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Cytokinetics Announces Primary Results From SEQUOIA-HCM Presented in Late Breaking Clinical Trial Session at the European Society of Cardiology Heart Failure…

Cytokinetics Announces Primary Results From SEQUOIA-HCM Presented in Late Breaking Clinical Trial Session at the European Society of Cardiology Heart Failure…
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Company to host investor eventStatistically significantClinically meaningful improvements observedPrimary efficacy endpointAll secondary endpointsResults consistent across all prespecifiedSustained improvements observedTreatment interruptions dueHost investor eventWebcast today

Cytokinetics Announces Primary Results From SEQUOIA-HCM Presented in Late Breaking Clinical Trial Session at the European Society of Cardiology Heart Failure 2024 Congress and Published in the New England Journal of Medicine

Cytokinetics Announces Primary Results From SEQUOIA-HCM Presented in Late Breaking Clinical Trial Session at the European Society of Cardiology Heart Failure 2024 Congress and Published in the New England Journal of Medicine
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United statesDiane weiserMartin maronFadyi malikCytokinetics incorporated nasdaqUs food drug administrationCorporate affairsHypertrophic cardiomyopathy centerResearch developmentGlobenewswire incEuropean society of cardiologyCompany to host investor eventNational medical products administrationJournal of the american college cardiologySymphony healthPestana palace lisboa hotel

Crinetics Once-Daily Oral Paltusotine Achieved the Primary and All Secondary Endpoints in the Phase 3 PATHFNDR-1 Study Evaluating Treatment of Patients with Acromegaly

Crinetics Once-Daily Oral Paltusotine Achieved the Primary and All Secondary Endpoints in the Phase 3 PATHFNDR-1 Study Evaluating Treatment of Patients with Acromegaly
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United statesCorey davisChas schultzCrinetics pharmaceuticals incCrinetics pharmaceuticalsIr corporate communicationsSecurities exchangeOnce daily oral paltusotine achievedAll secondary endpointsEvaluating treatmentPaltusotine maintainedWere maintainedAfter switchingInjected depot standardAcromegaly symptom diary scores were maintainedWas well tolerated

Alnylam Announces FDA Approval of AMVUTTRA™ (vutrisiran), an RNAi Therapeutic for the Treatment of the Polyneuropathy of Hereditary Transthyretin-Mediated Amyloidosis in Adults

Alnylam Announces FDA Approval of AMVUTTRA™ (vutrisiran), an RNAi Therapeutic for the Treatment of the Polyneuropathy of Hereditary Transthyretin-Mediated Amyloidosis in Adults
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United statesUnited kingdomChristine regan lindenboomJosh brodskyYvonne greenstreetMichael polydefkisIsabelle lousadaAlnylam pharmaceuticals incCompany expects to launch in earlyAlnylam pharmaceuticalsBrazilian health regulatory agencyJapanese pharmaceuticalsEuropean unionAmyloidosis research consortiumSubcutaneous administration once every three monthsDrug administration

Stock Market | FinancialContent Business Page

Stock Market | FinancialContent Business Page
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