According to GlobalData’s medical device pipeline database, 168 Acquired Gene or Chromosome Alterations devices are in various stages of development globally. GlobalData’s report Acquired Gene or Chromosome Alterations provides an overview of the segment’s pipeline landscape and offers detailed analysis of its products. Buy the report here.

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Of these devices, 25 are in active development, while the remaining 143 are in an inactive stage of development. There are 13 products in the early stages of development, and the remaining 12 are in the late stages of development.

Reagents which are used in genetic tests to detect cancer causing genes/related alterations like p53, k-ras, BRCA 1+2 etc.

Innovations in the medical devices sector are linked to the development of new approaches, processes, or technologies for treating, diagnosing, and managing disease in response to demand from healthcare for better patient outcomes and reduce healthcare costs.

Based on an analysis of GlobalData’s Medical Intelligence Center pipeline product database, these actively developed Acquired Gene or Chromosome Alterations pipeline devices are all expected to be approved within the next ten years.

Currently, private organizations, public entities and institutions are working on the development of Acquired Gene or Chromosome Alterations devices. Overall, most of these Acquired Gene or Chromosome Alterations pipeline devices are being developed by private entities.

Key players involved in the active development of Acquired Gene or Chromosome Alterations include Johns Hopkins University, Fred Hutchinson Cancer Research Center, H. Lee Moffitt Cancer Center & Research Institute, Telo Genomics, TheraDiag, Chinese University of Hong Kong, Chinese University of Hong Kong, Mayo Clinic, Interpace Biosciences and MolecularMD.

For a complete picture of the developmental pipeline for Acquired Gene or Chromosome Alterations devices, buy the report here.

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GlobalData, the leading provider of industry intelligence, provided the underlying data, research, and analysis used to produce this article. 

The medical devices pipeline data used in this article were obtained from the Medical Pipeline Products Database of GlobalData’s Medical Intelligence Center. The Pipeline Products database is a is a comprehensive source of information on medical devices, it covers 39K products which are in development stage and intended for diagnosis, treatment, and management of diseases/conditions/symptoms directly or indirectly. The pipeline products included in the database are sourced from reliable and authenticated sources, such as company websites, SEC filings, conference presentations, analyst presentations, news releases, clinical trial registries, and grants. The information is collected by following systematic research techniques and proprietary methodology.