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Macitentan for the treatment of inoperable chronic thromboembolic pulmonary hypertension (MERIT-1): results from the multicentre, phase 2, randomised, double-blind, placebo-controlled study.
Author: , D'ArminiAndrea M, FedulloPeter, GhofraniHossein-Ardeschir, HowardLuke S, JaïsXavier, JenkinsDavid P, JingZhi-Cheng, KimNick H, MadaniMichael M, MartinNicolas, MayerEckhard, PapadakisKelly, RichardDominik, SimonneauGérald
Original Abstract of the Article :
BACKGROUND: Macitentan is beneficial for long-term treatment of pulmonary arterial hypertension. The microvasculopathy of chronic thromboembolic pulmonary hypertension (CTEPH) and pulmonary arterial hypertension are similar. METHODS: The phase 2, double-blind, randomised, placebo-controlled MERIT-1...See full text at original site
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引用元:
https://doi.org/10.1016/S2213-2600(17)30305-3
データ提供:米国国立医学図書館(NLM)
Macitentan for Inoperable Chronic Thromboembolic Pulmonary Hypertension (CTEPH): A Phase 2 Study
Dr. Camel here, your guide through the often-challenging terrain of pulmonary hypertension! This study explores the potential of macitentan, a drug that targets the endothelin receptor, in treating inoperable chronic thromboembolic pulmonary hypertension (CTEPH), a condition that restricts blood flow through the lungs. It's like finding a new oasis in the vast and often-treacherous desert of pulmonary hypertension, seeking to provide relief for patients with this debilitating disease.
A Promising New Approach
The study demonstrates that macitentan significantly improved pulmonary vascular resistance (PVR) in patients with inoperable CTEPH, offering hope for a new treatment option for this challenging condition. The results are a beacon of hope for patients with limited treatment options, providing a potential path towards improved quality of life.
Navigating the Challenges of CTEPH
The study underscores the importance of continued research into new treatment options for CTEPH, a condition that often presents significant challenges for patients and their families. This research emphasizes the need to explore novel therapies and refine current treatment approaches to improve outcomes for those battling this complex disease. It's like finding a new way to navigate the often-difficult terrain of pulmonary hypertension, seeking to find better routes to treatment and better outcomes for patients.
Dr.Camel's Conclusion
This phase 2 study provides encouraging evidence for the efficacy of macitentan in treating inoperable CTEPH. The findings highlight the importance of continued research and development of new treatments for this challenging condition. It's like finding a wellspring of hope in the desert of pulmonary hypertension research, a source of optimism for future treatment options.
Date :
- Date Completed 2018-06-05
- Date Revised 2022-04-10
Further Info :
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