Event Group
Event Groups are part of the Adverse Events Module within the Results Section. They provide a way to organize and summarize adverse event data by grouping related events together.
Each Event Group typically represents a category or class of adverse events and includes statistical information such as the number of participants affected and at risk for different event types: deaths, serious events, and other events.
Event Group path is as follows:
Study -> Results Section -> Adverse Events Module -> Event Group
Event Group
Ignite Creation Date:
2025-12-24 @ 7:10 PM
Ignite Modification Date:
2025-12-25 @ 4:44 PM
NCT ID:
NCT05126303
Group ID:
EG000
Title:
RMC-035
Description:
RMC-035 is a concentrate (6.0 mg/mL) for solution for infusion for IV administration.
Dosing was done per kg bodyweight and at Subjects with eGFR ≥60 mL/min/1.73m2 will receive 1.3 mg/kg (per dose) for the first and second dose, followed by 0.65 mg/kg (per dose) for the third, fourth and fifth dose, while subjects with eGFR \>30 and \<60 mL/min/1.73m2 will receive 0.65 mg/kg (per dose) for all five doses Dosing occurs at time 0 and then after 6, 12, 24 and 48 hours.
RMC-035: Concentrate for Solution for Infusion
Deaths Number Affected:
1
Deaths Number At Risk:
None
Serious Number Affected:
20
Serious Number At Risk:
89
Other Number Affected:
75
Other Number At Risk:
89
Study:
NCT05126303
Results Section:
NCT05126303
Adverse Events Module:
NCT05126303