XEPTAGEN SpA (XEPTAGEN) is a medical device company, based in Italy. The company discovers novel molecular markers to produce diagnostic kits for the early detection, monitoring, and screening of cancerous cells. It develops the products for the treatments of liver cancer, colorectal cancer, prostate cancer and squamous cell carcinomas. XEPTAGEN products are marketed under the brand name HEPA AB, HEPA IC, HEPA AFPIC, COLONIC, PROSTATEIC and SCCALISA. The company uses proprietary platform technology called Combinatorial Proteomic to discover specific tumor markers. It develops an optoelectronic biochip for the determination of tumor molecular markers. The company partners with Associazione ABO, Olivetti I-jet S.p.A, University of Bologna, University of Brescia, University of Padova, ICS-UNIDO and University of Pisa among others. XEPTAGEN is headquartered in Marghera, Veneto, Italy.
This report is a source for data, analysis and actionable intelligence on the XEPTAGEN SpA portfolio of pipeline products. The report provides detailed analysis on each pipeline product with information on the indication, the development stage, trial phase, product milestones, pipeline territory, estimated approval date, and estimated launch date
Each pipeline product is profiled to cover information on product description, function, technology, indication, and application. The report is also supplemented with a detailed company profile and information on clinical trials, wherever applicable.
This report is built using data and information sourced from proprietary databases, primary and secondary research and in-house analysis by GlobalData’s team of industry experts.
Detailed company profile with information on business description, key company facts, major products and services, key competitors, key employees, locations and subsidiaries and recent developments.
Detailed coverage on all the pipeline products, by equipment type, by therapy area, by development stage, and by trial phase.
Information on product milestones and pipeline territory for each product, the estimated approval date, and estimated launch date.
Profile of each pipeline product with additional information on product description, function, technology, indication(s), and application.
Data on relevant clinical trials and product patent details, wherever applicable.
Information on clinical trial, wherever applicable, is supplemented with information on trial phase, trial status, trial objective, trial design, target patients, unique physician identifier, primary point, secondary point, acronym, participants inclusion, participants exclusion, interventions, trial results, trial start date, trial end date, study type, trial site, trial funding, age eligibility, and gender eligibility.
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