Olokizumab is under clinical development by R-Pharm and currently in Phase III for Idiopathic Interstitial Pneumonia (IIP). According to GlobalData, Phase III drugs for Idiopathic Interstitial Pneumonia (IIP) does not have sufficient historical data to build an indication benchmark PTSR for Phase III. GlobalData uses proprietary data and analytics to create drugs-specific PTSR and LoA in the Olokizumab 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.
Olokizumab overview
R-Pharm overview
R-Pharm (R Pharm) is a pharmaceutical company. It carries out the production of medicines, active pharmaceutical ingredients, laboratory equipment and high-tech medical systems. The company’s pipeline products portfolio comprises Nemonoxacin, narlaprevir, Cefilavancin, SCY 078, RPH-120 and Radotinib. R Pharm provides services such as production, commercialization, installation and maintenance of medical systems and staff training. The company offers products in the therapeutic areas of oncology, hematology, immune diseases, antibiotics, antivirals, neurology, cardiology, multiple sclerosis, hemophilia, Covid-19 and diabetes. It also carries out research and development of products and technologies in partnership with Russian and foreign institutes. The company supplies medicinal products and laboratory equipment for the hospitals, federal medical research centers, clinical hospitals, and regional curative and preventive care institutions. It has operations in Russia, the US, Azerbaijan, Uzbekistan, Kyrgyzstan, Kazakhstan, Belarus and Germany. R-Pharm is headquartered in Moscow, Russia.
For a complete picture of Olokizumab’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.
