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Selexipag

  • Effects of Selexipag and Its Active Metabolite in Contrasting The

    Effects of Selexipag and Its Active Metabolite in Contrasting The

  • Effect of Prostanoids on Human Platelet Function: an Overview

    Effect of Prostanoids on Human Platelet Function: an Overview

  • Nanosuspensions of Selexipag: Formulation, Characterization, and in Vitro Evaluation Rusul M

    Nanosuspensions of Selexipag: Formulation, Characterization, and in Vitro Evaluation Rusul M

  • Formulation and Optimization of Lyophilized Selexipag Nanocrystals to Improve the Saturation Solubility and Dissolution Rate

    Formulation and Optimization of Lyophilized Selexipag Nanocrystals to Improve the Saturation Solubility and Dissolution Rate

  • Report on Investigation Results

    Report on Investigation Results

  • AHRQ Healthcare Horizon Scanning System – Status Update

    AHRQ Healthcare Horizon Scanning System – Status Update

  • Prior Authorization PDL Implementation Schedule

    Prior Authorization PDL Implementation Schedule

  • Non-Steroidal Anti-Inflammatories

    Non-Steroidal Anti-Inflammatories

  • Queensland Health List of Approved Medicines

    Queensland Health List of Approved Medicines

  • Prostacyclin: an Inflammatory Paradox

    Prostacyclin: an Inflammatory Paradox

  • Prostanoid EP2 Receptors Are Up-Regulated in Human Pulmonary Arterial Hypertension: a Key Anti-Proliferative Target for Treprostinil in Smooth Muscle Cells

    Prostanoid EP2 Receptors Are Up-Regulated in Human Pulmonary Arterial Hypertension: a Key Anti-Proliferative Target for Treprostinil in Smooth Muscle Cells

  • UPTRAVI (Selexipag) Is a Selective Non-Prostanoid IP Prostacyclin Receptor Agonist

    UPTRAVI (Selexipag) Is a Selective Non-Prostanoid IP Prostacyclin Receptor Agonist

  • Selexipag Active Metabolite ACT-333679 Displays Strong Anticontractile and Antiremodeling Effects but Low B-Arrestin Recruitment and Desensitization Potential

    Selexipag Active Metabolite ACT-333679 Displays Strong Anticontractile and Antiremodeling Effects but Low B-Arrestin Recruitment and Desensitization Potential

  • Recent Advances in Targeting the Prostacyclin Pathway in Pulmonary Arterial Hypertension

    Recent Advances in Targeting the Prostacyclin Pathway in Pulmonary Arterial Hypertension

  • FDA Listing of Established Pharmacologic Class Text Phrases January 2021

    FDA Listing of Established Pharmacologic Class Text Phrases January 2021

  • Extract from the Clinical Evaluation Report for Selexipag

    Extract from the Clinical Evaluation Report for Selexipag

  • Selexipag / ACT-293987 Pulmonary Arterial Hypertension Protocol AC-065A309

    Selexipag / ACT-293987 Pulmonary Arterial Hypertension Protocol AC-065A309

  • Selexipag: a New Treatment Agent for Pulmonary Arterial Hypertension

    Selexipag: a New Treatment Agent for Pulmonary Arterial Hypertension

Top View
  • Clinical Use of Extended-Release Oral Treprostinil in the Treatment of Pulmonary Arterial Hypertension
  • Preferred Drug List Drug Class Review Announcement
  • Magellan Rx Report
  • FEP 5 Tier Rx Drug Formulary (607) Standard Option
  • Interactions with Experimental COVID-19 Therapies
  • Increased Role of E Prostanoid Receptor-3 in Prostacyclin
  • Beraprost Modified Release in Addition to Treprostinil for Pulmonary Arterial Hypertension
  • Preferred Drug List (PDL)
  • Reimbursement Criteria for Frequently Requested Drugs
  • Selexipag (Uptravi ) Issued by PHA’S Scientific Leadership Council
  • Mississippi Division of Medicaid Universal Preferred Drug
  • USP Category USP Class Example Part D Eligible Drugs* Salt/Ester
  • USP Medicare Model Guidelines V7.0 (With Example Part D Drugs)
  • Blue Cross and Blue Shield April 2021 Multi-Tier Basic Drug List
  • Therapeutic Drug Class
  • Diverse Pharmacology of Prostacyclin Mimetics: Implications for Pulmonary 5 Hypertension
  • EFFECTIVE 01/01/2017 Version 2017.1J
  • Quantity Limits — Select


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