Literature DB >> 26201504

Pharmacokinetics and bioequivalence of a liquid formulation of hydroxyurea in children with sickle cell anemia.

Jeremie H Estepp1, Chiara Melloni2, Courtney D Thornburg3, Paweł Wiczling4, Zora Rogers5, Jennifer A Rothman6, Nancy S Green7, Robert Liem8, Amanda M Brandow9, Shelley E Crary10, Thomas H Howard11, Maurine H Morris12, Andrew Lewandowski13, Uttam Garg14, William J Jusko15, Kathleen A Neville16.   

Abstract

Hydroxyurea (HU) is a crucial therapy for children with sickle cell anemia, but its off-label use is a barrier to widespread acceptance. We found HU exposure is not significantly altered by liquid vs capsule formulation, and weight-based dosing schemes provide consistent exposure. HU is recommended for all children starting as young as 9 months of age with sickle cell anemia (SCA; HbSS and HbSβspan(0) thalassemia); however; a paucity of pediatric data exists regarding the pharmacokinetics (PK) or the exposure-response relationship of HU. This trial aimed to characterize the PK of HU in children and to evaluate and compare the bioavailability of a liquid vs capsule formulation. This multicenter; prospective; open-label trial enrolled 39 children with SCA who provided 682 plasma samples for PK analysis following administration of HU. Noncompartmental and population PK models are described. We report that liquid and capsule formulations of HU are bioequivalent; weight-based dosing schemes provide consistent drug exposure; and age-based dosing schemes are unnecessary. These data support the use of liquid HU in children unable to swallow capsules and in those whose weight precludes the use of fixed capsule formulations. Taken with existing safety and efficacy literature; these findings should encourage the use of HU across the spectrum of age and weight in children with SCA; and they should facilitate the expanded use of HU as recommended in the National Heart; Lung; and Blood Institute guidelines for individuals with SCA.
© 2015, The American College of Clinical Pharmacology.

Entities:  

Keywords:  bioequivalent; hydroxyurea. children; sickle cell anemia

Mesh:

Substances:

Year:  2015        PMID: 26201504      PMCID: PMC4892120          DOI: 10.1002/jcph.598

Source DB:  PubMed          Journal:  J Clin Pharmacol        ISSN: 0091-2700            Impact factor:   3.126


  23 in total

1.  Do difficulties in swallowing medication impede the use of hydroxyurea in children?

Authors:  ElShadey Bekele; Courtney D Thornburg; Amanda M Brandow; Mukta Sharma; Arlene M Smaldone; Zhezhen Jin; Nancy S Green
Journal:  Pediatr Blood Cancer       Date:  2014-04-17       Impact factor: 3.167

2.  Isotope-dilution gas chromatography-mass spectrometry method for the analysis of hydroxyurea.

Authors:  Uttam Garg; David Scott; Clint Frazee; Gregory Kearns; Kathleen Neville
Journal:  Ther Drug Monit       Date:  2015-06       Impact factor: 3.681

3.  Hydroxycarbamide in very young children with sickle-cell anaemia: a multicentre, randomised, controlled trial (BABY HUG).

Authors:  Winfred C Wang; Russell E Ware; Scott T Miller; Rathi V Iyer; James F Casella; Caterina P Minniti; Sohail Rana; Courtney D Thornburg; Zora R Rogers; Ram V Kalpatthi; Julio C Barredo; R Clark Brown; Sharada A Sarnaik; Thomas H Howard; Lynn W Wynn; Abdullah Kutlar; F Daniel Armstrong; Beatrice A Files; Jonathan C Goldsmith; Myron A Waclawiw; Xiangke Huang; Bruce W Thompson
Journal:  Lancet       Date:  2011-05-14       Impact factor: 79.321

4.  Long-term hydroxyurea therapy for infants with sickle cell anemia: the HUSOFT extension study.

Authors:  Jane S Hankins; Russell E Ware; Zora R Rogers; Lynn W Wynn; Peter A Lane; J Paul Scott; Winfred C Wang
Journal:  Blood       Date:  2005-10-01       Impact factor: 22.113

5.  Pharmacokinetics of hydroxyurea 1,000 mg coated breakable tablets and 500 mg capsules in pediatric and adult patients with sickle cell disease.

Authors:  Mariane de Montalembert; Dora Bachir; Anne Hulin; Linda Gimeno; Agnès Mogenet; Jean Louis Bresson; Isabelle Macquin-Mavier; Françoise Roudot-Thoraval; Alain Astier; Frédéric Galactéros
Journal:  Haematologica       Date:  2006-12       Impact factor: 9.941

6.  Safety of hydroxyurea in children with sickle cell anemia: results of the HUG-KIDS study, a phase I/II trial. Pediatric Hydroxyurea Group.

Authors:  T R Kinney; R W Helms; E E O'Branski; K Ohene-Frempong; W Wang; C Daeschner; E Vichinsky; R Redding-Lallinger; B Gee; O S Platt; R E Ware
Journal:  Blood       Date:  1999-09-01       Impact factor: 22.113

7.  Organic anion transporting polypeptide 1B transporters modulate hydroxyurea pharmacokinetics.

Authors:  Aisha L Walker; Cynthia S Lancaster; David Finkelstein; Russell E Ware; Alex Sparreboom
Journal:  Am J Physiol Cell Physiol       Date:  2013-08-28       Impact factor: 4.249

8.  Parental and other factors associated with hydroxyurea use for pediatric sickle cell disease.

Authors:  Suzette O Oyeku; M Catherine Driscoll; Hillel W Cohen; Rebecca Trachtman; Farzana Pashankar; Craig Mullen; Patricia J Giardina; Nerissa Velazco; Andrew D Racine; Nancy S Green
Journal:  Pediatr Blood Cancer       Date:  2012-11-05       Impact factor: 3.167

Review 9.  Management of sickle cell disease: summary of the 2014 evidence-based report by expert panel members.

Authors:  Barbara P Yawn; George R Buchanan; Araba N Afenyi-Annan; Samir K Ballas; Kathryn L Hassell; Andra H James; Lanetta Jordan; Sophie M Lanzkron; Richard Lottenberg; William J Savage; Paula J Tanabe; Russell E Ware; M Hassan Murad; Jonathan C Goldsmith; Eduardo Ortiz; Robinson Fulwood; Ann Horton; Joylene John-Sowah
Journal:  JAMA       Date:  2014-09-10       Impact factor: 56.272

10.  A pilot study of hydroxyurea to prevent chronic organ damage in young children with sickle cell anemia.

Authors:  Courtney D Thornburg; Natalia Dixon; Shelly Burgett; Nicole A Mortier; William H Schultz; Sherri A Zimmerman; Melanie Bonner; Kristina K Hardy; Agustin Calatroni; Russell E Ware
Journal:  Pediatr Blood Cancer       Date:  2009-05       Impact factor: 3.167

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  9 in total

1.  A clinically meaningful fetal hemoglobin threshold for children with sickle cell anemia during hydroxyurea therapy.

Authors:  Jeremie H Estepp; Matthew P Smeltzer; Guolian Kang; Chen Li; Winfred C Wang; Christina Abrams; Banu Aygun; Russell E Ware; Kerri Nottage; Jane S Hankins
Journal:  Am J Hematol       Date:  2017-09-28       Impact factor: 10.047

2.  Model-based dosing with concentration feedback as an integral part of personalized hydroxycarbamide management.

Authors:  Min Dong; Patrick T McGann; Tomoyuki Mizuno; Russell E Ware; Alexander A Vinks
Journal:  Br J Clin Pharmacol       Date:  2018-04-17       Impact factor: 4.335

Review 3.  Hydroxyurea (hydroxycarbamide) for sickle cell disease.

Authors:  Angela E Rankine-Mullings; Sarah J Nevitt
Journal:  Cochrane Database Syst Rev       Date:  2022-09-01

4.  Compounded Nonsterile Preparations and FDA-Approved Commercially Available Liquid Products for Children: A North American Update.

Authors:  Richard H Parrish; Lisa D Ashworth; Raimar Löbenberg; Sandra Benavides; Jeffrey J Cies; Robert B MacArthur
Journal:  Pharmaceutics       Date:  2022-05-10       Impact factor: 6.525

5.  Mathematical Modeling of Hydroxyurea Therapy in Individuals with Sickle Cell Disease.

Authors:  Akancha Pandey; Jeremie H Estepp; Rubesh Raja; Guolian Kang; Doraiswami Ramkrishna
Journal:  Pharmaceutics       Date:  2022-05-16       Impact factor: 6.525

6.  Stability evaluation of compounded hydroxyurea 100 mg/mL oral liquids using a novel analytical method involving chemical derivatization.

Authors:  Daphné Coache; Mihaela Friciu; Ruth Bernine Marcellin; Lola Bonnemain; Annie Viau; V Gaëlle Roullin; Jean-Marc Forest; Grégoire Leclair
Journal:  PLoS One       Date:  2022-06-24       Impact factor: 3.752

Review 7.  Minireview: Prognostic factors and the response to hydroxurea treatment in sickle cell disease.

Authors:  Winfred C Wang
Journal:  Exp Biol Med (Maywood)       Date:  2016-03-29

8.  Hydroxycarbamide in children with sickle cell anaemia after first-dose vs. chronic therapy: pharmacokinetics and predictive models for drug exposure.

Authors:  Jeremie H Estepp; Paweł Wiczling; Joseph Moen; Guolian Kang; Joana Marie Mack; Robert Liem; Julie A Panepinto; Uttam Garg; Gregory Kearns; Kathleen A Neville
Journal:  Br J Clin Pharmacol       Date:  2017-11-28       Impact factor: 4.335

9.  Tolerability and age-dependent toxicokinetics following perinatal hydroxyurea treatment in Sprague Dawley rats.

Authors:  Madelyn C Huang; Katie J Turner; Molly Vallant; Veronica G Robinson; Yi Lu; Catherine J Price; Timothy R Fennell; Melanie A Silinski; Suramya Waidyanatha; Kristen R Ryan; Sherry R Black; Reshan A Fernando; Barry S McIntyre
Journal:  J Appl Toxicol       Date:  2020-11-25       Impact factor: 3.628

  9 in total

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