N-0877 is under clinical development by Eurofarma Laboratorios and currently in Phase II for Idiopathic (Essential) Hypertension. According to GlobalData, Phase II drugs for Idiopathic (Essential) Hypertension does not have sufficient historical data to build an indication benchmark PTSR for Phase II. GlobalData uses proprietary data and analytics to create drugs-specific PTSR and LoA in the N-0877 LoA Report. Buy the report here.

GlobalData tracks drug-specific phase transition and likelihood of approval scores, in addition to indication benchmarks based off 18 years of historical drug development data. Attributes of the drug, company and its clinical trials play a fundamental role in drug-specific PTSR and likelihood of approval.

N-0877 overview

N-0877 (fixed-dose combination of an angiotensin receptor blocker and thiazide diuretic) is under development for the treatment of essential arterial hypertension. The therapeutic candidate is administered through oral route as a tablet.

Eurofarma Laboratorios overview

Eurofarma Laboratorios (Eurofarma), is a pharmaceutical company that manufactures and markets therapeutics. The company offers prescription, over-the-counter (OTC), generic and cancer drugs, hospital drugs, and drugs exempt from prescription. Its products serve all medical specialties and cover various therapeutic classes. Eurofarma’s research and development projects focus on antibiotics, metabolism, and obesity, central nervous system, and oncology. The company operates in Argentina, Bolivia, Brazil, Chile, Colombia, Ecuador, Guatemala, Paraguay, Peru, Venezuela, Mexico, Mozambique and Uruguay. Eurofarma is headquartered in Sao Paulo, Brazil.

For a complete picture of N-0877’s drug-specific PTSR and LoA scores, buy the report here.

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GlobalData, the leading provider of industry intelligence, provided the underlying data, research, and analysis used to produce this article.

GlobalData’s Likelihood of Approval analytics tool dynamically assesses and predicts how likely a drug will move to the next stage in clinical development (PTSR), as well as how likely the drug will be approved (LoA). This is based on a combination of machine learning and a proprietary algorithm to process data points from various databases found on GlobalData’s Pharmaceutical Intelligence Center.