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Phenylalanine hydroxylase deficiency

ORPHA:708881疾病组中国目录 第1批 · 49暂无中文名

别名

PAH deficiency

近两年的全球研究 63L2

2024/08 起在 Europe PMC 检索所得,按发表时间倒序显示最近 20 篇。标题未译成中文——自动翻译需要接入 LLM 服务,尚未引入。

  • 2026-08预印本
    The spectrum of PAH variants and genotype-phenotype correlation in patients with phenylalanine hydroxylase deficiency in Inner Mongolia, China
    · DOI
  • 2026-07
    Genotype-Phenotype Relationships in Phenylalanine Hydroxylase Deficiency: Functional Annotation-Enhanced Analysis of 23,427 Individuals
    Genetics in medicine : official journal of the American College of Med · DOI · Europe PMC
  • 2026-07综述开放获取
    Mapping the Severity of Phenylalanine Hydroxylase Deficiency
    Journal of inherited metabolic disease · DOI · Europe PMC
  • 2026-06
    Factors affecting the success of follow-up and treatment of adults with phenylketonuria diagnosed by newborn screening
    Journal of pediatric endocrinology & metabolism : JPEM · DOI · Europe PMC
  • 2026-06
    Toward personalized treatment in phenylketonuria: Intra-individual variation of in vivo phenylalanine oxidation using the <sup>13</sup>C-phenylalanine breath test
    Molecular genetics and metabolism · DOI · Europe PMC
  • 2026-06
    A phenylketonuria mouse model exhibits EEG spike-wave discharges: Effects of sleep deprivation and low-Phe diet
    Neurobiology of disease · DOI · Europe PMC
  • 2026-06开放获取
    Molecular Genetic and Biochemical Characterization of Hyperphenylalaninemia Based on Expanded Neonatal Screening Data from 2023 to 2024 in the Russian Federation
    International journal of molecular sciences
  • 2026-05综述开放获取
    Phenylalanine-tyrosine-catecholamine axis disorders: pathways, molecular diagnosis, therapeutics, and emerging translational monitoring technologies
    Frontiers in molecular biosciences · DOI · Europe PMC
  • 2026-05开放获取
    Concurrent Phenylalanine Hydroxylase-Related Disorder and Celiac: A Rare Co-occurrence With Implications for Clinical Management
    Annals of internal medicine. Clinical cases · DOI · Europe PMC
  • 2026-05开放获取
    Real-Life Application of a Point-of-Care Biosensor for Phenylalanine in Patients With Phenylketonuria
    Journal of inherited metabolic disease · 被引 1 · DOI · Europe PMC
  • 2026-04开放获取
    Fe(II) with Tris(1-pyrazolyl)methane Complex Increases Thermal Stability In Vitro and Activity In Vivo of the Mutant 447R Form of Mouse Tryptophan Hydroxylase 2
    International journal of molecular sciences · DOI · Europe PMC
  • 2026-04开放获取
    Long-Term Safety and Efficacy of Pegvaliase in Japanese Adults With Phenylketonuria: Final Results of a Phase III Trial
    JIMD reports · DOI · Europe PMC
  • 2026-04
    Developmental and Phenotypic Outcomes in Mild Phenylalanine Hydroxylase Deficiency
    American journal of medical genetics. Part A · DOI · Europe PMC
  • 2026-03开放获取
    A Systematic Bioinformatic Analysis of the miRNA Pathway in Inborn Errors of Amino Acid Metabolism Disorders
    Molecular syndromology · DOI · Europe PMC
  • 2026-02荟萃分析系统综述综述开放获取
    The prevalence of phenylketonuria (PKU) and hyperphenylalaninemia (HPA) in Iran: a systematic review and meta-analysis
    Orphanet journal of rare diseases · DOI · Europe PMC
  • 2026-01综述开放获取
    Epidemiology of Hyperphenylalaninemia: A Systematic Review and Meta-Analysis
    Sage open pediatrics · DOI · Europe PMC
  • 2026-01综述开放获取
    Mass Spectrometry-Based Metabolomics in Pediatric Health and Disease
    Metabolites · 被引 1 · DOI · Europe PMC
  • 2026-01
    Correspondence on "Phenylalanine hydroxylase deficiency diagnosis and management: A 2023 evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG)" by Smith et al
    Genetics in medicine : official journal of the American College of Med · 被引 1 · DOI · Europe PMC
  • 2026-01
    Phenylalanine hydroxylase deficiency diagnosis and management: A 2023 evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG)
    Genetics in medicine : official journal of the American College of Med · DOI · Europe PMC
  • 2025-12综述开放获取
    Expert consensus on the combined screening of genes and biomarkers for neonatal diseases
    World journal of pediatrics : WJP · DOI · Europe PMC

境外已获批用于本病的药物 5L2

欧盟 2 项、美国 3 项。同一药物在两地各批一次的,会分别列出。

「境外已获批」不等于「在中国能用」。中间隔着进口注册、临床急需境外新药通道、海南博鳌乐城国际医疗旅游先行区等几条路径,各有各的条件与费用。这一节能确定地告诉你的只有一件事:这个病在世界范围内已经有获得批准的药物,它叫什么名字。拿这个名字去问主治医生,是下一步最省力的做法。

药名一律保留英文原文,不作翻译——中国的药品通用名与英文名的音译经常不一致,译错会让人去找一个不存在的药。

已获孤儿药资格、尚未获批的在研药物(8 项)

孤儿药资格只是一种监管身份——它意味着监管机构认可这是罕见病用药并给予研发激励,不代表这个药已被证明有效,也不代表将来一定能上市。绝大多数最终不会成药。列在这里是为了看清有哪些方向正在被尝试。

  • 5,6,7,8-Tetrahydrobiopterin欧盟2003-10-02
    Treatment of hyperphenylalaninaemia
    官方记录
  • particles comprised of methacrylic acid based co-polymer, cross-linked欧盟2016-11-18
    Treatment of hyperphenylalaninaemia
    官方记录
  • Escherichia coli, strain Nissle 1917, expressing high affinity phenyla欧盟2023-04-21
    Treatment of hyperphenylalaninaemia
    官方记录
  • 2,4-Diamino-5-[[5-(1H-pyrazol-5-yl)-2-thienyl]methyl]-1H-pyrimidin-6-o欧盟2024-05-24
    Treatment of hyperphenylalaninaemia
    官方记录
  • (R)-3-(1-Cyclopropyl-3-(2-fluoro-4-(trifluoromethoxy)benzyl)ureido)pip欧盟2024-06-28
    Treatment of hyperphenylalaninaemia
    官方记录
  • adeno-associated virus vector serotype SNY001 containing the human PAH欧盟2025-02-26
    Treatment of hyperphenylalaninaemia
    官方记录
  • Valine, isoleucine and leucine美国1996-01-05
    Treatment of hyperphenylalaninemia
    官方记录
  • Particles comprised ofmethacrylic acid based co-polymer, cross-linked 美国2020-02-27
    Treatment of hyperphenylalaninemia
    官方记录

数据来自欧洲药品管理局(EMA)的药品与孤儿药资格公开导出表,以及美国 FDA 孤儿药资格数据库。两边口径不同:欧盟一侧取的是当前状态仍为「已授权」的药品;美国一侧记录的是「曾获批准」这一事实,FDA 的公开表不追踪药物此后是否退市(例如 Relyvrio 于 2024 年撤市,表中仍记为已获批)。请以官方记录页为准。

在中国开展的临床试验 7L2

按病名在 ClinicalTrials.gov 检索、并校验研究中心含中国大陆而来。登记状态不等于现在真的能入组——务必按 NCT 号到原站核实,并与主治医生商量。

登记为可入组 4

  • 招募中NCT06687733
    Safety and Efficacy Study of NGGT002 in Adult Patients With Phenylketonuria
    I 期、II 期 · 干预性 · 2024/07/16NGGT (Suzhou) Biotechnology Co., Ltd.
    中国研究中心 2 个:Bengbu、Shanghai
  • 招募中NCT07672756
    A Clinical Study on the Safety and Tolerability of PL54 Injection in Adult Patients With Phenylketonuria (PKU)
    I 期 · 干预性 · 2025/07/20Chongqing Peg-Bio Biopharm Co., Ltd.
    中国研究中心 1 个:Hefei
  • 尚未开始招募NCT07318909
    To Evaluate the Safety and Efficacy of GS1168 Injection in Adult Phenylketonuria
    早期 I 期 · 干预性 · 2025/12/31Gritgen Therapeutics Co., Ltd.
    中国研究中心 1 个:Hefei
  • 招募中NCT07685210
    GenSci144 Tablets Phase I Clinical Trial
    I 期 · 干预性 · 2026/06/22Changchun GeneScience Pharmaceutical Co., Ltd.
    中国研究中心 1 个:Jinan
其他状态的试验(3 项)
  • 已完成NCT03864029
    Retrospective Observational Safety Effectiveness With Kuvan in hpA
    观察性 · 2017/10/10BioMarin Pharmaceutical
    中国研究中心 1 个:Chengdu
  • 进行中·不再招募NCT06061614
    Safety and Efficacy Study of NGGT002 in PKU Adult Subjects
    早期 I 期 · 干预性 · 2023/03/30The First Affiliated Hospital of Bengbu Medical University
    中国研究中心 1 个:Bengbu
  • 已完成NCT05948020
    Efficacy and Safety of Orally Administered Engineered Probiotics (CBT102-A) for the Treatment of Children With Phenylketonuria
    早期 I 期 · 干预性 · 2023/09/02Children's Hospital of Fudan University
    中国研究中心 1 个:Shanghai

中国境外的在招试验 35L2

这些试验在中国没有研究中心,通常无法直接报名——入组一般要求在当地居住并接受随访。列在这里是因为它另有用处:看清楚全世界正在试哪些药、做到了哪一期、由谁在做。把药名和 NCT 编号记下来去问主治医生,或据此进一步查该药是否已在境外获批、是否有拓展性用药(expanded access)通道。

美国15法国5英国4澳大利亚4波兰3德国3加拿大2瑞士2意大利2捷克1日本1荷兰1西班牙1土耳其1另有 4 个国家/地区

CT.gov 报告命中 35 项,此处取回并展示最近的 15 项。

  • 招募中NCT07713758
    A Trial to Examine if Repinatrabit is Processed Differently in Adults With Reduced Liver or Kidney Function Compared to Adults With Normal Liver and Kidney Function
    I 期 · 干预性 · 2026/07/17Otsuka Pharmaceutical Development & Commercialization, Inc.
    美国
  • 尚未开始招募NCT07671859
    PKU Microtablets Case Studies
    不适用 · 干预性 · 2026/07/01Nutricia UK Ltd
    英国
  • 招募中NCT07694440
    A Study of MZE782 in Adults With PKU
    II 期 · 干预性 · 2026/06/23Maze Therapeutics
    美国
  • 招募中NCT07477691
    Immune Modulation During Palynziq® Treatment in Adults (IMPALA)
    IV 期 · 干预性 · 2026/05/29BioMarin Pharmaceutical
    美国
  • 尚未开始招募NCT07551921
    PheCheck™ Validation Study
    观察性 · 2026/05/20Aptatek BioSciences, Inc
  • 招募中NCT07241234
    A Study to Evaluate Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of AG-181 in Subjects With Phenylketonuria
    I 期 · 干预性 · 2026/04/17Agios Pharmaceuticals, Inc.
    波兰、美国
  • 招募中NCT07446400
    A Trial to Examine the Interaction of Repinatrabit With Ethinyl Estradiol/Norethindrone, Metformin,Carbamazepine, Rosuvastatin, and Methotrexate When Administered Together
    I 期 · 干预性 · 2026/03/31Otsuka Pharmaceutical Development & Commercialization, Inc.
    澳大利亚
  • 招募中NCT07484945
    Multiomics Approach in Adult Patients With Phenylketonuria
    观察性 · 2026/03/23University Hospital, Tours
    法国
  • 尚未开始招募NCT07406009
    The Psychosocial Functioning of Adults With Phenylketonuria.
    观察性 · 2026/01/15Central Hospital, Nancy, France
  • 招募中NCT07220265
    Impact of Phenylalanine Elevations on Brain and Cognition in Adult PKU Carriers
    不适用 · 干预性 · 2025/12/19University of Missouri-Columbia
    美国
  • 招募中NCT07698743
    Eating Disorders in Patients With Phenylketonuria
    观察性 · 2025/12/04Central Hospital, Nancy, France
    法国
  • 招募中NCT06971731
    A Study of JNT-517 in Participants With Phenylketonuria (PKU)
    III 期 · 干预性 · 2025/10/20Otsuka Pharmaceutical Development & Commercialization, Inc.
    澳大利亚、加拿大、捷克、法国、德国、日本、荷兰、波兰 等 10 国
  • 招募中NCT07526909
    Effect of Different Meal Types Given Before Exercise on Plasma Amino Acid Levels and Metabolic Control Parameters in Classical Phenylketonuria Patients Undergoing Aerobic and Resistance Exercises
    不适用 · 干预性 · 2025/10/01Hacettepe University
    土耳其
  • 招募中NCT07728032
    Impact Of A Phe-Restricted Diet On Gut Health In Children With PKU
    观察性 · 2025/10/01Birmingham Women's and Children's NHS Foundation Trust
    英国
  • 招募中NCT06628128
    A Long-Term Study of JNT-517 in Participants With Phenylketonuria
    III 期 · 干预性 · 2025/08/11Otsuka Pharmaceutical Development & Commercialization, Inc.
    澳大利亚、美国

外部标识与链接

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本页数据来源

  • 疾病定义、同义词、基因、表型、流行病学:Orphanet(CC BY 4.0)
  • 中文病名:Orphanet 中文包,冻结于 2020-06-01;本条目在该版本中无中文名
  • 表型中文标签:HPO 简体中文翻译(CHPO 上游成果)