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 @ 7:25 PM
Ignite Modification Date: 2025-12-25 @ 5:06 PM
NCT ID: NCT01587703
Term: Prothrombin time prolonged
Organ System: Investigations
Assessment Type: SYSTEMATIC_ASSESSMENT
Source Vocabulary: MedDRA 21.0
Notes: None
Study: NCT01587703
Study Brief: A Study to Investigate the Safety, Pharmacokinetics, Pharmacodynamics, and Clinical Activity of GSK525762 in Subjects With NUT Midline Carcinoma (NMC) and Other Cancers
Serious Event Stats (If Any):

Serious Event Stats

Group ID # Events # Affected # At Risk View
EG000 0 0 4 View
EG001 0 0 1 View
EG002 0 0 3 View
EG003 0 0 4 View
EG004 0 0 9 View
EG005 0 0 32 View
EG006 0 0 9 View
EG007 0 0 4 View
EG008 0 0 10 View
EG009 0 0 5 View
EG011 0 0 14 View
EG012 0 0 23 View
EG013 0 0 3 View
EG014 0 0 19 View
EG016 0 0 13 View
EG017 0 0 5 View
EG018 0 0 5 View
EG010 2 1 12 View
EG015 0 0 21 View