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Clinical Pharmacology in Drug Development 期刊封面 医学
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Review Cycle Records

Clinical Pharmacology in Drug Development

Wiley SCIE 非OA
2026新锐 4区2025中科院 4区2025 JCR Q3
135.9平均天数
119中位天数
43最短天数
296最长天数
1402025发文量

Paper Review Records

全部论文审稿周期

19 篇有效样本 · 按发表日期由新到旧排列
审稿天数=录用日期-收稿日期;保留 PDF/DOI/网页源链接

88 天

Open‐Label, Balanced, Randomized, Single‐Dose, Three‐Treatment, Three‐Sequence, Three‐Period, Three‐Way Crossover Oral Bioequivalence Study of Desmopressin Acetate Oral Solution

作者Adam Christensen; Axay Parth; Mansi Kotak; Danka Radosavjevic; Catherine Gorman Moore; Byung‐Woun Seo

作者单位1. Eton Pharmaceuticals Deer Park IL USA; 2. Veeda Clinical Research, Mehsana Panchot India; 3. Veeda Clinical Research Ahmedabad Gujarat India

PDF源文件 DOI 网页
87 天

Safety, Tolerability, Pharmacokinetics, Food Effect of Ribitol, and Its Effect on QTcF in Healthy Adults: First‐in‐Human, Randomized, Double‐Blind (Sponsor Unblinded), Placebo‐Controlled Studies

作者Daniel D. Gretler; Athiwat Hutchaleelaha; Uma Sinha; Kristen Rickert; Doug Sproule

作者单位1. Bridgebio Pharma, Inc. Palo Alto CA USA

PDF源文件 DOI 网页
55 天

Phase 1 Study of Paltusotine, a Novel Oral Once‑Daily, Nonpeptide Selective Somatostatin Receptor 2 Agonist, in Healthy Japanese Adults

作者Fumio Otsuka; Keiko Hanabara; Seigo Akari; Katsunori Kitamoto; Yosuke Inagaki; Dylan Glatt; Harumi Murakami; Naoki Uchida

作者单位1. Department of General Medicine Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences Okayama Japan; 2. Medical Affairs Group Medical Affairs Department Sanwa Kagaku Kenkyusho Co., Ltd. Nagoya Japan; 3. Project Management Group Project Management Department Sanwa Kagaku Kenkyusho Co., Ltd. Nagoya Japan; 4. Clinical Development Department Sanwa Kagaku Kenkyusho Co., Ltd. Nagoya Japan; 5. Crinetics Pharmaceuticals, Inc. San Diego USA; 6. Souseikai Sumida Hospital Tokyo Japan; 7. Division of Clinical Pharmacology Department of Pharmacology Showa Medical University School of Medicine Tokyo Japan

PDF源文件 DOI 网页
43 天

Comparative bioavailability of a novel fixed‐dose combination of ticagrelor and acetylsalicylic acid

作者Susana Tera‐Ponce; Perla E. Castañeda‐Tera; Elva J. García‐Real; Francisco Ávila‐García; Kevin F. Rios‐Brito; Laura A. Lugo‐Sánchez; Daniel E. Sandoval‐Colin; Paola M. Medina‐Cárdenas; Jorge González‐Canudas

作者单位1. Department of Pharmacology Faculty of Medicine National Autonomous University of Mexico (UNAM) Mexico City Mexico; 2. Unidad Clínica Farmacológica Bioemagno S. A. de C. V Mexico City Mexico; 3. Bioanalit Laboratorios S.A. de C.V Mexico City Mexico; 4. Research and Development Department Laboratorios Silanes S.A. de C.V. Mexico City Mexico; 5. Mexican Social Security Institute (IMSS) Centro Médico Nacional Siglo XXI Mexico City Mexico

PDF源文件 DOI 网页
73 天

Pharmacokinetics and Bioequivalence of Tamsulosin Hydrochloride Extended‐Release Capsules in Healthy Chinese Volunteers: A Randomized, Open‐Label, Crossover Study Under Fasting and Fed Conditions

作者Lijie Du; Xiaolu Wang; Yi Zhang; Jiamin Yang; Fangliang Gan; Yaxun Pang

作者单位1. School of Pharmacy Hubei University of Science and Technology Xianning China; 2. Phase I Clinical Research Center Xianning Central Hospital The First Affiliated Hospital of Hubei University of Science and Technology Xianning China; 3. Department of Neurosurgery Xianning Central Hospital The First Affiliated Hospital of Hubei University of Science and Technology Xianning China

PDF源文件 DOI 网页
98 天

Pharmacokinetics and Bioequivalence Study of Levodopa and Benserazide Tablets in Healthy Chinese Subjects Under Fasting and High‐Fat Meal Conditions

作者Yufei Liang; Yanchao Wang; Rui Shi; Yingzi Pei; Xiao Zhao; Qian Wang; Yanping Ren; Zekang Xie; Kexin Zhao

作者单位1. Phase I Clinical Trials Center Hebei PetroChina Central Hospital Langfang China; 2. Department of Clinical Research Beijing Foyou Pharmaceutical Co., Ltd. Beijing China

PDF源文件 DOI 网页
119 天

Bioequivalence of Two Firsekibart Subcutaneous Formulations: A Randomized, Double‐Blind, Single‐Dose, Parallel‐Group Study in Healthy Chinese Participants

作者Yehua Xie; Xiao Li; Yushi Chen; Guangli Ma; Fei Gu; Yuling Lian; Xu Zhang; Xiaolan Yong

作者单位1. Changchun GeneScience Pharmaceutical Co., Ltd. Shanghai China; 2. Phase I Clinical Trial Center Chengdu Xinhua Hospital Chengdu China

PDF源文件 DOI 网页
152 天

Comparison of ABBV‐552 Safety and Pharmacokinetics in Healthy Asian and Western Adults

作者Nick Miles; Brian McNamee; Cindy Zadikoff; Joey Boiser; Mohamad Shebley; Ramesh Boinpally

作者单位1. Clinical Pharmacology AbbVie Inc. North Chicago IL USA; 2. Clinical Development Neuroscience AbbVie Inc. North Chicago IL USA; 3. Pharmacovigilance and Patient Safety AbbVie Inc. North Chicago IL USA

PDF源文件 DOI 网页
56 天

A Phase 1 Study to Assess the Relative Bioavailability of Brigatinib Administered as an Oral Solution Versus an Immediate‐Release Tablet in Healthy Adults

作者Michael J. Hanley; Ronald Gounden; Bradley Hupf; Saurabh Sarkar; Robert J. Fram; Neeraj Gupta

作者单位1. Takeda Development Center Americas, Inc. Cambridge MA USA

PDF源文件 DOI 网页

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我是环境工程专业,需要一篇 SCI,希望 3 个月内见刊。没有基金,也没有大牛挂名,可以投哪些期刊?

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可以。先按 90 天时限做可行性筛选,同步查找无基金、无知名作者挂靠的典型论文案例,作为选刊依据。重点核对研究质量与期刊 scope。

拟题建议
《融合机器学习与生命周期评价的城市污水处理碳排放预测与优化》

样本口径2026 年最近 5 篇有效论文样本

平均审稿96.4 天

中位数77 天

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