NCT04165031 · OUTCOME
Phase 2: Overall Response Rate (ORR): Percentage of Participants Who Achieve Complete Response (CR) or Partial Response (PR) in Colorectal Cancer (CRC) Cohorts and Other Tumors Cohort
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- Measure
- Not reported
- Unit
- Not reported
- Interval / dispersion
- Not reported
- Time frame
- Baseline through Measured Progressive Disease
What was measured
ORR is defined as percentage of participants who achieved a CR or PR out of all the participants treated. Tumor responses were measured and record using Response Evaluation Criteria in Solid Tumors v1.1 (RECIST) v1.1 guidelines. CR is defined as the disappearance of all targeted and non-target lesions and no appearance of new lesions. PR is defined as at least a 30% decrease in the sum of the longest diameter (LD) of target lesions (taking as reference the baseline sum LD), no progression of non-target lesions and no appearance of new lesions.
Analysis population: Zero participants were analyzed due to early termination of study.
Groups in this outcome
LY3499446 Monotherapy + Combination Drugs Phase 2
LY3499446 combined with either abemaciclib (orally), erlotinib (orally), or cetuximab (IV).
Docetaxel Phase 2
Docetaxel IV infusion.
| Group | Source count |
|---|---|
| LY3499446 Monotherapy + Combination Drugs Phase 2 | 0 |
| Docetaxel Phase 2 | 0 |
Reported measurements
No numerical measurement classes were posted for this outcome. Missing is not zero.
Complete source fields
- denoms
- counts
- group Id
- OG000
- value
- 0
- group Id
- OG001
- value
- 0
- units
- Participants
- description
- ORR is defined as percentage of participants who achieved a CR or PR out of all the participants treated. Tumor responses were measured and record using Response Evaluation Criteria in Solid Tumors v1.1 (RECIST) v1.1 guidelines. CR is defined as the disappearance of all targeted and non-target lesions and no appearance of new lesions. PR is defined as at least a 30% decrease in the sum of the longest diameter (LD) of target lesions (taking as reference the baseline sum LD), no progression of non-target lesions and no appearance of new lesions.
- groups
- description
- LY3499446 combined with either abemaciclib (orally), erlotinib (orally), or cetuximab (IV).
- id
- OG000
- title
- LY3499446 Monotherapy + Combination Drugs Phase 2
- description
- Docetaxel IV infusion.
- id
- OG001
- title
- Docetaxel Phase 2
- population Description
- Zero participants were analyzed due to early termination of study.
- reporting Status
- POSTED
- time Frame
- Baseline through Measured Progressive Disease
- title
- Phase 2: Overall Response Rate (ORR): Percentage of Participants Who Achieve Complete Response (CR) or Partial Response (PR) in Colorectal Cancer (CRC) Cohorts and Other Tumors Cohort
- type
- PRIMARY
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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