NCT02917941 · OUTCOME
Number of Participants With NCI CTCAE Grade 3 or Higher TEAEs Related Laboratory Parameters
A Study of Ixazomib Plus Lenalidomide and Dexamethasone in Adult Japanese Participants With Relapsed and/or Refractory Multiple Myeloma · Source last updated 2021-01-12
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
- Up to approximately 33 months
What was measured
Laboratory parameters included chemistry and hematology. An AE is any unfavorable or unintended sign (including an abnormal laboratory finding), symptom, or disease temporally associated with the use of a medicinal (investigational) product whether or not it was related to the medicinal product. A TEAE is defined as any AE that occurred after administration of the first dose of any study drug through 30 days after the last dose of any study drug. An AE was graded as per NCI CTCAE.
Analysis population: Safety analysis set included all participants who received at least one dose of study drug during the treatment period. Number analyzed is the number of participants with data available for analyses for the specific category.
Groups in this outcome
Ixazomib 4 mg + Lenalidomide 25 mg + Dexamethasone 40 mg
Ixazomib 4 mg, capsules, orally on Days 1, 8, and 15 plus lenalidomide 25 mg, capsule, orally, once daily on Days 1 through 21 and dexamethasone 40 mg, tablet, orally on Days 1, 8, 15, and 22 of a 28-day cycle up to 32 cycles.
Group identifiers and denominators belong to this outcome only. They may differ in another outcome or in safety reporting.
Analysis denominator · Participants
| Group | Source count |
|---|
| Ixazomib 4 mg + Lenalidomide 25 mg + Dexamethasone 40 mg | 34 |
|---|
Reported measurements
Platelet count decreased
Analysis denominator · Participants
| Group | Source count |
|---|
| Ixazomib 4 mg + Lenalidomide 25 mg + Dexamethasone 40 mg | 34 |
|---|
Values in Participants · Interval/dispersion: Not reported| Group | Value | Spread | Lower | Upper | Comment |
|---|
| Ixazomib 4 mg + Lenalidomide 25 mg + Dexamethasone 40 mg | 7 | Not reported | Not reported | Not reported | Not reported |
|---|
Neutrophil count decreased
Analysis denominator · Participants
| Group | Source count |
|---|
| Ixazomib 4 mg + Lenalidomide 25 mg + Dexamethasone 40 mg | 34 |
|---|
Values in Participants · Interval/dispersion: Not reported| Group | Value | Spread | Lower | Upper | Comment |
|---|
| Ixazomib 4 mg + Lenalidomide 25 mg + Dexamethasone 40 mg | 6 | Not reported | Not reported | Not reported | Not reported |
|---|
White blood cell count decreased
Analysis denominator · Participants
| Group | Source count |
|---|
| Ixazomib 4 mg + Lenalidomide 25 mg + Dexamethasone 40 mg | 34 |
|---|
Values in Participants · Interval/dispersion: Not reported| Group | Value | Spread | Lower | Upper | Comment |
|---|
| Ixazomib 4 mg + Lenalidomide 25 mg + Dexamethasone 40 mg | 3 | Not reported | Not reported | Not reported | Not reported |
|---|
Lymphocyte count decreased
Analysis denominator · Participants
| Group | Source count |
|---|
| Ixazomib 4 mg + Lenalidomide 25 mg + Dexamethasone 40 mg | 34 |
|---|
Values in Participants · Interval/dispersion: Not reported| Group | Value | Spread | Lower | Upper | Comment |
|---|
| Ixazomib 4 mg + Lenalidomide 25 mg + Dexamethasone 40 mg | 1 | Not reported | Not reported | Not reported | Not reported |
|---|
Alanine aminotransferase increased
Analysis denominator · Participants
| Group | Source count |
|---|
| Ixazomib 4 mg + Lenalidomide 25 mg + Dexamethasone 40 mg | 34 |
|---|
Values in Participants · Interval/dispersion: Not reported| Group | Value | Spread | Lower | Upper | Comment |
|---|
| Ixazomib 4 mg + Lenalidomide 25 mg + Dexamethasone 40 mg | 1 | Not reported | Not reported | Not reported | Not reported |
|---|
Aspartate aminotransferase increased
Analysis denominator · Participants
| Group | Source count |
|---|
| Ixazomib 4 mg + Lenalidomide 25 mg + Dexamethasone 40 mg | 34 |
|---|
Values in Participants · Interval/dispersion: Not reported| Group | Value | Spread | Lower | Upper | Comment |
|---|
| Ixazomib 4 mg + Lenalidomide 25 mg + Dexamethasone 40 mg | 1 | Not reported | Not reported | Not reported | Not reported |
|---|
Lipase increased
Analysis denominator · Participants
| Group | Source count |
|---|
| Ixazomib 4 mg + Lenalidomide 25 mg + Dexamethasone 40 mg | 33 |
|---|
Values in Participants · Interval/dispersion: Not reported| Group | Value | Spread | Lower | Upper | Comment |
|---|
| Ixazomib 4 mg + Lenalidomide 25 mg + Dexamethasone 40 mg | 1 | Not reported | Not reported | Not reported | Not reported |
|---|
Blood creatine phosphokinase increased
Analysis denominator · Participants
| Group | Source count |
|---|
| Ixazomib 4 mg + Lenalidomide 25 mg + Dexamethasone 40 mg | 34 |
|---|
Values in Participants · Interval/dispersion: Not reported| Group | Value | Spread | Lower | Upper | Comment |
|---|
| Ixazomib 4 mg + Lenalidomide 25 mg + Dexamethasone 40 mg | 1 | Not reported | Not reported | Not reported | Not reported |
|---|
Complete source fields
- classes
- title
- Platelet count decreased
- title
- Neutrophil count decreased
- title
- White blood cell count decreased
- title
- Lymphocyte count decreased
- title
- Alanine aminotransferase increased
- title
- Aspartate aminotransferase increased
- title
- Lipase increased
- title
- Blood creatine phosphokinase increased
- description
- Laboratory parameters included chemistry and hematology. An AE is any unfavorable or unintended sign (including an abnormal laboratory finding), symptom, or disease temporally associated with the use of a medicinal (investigational) product whether or not it was related to the medicinal product. A TEAE is defined as any AE that occurred after administration of the first dose of any study drug through 30 days after the last dose of any study drug. An AE was graded as per NCI CTCAE.
- groups
- description
- Ixazomib 4 mg, capsules, orally on Days 1, 8, and 15 plus lenalidomide 25 mg, capsule, orally, once daily on Days 1 through 21 and dexamethasone 40 mg, tablet, orally on Days 1, 8, 15, and 22 of a 28-day cycle up to 32 cycles.
- id
- OG000
- title
- Ixazomib 4 mg + Lenalidomide 25 mg + Dexamethasone 40 mg
- param Type
- COUNT_OF_PARTICIPANTS
- population Description
- Safety analysis set included all participants who received at least one dose of study drug during the treatment period. Number analyzed is the number of participants with data available for analyses for the specific category.
- reporting Status
- POSTED
- time Frame
- Up to approximately 33 months
- title
- Number of Participants With NCI CTCAE Grade 3 or Higher TEAEs Related Laboratory Parameters
- type
- SECONDARY
- unit Of Measure
- Participants
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice