Boston, MA -- (SBWIRE) -- 02/23/2013 -- Nanospectra Biosciences, Inc. (Nanospectra) is a medical device company, based in the US. The company develops and commercializes particle-based therapies for the selective and precise thermal destruction of solid tumors. It provides AuroLase Therapy, a medical device that is applicable to the ablation of various solid tumors. The company also offers research-use-only nanoparticles with specific optical characteristics. It has an open investigational device exemption (IDE) to evaluate the safety and efficacy of aurolase therapy for the treatment of refractory head and neck cancers. The company was awarded SAIC contract for toxicity studies of Gold Nanorods. Nanospectra is headquartered in Houston, Texas, the US.
This report is a source for data, analysis and actionable intelligence on the Nanospectra Biosciences, 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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