Donidalorsen Sodium is an antisense oligonucleotide commercialized by Ionis Pharmaceuticals, with a leading Phase III program in Hereditary Angioedema (HAE) (C1 Esterase Inhibitor [C1-INH] Deficiency). According to Globaldata, it is involved in 7 clinical trials, of which 4 were completed, and 3 are ongoing. GlobalData uses proprietary data and analytics to provide a complete picture of Donidalorsen Sodium’s valuation in its risk-adjusted NPV model (rNPV). Buy the model here.

Smarter leaders trust GlobalData

The revenue for Donidalorsen Sodium is expected to reach an annual total of $399 mn by 2034 in the US based off GlobalData’s Expiry Model. The drug’s revenue forecasts along with estimated costs are used to measure the value of an investment opportunity in that drug, otherwise known as net present value (NPV). Applying the drug’s phase transition success rate to remaining R&D costs and likelihood of approval (LoA) to sales related costs provides a risk-adjusted NPV model (rNPV). The rNPV model is a more conservative valuation measure that accounts for the risk of a drug in clinical development failing to progress.

Donidalorsen Sodium Overview

Donidalorsen sodium (IONIS-PKKLRx) is under development for the treatment of hereditary angioedema(HAE). It is administered through subcutaneous route. The therapeutic candidate acts by targeting plasma kallikrein. It is developed based on ligand-conjugated anti-sense(LICA) technology, designed to enhance the delivery of the drugs to particular tissues.

It was under development for Coronavirus disease 2019 (COVID-19).

Ionis Pharmaceuticals Overview

Ionis Pharmaceuticals (Ionis), formerly Isis Pharmaceuticals, focuses on the discovery and development of RNA-targeted drugs. The company develops medicines to treat various diseases including cancer, pulmonary, cardiovascular diseases, neurological and infectious diseases. Its major products include Spinraza for spinal muscular atrophy, Tegsedi for neuropathy, Waylivra for familial chylomicronemia syndrome, Qalsody for superoxide dismutase 1 amyotrophic lateral sclerosis (SOD1-ALS), and Wainua for polyneuropathy of hereditary transthyretin-mediated amyloidosis (ATTRv-PN). Ionis also has a pipeline of products in different phases of clinical trials. It develops products based on its proprietary antisense technology. The company partnered with other pharmaceutical companies to develop a range of products in different therapeutic areas. The company sells its products in North America and Europe. Ionis is headquartered in Carlsbad, California, the US.
The company reported revenues of (US Dollars) US$787.7 million for the fiscal year ended December 2023 (FY2023), an increase of 34.1% over FY2022. The operating loss of the company was US$340.3 million in FY2023, compared to an operating loss of US$410.2 million in FY2022. The net loss of the company was US$366.3 million in FY2023, compared to a net loss of US$269.7 million in FY2022. The company reported revenues of US$119.5 million for the first quarter ended March 2024, a decrease of 63.2% over the previous quarter.

For a complete picture of Donidalorsen Sodium’s valuation, buy the drug’s risk-adjusted NPV model (rNPV) here.

This content was updated on 24 July 2024

Data Insights

From

The gold standard of business intelligence.

Blending expert knowledge with cutting-edge technology, GlobalData’s unrivalled proprietary data will enable you to decode what’s happening in your market. You can make better informed decisions and gain a future-proof advantage over your competitors.

GlobalData

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

To create this model, GlobalData takes into account factors including patent law, known and projected regulatory approval processes, cash flows, drug margins and company expenses. Combining these data points with GlobalData’s world class analysis creates high value models that companies can use to help in evaluation processes for each drug or company.

The rNPV method integrates the probability of a drug reaching a clinical stage into the cash flow at that time, which provides a more accurate valuation, as it considers the probability that the drug never makes it through the clinical pathway to commercialization. GlobalData’s rNPV model uses proprietary likelihood of approval (LoA) and phase transition success rate (PTSR) data for the indication in the highest development stage, which can be found on GlobalData’s Pharmaceutical Intelligence Center.