Regenicin, Inc.(Regenicin), formerly Windstar, Inc., is a development-stage biotechnology company. It develops and commercializes regenerative cell therapies to restore the health of damaged tissues and organs. The company's first prodcut PermaDerm, is a tissue-engineered skin prepared from autologous skin cells used for burns, chronic wounds, and reconstructive surgery; while it expects its second product to be, TempaDerm which would provide a continuous supply of non-allogenic skin substitutes. It received Orphan Status grant for the PermaDerm product from Food and Drug Administration (FDA). The company intends to diversify certain intrinsic elements of PermaDerm be used for a variety of applications including a protective healing agent for wounds, a carrier for stem cells, protection for organs and tendons, and a barrier for hormones or medicines. It entered into an agreement with Lonza Walkersville, Inc. for the license to develop and seek approval by the U.S. Food and Drug Administration (“FDA”) for the commercial sale of engineered skin substitute products. Regenicin is headquartered in Little Falls, the US.
This report is a source for data, analysis and actionable intelligence on the Regenicin, 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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