(Amlodipine + indapamide + telmisartan) is under clinical development by George Medicines and currently in Pre-Registration for Hypertension. According to GlobalData, Pre-Registration drugs for Hypertension have an 82% phase transition success rate (PTSR) indication benchmark for progressing into Marketed. GlobalData’s report assesses how (Amlodipine + indapamide + telmisartan)’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.
(Amlodipine + indapamide + telmisartan) overview
Amlodipine in fixed dose combination with indapamide and telmisartan is under development for the treatment of hypertension. It is administered through oral route as tablet. Telmisartan acts by targeting angiotensin II, amlodipine acts by targeting calcium channel and indapamide acts by targeting potassium channel.
For a complete picture of (Amlodipine + indapamide + telmisartan)’s drug-specific PTSR and LoA scores, buy the report here.
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