A Phase 2 interventional study of lenalidomide in Kidney Cancer, sponsored by The Cleveland Clinic. Completed at 1 site in United States. Open to participants aged 18 Years to 120 Years. Per ClinicalTrials.gov, last updated 2026-07-02.
Sponsored by The Cleveland Clinic · Phase 2, Interventional, and Treatment
RATIONALE: Lenalidomide may stop the growth of kidney cancer by blocking blood flow to the tumor.
PURPOSE: This phase II trial is studying how well lenalidomide works in treating patients with advanced or unresectable kidney cancer.
OBJECTIVES:
OUTLINE: This is an open-label study.
Patients receive oral lenalidomide daily on days 1-21. Courses repeat every 28 days in the absence of unacceptable toxicity or disease progression.
After completion of study treatment, patients are followed every 3 months.
PROJECTED ACCRUAL: A total of 26 patients will be accrued for this study.
956 studies on the registry are indexed under Kidney Neoplasms; 210 are open to participants now.
This study's enrollment of 28 is below the median of 43 across 650 interventional studies indexed under Kidney Neoplasms.
Browse Kidney Neoplasms studies →The Cleveland Clinic is the lead sponsor of 818 studies on the registry; 118 are open to participants now.
Of its 89 completed or terminated interventional studies of FDA-regulated products, 72 (81%) have results posted.
Counted across the registry records on this site, refreshed daily.
DISEASE CHARACTERISTICS:
Histologically or cytologically confirmed renal cell carcinoma (RCC)
No brain metastases
PATIENT CHARACTERISTICS:
No uncontrolled intercurrent illness including, but not limited to, any of the following:
PRIOR CONCURRENT THERAPY:
25 mg/day Lenalidomide for 21 days per cycle.
Drug: lenalidomide
drug
Also known as: CC-5013
Objective Response Rate
The objective response rate was defined by RECIST.
Time frame: Baseline and every 2 weeks until study completion, up to 1.5 years
Toxicity--Most Common AEs
Most commonly reported Serious Adverse Events
Time frame: Baseline and every 2 weeks until study completion. Number of cycles is open ended.
Overall Survival
Time frame: 1 to 16 cycles, until patient expires, is lost to follow up or withdraws consent
| Milestone | Lenalidomide for Advanced RCC |
|---|---|
| Started | 28 |
| Completed | 28 |
| Not completed | 0 |
The objective response rate was defined by RECIST.
| Participants | Lenalidomide for Advanced RCC |
|---|---|
| Objective Response Rate | 3 |
Most commonly reported Serious Adverse Events
| percentage of participants | Lenalidomide for Advanced RCC |
|---|---|
| Fatigue | 11 |
| Skin Toxicity | 11 |
| Neutropenia | 36 |
| Participants | Lenalidomide for Advanced RCC |
|---|---|
| Overall Survival | 17 |
Non-serious events are listed at a 0% frequency threshold.
| Group | Deaths | Serious | Other |
|---|---|---|---|
| Lenalidomide for Advanced RCC | 11/28 (39.3%) | 16/28 (57.1%) | 28/28 (100%) |
| Event | Lenalidomide for Advanced RCC |
|---|---|
| NeutropeniaBlood and lymphatic system disorders | 10/28 |
| FatigueGeneral disorders | 3/28 |
| Skin ReactionSkin and subcutaneous tissue disorders | 3/28 |
| Event | Lenalidomide for Advanced RCC |
|---|---|
| FatigueGeneral disorders | 21/28 |
| Skin ReactionsSkin and subcutaneous tissue disorders | 16/28 |
| Nausea/EmesisGastrointestinal disorders | 10/28 |
| ConstipationGastrointestinal disorders | 8/28 |
| DiarrheaGastrointestinal disorders | 8/28 |
| EdemaGeneral disorders | 6/28 |
| Cough/DyspneaRespiratory, thoracic and mediastinal disorders | 4/28 |
| DizzinessGeneral disorders | 4/28 |
| NeuropathyNervous system disorders | 3/28 |
| Age, Continuous(years) | Lenalidomide for Advanced RCC |
|---|---|
| Mean | 63.5 ± 9.3 |
| Sex: Female, Male(Participants) | Lenalidomide for Advanced RCC |
|---|---|
| Female | 9 |
| Male | 19 |
This study is completed, as verified in Jul 2026. You cannot join it, but the record below documents what was studied.
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