NCT00923481 · OUTCOME
Number of Participants With Adverse Events
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- Measure
- NUMBER
- Unit
- Participants
- Interval / dispersion
- Not reported
- Time frame
- 23 months
What was measured
Here is the number of participants with adverse events. For the detailed list of adverse events see the adverse event module.
Groups in this outcome
Multi-kinase Inhibitor Fosamatinib Disodium
200 mg BID was the administered dose for the initial part of the study and then a phase I dose escalation was added with 100 mg as the starting dose.
| Group | Source count |
|---|---|
| Multi-kinase Inhibitor Fosamatinib Disodium | 37 |
Reported measurements
Source class 1
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Multi-kinase Inhibitor Fosamatinib Disodium | 37 | Not reported | Not reported | Not reported | Not reported |
Complete source fields
- classes
- categories
- measurements
- group Id
- OG000
- value
- 37
- denoms
- counts
- group Id
- OG000
- value
- 37
- units
- Participants
- description
- Here is the number of participants with adverse events. For the detailed list of adverse events see the adverse event module.
- groups
- description
- 200 mg BID was the administered dose for the initial part of the study and then a phase I dose escalation was added with 100 mg as the starting dose.
- id
- OG000
- title
- Multi-kinase Inhibitor Fosamatinib Disodium
- param Type
- NUMBER
- reporting Status
- POSTED
- time Frame
- 23 months
- title
- Number of Participants With Adverse Events
- type
- SECONDARY
- unit Of Measure
- Participants
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
Triangle