Literature DB >> 25239269

Eliglustat: first global approval.

Raewyn M Poole1.   

Abstract

Eliglustat [Cerdelga™ (US, EU)], a small-molecule oral glucosylceramide analogue that inhibits the enzyme glucosylceramide synthase has been developed by Genzyme Corporation (a subsidiary of Sanofi) for the treatment of Gaucher disease type 1 in adults. Inhibition of this enzyme reduces the accumulation of the lipid glucosylceramide in the liver, spleen, bone marrow and other organs. Eliglustat received its first global approval in this indication in the US, for use in treatment-naïve and treatment-experienced adult patients. It is also under regulatory review in the EU and Japan. This article summarizes the milestones in the development of eliglustat leading to this first approval for Gaucher disease type 1.

Entities:  

Mesh:

Substances:

Year:  2014        PMID: 25239269     DOI: 10.1007/s40265-014-0296-3

Source DB:  PubMed          Journal:  Drugs        ISSN: 0012-6667            Impact factor:   9.546


  12 in total

1.  The substrate is down: is the IV out?

Authors:  Jeff Szer
Journal:  Blood       Date:  2010-08-12       Impact factor: 22.113

Review 2.  Oral small molecule therapy for lysosomal storage diseases.

Authors:  Neal J Weinreb
Journal:  Pediatr Endocrinol Rev       Date:  2013-11

3.  A phase 2 study of eliglustat tartrate (Genz-112638), an oral substrate reduction therapy for Gaucher disease type 1.

Authors:  Elena Lukina; Nora Watman; Elsa Avila Arreguin; Maryam Banikazemi; Marta Dragosky; Marcelo Iastrebner; Hanna Rosenbaum; Mici Phillips; Gregory M Pastores; Daniel I Rosenthal; Mathilde Kaper; Tejdip Singh; Ana Cristina Puga; Peter L Bonate; M Judith Peterschmitt
Journal:  Blood       Date:  2010-05-03       Impact factor: 22.113

4.  Safety, tolerability, and pharmacokinetics of eliglustat tartrate (Genz-112638) after single doses, multiple doses, and food in healthy volunteers.

Authors:  M Judith Peterschmitt; Amy Burke; Larry Blankstein; Sharon E Smith; Ana Cristina Puga; William G Kramer; James A Harris; David Mathews; Peter L Bonate
Journal:  J Clin Pharmacol       Date:  2010-09-23       Impact factor: 3.126

Review 5.  Gaucher disease and its treatment options.

Authors:  Lunawati L Bennett; Devipriya Mohan
Journal:  Ann Pharmacother       Date:  2013-09       Impact factor: 3.154

6.  Immunosurveillance of alglucerase enzyme therapy for Gaucher patients: induction of humoral tolerance in seroconverted patients after repeat administration.

Authors:  M Rosenberg; W Kingma; M A Fitzpatrick; S M Richards
Journal:  Blood       Date:  1999-03-15       Impact factor: 22.113

7.  Antibody response in patients with Gaucher disease after repeated infusion with macrophage-targeted glucocerebrosidase.

Authors:  S M Richards; T A Olson; J M McPherson
Journal:  Blood       Date:  1993-09-01       Impact factor: 22.113

Review 8.  The design and clinical development of inhibitors of glycosphingolipid synthesis: will invention be the mother of necessity?

Authors:  James A Shayman
Journal:  Trans Am Clin Climatol Assoc       Date:  2013

9.  Clinical response to eliglustat in treatment-naïve patients with Gaucher disease type 1: Post-hoc comparison to imiglucerase-treated patients enrolled in the International Collaborative Gaucher Group Gaucher Registry.

Authors:  Jennifer Ibrahim; Lisa H Underhill; John S Taylor; Jennifer Angell; M Judith Peterschmitt
Journal:  Mol Genet Metab Rep       Date:  2016-06-27

10.  Skeletal improvement in patients with Gaucher disease type 1: a phase 2 trial of oral eliglustat.

Authors:  Ravi S Kamath; Elena Lukina; Nora Watman; Marta Dragosky; Gregory M Pastores; Elsa Avila Arreguin; Hanna Rosenbaum; Ari Zimran; Rasha Aguzzi; Ana Cristina Puga; Andrea M Norfleet; M Judith Peterschmitt; Daniel I Rosenthal
Journal:  Skeletal Radiol       Date:  2014-05-10       Impact factor: 2.199

View more
  12 in total

Review 1.  Lysosomal storage diseases.

Authors:  Frances M Platt; Alessandra d'Azzo; Beverly L Davidson; Elizabeth F Neufeld; Cynthia J Tifft
Journal:  Nat Rev Dis Primers       Date:  2018-10-01       Impact factor: 52.329

2.  A peptide-linked recombinant glucocerebrosidase for targeted neuronal delivery: Design, production, and assessment.

Authors:  Paul A Gramlich; Wendy Westbroek; Ricardo A Feldman; Ola Awad; Nicholas Mello; Mary P Remington; Ying Sun; Wujuan Zhang; Ellen Sidransky; Michael J Betenbaugh; Paul S Fishman
Journal:  J Biotechnol       Date:  2016-01-18       Impact factor: 3.307

3.  Ubiquitous transgene expression of the glucosylceramide-synthesizing enzyme accelerates glucosylceramide accumulation and storage cells in a Gaucher disease mouse model.

Authors:  Sonya Barnes; You-Hai Xu; Wujuan Zhang; Benjamin Liou; Kenneth D R Setchell; Liming Bao; Gregory A Grabowski; Ying Sun
Journal:  PLoS One       Date:  2014-12-31       Impact factor: 3.240

4.  Attitudes of Individuals with Gaucher Disease toward Substrate Reduction Therapies.

Authors:  Victoria F Wagner; Hope Northrup; S Shahrukh Hashmi; Joanne M Nguyen; Mary Kay Koenig; Jessica M Davis
Journal:  J Genet Couns       Date:  2017-08-13       Impact factor: 2.537

Review 5.  Induced pluripotent stem cell models of lysosomal storage disorders.

Authors:  Daniel K Borger; Benjamin McMahon; Tamanna Roshan Lal; Jenny Serra-Vinardell; Elma Aflaki; Ellen Sidransky
Journal:  Dis Model Mech       Date:  2017-06-01       Impact factor: 5.758

Review 6.  Protection against Shiga Toxins.

Authors:  Simona Kavaliauskiene; Anne Berit Dyve Lingelem; Tore Skotland; Kirsten Sandvig
Journal:  Toxins (Basel)       Date:  2017-02-03       Impact factor: 4.546

7.  Visualization of Active Glucocerebrosidase in Rodent Brain with High Spatial Resolution following In Situ Labeling with Fluorescent Activity Based Probes.

Authors:  Daniela Herrera Moro Chao; Wouter W Kallemeijn; Andre R A Marques; Marie Orre; Roelof Ottenhoff; Cindy van Roomen; Ewout Foppen; Maria C Renner; Martina Moeton; Marco van Eijk; Rolf G Boot; Willem Kamphuis; Elly M Hol; Jan Aten; Hermen S Overkleeft; Andries Kalsbeek; Johannes M F G Aerts
Journal:  PLoS One       Date:  2015-09-29       Impact factor: 3.240

Review 8.  Eliglustat tartrate for the treatment of adults with type 1 Gaucher disease.

Authors:  Lunawati L Bennett; Kelsey Turcotte
Journal:  Drug Des Devel Ther       Date:  2015-08-18       Impact factor: 4.162

9.  Targeting glucosylceramide synthase upregulation reverts sorafenib resistance in experimental hepatocellular carcinoma.

Authors:  Milica Stefanovic; Anna Tutusaus; Guillermo A Martinez-Nieto; Cristina Bárcena; Estefania de Gregorio; Catia Moutinho; Elisabet Barbero-Camps; Alberto Villanueva; Anna Colell; Montserrat Marí; Carmen García-Ruiz; Jose C Fernandez-Checa; Albert Morales
Journal:  Oncotarget       Date:  2016-02-16

10.  Rare GBA1 genotype associated with severe bone disease in Gaucher disease type 1.

Authors:  Livia d'Avila Paskulin; Rodrigo Tzovenos Starosta; Vitória Schütt Zizemer; Suélen Basgalupp; Débora Bertholdo; Filippo Pinto E Vairo; Marina Siebert; Kristiane Michelin-Tirelli; Ida Vanessa Doederlein Schwartz
Journal:  Mol Genet Metab Rep       Date:  2019-11-22
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.