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A Study of LY2510924 and Sunitinib in Patients With Metastatic Renal Cell Carcinoma

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ClinicalTrials.gov Identifier: NCT01391130
Recruitment Status : Terminated (Study Terminated due to Insufficient Efficacy)
First Posted : July 11, 2011
Last Update Posted : April 24, 2017
Sponsor:
Information provided by (Responsible Party):
Eli Lilly and Company

Brief Summary:
To compare the progression free survival of LY2510924 plus sunitinib therapy versus sunitinib in the first-line setting for patients with metastatic clear-cell renal cell carcinoma.

Condition or disease Intervention/treatment Phase
Metastatic Clear Cell Renal Cell Carcinoma Drug: LY2510924 Drug: Sunitinib Phase 2

Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 108 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Randomized, Multicenter, Open-label, Active-Controlled, Phase 2 Study of LY2510924 and Sunitinib Versus Sunitinib in Patients With Metastatic Renal Cell Carcinoma
Study Start Date : August 2011
Actual Primary Completion Date : September 2014
Actual Study Completion Date : February 2017


Arm Intervention/treatment
Experimental: LY2510924 + Sunitinib
LY2510924: 20 milligram administered subcutaneously once daily, given every day of the 6 week cycle. Sunitinib: 50 milligram administered orally once daily, on a schedule of 4 weeks on treatment followed by 2 weeks off treatment. Treatment cycles will continue until disease progression, unacceptable toxicity, or another withdrawal criterion is met.
Drug: LY2510924
Administered subcutaneously

Drug: Sunitinib
Administered orally

Active Comparator: Sunitinib
50 milligram administered orally once daily, on a schedule of 4 weeks on treatment followed by 2 weeks off treatment. Treatment cycles will continue until disease progression, unacceptable toxicity, or another withdrawal criterion is met.
Drug: Sunitinib
Administered orally




Primary Outcome Measures :
  1. Progression free survival [ Time Frame: Baseline to measured progressive disease or date of death from any cause (approximately 2 years) ]

Secondary Outcome Measures :
  1. Objective tumor response (Objective Response Rate [ORR]) [ Time Frame: Baseline to best response (approximately 2 years) ]
  2. Overall survival [ Time Frame: Baseline to date of death from any cause (approximately 2 years) ]
  3. Duration of overall response [ Time Frame: Date of first response to date of progressive disease (approximately 2 years) ]
  4. Duration of complete response [ Time Frame: Date of complete response to the date of progressive disease (approximately 2 years) ]


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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Evidence of histologically confirmed renal cell carcinoma (RCC) with metastases with a component of clear (conventional) cell histology
  • A diagnosis of metastatic renal cell carcinoma (RCC) and have not received prior treatment with systemic (adjuvant or neoadjuvant) therapy for renal cell carcinoma (RCC) (including targeted therapy such as tyrosine kinase inhibitors or bevacizumab, immunotherapy, chemotherapy, hormonal, or investigational therapy)
  • Evidence of measurable disease as defined by Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1. Computed tomography (CT) or magnetic resonance imaging (MRI) should be performed within 4 weeks prior to study entry
  • Participants who have or have not had their primary tumor removed by nephrectomy are allowed. Participants who have not had a nephrectomy should not be considered to need a nephrectomy as part of their overall therapy at the time of enrollment
  • Performance status score of 0 or 1 on the Eastern Cooperative Oncology Group (ECOG) scale
  • Adequate bone marrow, liver, and renal function, as assessed by the following laboratory requirements, to be conducted within seven days prior to treatment: (upper limit of normal/lower limit of normal [ULN/LLN])

    • hemoglobin (greater than) >8.0 g/dL (grams per deciliter)
    • absolute neutrophil count (ANC) (greater than or equal to) ≥1.5 × 10^9/L (liter)
    • platelet count (greater than or equal to) ≥100 × 10^9/L (liter)
    • total bilirubin (less than or equal to) ≤ 1.5 × ULN (upper limit of normal)
    • serum creatinine (less than or equal to) ≤2 × ULN (upper limit of normal)
    • alanine aminotransferase (ALT) and aspartate aminotransferase (AST) (less than or equal to) ≤2.5 × ULN (upper limits of normal) [or (less than or equal to) ≤5 × ULN (upper limits of normal) for patients with liver involvement of their cancer]
    • Prothrombin Time (PT) or International Normalized Ratio (INR) and activated Partial Thromboplastin Time (aPTT) (less than or equal to) ≤1.5 x ULN (upper limit of normal)
  • For women: Must be surgically sterile (surgical procedure: bilateral tubal ligation, hysterectomy, bilateral oophorectomy), post-menopausal (at least 12 consecutive months of amenorrhea), or have a negative pregnancy test. Women of childbearing potential should be compliant with a medically approved contraceptive regimen (intrauterine device [IUD], birth control pills, or barrier device) during and for 3 months after the treatment period; must have a negative serum pregnancy test within 7 days before study enrollment, and must not be breastfeeding
  • For men: Must be surgically sterile or compliant with a contraceptive regimen during and for 3 months after the treatment period
  • Estimated life expectancy of at least 12 weeks
  • Provide written informed consent/assent prior to any study-specific procedures
  • No prior malignancies with the exception of stage 1 cancers definitively treated, carcinoma in situ (any primary site), treated non-melanoma skin cancer, superficial bladder tumors (Ta, Tis, and T1) or any cancer curatively treated 5 or more years prior to study entry
  • Capable and willing to learn to self-administer LY2510924, or have a caregiver who is willing to learn and able to administer LY2510924 by subcutaneous (SC) injection and are able to swallow tablets
  • Left ventricular ejection fraction (LVEF) greater than or equal to LLN as defined by the institution performing the scan, as assessed by Multiple Gated Acquisition (MUGA) scan, or from echocardiogram to be performed within 28 days prior to start of treatment

Exclusion Criteria:

  • Received prior treatment with sunitinib or LY2510924
  • Received treatment within the last 30 days with a drug that has not received regulatory approval for any indication at the time of study entry
  • History of active cardiovascular disease within the previous 12 months, including any of the following:

    • Myocardial infarction
    • Unstable angina
    • Coronary artery/peripheral artery bypass graft
    • Congestive heart failure
    • Malignant hypertension
    • Cerebrovascular accident or transient ischemic attack
    • Symptomatic cardiac arrhythmias (Patients with chronic, stable, rate- controlled atrial fibrillation are eligible)
  • Exhibit uncontrolled hypertension ( [greater than] >150/100 [millimeters of mercury] mm/Hg despite optimal medical therapy), or history of poor compliance with antihypertensive treatment
  • Evidence of bleeding diathesis, National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) Grade 3 hemorrhage (less than) <4 weeks of starting the study treatment, coagulopathy, or thromboembolic event
  • Significant surgery (less than) <4 weeks of starting study treatment or a minor surgical procedure (less than) < 7 days prior to study treatment (Placement of a portacath or other venous access device does not require a waiting period)
  • Suffer from medical, psychological, or social conditions that may interfere with the patient's participation in the study or evaluation of the study results
  • Known or suspected allergy to any agent given in association with this trial
  • Prior palliative radiotherapy to metastatic lesion(s) is/are permitted, provided there is at least 1 measurable lesion that has not been irradiated. Radiotherapy must have been completed (greater than) >2 weeks prior to starting study treatment, and radiation-related side effects must have resolved
  • Pregnant or lactating women
  • Impairment of the gastrointestinal (GI) function or GI disease that may significantly alter the absorption of sunitinib
  • Current or recent (within 10 days of first dose of study treatment) daily use of aspirin ( [greater than] >325 [milligram] mg/day )
  • Serious nonhealing wounds, acute or nonhealing ulcers, or bone fractures

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01391130


  Show 21 Study Locations
Sponsors and Collaborators
Eli Lilly and Company
Investigators
Study Director: Call 1-877-CTLILLY (1-877-285-4559) or 1-317-615-4559 Mon - Fri 9 AM - 5 PM Eastern time (UTC/GMT - 5 hours, EST) Eli Lilly and Company

Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: Eli Lilly and Company
ClinicalTrials.gov Identifier: NCT01391130     History of Changes
Other Study ID Numbers: 14241
I2V-MC-CXAB ( Other Identifier: Eli Lilly and Company )
First Posted: July 11, 2011    Key Record Dates
Last Update Posted: April 24, 2017
Last Verified: April 2017

Keywords provided by Eli Lilly and Company:
Cancer
Tumor
Metastasis

Additional relevant MeSH terms:
Carcinoma
Carcinoma, Renal Cell
Neoplasms, Glandular and Epithelial
Neoplasms by Histologic Type
Neoplasms
Adenocarcinoma
Kidney Neoplasms
Urologic Neoplasms
Urogenital Neoplasms
Neoplasms by Site
Kidney Diseases
Urologic Diseases
Sunitinib
Antineoplastic Agents
Angiogenesis Inhibitors
Angiogenesis Modulating Agents
Growth Substances
Physiological Effects of Drugs
Growth Inhibitors