Found 0 matching trials
Evaluating the Safety and Efficacy of AD17002 Intranasal Spray in Treating Participants With Mild to Moderate COVID-19
PHASE2AD17002 enhances nasal mucosal innate immunity and has met safety and effic...
Location
RSPI Sulianti Saroso
Phase IIa Clinical Study of N-Rephasin® SAL200
PHASE2This study is performed to evaluate safety and to explore the efficacy of a...
Location
Seoul National University Bundang Hospital
Evaluating Safety, Tolerability, and Potential Efficacy of Intranasal AD17002 in Adults With Mild to Moderate COVID-19
PHASE1AD17002 has demonstrated superior safety and efficacy as a nasal adjuvant f...
Location
Advagene Biopharma
Dose Regimen Study of SLI-F06 in Healthy Volunteers
PHASE2Multi-center, dose-regimen, double-blind study evaluating the safety and ef...
Location
California Dermatology & Clinical Research Institute
Safety and Immunogenicity Study of tgAAC09, an HIV Vaccine in an Adeno-associated Virus (AAV) Capsid
PHASE2This phase 2 study will evaluate the safety, immunogenicity and optimal tim...
Location
Desmond Tutu HIV Centre Cape Town
A Study to Evaluate the Safety, Tolerability and Immunogenicity of Ad26.RSV.FA2 Followed by Ad35.RSV.FA2 in Healthy Adult Volunteers
PHASE1The purpose of this study is to assess the safety and tolerability of intra...
Location
Multiple Locations
Bioavailability and Pharmacokinetics of Lefamulin When Administered to Fed and Fasted Healthy Subjects
PHASE1A Phase 1 study to assess the bioavailability and pharmacokinetics of a 600...
Location
Quotient Clinical
AXER-204 in Participants With Chronic Spinal Cord Injury
PHASE1This two-part trial will assess the safety, tolerability, pharmacokinetics,...
Location
Keck Medicine of USC
Pharmacokinetics and Safety of Subcutaneous CSL324 in Healthy Japanese and White Subjects
PHASE1Study CSL324\_1003 is a single center, randomized, double-blind, placebo-co...
Location
Scientia Clinical Research Ltd
A Trial Investigating the Safety, Tolerability and Efficacy of TransCon PTH Administered Daily in Adults With Hypoparathyroidism
PHASE3During the first 26 weeks of the trial, participants were randomly assigned...
Location
Ascendis Pharma Investigational Site