Ascorbic acid is under clinical development by Renovion and currently in Phase II for Bronchiectasis. According to GlobalData, Phase II drugs for Bronchiectasis 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 Ascorbic acid LoA Report. Buy the report here.
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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.
Ascorbic acid overview
Ascorbic acid is under development for the treatment of lung dysfunction in lung transplant patients, patients with tracheostomy and non-CF bronchiectasis, bronchiolitis obliterans syndrome (BOS) progression in participants with a bilateral lung transplant and chronic obstructive pulmonary disease (COPD). It is administered through inhalational route. The drug candidate is developed as a nebulized therapy.
It was under development for primary ciliary dyskinesia (PCD), cystic fibrosis and alpha-1 anti-trypsin deficiency (A1AD).
For a complete picture of Ascorbic acid’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.
