Nuclea Biotechnologies Inc. - Product Pipeline Analysis - New Report Available

Boston, MA -- (SBWIRE) -- 03/20/2013 -- Nuclea Biotechnologies Inc. (Nuclea) is a translational medicine company. It carries out the discovery of proprietary biomarkers and in vitro companion diagnostic assays. The company's vitro companion diagnostics are used in therapeutic and medical imaging applications: colon, stomach, leukemia, lung and prostate. Nuclea develops companion diagnostics for other disease indications such as cardiovascular, inflammation, metabolic disorders and neurological. It conducts research leading to novel molecular oncology therapeutics and diagnostics for the pharmaceutical and biotechnology industries. Nuclea is headquartered in Pittsfield, Massachusetts, the US.

Nuclea aims to expand its product offering and drive significant licensing revenue. To this end, the company acquired a portfolio containing six patents and applications related to tissue microarrays from Laurus Master Fund, Ltd.

This report is a source for data, analysis and actionable intelligence on the Nuclea Biotechnologies 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

View Full Report Details and Table of Contents

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.

Scope

- 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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