Neurocrine Biosciences, Inc. Selects PANTHERxRare Specialty Pharmacy for Distribution of Crenessity (Crinecerfont)
Neurocrine Biosciences, Inc. Selects PANTHERxRare Specialty Pharmacy for Distribution of Crenessity (Crinecerfont)
PITTSBURGH, Dec. 23, 2024 /PRNewswire/ -- PANTHERx Rare, a leader in rare disease product patient access and support services in the United States, is pleased to announce that it was selected by Neurocrine Biosciences, Inc. for the distribution of CRENESSITY (crinecerfont), an oral selective corticotropin-releasing factor type 1 (CRF1) receptor antagonist indicated to improve androgen control and enable a reduced glucocorticoid dose in patients 4 years of age and older with classic congenital adrenal hyperplasia (CAH). CRENESSITY is the first non-steroidal treatment approved for classic CAH and a first-in-class therapy that provides a novel approach to treatment for this rare disorder.
匹茲堡,2024年12月23日 /PRNewswire/ — 美國罕見病產品患者准入和支持服務領域的領導者PantherX Rare欣然宣佈,它被Neurocrine Biosciences, Inc.選中分銷CRENESSITY(crinecerfont),這是一種口服選擇性促腎上腺素釋放因數(CRF1)受體拮抗劑,旨在改善雄激素控制和可以減少 4 歲及以上典型先天性腎上腺增生 (CAH) 患者的糖皮質激素劑量。CRENESSITY是第一種獲准用於經典CAH的非甾體療法,也是同類首創的療法,爲這種罕見疾病的治療提供了一種新方法。
CAH is a rare, autosomal recessive genetic disorder that results from deficiency of one of the enzymes needed for adrenal hormone production. The most common cause of CAH is 21-hydroxylase (21-OHD) deficiency, which accounts for approximately 95% of cases.2 21-OHD deficiency prevents the body from producing cortisol, which is essential to respond to stress and illness. In about 75% of cases, aldosterone production is also affected, which impairs the body's ability to regulate salt and water levels, and thereby blood pressure.2,3 In response to low levels of cortisol and aldosterone, the hypothalamus-pituitary-adrenal (HPA) axis is activated, leading to overproduction of androgens.2 Excess androgen production can cause a variety of symptoms, including anxiety, acne, hirsutism, atypical genital development in affected females, fertility issues, early-onset puberty, and rapid growth followed by premature completion resulting in short stature.3 These symptoms can significantly impact both the physical and mental health of those affected with CAH.
CAH 是一種罕見的常染色體隱性遺傳疾病,由缺乏產生腎上腺激素所需的一種酶引起。CAH 的最常見原因是 21-羥化酶(21-OHD)缺乏,約佔病例的 95%。2 21-OHD 缺乏會阻止人體產生皮質醇,而皮質醇對應對壓力和疾病至關重要。在大約 75% 的病例中,醛固酮的產生也會受到影響,這會損害人體調節鹽和水水平的能力,從而降低血壓。2,3 針對皮質醇和醛固酮的低水平,下丘腦-垂體-腎上腺(HPA)軸被激活,導致雄激素過度產生。2 雄激素分泌過多會導致各種症狀,包括焦慮、痤瘡、毛孔自閉症、受影響女性的非典型生殖器發育、生育問題、早發的青春期以及隨之而來的快速成長導致的過早完成身材矮小3 這些症狀會嚴重影響 CAH 患者的身心健康。
"We are proud to partner with Neurocrine Biosciences for the distribution of CRENESSITY. This collaboration underscores PANTHERx's dedication to providing personalized care and seamless access to transformative therapies for patients with rare and complex conditions," said Rob Snyder, Executive Chair, PANTHERx Rare Pharmacy.
「我們很榮幸能與Neurocrine Biosciences合作發行CRENESSITY。這種合作凸顯了PantherX致力於爲罕見和複雜疾病的患者提供個性化護理和無縫獲得變革性療法的決心。」 PantherX稀有藥房執行主席羅布·斯奈德說。
About PANTHERx Rare
PANTHERx Rare is a dual-accredited specialty pharmacy focused on rare and orphan disease, distributing several orphan products and providing access and support services to those needing them most. PANTHERx transforms lives by delivering medicine breakthroughs, clinical excellence, and access solutions to people living with rare and devastating conditions. While each rare condition affects few people, together all rare diseases impact an estimated 25 to 30 million Americans.3 Currently over 7,000 rare diseases have been identified and more than 90% of rare diseases are still without an FDA-approved treatment. 3 Changes in federal policy and advances in science have led to a surge in FDA orphan drug approvals, providing tremendous hope to the rare disease community.
關於 PantherX Rare
PantherX Rare是一家雙重認證的專業藥房,專注於罕見病和孤兒病,分發多種孤兒產品,併爲最需要這些產品的人提供准入和支持服務。PantherX 通過爲患有罕見和毀滅性疾病的人們提供醫學突破、卓越的臨牀表現和可獲得的解決方案,從而改變生活。儘管每種罕見病影響的人數很少,但所有罕見疾病加起來影響估計有25至3000萬美國人。3目前已發現超過7,000種罕見疾病,90%以上的罕見疾病仍未獲得美國食品藥品管理局批准的治療方法。3 聯邦政策的變化和科學的進步導致美國食品藥品管理局孤兒藥批准量激增,爲罕見病界帶來了巨大的希望。
PANTHERx is a dual-accredited specialty pharmacy, holding distinctions in rare disease including the Accreditation Commission for Health Care (ACHC) Distinction in Orphan Drugs and Utilization Review Accreditation Commission (URAC) Rare Disease Center of Excellence. As a pharmacy focused on patient satisfaction, PANTHERx is now a six-time winner of the prestigious MMIT Patient Choice Award, including the 2023 honor. PANTHERx is headquartered in Pittsburgh, Pennsylvania and is licensed in all 50 states and US territories.
PantherX是一家獲得雙重認證的專業藥房,在罕見病領域擁有榮譽,包括醫療保健認證委員會(ACHC)孤兒藥區別和利用審查認證委員會(URAC)罕見病卓越中心。作爲一家注重患者滿意度的藥房,PantherX現已六次獲得久負盛名的麻省理工學院患者選擇獎,包括2023年的榮譽。PantherX 總部位於賓夕法尼亞州匹茲堡,在美國所有 50 個州和地區均獲得許可。
1. CRENESSITY (crinecerfont) [package insert]. Neurocrine Biosciences, Inc. 2024.
2. Congenital Adrenal Hyperplasia (CAH). Neurocrine Biosciences, Inc. Accessed October 21, 2024.
3. Congenital Adrenal Hyperplasia. NORD (National Organization for Rare Disorders). Published June 8, 2023. Accessed October 21, 2024.
1。CRENESSITY (crinecerfont) [包裝說明書]。Neurocrine Biosciences, Inc. 2024.
2。先天性腎上腺皮質增生(CAH)。Neurocrine Biosciences, Inc. 於 2024 年 10 月 21 日訪問。
3.先天性腎上腺皮質增生。NORD(全國罕見疾病組織)。發佈於 2023 年 6 月 8 日。已於 2024 年 10 月 21 日訪問。
For more information, please contact [email protected]
欲了解更多信息,請聯繫 [email protected]
SOURCE PANTHERx Rare Pharmacy
來源 PantherX 稀有藥房
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