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Healthy Male Volunteers clinical trials

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NCT ID: NCT04086719 Completed - Clinical trials for Healthy Male Volunteers

An Investigational Study to Determine the Drug Level Profile of BMS-986165 in Healthy Male Volunteers Following Transporter Inhibition.

Start date: September 12, 2019
Phase: Phase 1
Study type: Interventional

Study of what the body does to drug BMS-986165 when it is taken together with pyrimethamine

NCT ID: NCT03941340 Completed - Clinical trials for Healthy Male Volunteers

Study Evaluating the Mass Balance And Biotransformation of Single Dose[14C] AST2818 in Chinese Healthy Male Volunteers

Start date: April 8, 2019
Phase: Phase 1
Study type: Interventional

Study to Evaluate the Mass Balance and Biotransformation of Single Dose[14C] AST2818 in Chinese Healthy Male Volunteers

NCT ID: NCT03926182 Completed - Clinical trials for Healthy Male Volunteers

Study to Determine the Effect of Food on the Blood Levels of AST2818 Following Single Oral Doses in Healthy Male Volunteers

Start date: February 19, 2019
Phase: Phase 1
Study type: Interventional

To assess the Effect of Food on the Blood Levels of AST2818 Following Single Oral Doses in Healthy Male Volunteers in Fasting State or Following a High Fat Meal

NCT ID: NCT03810664 Completed - Clinical trials for Healthy Male Volunteers

A Clinical Study Investigating the Comparability of Somatrogon in Two Different Drug Product Presentations

Start date: January 18, 2019
Phase: Phase 1
Study type: Interventional

This is a Phase 1, single-center, open-label randomized, 2×2 crossover (Ref Test | Test Ref) study with a washout of two weeks to establish bioequivalence between single dose of somatrogon in a PEN to somatrogon in VIAL administered sc in healthy male volunteers.

NCT ID: NCT03686501 Completed - Clinical trials for Healthy Male Volunteers

D1 Receptor Occupancy (RO) Following a Single Dose of PF-06412562

Start date: September 10, 2018
Phase: Early Phase 1
Study type: Interventional

To assess the D1 receptor occupancy (D1 RO) in striatum after a single oral administration of PF-06412562.

NCT ID: NCT03532854 Completed - Clinical trials for Healthy Male Volunteers

Evaluating a Pharmacokinetic Drug Interaction Between LGEV1801 and LGEV1802

Start date: May 28, 2018
Phase: Phase 1
Study type: Interventional

The purpose of this study is to evaluate the drug-drug interaction between LGEV1801 and LGEV1802 in healthy male volunteers.

NCT ID: NCT03468725 Completed - Clinical trials for Healthy Male Volunteers

Safety, Tolerability, Pharmacokinetics and Effects on Transcranial Magnetic Stimulation of Oral Doses of XEN1101

Start date: February 13, 2018
Phase: Phase 1
Study type: Interventional

The XEN1101 Phase 1 clinical trial is a randomized, double-blind, placebo-controlled study that will eventuate the safety, tolerability, pharmacokinetics (PK) and effects on transcranial magnetic stimulation (TMS) of oral doses of XEN1101 in healthy male subjects.The TMS procedure is designed to demonstrate delivery of XEN1101 into the central nervous system and to observe a change in cortical excitability as measured by EEG and/or EMG activity. It is estimated there will be approximately 15 subjects in the planned study.

NCT ID: NCT03464227 Completed - Clinical trials for Healthy Male Volunteers

A Study to Test the Safety, Pharmacokinetics, and Pharmacodynamics of Single Ascending Intravenous Doses of UCB0107 in Healthy Male Subjects

Start date: February 16, 2018
Phase: Phase 1
Study type: Interventional

The purpose of the study is to evaluate the safety and tolerability of single ascending doses of UCB0107 administered by intravenous (iv) infusion in healthy male subjects.

NCT ID: NCT03378284 Completed - Clinical trials for Healthy Male Volunteers

A Study to Evaluate Safety, Tolerability, and PD of Tegoprazan on Healthy Male Volunteers

Start date: December 10, 2017
Phase: Phase 1
Study type: Interventional

A randomized, open-label, active-controlled, multiple dose phase 1 clinical trial to evaluate safety, tolerability, and pharmacodynamics of tegoprazan after oral administration in healthy male volunteers

NCT ID: NCT03355014 Completed - Clinical trials for Healthy Male Volunteers

BE Study of the Combinations of Gemigliptin/Metformin HCl Extended Release 50/1000mg(25/500mg x 2 Tablets) in Comparison to Each Component Administered Alone

Start date: December 13, 2017
Phase: Phase 1
Study type: Interventional

This study is to compare the safety/tolerability and pharmacokinetics/pharmacodynamics of the fixed-dose combinations of gemigliptin/metformin HCl sustained release 50/1000 mg (25/500 mg x 2 tablets) in comparison to each component gemigliptin 50 mg and metformin HCl extended release 1000 mg (500mg x 2 tablets) under fasting and fed conditions in healthy male volunteers.