Octanorm is under clinical development by Octapharma and currently in Phase III for Primary Immune Deficiency (PID). According to GlobalData, Phase III drugs for Primary Immune Deficiency (PID) have a 67% phase transition success rate (PTSR) indication benchmark for progressing into Pre-Registration. GlobalData’s report assesses how Octanorm’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. 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.

Octanorm overview

Immunoglobulin G (Human) (Octonorm) contains mainly normal human immunoglobulin G (IgG) with a broad spectrum of antibodies against infectious agents. It is formulated as injectable solution for subcutaneous and intramuscular route of administration. It is formulated as injectable solution for intravenous or intramuscular or subcutaneous route of administration. Human normal immunoglobulin is used for the treatment of primary immunodeficiency syndromes such as congenital agammaglobulinaemia and hypogammaglobulinaemia, severe combined immunodeficiencies, Wiskott Aldrich syndrome, chronic lymphatic leukaemia with severe secondary hypogammaglobulinaemia and recurrent infections and children with congenital AIDS who have repeated bacterial infections.

Immune globulin (Newnorm) is under development for treatment of primary immune deficiency disorders (PID). The drug candidate is administered subcutaneously. It was under development for the treatment of dermatomyositis.

Octapharma overview

Octapharma is a human protein product manufacturer that focuses on developing and producing medicines through human proteins from human plasma and cell lines. The company treats patients worldwide with products across immunotherapy, hematology, and critical care therapeutic areas. It sources plasma from company-owned plasma donation centers and other external sources. Octapharma owns plasma donation centers in the US and Germany and owns production facilities in Austria, Germany, France, Mexico, and Sweden. The company’s production plants carry out plasma fractionation and purification, pharmaceutical production, research and development, product labeling, packaging, storage, and distribution. Octapharma is headquartered in Lachen, Switzerland.

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


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 its clinical pathway (PTSR), as well as how likely the drug will be approved (LoA). This is based on a proprietary algorithm built from the drugs’ sales forecast, regulatory milestones, cost forecasts, WACC rate and other proprietary data sources found on GlobalData’s Pharmaceutical Intelligence Center.