NCT01797523 · OUTCOME
Percentage of Participants With Toxicities Associated With RAD001, Letrozole, and Metformin
A Phase II, Single-Arm Study of RAD001 (Everolimus), Letrozole, and Metformin in Patients With Advanced or Recurrent Endometrial Carcinoma · Source last updated 2026-07-30
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- Measure
- NUMBER
- Unit
- percentage of participants
- Interval / dispersion
- Not reported
- Time frame
- 93 months
What was measured
To determine the frequency and severity of toxicities associated with RAD001, letrozole, and metformin in this cohort of patients.
Analysis population: 59 patients who had at least one dose of treatment and had a follow up evaluation for side effects
Groups in this outcome
Rad-Let-Met
Everolimus 10 mg PO daily + Letrozole 2.5 mg PO daily + Metformin 500 mg PO twice daily on a 4 week schedule
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 |
|---|
| Rad-Let-Met | 59 |
|---|
Reported measurements
Anemia (Grade 2)
Values in percentage of participants · Interval/dispersion: Not reported| Group | Value | Spread | Lower | Upper | Comment |
|---|
| Rad-Let-Met | 85 | Not reported | Not reported | Not reported | Not reported |
|---|
Anemia (Grade 3)
Values in percentage of participants · Interval/dispersion: Not reported| Group | Value | Spread | Lower | Upper | Comment |
|---|
| Rad-Let-Met | 24 | Not reported | Not reported | Not reported | Not reported |
|---|
Hypertriglyceridemia
Values in percentage of participants · Interval/dispersion: Not reported| Group | Value | Spread | Lower | Upper | Comment |
|---|
| Rad-Let-Met | 15 | Not reported | Not reported | Not reported | Not reported |
|---|
Hyperglycemia
Values in percentage of participants · Interval/dispersion: Not reported| Group | Value | Spread | Lower | Upper | Comment |
|---|
| Rad-Let-Met | 9 | Not reported | Not reported | Not reported | Not reported |
|---|
Hyponatremia
Values in percentage of participants · Interval/dispersion: Not reported| Group | Value | Spread | Lower | Upper | Comment |
|---|
| Rad-Let-Met | 7 | Not reported | Not reported | Not reported | Not reported |
|---|
Fatigue
Values in percentage of participants · Interval/dispersion: Not reported| Group | Value | Spread | Lower | Upper | Comment |
|---|
| Rad-Let-Met | 6 | Not reported | Not reported | Not reported | Not reported |
|---|
Thrombocytopenia
Values in percentage of participants · Interval/dispersion: Not reported| Group | Value | Spread | Lower | Upper | Comment |
|---|
| Rad-Let-Met | 6 | Not reported | Not reported | Not reported | Not reported |
|---|
Complete source fields
- classes
- title
- Anemia (Grade 2)
- title
- Anemia (Grade 3)
- title
- Hypertriglyceridemia
- title
- Hyperglycemia
- title
- Hyponatremia
- title
- Fatigue
- title
- Thrombocytopenia
- description
- To determine the frequency and severity of toxicities associated with RAD001, letrozole, and metformin in this cohort of patients.
- groups
- description
- Everolimus 10 mg PO daily + Letrozole 2.5 mg PO daily + Metformin 500 mg PO twice daily on a 4 week schedule
- id
- OG000
- title
- Rad-Let-Met
- param Type
- NUMBER
- population Description
- 59 patients who had at least one dose of treatment and had a follow up evaluation for side effects
- reporting Status
- POSTED
- time Frame
- 93 months
- title
- Percentage of Participants With Toxicities Associated With RAD001, Letrozole, and Metformin
- type
- SECONDARY
- unit Of Measure
- percentage of participants
Download exact source JSON → · Snapshot ctgov-results-191f4516d4760045304b24a0
Preserved source evidence · Independent clinical review pending · Not medical advice