Correction to: An open-label, single-dose study to evaluate the safety, tolerability, pharmacokinetics, and pharmacodynamics of cinacalcet in pediatric subjects aged 28 days to < 6 years with chronic kidney disease receiving dialysis

被引:0
|
作者
Winnie Y. Sohn
Anthony A. Portale
Isidro B. Salusky
Hao Zhang
Lucy L. Yan
Bella Ertik
Shahnaz Shahinfar
Edward Lee
Bastian Dehmel
Bradley A. Warady
机构
[1] Amgen,
[2] Inc.,undefined
[3] UCSF Benioff Children’s Hospital,undefined
[4] David Geffen School of Medicine at UCLA,undefined
[5] S. Shahinfar Consulting and Childrens Hospital of Philadelphia,undefined
[6] Children’s Mercy Hospital,undefined
来源
Pediatric Nephrology | 2019年 / 34卷
关键词
D O I
暂无
中图分类号
学科分类号
摘要
The original version of this article unfortunately contained three mistakes. In Table 1, the last line under “Key Inclusion Criteria” should read “Normal or clinically acceptable ECGs at screening and at day − 1.” In addition, the abbreviation “IP” in the legend to Table 1 stands for “investigational product.”
引用
收藏
页码:739 / 740
页数:1
相关论文
共 50 条
  • [41] Single-Dose, Open-Label Study of the Differences in Pharmacokinetics of Colchicine in Subjects with Renal Impairment, Including End-Stage Renal Disease
    Yalcin Solak
    Seyyid Bilal Acikgoz
    Mehmet Yildirim
    Clinical Drug Investigation, 2015, 35 : 149 - 149
  • [42] Single-Dose, Open-Label Study of the Differences in Pharmacokinetics of Colchicine in Subjects with Renal Impairment, Including End-Stage Renal Disease
    Solak, Yalcin
    Acikgoz, Seyyid Bilal
    Yildirim, Mehmet
    CLINICAL DRUG INVESTIGATION, 2015, 35 (02) : 149 - 149
  • [43] Single-Dose, Open-Label Study of the Differences in Pharmacokinetics of Colchicine in Subjects with Renal Impairment, Including End-Stage Renal Disease
    Wason, Suman
    Mount, David
    Faulkner, Robert
    CLINICAL DRUG INVESTIGATION, 2014, 34 (12) : 845 - 855
  • [44] Single-Dose, Open-Label Study of the Differences in Pharmacokinetics of Colchicine in Subjects with Renal Impairment, Including End-Stage Renal Disease
    Suman Wason
    David Mount
    Robert Faulkner
    Clinical Drug Investigation, 2014, 34 : 845 - 855
  • [45] A randomized, open-label, single-dose, two-cycle crossover study to evaluate the bioequivalence and safety of lenvatinib and Lenvima® in Chinese healthy subjects
    Xu, Zhongnan
    Wang, Yanli
    Liu, Guangwen
    Chen, Jiahui
    Wang, Wanhua
    Cheng, Yang
    Ren, Qing
    Cui, Yingzi
    Yang, Wei
    Liu, Zhengzhi
    Chen, Xuesong
    Xue, Jinling
    Chang, Tianying
    Qu, Xinyao
    Yu, Shuang
    Zhou, Yannan
    Xu, Kaibo
    Su, Zhengjie
    Deng, Qiaohuan
    Zhao, Yicheng
    Yang, Haimiao
    EXPERT OPINION ON INVESTIGATIONAL DRUGS, 2022, 31 (07) : 737 - 746
  • [46] An Open-Label, Single-Dose, Parallel-Group, Dose-Increasing Study Comparing the Pharmacokinetics and Tolerability of Pilsicainide Hydrochloride in Healthy Korean and Japanese Male Subjects
    Kim, Bo-Hyung
    Kim, Jung-Ryul
    Lim, Kyoung Soo
    Kim, Jae Woo
    Kim, Kyu-pyo
    Hong, Jang-Hee
    Jang, In-Jin
    Shin, Sang-Goo
    Yu, Kyung-Sang
    Tanaka, Takanori
    CLINICAL THERAPEUTICS, 2009, 31 (03) : 609 - 618
  • [47] PHASE I, OPEN-LABEL, RANDOMIZED, SINGLE-DOSE STUDY TO ASSESS SAFETY AND PHARMACOKINETICS OF SUBCUTANEOUS ROZIBAFUSP ALFA IN HEALTHY JAPANESE SUBJECTS.
    Abuqayyas, L.
    Cheng, L.
    Simiens, M.
    Dutta, S.
    Houk, B.
    CLINICAL PHARMACOLOGY & THERAPEUTICS, 2021, 109 : S53 - S53
  • [48] Pharmacokinetics and Safety of DS-8500a, an Antidiabetic Drug, in Japanese Subjects with Hepatic or Renal Impairment: A Single-Center, Open-Label, Single-Dose Study
    Kato, Manabu
    Ishizuka, Hitoshi
    Taguchi, Takashi
    Shiosakai, Kazuhito
    Kamiyama, Emi
    Sata, Michio
    Yoshida, Takafumi
    ADVANCES IN THERAPY, 2018, 35 (08) : 1239 - 1250
  • [49] Pharmacokinetics and Safety of DS-8500a, an Antidiabetic Drug, in Japanese Subjects with Hepatic or Renal Impairment: A Single-Center, Open-Label, Single-Dose Study
    Manabu Kato
    Hitoshi Ishizuka
    Takashi Taguchi
    Kazuhito Shiosakai
    Emi Kamiyama
    Michio Sata
    Takafumi Yoshida
    Advances in Therapy, 2018, 35 : 1239 - 1250
  • [50] The Pharmacokinetics, Safety, and Tolerability of Rimegepant 75 mg are Similar in Elderly and Nonelderly Adults: a Phase 1, Open-Label, Parallel-Group, Single-Dose Study
    Croop, R.
    Stringfellow, J.
    Ivans, A.
    Coric, V
    HEADACHE, 2019, 59 : 177 - 178