跳至主要内容
临床试验/ACTRN12617001330336
ACTRN12617001330336已完成1 期

A Phase 1, Single-Center, Randomized, Placebo-Controlled, Ascending Single-Dose Study of the Pharmacokinetics, Safety, and Tolerability of Oral XG005 in Healthy Volunteers

Xgene Pharmaceutical Inc.0 个研究点目标入组 50 人开始时间: 2017年9月18日最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
发起方
入组人数
50

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 Years 至 55 Years(—)
性别
All

入选标准

  • 未提供

排除标准

  • 未提供

研究者

发起方
Xgene Pharmaceutical Inc.

相似试验

已完成
1 期
A Phase 1 Single-Center, Randomized, Placebo-Controlled, Double-Blind Pilot Study to Evaluate the Safety, Tolerability and Preliminary Efficacy of a Candidate Topical Antimicrobial (NEO101) in the Reduction of Propionibacterium acnes among Healthy Young Adult MePropionibacterium acnes amongst healthy volunteersSkin - Dermatological conditions
ACTRN12606000424505eosil, Inc.30
已完成
1 期
A phase 1, randomized, placebo-controlled study to evaluate the safety, tolerability, and pharmacokinetic profiles of OLX10010 in healthy subjects compared to placebo
ISRCTN64317949OliX Pharmaceuticals, Inc.48
已完成
不适用
A Phase 1, Single-Center, Single-Blind, Placebo and Propofol Controlled Study in Healthy Subjects to Assess the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Single Ascending Intravenous (IV) Infusion Doses of ABP-700anesthesia
NL-OMON41980Annovation Biopharma, Inc. (a wholly owned subsidiary of The Medicines Company, Inc.)72
已完成
1 期
A Phase 1 Randomized, Placebo-Controlled, Single & Multiple Ascending Dose Study to Evaluate the Safety and Tolerability of GLY-200 in Healthy Adult SubjectsMetabolic and Endocrine - DiabetesType 2 Diabetes
ACTRN12621000800820Glyscend Pty Ltd64
已完成
不适用
Phase I, Single-Center, Randomized, Placebo-Controlled, Double-Blinded Study with Single Ascending Doses, Evaluating the Safety and Tolerability of T20K, Administered by a 1-hr IV Infusion in Healthy Male VolunteersMultiple Sclerosis
NL-OMON48273Cyxone AB40