Cytograft Tissue Engineering, Inc. - Product Pipeline Analysis, 2013 Update - New Market Report

From: Fast Market Research, Inc.
Published: Mon Jun 03 2013

Cytograft Tissue Engineering, Inc. (CTE) is a genetic engineering company. The company develops cell-based solutions for the treatment of cardiovascular diseases. It has developed a regenerative medicine platform, Tissue Engineering by Self-Assembly, or TESA. CTE's product portfolio includes tissue engineered blood vessel, covered stent, patch, percutaneous bypass and valve. The company's technologies include sheet-based tissue engineering, thread-based tissue engineering and particle-based tissue engineering. It repairs diseased cardiovascular tissues and organs. CTE transforms cardiovascular medicine by developing cell-based therapies to repair and rebuild diseased tissues and organs. The company conducts ongoing clinical trials in Europe and South America. CTE is headquartered in Novato, California, the US.

This report is a source for data, analysis and actionable intelligence on the Cytograft Tissue Engineering, 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.

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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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