A Phase 1 Study to Evaluate the Bioequivalence of Oral Tablet and Orally Dissolving Tablet Formulations of Rimegepant in Healthy Adult Subjects Under Fasting Conditions

Croop R.; Ivans A.; Stock D.; Hould J.; Morris B. A.; Stringfellow J.; Moulin J.; Larouche R.; Tanguay M.; Coric V; Lipton R. B.

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A Phase 1 Study to Evaluate the Bioequivalence of Oral Tablet and Orally Dissolving Tablet Formulations of Rimegepant in Healthy Adult Subjects Under Fasting Conditions

机译：第1阶段研究，以评估口服片剂的生物等效性，在禁食条件下健康成人受试者中的重新溶解矿床

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来源
《Headache 》 |2018年第8期| 共2页
作者
Croop R.; Ivans A.; Stock D.; Hould J.; Morris B. A.; Stringfellow J.; Moulin J.; Larouche R.; Tanguay M.; Coric V; Lipton R. B.;
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作者单位

Biohaven Pharmaceut Inc New Haven CT USA;

Biohaven Pharmaceut Inc New Haven CT USA;

Biohaven Pharmaceut Inc New Haven CT USA;

Biohaven Pharmaceut Inc New Haven CT USA;

Biohaven Pharmaceut Inc New Haven CT USA;

Syneos Hlth Quebec City PQ Canada;

Syneos Hlth Quebec City PQ Canada;

Syneos Hlth Quebec City PQ Canada;

Biohaven Pharmaceut Inc New Haven CT USA;

Albert Einstein Coll Med Bronx NY 10467 USA;

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正文语种 eng
中图分类诊断学 ;
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1. A Phase 1 Study to Evaluate the Bioequivalence of Oral Tablet and Orally Dissolving Tablet Formulations of Rimegepant in Healthy Adult Subjects Under Fasting Conditions [J] . Croop R., Ivans A., Stock D., Headache . 2018 ,第8期

机译：第1阶段研究，以评估口服片剂的生物等效性，在禁食条件下健康成人受试者中的重新溶解矿床
2. A comparative, bioequivalence study to evaluate the safety and pharmacokinetic profile of single dose Ivabradine 7.5mg tablets in healthy, adult, human subjects under fasting condition [J] . RandDCenterMacleodsPharmaceuticalsLtd, SchoolofPharmacyandTechnologyManagementNarseeMonjeeInstituteofManagementandHigherStudies Research journal of pharmacy and technology . 2012 ,第5期

机译：一项比较性的生物等效性研究，评估禁食条件下健康，成人，人类受试者中单剂量伊伐布雷定7.5mg片剂的安全性和药代动力学
3. Pilot study of relative bioavailability of two oral formulations of ketoprofen 25 mg in healthy subjects. A fast-dissolving lyophilized tablet as compared to immediate release tablet. [J] . Ahmed IS, Fatahalla FA Drug development and industrial pharmacy . 2007 ,第5期

机译：两种酮洛芬25毫克口服制剂在健康受试者中的相对生物利用度的初步研究。与速释片剂相比，速溶冻干片剂。
4. Formulation And Evaluation Of Sustained Release Orally Disintegrating Tablets OfMetoclopramide Hydrochloride Intended For Gastro retention [C] . Shidhaye.S, Malke .S, Kadam.V, Annual meeting exposition of the Controlled Release Society . 2009

机译：胃胃retention留用盐酸甲氧氯普胺缓释口腔崩解片的研制与评价
5. 1. A novel self-sealing chewable sustained release tablet of acetaminophen, 2. Development and evaluation of novel itraconazole oral formulations, 3. A novel zero order release matrix tablet. [D] . Rakkanka, Vipaporn. 2003

机译：1.新型对乙酰氨基酚自密封咀嚼型缓释片剂，2.新型伊曲康唑口服制剂的开发和评估，3.新型零级释放基质片剂。
6. Bioequivalence Evaluation of Two Formulations of Tenofovir Alafenamide Tablets in Healthy Subjects Under Fasting and Fed Conditions [O] . Qiuying Li, Lihui Jia, Wenli Hu, 2021

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7. Bioequivalence of Two Oral Formulations of Modafinil Tablets in Healthy Male Subjects under Fed and Fasting Conditions [O] . AlSayed Sallam Isam I 2015

机译：在喂养和禁食条件下健康男性对母体受试者中制剂两种口服配方的生物等效性

A Phase 1 Study to Evaluate the Bioequivalence of Oral Tablet and Orally Dissolving Tablet Formulations of Rimegepant in Healthy Adult Subjects Under Fasting Conditions

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