Biowaiver Monograph for Immediate-Release Solid Oral Dosage Forms: Sitagliptin Phosphate Monohydrate

被引:9
作者
Charoo, Naseem A. [1 ]
Abdallah, Daud B. [2 ]
Bakheit, Ahmed Abdalla [2 ]
Ul Haque, Kashif [1 ]
Hassan, Hassan Ali [3 ]
Abrahamsson, Bertil [4 ]
Cristofoletti, Rodrigo [5 ]
Langguth, Peter [6 ]
Mehta, Mehul [7 ]
Parr, Alan [8 ]
Polli, James E. [9 ]
Shah, Vinod P. [10 ]
Tajiri, Tomokazu [11 ]
Dressman, Jennifer [12 ]
机构
[1] Succor Pharma Solut, Dubai Sci Pk, Dubai, U Arab Emirates
[2] Natl Ribat Univ, Fac Pharm, Dept Pharmaceut, Khartoum, Sudan
[3] Univ Khartoum, Fac Pharm, Dept Pharmaceut, Khartoum, Sudan
[4] Operat AstraZeneca, Pharmaceut Technol & Dev, Oral Prod Dev, Gothenburg, Sweden
[5] Brazilian Hlth Surveillance Agcy ANVISA, Div Bioequivalence, Brasilia, DF, Brazil
[6] Johannes Gutenberg Univ Mainz, Dept Pharmaceut Technol & Biopharmaceut, Mainz, Germany
[7] US FDA, Ctr Drug Evaluat & Res, Silver Spring, MD USA
[8] Bioceut LCC, Raleigh, NC USA
[9] Univ Maryland, Sch Pharm, Dept Pharmaceut Sci, Baltimore, MD 21201 USA
[10] Int Pharmaceut Federat FIP, The Hague, Netherlands
[11] Astellas Pharma Inc, Analyt Res Labs, Yaizu, Japan
[12] Fraunhofer Inst Translat Med & Pharmacol ITMP, Frankfurt, Germany
关键词
Sitagliptin phosphate monohydrate; Solubility; Therapeutic index; Pharmacokinetics; Biopharmaceutics classification system; Pharmacodynamics; Biowaiver; Permeability; DIPEPTIDYL PEPTIDASE-4 INHIBITOR; GENERAL MEDICINE; SURGERY PATIENTS; IV INHIBITOR; DOUBLE-BLIND; EFFICACY; SAFETY; PHARMACOKINETICS; BIOAVAILABILITY; MANAGEMENT;
D O I
10.1016/j.xphs.2021.09.031
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Sitagliptin is an antihyperglycemic drug used in adults for the treatment of diabetes Type 2. Literature data and in-house experiments were applied in this monograph to assess whether methods based on the Biopharmaceutics Classification System (BCS) could be used to assess the bioequivalence of solid immediate-release (IR) oral dosage forms containing sitagliptin phosphate monohydrate, as an alternative to a pharmacokinetic study in human volunteers. The solubility and permeability characteristics of sitagliptin were reviewed according to the BCS, along with dissolution, therapeutic index, therapeutic applications, pharmacokinetics, pharmacodynamic characteristics, reports of bioequivalence (BE) / bioavailability problems, data on interactions between the drug and excipients and other data germane to the subject. All data reviewed in this monograph unambiguously support classification of sitagliptin as a BCS Class 1 drug. In light of its broad therapeutic index and lack of severe adverse effects, the clinical risks associated with moderately supraoptimal doses were deemed inconsequential, as were the risks associated with moderately suboptimal doses. Taking all evidence into consideration, it was concluded that the BCS-based biowaiver can be implemented for solid IR oral drug products containing sitagliptin phosphate monohydrate, provided (a) the test product is formulated solely with excipients commonly present in solid IR oral drug products approved in ICH or associated countries and used in amounts commonly applied in this type of product, (b) data in support of the BCS-based biowaiver are obtained using the methods recommended by the WHO, FDA, EMA or ICH and (c) the test product and the comparator product (which is the innovator product in this case) meet all in vitro dissolution specifications provided in the WHO, FDA, EMA or ICH guidance. (C) 2021 American Pharmacists Association. Published by Elsevier Inc. All rights reserved.
引用
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页码:2 / 13
页数:12
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