Obicetrapib calcium is under clinical development by NewAmsterdam Pharma Company and currently in Phase III for Heterozygous familial hypercholesterolemia (heFH). According to GlobalData, Phase III drugs for Heterozygous familial hypercholesterolemia (heFH) have a 73% phase transition success rate (PTSR) indication benchmark for progressing into Pre-Registration. GlobalData’s report assesses how Obicetrapib calcium’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.
Obicetrapib calcium overview
Obicetrapib calcium (AMG-899, DEZ-001, TA-8995) is under development for Alzheimer’s disease, atherosclerosis, dyslipidemia and heterozygous familial hypercholesterolemia (HeFH). It is administered orally as once daily formulation. The drug candidate acts by targeting cholesteryl ester transfer protein (CETP).
It was under development for was under development for the treatment of mild dyslipidemia by Amgen and diabetes.
NewAmsterdam Pharma Company overview
NewAmsterdam Pharma Company (NAP), a clinical stage biotechnology company focused on the research and development of transformative therapies for cardio-renal diseases. The company is headquartered in the Netherlands.
For a complete picture of Obicetrapib calcium’s drug-specific PTSR and LoA scores, buy the report here.
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