Neoplasm Metastasis Clinical Trial
Official title:
An Exploratory Phase II, Multicenter, Open-label Trial Evaluating the Activity and Tolerability of FK228 in Patients With Metastatic Renal Cell Carcinoma That is Progressive Following or During Immunotherapy
Verified date | October 2019 |
Source | Celgene |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to evaluate the activity of FK228 in metastatic renal cell carcinoma (RCC) patients who have developed progressive disease (PD) following or during treatment with immunotherapy.
Status | Completed |
Enrollment | 30 |
Est. completion date | August 1, 2004 |
Est. primary completion date | August 1, 2004 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: Patients must fulfill all of the following criteria to be eligible for study participation: - Age = 18 years; - Histologically confirmed Renal Cell Carcinoma (RCC); - Metastatic disease, with measurable lesions according to the Response Evaluation Criteria in Solid Tumors (RECIST); - Failure of prior cytokine therapy; - Documented progressive disease; Exclusion Criteria: Patients are ineligible for entry if any of the following criteria are met: - Significant cardiac disease including congestive heart failure, history of myocardial infarction within one year, uncontrolled dysrhythmias, or poorly controlled angina - History of serious ventricular arrhythmia - Corrected QT interval (QTc) = 500 msec - Known infection with Human Immunodeficiency Virus (HIV), Hepatitis B, or Hepatitis C; - Previous extensive radiotherapy involving = 30% of bone marrow - Coexistent second malignancy or history of prior malignancy within previous 5 years |
Country | Name | City | State |
---|---|---|---|
United States | University of Chicago | Chicago | Illinois |
United States | City of Hope National Medical Center | Duarte | California |
United States | Seattle Cancer Care Alliance | Seattle | Washington |
Lead Sponsor | Collaborator |
---|---|
Celgene |
United States,
Mansfield AS, Jen J. Predicting Treatment Response Based on RNA Expression in Large Datasets. Clin Cancer Res. 2019 Mar 1;25(5):1443-1445. doi: 10.1158/1078-0432.CCR-18-2823. Epub 2018 Nov 16. — View Citation
Moreno L, Casanova M, Chisholm JC, Berlanga P, Chastagner PB, Baruchel S, Amoroso L, Gallego Melcón S, Gerber NU, Bisogno G, Fagioli F, Geoerger B, Glade Bender JL, Aerts I, Bergeron C, Hingorani P, Elias I, Simcock M, Ferrara S, Le Bruchec Y, Slepetis R, Chen N, Vassal G. Phase I results of a phase I/II study of weekly nab-paclitaxel in paediatric patients with recurrent/refractory solid tumours: A collaboration with innovative therapies for children with cancer. Eur J Cancer. 2018 Sep;100:27-34. doi: 10.1016/j.ejca.2018.05.002. Epub 2018 Jun 21. — View Citation
Pal SK, Forero-Torres A, Thompson JA, Morris JC, Chhabra S, Hoimes CJ, Vogelzang NJ, Boyd T, Bergerot PG, Adashek JJ, Li H, Yu X, Gartner EM, Carret AS, Smith DC. A phase 1 trial of SGN-CD70A in patients with CD70-positive, metastatic renal cell carcinoma. Cancer. 2019 Apr 1;125(7):1124-1132. doi: 10.1002/cncr.31912. Epub 2019 Jan 9. — View Citation
Stadler W, et al. A phase II study of depsipeptide (Dep) in patients (pts) with metastatic renal cell cancer (RCC). J Clin Oncol. 2005 Jun; 23(16_suppl):4669.
Stadler WM, Margolin K, Ferber S, McCulloch W, Thompson JA. A phase II study of depsipeptide in refractory metastatic renal cell cancer. Clin Genitourin Cancer. 2006 Jun;5(1):57-60. — View Citation
Wolchok J. Putting the Immunologic Brakes on Cancer. Cell. 2018 Nov 29;175(6):1452-1454. doi: 10.1016/j.cell.2018.11.006. Review. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | To evaluate the rate of objective response (the best response of Complete Response (CR), Partial Response (PR)). | Up to 6 months | ||
Secondary | Rate of disease control, Complete Response, Partial Response, or Stable Disease | Up to 6 months | ||
Secondary | Time to objective disease progression. | Up to 6 months | ||
Secondary | Number of Participants with Adverse Events | Up to 6 months | ||
Secondary | Change from screening assessment to the final study visit in Karnofsky performance status. | Up to 6 months | ||
Secondary | Steady state plasma concentrations | Up to 6 months |
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