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Adult Healthy Volunteers clinical trials

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NCT ID: NCT06204250 Recruiting - Vasomotor Symptoms Clinical Trials

A Study to Assess Safety and Tolerability of GS1-144 in Healthy Volunteers

Start date: February 27, 2024
Phase: Phase 1
Study type: Interventional

The primary purpose of this study is to assess the safety and tolerability of single ascending doses of GS1-144 in healthy participants in Part 1 and to assess the safety and tolerability of multiple ascending doses of GS1-144 in healthy postmenopausal female participants in Part 2.

NCT ID: NCT05852275 Recruiting - Clinical trials for Adult Healthy Volunteers

O-LIVE: Impact of a Portuguese Olive Oil in Health Biomarkers

O-LIVE
Start date: September 1, 2022
Phase: N/A
Study type: Interventional

This research project, approved and funded, is part of a larger project, entitled "Healthy Soil for Food", which completes several work packages, one of which is a clinical research submitted to Ethics Committee entitled "O-LIVE: Impact of olive oil Portuguese in biomarkers of healthy volunteers". The main objective of this work is to evaluate the impact of ingestion of an olive oil rich in polyphenols on clinical biomarkers and parameters, such as anthropometric measurements, on inflammatory gene expression regulation and on the composition of the intestinal microbiota.

NCT ID: NCT01885624 Completed - Clinical trials for Adult Healthy Volunteers

Open Label Phase 1 Pharmacokinetics and Tolerability Study of Single TAB08 Administration in Healthy Volunteers

Start date: November 2011
Phase: Phase 1
Study type: Interventional

The purpose of this study is to assess safety and tolerability of ascending dosed of TAB08 after single i.v. infusion to the adult healthy volunteers. Additionally were assessed infusion speed tolerability, pharmacokinetics and pharmacodynamics of TAB08 after single i.v. infusion and to explore TAB mechanism-of-action biomarkers.

NCT ID: NCT01495442 Completed - Clinical trials for Adult Healthy Volunteers

Evaluation of a Dry Powder Aerosol Dispersion Mechanism by Radiolabeling Techniques

DPI
Start date: December 2011
Phase: N/A
Study type: Interventional

The primary objective is to admix a radiolabel with albuterol sulphate for incorporation into the Handihaler® device for inhalation studies. This will allow for the investigators to determine the regional lung deposition of drug inhaled from the standard Handihaler® device compared to a novel modification of the device to provide more effective dispersion and aerosolization of the coated albuterol powder. The new mechanism of action for proof-of-concept testing consists of a bead (5.1 mm; expanded polystyrene foam) coated with drug powder, as opposed to the standard lactose formulation-filled capsule.