIMULATION OF PERCUTANEOUS CARDIAC INTERVENTIONS AND THE TRAINING OF HEALTHCARE STAFF
Grupo: Cardiología Clínica
Tipo: Software
ReMindCare: una plataforma para la evaluación del estado clínico del paciente y la comunicación entre paciente y médico en psiquiatría
Grupo: Psiquiatría y Enfermedades Neurodegenerativas
Tipo: Software
Método de evaluación de la actividad de la nicotinamida N-metil transferasa. Metabotest
Grupo: Cáncer colorrectal y nuevos desarrollos terapéuticos en tumores sólidos
Tipo: Patente
MOLECULAR TOOLS FOR THE DIAGNOSIS AND PROGNOSIS OF SPITZOID MELANOCYTIC TUMOURS
Grupo: Cáncer Cutáneo
Tipo: Patente
Haloperidol para el tratamiento de la atrofia muscular espinal
Grupo: Genómica Traslacional Humana
Tipo: Patente
Material inyectable para la regeneración del cartílago articular
Grupo: Histopatología e Ingeniería Tisular
Tipo: Patente
AMMON-OHE: A Machine Learning Model to Predict Occurrence of Overt Hepatic Encephalopathy in Patients with Cirrhosis
Grupo: Research Group on Neurological Impairment
Type: Patent
SepAsT: Software for early sepsis diagnosis of sepsis and patients clinical clourse and septic shock
Group: Research Group on Epigenomics and Translational Epigenetics
Type: Software
Musashi 2 (MSI2) como diana terapéutica para el tratamiento de la distrofia miotónica tipo 1 y 2
Group: Research Group on Human Translational Genomics
Type: Patent
Method for minimal residual disease detection in cancer patients
Group: : Research Group of Innovative Diagnostic and Therapeutical Developments in Solid Tumors
Type: Patent
Nanoparticles-based therapy for ischemic cardiopathies
Grupo: Grupo de Investigación Traslacional en Cardiopatía Isquémica
Type: Patent
Microbiological Information Bulletin(BIMIC)
Group: Grupo de Investigación en Microbiología Molecular y Patogénesis Microbiana
Type: Software
i2024/30 EndosCitas y EndosNet
Grupo: Servicio de Medicina Digestiva / Unidad de endoscopias
Tipo: Software
Angiopath
Grupo: Grupo de Investigación Translacional de Tumores Sólidos Pediátricos
Tipo: Software
Spin-Off technology-based companies:
Seqplexing is a company created in 2013, which was born from the idea of generating solutions for research and clinical applications, using as a basis the introduction of new advanced genetic techniques and platforms, mainly next generation sequencing (NGS). Seqplexing aims to cover the need for reliable protocols for the sequencing of amplicons or genes. To this end, it develops closed solutions that are easy to use and implement in its own laboratories.
Seqplexing’s mission is focused on providing a service to those laboratories that, due to their daily routine, do not have time to carry out the development of suitable protocols for the sequencing of genes or regions of interest. Seqplexing is transforming into a commercial kit all the necessary elements to carry out these techniques, providing a comprehensive service from the beginning of the sample preparation to the final analysis of the results.
Epidisease was created in 2014 because of a project led by INCLIVA researchers and the Center for Biomedical Research Network (CIBER) of Rare Diseases to transfer knowledge in the field of epigenetics and biomedical sciences to the service of society.
Epigenetics studies all those factors and mechanisms involved in the control of gene expression. The importance of this science is growing, as demonstrated by some of the conclusions of the Human Genome Project, thanks to which scientist have realised that the molecular bases of cellular functioning, development, ageing and many diseases goes far beyond the DNA sequence. Proof of this are recent findings from the Epigenome Road Map project.
Epidiseases’s mission is to leverage its expensive expertise in the field of epigenetics to provide its customers with biomedical solutions, diagnostic tools and new therapies, as well as to stimulate translational research with the goal of improving people’s health and well-being.
Nela BioDynamics is a young technology development company in biomedicine, which arises from Valencian university collaboration, formed by a group of multidisciplinary researchers with expertise in biomedicine and engineering. The company arises from the results of a master’s Thesis in Biomedical Engineering, which led to the obtaining of two patents on a novel intramedullary fixation device for joint arthroplasty, nails for fractures and exo-prosthetization; and a percutaneous collar for ostomies.
NELA spinal implant technology allows for a customised fit for each patient and avoids conventional techniques based on impact pressure fitting or the use of bone cement to achieve fixation. All this translates into a shorter surgical time, less pain, higher success rates and better quality of life for the patient. NELAS’s mission is to respond to different unmet medical need, while providing a positive socio-economic impact.
ARTHEx BIOTECH is a spin-off company of the University of Valencia that develops advanced RNA treatments against genetic diseases. The team has a solid experience in drug discovery and the involvement of microRNAs in neuromuscular diseases. They are supported by world-renowned scientific and clinical advisors who will facilitate the successful development of their products.
ARTHEx Biotech mission is to find effective treatments for unmet medical needs. The company’s first objective will be to investigate anti-miRNAs for the treatment of myotonic dystrophy type 1 (DM1), which is an orphan disease affecting more than 900 000 people worldwide (estimated prevalence 1/8000).



