Effect of Renal Impairment on the Pharmacokinetics, Efficacy, and Safety of Albiglutide

被引:26
|
作者
Young, Malcolm A. [1 ,2 ]
Wald, Jeffrey A. [1 ]
Matthews, Jessica E. [2 ]
Yang, Fred [3 ]
Reinhardt, Rickey R. [4 ]
机构
[1] GlaxoSmithKline, Clin Pharmacol Modeling & Simulat, Res Triangle Pk, NC 27709 USA
[2] GlaxoSmithKline, Res Triangle Pk, NC 27709 USA
[3] GlaxoSmithKline, Biostat & Data Sci, Upper Merion, PA USA
[4] GlaxoSmithKline, Clin Dev, Upper Merion, PA USA
关键词
albiglutide; GLP-1; agonist; renal impairment; hemodialysis; pharmacokinetics; efficacy; safety; 52-WEEK EFFICACY; SERUM-ALBUMIN; GLP-1; ANALOG; TYPE-2; LIRAGLUTIDE; PHARMACODYNAMICS; TOLERABILITY; EXENATIDE; METFORMIN; AGONIST;
D O I
10.3810/pgm.2014.05.2754
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Chronic kidney disease is frequently present in patients with type 2 diabetes mellitus (T2DM). New therapeutic options in this patient subpopulation are needed. Objectives: Assess the effect of renal impairment on the pharmacokinetics (PK), efficacy, and safety of albiglutide in single-and multiple-dose studies. Methods: Pharmacokinetics, safety, and efficacy of once weekly albiglutide in patients with T2DM was assessed from a single-dose (30 mg), nonrandomized, open-label study (N = 41) including subjects with normal and varying degrees of renal impairment, including hemodialysis, and a pooled analysis of 4 phase 3, randomized, double-blind (1 open-label), active or placebo-controlled multiple-dose studies. The pooled analysis of the latter 4 studies (N = 1113) was part of the population PK analysis, which included subjects with normal and varying degrees of renal impairment (mild, moderate, severe) treated with albiglutide (30 to 50 mg) to primary end points of 26 to 52 weeks. Results: Single-dose PK showed area-under-the-curve ratios (and 90% CIs) of 1.32 (0.96-1.80), 1.39 (1.03-1.89), and 0.99 (0.63-1.57) for the moderate, severe, and hemodialysis groups, respectively, relative to the normal group. Results indicate that modest increases in plasma concentration of albiglutide were observed with the severity of renal impairment. There was a trend for more glycemic lowering as the estimated glomerular filtration rate decreased. The severe group had a higher frequency of gastrointestinal (eg, diarrhea, constipation, nausea, and vomiting) and hypoglycemic (with background sulfonylurea use) events compared with patients with mild or moderate renal impairment. Conclusion: The PK, efficacy, and safety data indicate that albiglutide has a favorable benefit/risk ratio in patients with T2DM and varying degrees of renal impairment, and the need for a dose adjustment is not suggested. Experience in patients with more severe renal impairment is very limited, so the recommendation is to use albiglutide carefully in this population.
引用
收藏
页码:35 / 46
页数:12
相关论文
共 50 条
  • [41] The Pharmacokinetics and Safety Of Idelalisib In Subjects With Severe Renal Impairment
    Jin, Feng
    Robeson, Michelle
    Zhou, Huafeng
    Hisoire, Grace
    Ramanathan, Srini
    BLOOD, 2013, 122 (21)
  • [42] Pharmacokinetics and Safety of Momelotinib in Subjects With Hepatic or Renal Impairment
    Xin, Yan
    Kawashima, Jun
    Weng, Winnie
    Kwan, Ellen
    Tarnowski, Thomas
    Silverman, Jeffrey A.
    JOURNAL OF CLINICAL PHARMACOLOGY, 2018, 58 (04): : 522 - 532
  • [43] Pharmacokinetics, Safety, and Tolerability of Faldaprevir in Patients with Renal Impairment
    Huang, Fenglei
    Moschetti, Viktoria
    Lang, Benjamin
    Halabi, Atef
    Petersen-Sylla, Marc
    Yong, Chan-Loi
    Elgadi, Mabrouk
    ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2015, 59 (01) : 251 - 257
  • [44] Pharmacokinetics and safety of the ketolide telithromycin in patients with renal impairment
    Shi, J
    Montay, G
    Chapel, S
    Hardy, P
    Barrett, JS
    Sack, M
    Marbury, T
    Swan, SK
    Vargas, R
    Leclerc, V
    Leroy, B
    Bhargava, VO
    JOURNAL OF CLINICAL PHARMACOLOGY, 2004, 44 (03): : 234 - 244
  • [45] The pharmacokinetics and safety of idelalisib in subjects with severe renal impairment
    Jin, F.
    Robeson, M.
    Zhou, H.
    Hisoire, G.
    Ramanathan, S.
    CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2015, 76 (06) : 1133 - 1141
  • [46] The pharmacokinetics and safety of desvenlafaxine in subjects with chronic renal impairment
    Nichols, A. I.
    Richards, L. S.
    Behrle, J. A.
    Posener, J. A.
    McGrory, S. B.
    Paul, J.
    INTERNATIONAL JOURNAL OF CLINICAL PHARMACOLOGY AND THERAPEUTICS, 2011, 49 (01) : 3 - 13
  • [47] EFFICACY, SAFETY AND PHARMACOKINETICS OF INCLISIRAN BY RENAL FUNCTION
    Kallend, D.
    Collins, M.
    Kastelein, J.
    Landmesser, U.
    Leiter, L.
    Ray, K.
    Robson, R.
    Stoekenbroek, R.
    Wright, R. S.
    Wijngaard, P.
    ATHEROSCLEROSIS, 2019, 287 : E38 - E38
  • [48] Effect of renal impairment on the pharmacokinetics and safety of alfuzosin 10 mg OD formulation.
    Pinquier, JL
    Rauch-Desanti, C
    Miller, RP
    Stasiak, E
    Blum, RA
    Marbury, TC
    Brohier, S
    CLINICAL PHARMACOLOGY & THERAPEUTICS, 2000, 67 (02) : 111 - 111
  • [49] MILD RENAL IMPAIRMENT AND THE EFFICACY AND SAFETY OF LIRAGLUTIDE
    Davidson, Jaime A.
    Brett, Jason
    Falahati, Ali
    Scott, David
    ENDOCRINE PRACTICE, 2011, 17 (03) : 345 - 355
  • [50] The effect of renal impairment on risedronate pharmacokinetics.
    Mitchell, DY
    StPeter, JV
    Eusebio, RA
    Pallone, KA
    Kelly, SC
    Nesbitt, JD
    Russell, DA
    Powell, JH
    JOURNAL OF BONE AND MINERAL RESEARCH, 1997, 12 : F472 - F472