NCT03945019 · OUTCOME
Percentage of Patients Achieving CDAI-100 Response at Week 54
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- Measure
- COUNT_OF_PARTICIPANTS
- Unit
- Participants
- Interval / dispersion
- Not reported
- Time frame
- Week 54
What was measured
Crohn's Disease Activity Index (CDAI)-100 response was defined as a decrease in CDAI score of 100 points or more from the baseline value. The total CDAI scores range from 0 to over 600 with higher scores indicating increased severity of disease. The index is the sum of 8 components; number of liquid or very soft stools, abdominal pain, general well-being, CD complications, taking antidiarrheal drugs, abdominal mass, hematocrit, and weight. Patients with dose adjustment to CT-P13 SC 240 mg prior to Week 54 were considered as non-responder.
Analysis population: All-randomized population
Groups in this outcome
CT-P13 SC 120 mg
CT-P13 SC 120 mg
Placebo
Placebo
| Group | Source count |
|---|---|
| CT-P13 SC 120 mg | 231 |
| Placebo | 112 |
Reported measurements
Source class 1
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| CT-P13 SC 120 mg | 152 | Not reported | Not reported | Not reported | Not reported |
| Placebo | 43 | Not reported | Not reported | Not reported | Not reported |
Complete source fields
- classes
- categories
- measurements
- group Id
- OG000
- value
- 152
- group Id
- OG001
- value
- 43
- denoms
- counts
- group Id
- OG000
- value
- 231
- group Id
- OG001
- value
- 112
- units
- Participants
- description
- Crohn's Disease Activity Index (CDAI)-100 response was defined as a decrease in CDAI score of 100 points or more from the baseline value. The total CDAI scores range from 0 to over 600 with higher scores indicating increased severity of disease. The index is the sum of 8 components; number of liquid or very soft stools, abdominal pain, general well-being, CD complications, taking antidiarrheal drugs, abdominal mass, hematocrit, and weight. Patients with dose adjustment to CT-P13 SC 240 mg prior to Week 54 were considered as non-responder.
- groups
- description
- CT-P13 SC 120 mg
- id
- OG000
- title
- CT-P13 SC 120 mg
- description
- Placebo
- id
- OG001
- title
- Placebo
- param Type
- COUNT_OF_PARTICIPANTS
- population Description
- All-randomized population
- reporting Status
- POSTED
- time Frame
- Week 54
- title
- Percentage of Patients Achieving CDAI-100 Response at Week 54
- type
- SECONDARY
- unit Of Measure
- Participants
Download exact source JSON → · Snapshot ctgov-results-191f4516d4760045304b24a0
Preserved source evidence · Not medical advice
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