Literature DB >> 26536331

Oral Delivery of Therapeutic Proteins and Peptides: An Overview of Current Technologies and Recommendations for Bridging from Approved Intravenous or Subcutaneous Administration to Novel Oral Regimens.

M Philippart1, J Schmidt2, B Bittner2.   

Abstract

Since the early 1980s, therapeutic proteins and peptides have become established as an important class of pharmaceuticals. Due to their low oral bioavailability, which results from pre-systemic degradation and poor gastrointestinal absorption, most therapeutic proteins and peptides are administered intravenously. While subcutaneous formulations of some therapeutic proteins and peptides have been shown to improve patient convenience and reduce medical resource utilization, oral administration is generally the preferred administration route. Some therapeutic proteins and peptides employing novel oral delivery technologies have reached late-stage clinical development. To develop a new oral formulation of a therapeutic protein or peptide currently marketed as an injectable product, technical, nonclinical, and clinical studies are required to demonstrate similar safety and efficacy compared with the existing administration route. Since there is little experience with oral therapeutic proteins and peptides, this review provides recommendations for bridging from an approved intravenous or subcutaneous regimen to novel oral administration of the same therapeutic protein or peptide, based on precedents from intravenous-to-subcutaneous bridging approaches for trastuzumab, rituximab, tocilizumab, and bortezomib. If the pharmacokinetic/pharmacodynamic relationship is well characterized, demonstration of comparability in prespecified pharmacokinetic parameters might form a basis for establishing similar efficacy and safety of the oral formulation vs. the reference product. Although oral administration of therapeutic proteins and peptides remains challenging, given recent progress with novel delivery technologies, intravenous/subcutaneous-to-oral nonclinical and clinical bridging programs may soon be utilized to support approval of new oral formulations. © Georg Thieme Verlag KG Stuttgart · New York.

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Year:  2015        PMID: 26536331     DOI: 10.1055/s-0035-1559654

Source DB:  PubMed          Journal:  Drug Res (Stuttg)        ISSN: 2194-9379


  10 in total

1.  Effect of Additional Oral Semaglutide vs Sitagliptin on Glycated Hemoglobin in Adults With Type 2 Diabetes Uncontrolled With Metformin Alone or With Sulfonylurea: The PIONEER 3 Randomized Clinical Trial.

Authors:  Julio Rosenstock; Dale Allison; Andreas L Birkenfeld; Thalia Marie Blicher; Srikanth Deenadayalan; Jacob Bonde Jacobsen; Pierre Serusclat; Rafael Violante; Hirotaka Watada; Melanie Davies
Journal:  JAMA       Date:  2019-04-16       Impact factor: 56.272

2.  In silico approaches for predicting the half-life of natural and modified peptides in blood.

Authors:  Deepika Mathur; Sandeep Singh; Ayesha Mehta; Piyush Agrawal; Gajendra P S Raghava
Journal:  PLoS One       Date:  2018-06-01       Impact factor: 3.240

Review 3.  Oral delivery of protein and peptide drugs: from non-specific formulation approaches to intestinal cell targeting strategies.

Authors:  Guanyu Chen; Weirong Kang; Wanqiong Li; Shaomeng Chen; Yanfeng Gao
Journal:  Theranostics       Date:  2022-01-01       Impact factor: 11.556

Review 4.  Oral GLP-1 analogue: perspectives and impact on atherosclerosis in type 2 diabetic patients.

Authors:  José Francisco Kerr Saraiva; Denise Franco
Journal:  Cardiovasc Diabetol       Date:  2021-12-15       Impact factor: 9.951

5.  Quality by Design Approach for the Development of Liposome Carrying Ghrelin for Intranasal Administration.

Authors:  Cecília de Barros; Norberto Aranha; Patrícia Severino; Eliana B Souto; Aleksandra Zielińska; André Lopes; Alessandra Rios; Fernando Batain; Kessi Crescencio; Marco Chaud; Thais Alves
Journal:  Pharmaceutics       Date:  2021-05-10       Impact factor: 6.321

6.  Dispersive effects and focused biodistribution of recombinant human hyaluronidase PH20: A locally acting and transiently active permeation enhancer.

Authors:  David W Kang; Beate Bittner; Barry J Sugarman; Monica L Zepeda; Marie A Printz
Journal:  PLoS One       Date:  2021-07-22       Impact factor: 3.240

7.  TRPA1-dependent reversible opening of tight junction by natural compounds with an α,β-unsaturated moiety and capsaicin.

Authors:  Yusuke Kanda; Youhei Yamasaki; Yoshie Sasaki-Yamaguchi; Noriko Ida-Koga; Shinji Kamisuki; Fumio Sugawara; Yoko Nagumo; Takeo Usui
Journal:  Sci Rep       Date:  2018-02-02       Impact factor: 4.379

8.  Therapeutic hexapeptide (PGPIPN) prevents and cures alcoholic fatty liver disease by affecting the expressions of genes related with lipid metabolism and oxidative stress.

Authors:  Nan Qi; Chen Liu; Haoran Yang; Wanrong Shi; Shenyi Wang; Yan Zhou; Cai Wei; Fang Gu; Yide Qin
Journal:  Oncotarget       Date:  2017-09-30

Review 9.  GLP-1 Analogs and DPP-4 Inhibitors in Type 2 Diabetes Therapy: Review of Head-to-Head Clinical Trials.

Authors:  Matthew P Gilbert; Richard E Pratley
Journal:  Front Endocrinol (Lausanne)       Date:  2020-04-03       Impact factor: 5.555

10.  Crotoxin Conjugated to SBA-15 Nanostructured Mesoporous Silica Induces Long-Last Analgesic Effect in the Neuropathic Pain Model in Mice.

Authors:  Morena Brazil Sant'Anna; Flavia Souza Ribeiro Lopes; Louise Faggionato Kimura; Aline Carolina Giardini; Osvaldo Augusto Sant'Anna; Gisele Picolo
Journal:  Toxins (Basel)       Date:  2019-11-20       Impact factor: 4.546

  10 in total

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