A Phase III Randomized, Double-blind, Placebo-controlled Multicenter Study in Adults to Determine the Safety, Efficacy, and Immunogenicity of AZD1222, a Non-replicating ChAdOx1 Vector Vaccine, for the Prevention of COVID-19 (Bronx)
		
	
		
			
				| Sponsor: | AstraZeneca | 
			
			
				| Enrolling: | Male and Female Patients | 
							
					| Study Length: | 24 Months | 
						
							
					| Clinic Visits: | 7 | 
			
			
                            
                    | IRB Number: | AAAT2402 | 
            
			 
				
					| U.S. Govt. ID: | NCT04516746 | 
					
			
				| Contact: | Logan Posey: 347-590-7280 / lp2907@cumc.columbia.edu | 
		
	
		The aim of the study is to assess the safety, efficacy, and immunogenicity of AZD1222 for the prevention of COVID-19. The COVID-19 pandemic has caused major disruption to healthcare systems with significant socioeconomic impacts. Currently, there are no specific treatments available against COVID-19 and accelerated vaccine development is urgently needed. A safe and effective vaccine for COVID-19 prevention would have significant public health impact.
	
			This study is closed
	
	   	
		Investigator
		
		Jessica Justman, MD
		
					   
	
		
		
		
			
				
					| Are you 18 years old or older? | Yes | No | 
				
									
						| Have you ever tested positive for Sars-Co-V-2 (Covid-19)? | Yes | No | 
								
									
						| Are you currently pregnant? If N/A select No. | Yes | No | 
				
									
						| Are you preventing pregnancy (i.e. birth control)? If N/A select Yes. | Yes | No | 
				
									
						| Are you willing to travel to the South Bronx for participation in this study? | Yes | No |