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Elagolix in endometriosis-related pain: a profile of its use as approved in the USA

机译:Elagolix在子宫内膜异位症相关的痛苦:它在美国批准的用途

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摘要

Elagolix (Orilissa?), an oral non-peptide gonadotropin-releasing hormone receptor antagonist, is approved for the management of moderate to severe pain associated with endometriosis in the USA and Canada. It reduces levels of gonadotropins, thereby suppressing ovarian sex hormones, ovulation, and endometrial proliferation. In phase 3 trials in women with moderate to severe endometriosis-related pain, elagolix 150 mg once daily and 200 mg twice daily improved clinical response rates for dysmenorrhea and non-menstrual pelvic pain to a significantly greater extent than placebo at 3 and 6 months of treatment. Improvements from baseline in several other endometriosis pain-related outcomes were also better with elagolix than with placebo, with the benefits of treatment being maintained with treatment for an additional 6 months in extension studies. Elagolix is generally well tolerated, with most adverse events being of mild to moderate severity. However, elagolix is associated with a dosage-dependent risk of bone loss, which limits its duration of therapy, use in at-risk patients, and concomitant use with certain drugs.
机译:Elagolix(Orilissa?)是一种口腔非肽促性腺激素 - 释放激素受体拮抗剂,被批准用于管理中度至美国和加拿大的子宫内膜异位症相关的严重疼痛。它减少了促性腺激素的水平,从而抑制卵巢性激素,排卵和子宫内膜增殖。在适度至严重子宫内膜异位症相关疼痛的女性的第3阶段试验中,Elagolix每日150毫克,每日200毫克两次改善痛经和非月经骨盆疼痛的临床反应率,在3和6个月的安慰剂中显着更大程度地变得更大的程度。治疗。在其他几个子宫内膜异位症疼痛相关结果中的基线的改善也比Elagolix更好,而不是安慰剂,在延长研究中治疗治疗的效果额外6个月。 Elagolix通常是耐受性的,大多数不良事件是轻度到中度严重程度。然而,Elagolix与剂量依赖性的骨质损失风险有关,这限制了其治疗的持续时间,在风险患者中使用,以及与某些药物的伴随使用。

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