Itepekimab is under clinical development by and currently in Phase II for Bronchiectasis. According to GlobalData, Phase II drugs for Bronchiectasis have a 44% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how Itepekimab’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks.

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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.

Itepekimab overview

Itepekimab is under development for the treatment of chronic obstructive pulmonary disease, non-cystic fibrosis bronchiectasis. It is administered intravenously and subcutaneously. The drug candidate is a fully human monoclonal antibody which acts by targeting the interleukin-33 (IL-33). The drug candidate is a new molecular entity developed based on VelocImmune technology.

The drug candidate was also under development for the treatment of atopic dermatitis and asthma.

Regeneron Pharmaceuticals overview

(Regeneron) discovers, develops, manufactures, and markets medicines for the treatment of serious medical conditions. Its products are focused on helping patients suffering from cancer, allergic and inflammatory diseases, eye diseases, metabolic and cardiovascular diseases, infectious diseases, neuromuscular diseases, hematologic conditions, pain, and rare diseases. Regeneron develops products using its Trap and VelociSuite technology platforms, which include VelocImmune, VelociGene, VelociMouse, VelociMab, Veloci-Bi, VelociT, and other related technologies. The company operates manufacturing facilities in Rensselaer, New York, and Limerick. It also collaborates with strategic partners to develop, manufacture and commercialize its products. The company sells its products to specialty pharmacies and distributors. It operates in the US, the Netherlands, Bermuda, Ireland, Spain, India, Japan and the UK. Regeneron is headquartered in Tarrytown, New York, the US.

For a complete picture of Itepekimab’s drug-specific PTSR and LoA scores,

This content was updated on 16 July 2024

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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 .