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: 2025-12-24 @ 2:03 PM
Ignite Modification Date: 2025-12-25 @ 12:47 PM
NCT ID: NCT02799095
Term: Supraventricular extrasystoles
Organ System: Cardiac disorders
Assessment Type: SYSTEMATIC_ASSESSMENT
Source Vocabulary: MedDRA version 25.0
Notes: None
Study: NCT02799095
Study Brief: A Study of the Effects of ALKS 4230 (Nemvaleukin Alfa) on Subjects With Solid Tumors
Serious Event Stats (If Any):

Serious Event Stats

Group ID # Events # Affected # At Risk View
EG000 0 0 5 View
EG001 0 0 4 View
EG002 0 0 7 View
EG003 0 0 8 View
EG004 0 0 12 View
EG005 0 0 3 View
EG006 0 0 7 View
EG007 0 0 47 View
EG008 0 0 27 View
EG009 0 0 3 View
EG010 1 1 42 View
EG011 1 1 26 View
EG012 1 1 26 View
EG013 0 0 43 View
EG014 0 0 3 View
EG015 0 0 21 View
EG016 0 0 2 View