HTG Molecular Diagnostics, Inc. (HTG) is a life sciences company. It provides wide range of services to biomarker discovery and companion diagnostic developers. HTG provides extraction-free gene expression profiles which can measure miRNA and mRNA from source material for diagnostic applications. The company's HTG Molecular Diagnostics EDGE system offers extraction-free gene expression results from FFPE tissue samples. HTG is headquartered in Washington, the US.
The company intends to expand its customer base. To this end, the company introduced EDGE system for clinical and research laboratories that offers nucleic acid extraction-free gene expression results. This launch will mark an shift in industry in workflow optimization and significant necessary move toward more accessible and accurate answers for laboratorians and patients.
This report is a source for data, analysis and actionable intelligence on the HTG Molecular Diagnostics, Inc. 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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