Boston, MA -- (SBWIRE) -- 07/17/2013 -- TcLand Expression (TcLand) is a biotechnology company. The company develops companion diagnostics (CDx) in immune mediated disorders and biomarkers in solid organ transplantation. Its research and development platform develops, and validates invasive multi-genes molecular diagnostic blood tests. TcLand's clinical development programs include RA-INF-Dx Test, and L-TolX test. The company's research and development process alsdo combines biological process with data driven approaches. It has strategic alliance with Val d'Hebron Hospital, Hospital Clinic Barcelona, Institut National de la Recherche Medicale, and IMI JU. The company partners with academic centers and industry organizations to develop and distribute genomic-based testing services. TcLand is headquartered in Nantes, France.

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This report is a source for data, analysis and actionable intelligence on the TcLand Expression 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.

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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