The Hypophosphatasia drugs in development market research report provides comprehensive information on the therapeutics under development for Hypophosphatasia, complete with analysis by stage of development, drug target, mechanism of action (MoA), route of administration (RoA), and molecule type. GlobalData’s report assesses key aspects of the companies and drugs in development for Hypophosphatasia. Buy the report here.

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Data Insights Hypophosphatasia - Drugs In Development, 2024

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The report also covers the descriptive pharmacological action of the therapeutics and the latest news and press releases. Additionally, the report provides an overview of the key players involved in therapeutic development for Hypophosphatasia and features dormant and discontinued products.

GlobalData tracks seven drugs in development for Hypophosphatasia by seven companies/universities/institutes. The top development phase for Hypophosphatasia is preclinical with four drugs in that stage. The Hypophosphatasia pipeline has six drugs in development by companies and one by universities/ institutes. Some of the companies in the Hypophosphatasia pipeline products market are: Nippon Medical School Hospital, Alexion Pharmaceuticals and Am-Pharma.

The key targets in the Hypophosphatasia pipeline products market include Alkaline Phosphatase, Alkaline Phosphatase Tissue Nonspecific Isozyme, and Ectonucleotide Pyrophosphatase/Phosphodiesterase Family Member 1.

The key mechanisms of action in the Hypophosphatasia pipeline product include Alkaline Phosphatase Replacement with two drugs in Phase III. The Hypophosphatasia pipeline products include three routes of administration with the top ROA being Intravenous and four key molecule types in the Hypophosphatasia pipeline products market including Gene-Modified Cell Therapy, and Recombinant Enzyme.

Hypophosphatasia overview

Hypophosphatasia (HOPS) is a rare inherited disorder characterized by the deficiency of alkaline phosphatase. It is also referred as phosphoethanolaminuria or Rathbun disease. HOPS is caused by mutations in the ALPL gene, which is responsible for making tissue non-specific alkaline phosphatase (TNSALP). ALP plays an important role in the mineralization of the skeleton and teeth. HOPS weakens and softens the bones, resulting in the skeletal abnormalities. Affected infants are born with short limbs, an abnormally shaped chest, and soft skull bones. The forms of hypophosphatasia that appear in childhood or adulthood are typically less severe than those that appear in infancy.

For a complete picture of Hypophosphatasia’s pipeline drug market, buy the report here.

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GlobalData’s pipeline drugs offers detailed profiles of pharmaceutical drugs in all stages of pre-clinical and clinical development, from discovery through to pre-registration. Coverage is limited to novel human medicinal drugs and biosimilars seeking market approval proprietary and is one of two primary repositories of pharmaceutical drug information offered by GlobalData through its Pharmaceutical Intelligence Center.