Nicht-interventionelle Studie (Anwendungsbeobachtung) NIS-Nr.: 569
		Studiencode: CRTH258A2402
Allgemeine Angaben
		
			
			
				| Institution: | Novartis Pharma GmbH |  |  | 
			
				| Titel der NIS: | A non-interventional study to assess the influence of automated optical coherence tomography (OCT) image enrichment with segmentation information on disease activity assessment in patients treated with licensed anti-VEGF injections (RAZORBILL) | 
			
				| Ziel der NIS: | The primary research question to be addressed by this study is: Does automated OCT image enrichment with segmentation information influence disease activity assessment in patients treated with licensed anti-VEGF injections for nAMD?Primary objective: To assess the influence of automated OCT image enrichment with segmentation information on disease activity assessment in patients treated with licensed anti-VEGF injections for nAMD.
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				| Ort der Durchführung: | multinational | NIS angefordert: | nein | 
			
				| Patientenanzahl insgesamt: | 476 | Anzahl Ärzte insgesamt: | 17 | 
			
				| Patientenanzahl in Deutschland: | 181 | Ärzte in Deutschland: | 6 | 
			
		
		Weitere Angaben und Unterlagen
		
			
				
					| Anzeige am: | 16.02.2021 | Geplanter Beginn: | 23.02.2021 | Geplantes Ende: | 21.06.2023 | 
				
					| Angezeigtes Ende der NIS am: 21.06.2023 | 
			
		
		Angaben zu den beobachteten Arzneimitteln, soweit angezeigt
		
			
				
					| Arzneimittelbezeichnung | INN | Zulassungs-Nr. | ATC-Code | Substanzklasse | 
			
			
				
					| All licensed anti-VEGF injections: |  |  |  |  | 
				
					| Beovu | Brolucizumab | EU/1/19/1417/001-002 | S01LA06 | anti-VEGF | 
				
					| Lucentis | Ranibizumab | EU/1/06/374/002, EU/1/06/374/004 | S01LA04 | anti-VEGF | 
				
					| Eylea | Aflibercept | EU/1/12/797/002 | S01LA05 | anti-VEGF | 
			
		
		Verfügbare Dokumente
		
			
				
					
						| Art des Dokuments |  | 
				
				
					
						| Beobachtungsplan, NIS 569 | pdf 1MB
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						| Abschlussbericht, NIS 569 | pdf 1MB
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