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Idorsia submits NDA for clazosentan to Japanese PMDA


Press release content from Globe Newswire. The AP news staff was not involved in its creation.
Idorsia submits NDA for clazosentan to Japanese PMDA
Idorsia Pharmaceuticals LtdMarch 1, 2021 GMT
Allschwil, Switzerland – March 1, 2021
Idorsia Ltd (SIX: IDIA) today announced the submission of a New Drug Application (NDA) to the Japanese Pharmaceuticals and Medical Devices Agency (PMDA) for clazosentan, a fast-acting, selective endothelin A (ETA) receptor antagonist, for the prevention of cerebral vasospasm, vasospasm-related cerebral infarction and cerebral ischemic symptoms after aneurysmal subarachnoid hemorrhage (aSAH).
The application is supported by replicated results from the Japanese registration program which consisted of two double-blind, randomized, placebo-controlled studies assessing the efficacy and safety of clazosentan in reducing vasospasm-related morbidity and all-cause mortality events in adult Japanese patients following aSAH. Patients were ra ....

Switzerland General , Andrewc Weiss , Satoshi Tanaka , Idorsia Ltd , Head Of Investor Relations Corporate Communications , Swiss Exchange , Japanese Pharmaceuticals , Idorsia Pharmaceuticals Ltd , Life Sciences , Idorsia Pharmaceuticals Japan , Devices Agency , New Drug Application , Medical Devices Agency , Cerebrovascular Diseases , Pharmacol Exp Ther , Pharmaceuticals Japan , Vice President , Investor Relations , Corporate Communications , Pharmaceuticals Ltd , Products And Services , Coronavirus Pandemic , Product Testing , Globe Newswire , Pharmaceutical Manufacturing , Health Care Industry ,

Idorsia Pharmaceuticals Ltd: Idorsia submits NDA for clazosentan to Japanese PMDA


Idorsia Pharmaceuticals Ltd: Idorsia submits NDA for clazosentan to Japanese PMDA
Allschwil, Switzerland - March 1, 2021
Idorsia Ltd (SIX: IDIA) today announced the submission of a New Drug Application (NDA) to the Japanese Pharmaceuticals and Medical Devices Agency (PMDA) for clazosentan, a fast-acting, selective endothelin A (ET
A) receptor antagonist, for the prevention of cerebral vasospasm, vasospasm-related cerebral infarction and cerebral ischemic symptoms after aneurysmal subarachnoid hemorrhage (aSAH).
The application is supported by replicated results from the Japanese registration program which consisted of two double-blind, randomized, placebo-controlled studies assessing the efficacy and safety of clazosentan in reducing vasospasm-related morbidity and all-cause mortality events in adult Japanese patients following aSAH. Patients were randomized to receive continuous infusion of either 10 mg/hr clazosentan or placebo for up to 15 days following the ons ....

Switzerland General , Andrewc Weiss , Satoshi Tanaka , Idorsia Ltd , Head Of Investor Relations Corporate Communications , Swiss Exchange , Japanese Pharmaceuticals , Idorsia Pharmaceuticals Ltd , Life Sciences , Idorsia Pharmaceuticals Japan , Devices Agency , New Drug Application , Medical Devices Agency , Cerebrovascular Diseases , Pharmacol Exp Ther , Pharmaceuticals Japan , Vice President , Investor Relations , Pharmaceuticals Ltd , சுவிட்சர்லாந்து ஜநரல் , சதோஷி தனகா , தலை ஆஃப் முதலீட்டாளர் உறவுகள் பெருநிறுவன தகவல்தொடர்புகள் , சுவிஸ் பரிமாற்றம் , ஜப்பானிய மருந்துகள் , வாழ்க்கை அறிவியல் , புதியது மருந்து விண்ணப்பம் ,