Serious Event

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Serious Event

Serious Adverse Events (SAEs) are adverse events that result in death, are life-threatening, require or prolong hospitalization, cause persistent or significant disability/incapacity, or are congenital anomalies/birth defects. Each serious event is categorized by term, organ system, assessment type, and source vocabulary to provide standardized reporting across clinical trials.

Serious Event path is as follows:

Study -> Results Section -> Adverse Events Module -> Serious Event

Study -> Results Section -> Adverse Events Module -> Serious Event -> Serious Event Stats

Serious Event

Ignite Creation Date: 2025-12-25 @ 2:33 AM
Ignite Modification Date: 2025-12-26 @ 1:09 AM
NCT ID: NCT02966834
Term: Lower respiratory tract infection
Organ System: Infections and infestations
Assessment Type: SYSTEMATIC_ASSESSMENT
Source Vocabulary: MedDRA 23.0
Notes: None
Study: NCT02966834
Study Brief: Dose Response Study of GSK2330672 for the Treatment of Pruritus in Participants With Primary Biliary Cholangitis
Serious Event Stats (If Any):

Serious Event Stats

Group ID # Events # Affected # At Risk View
EG000 0 0 36 View
EG001 0 0 16 View
EG002 0 0 23 View
EG003 0 0 27 View
EG004 0 0 23 View
EG005 0 0 22 View
EG006 0 0 35 View
EG007 0 0 16 View
EG008 0 0 19 View
EG009 0 0 19 View
EG010 0 0 21 View
EG011 0 0 17 View
EG012 0 0 35 View
EG013 1 1 16 View
EG014 0 0 23 View
EG015 0 0 27 View
EG016 0 0 22 View
EG017 0 0 22 View