Table 3.

Frequency of drug-related TEAEs, by dose cohort and system organ class

Category of event*Vedolizumab 75 mg (n = 3)Vedolizumab 300 mg (n = 21)Total (N = 24)
Participants with any drug-related TEAE 2 (66.7) 6 (28.6) 8 (33.3) 
Blood and lymphatic system disorders    
 Total 0 (0) 2 (9.5) 2 (8.3) 
 Anemia 0 (0) 1 (4.8) 1 (4.2) 
 Febrile neutropenia 0 (0) 1 (4.8) 1 (4.2) 
Nervous system disorders    
 Total 0 (0) 2 (9.5) 2 (8.3) 
 Headache 0 (0) 1 (4.8) 1 (4.2) 
 Cognitive disorder 0 (0) 1 (4.8) 1 (4.2) 
Musculoskeletal and connective tissue disorders    
 Total 1 (33.3) 1 (4.8) 2 (8.3) 
 Arthralgia 0 (0) 1 (4.8) 1 (4.2) 
 Musculoskeletal pain 1 (33.3) 0 (0) 1 (4.2) 
Investigations    
 Total 1 (33.3) 1 (4.8) 2 (8.3) 
 Alanine aminotransferase increased 1 (33.3) 0 (0) 1 (4.2) 
 Aspartate aminotransferase increased 0 (0) 1 (4.8) 1 (4.2) 
Infections and infestations    
 CMV infection 0 (0) 1 (4.8) 1 (4.2) 
Vascular disorders    
 Hypotension 0 (0) 1 (4.8) 1 (4.2) 
Respiratory, thoracic, and mediastinal disorders    
 Dyspnea exertional 0 (0) 1 (4.8) 1 (4.2) 
Skin and subcutaneous tissue disorders    
 Rash pruritic 0 (0) 1 (4.8) 1 (4.2) 
General disorders and administration site conditions    
 Pyrexia 0 (0) 1 (4.8) 1 (4.2) 
Participants with at least 1 serious drug-related TEAE 0 (0) 1 (4.8) 1 (4.2) 
Blood and lymphatic system disorders    
 Febrile neutropenia 0 (0) 1 (4.8) 1 (4.2) 
Vascular disorders    
 Hypotension 0 (0) 1 (4.8) 1 (4.2) 
Category of event*Vedolizumab 75 mg (n = 3)Vedolizumab 300 mg (n = 21)Total (N = 24)
Participants with any drug-related TEAE 2 (66.7) 6 (28.6) 8 (33.3) 
Blood and lymphatic system disorders    
 Total 0 (0) 2 (9.5) 2 (8.3) 
 Anemia 0 (0) 1 (4.8) 1 (4.2) 
 Febrile neutropenia 0 (0) 1 (4.8) 1 (4.2) 
Nervous system disorders    
 Total 0 (0) 2 (9.5) 2 (8.3) 
 Headache 0 (0) 1 (4.8) 1 (4.2) 
 Cognitive disorder 0 (0) 1 (4.8) 1 (4.2) 
Musculoskeletal and connective tissue disorders    
 Total 1 (33.3) 1 (4.8) 2 (8.3) 
 Arthralgia 0 (0) 1 (4.8) 1 (4.2) 
 Musculoskeletal pain 1 (33.3) 0 (0) 1 (4.2) 
Investigations    
 Total 1 (33.3) 1 (4.8) 2 (8.3) 
 Alanine aminotransferase increased 1 (33.3) 0 (0) 1 (4.2) 
 Aspartate aminotransferase increased 0 (0) 1 (4.8) 1 (4.2) 
Infections and infestations    
 CMV infection 0 (0) 1 (4.8) 1 (4.2) 
Vascular disorders    
 Hypotension 0 (0) 1 (4.8) 1 (4.2) 
Respiratory, thoracic, and mediastinal disorders    
 Dyspnea exertional 0 (0) 1 (4.8) 1 (4.2) 
Skin and subcutaneous tissue disorders    
 Rash pruritic 0 (0) 1 (4.8) 1 (4.2) 
General disorders and administration site conditions    
 Pyrexia 0 (0) 1 (4.8) 1 (4.2) 
Participants with at least 1 serious drug-related TEAE 0 (0) 1 (4.8) 1 (4.2) 
Blood and lymphatic system disorders    
 Febrile neutropenia 0 (0) 1 (4.8) 1 (4.2) 
Vascular disorders    
 Hypotension 0 (0) 1 (4.8) 1 (4.2) 

Data are presented as n (%).

*

MedDRA (version 21.0) terms were used for coding AEs.

Participants with 1 or more events within a level of MedDRA term are counted only once in that level.

Investigator reported this event as “CMV reactivation.”

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