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Selexipag for the Treatment of Pulmonary Arterial Hypertension.
Author: , AdzerikhoIgor, ChannickRichard, ChinKelly M, Di ScalaLilla, FreyAline, GaineSean, GalièNazzareno, GhofraniHossein-Ardeschir, HoeperMarius M, LangIrene M, LiuJinming, McLaughlinVallerie V, MoiseevaOlga, PreissRalph, RubinLewis J, SimonneauGérald, SitbonOlivier, TapsonVictor, ZengXiaofeng
Original Abstract of the Article :
BACKGROUND: In a phase 2 trial, selexipag, an oral selective IP prostacyclin-receptor agonist, was shown to be beneficial in the treatment of pulmonary arterial hypertension. METHODS: In this event-driven, phase 3, randomized, double-blind, placebo-controlled trial, we randomly assigned 1156 patien...See full text at original site
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引用元:
https://doi.org/10.1056/NEJMoa1503184
データ提供:米国国立医学図書館(NLM)
Selexipag: A New Weapon in the Fight Against Pulmonary Arterial Hypertension
Pulmonary arterial hypertension (PAH) is a serious condition that can be as challenging to treat as crossing a vast desert. This study investigates the effectiveness of selexipag, a new oral medication, in the treatment of PAH. Selexipag works by activating the IP prostacyclin receptor, a crucial player in regulating blood pressure and blood vessel function.The study, a large-scale randomized controlled trial, found that selexipag significantly reduced the risk of death or PAH-related complications compared to placebo. The study also found that selexipag was well-tolerated, with the most common side effects being consistent with known side effects of prostacyclin, such as headache and diarrhea.
A Promising New Treatment for PAH
This study offers a promising new treatment option for patients with PAH. Selexipag demonstrates the potential of targeting the IP prostacyclin receptor to improve outcomes in patients with this challenging condition. This research highlights the importance of developing new therapies that target specific pathways to improve treatment effectiveness and patient outcomes.Navigating the Desert of PAH
This research underscores the importance of continued research and development of new treatments for PAH. Selexipag represents a promising new therapy, but further research is needed to fully understand its long-term effectiveness and safety. This research emphasizes the importance of a multi-pronged approach to treating complex conditions like PAH, combining medication, lifestyle modifications, and supportive care.Dr. Camel's Conclusion
This study on selexipag provides a promising insight into the treatment of pulmonary arterial hypertension (PAH). Selexipag's effectiveness in reducing the risk of death or PAH-related complications highlights the potential of targeting the IP prostacyclin receptor to improve outcomes in patients with this challenging condition. This research underscores the importance of continued research and development of new therapies for PAH, offering hope for those navigating the complexities of this disease.Date :
- Date Completed 2015-12-31
- Date Revised 2022-04-10
Further Info :
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