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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00106613
Other study ID # FJ-228-0001
Secondary ID
Status Completed
Phase Phase 2
First received
Last updated
Start date May 1, 2003
Est. completion date August 1, 2004

Study information

Verified date October 2019
Source Celgene
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Other known NCT identifiers
  • NCT00058630
  • NCT00060216

Recruitment information / eligibility

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

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
FK228 (romidepsin)
Patients receive 13 mg/m2 of romidepsin (FK228) intravenously over 4 hours on Days 1, 8, and 15 of each 28-day cycle.

Locations

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

Sponsors (1)

Lead Sponsor Collaborator
Celgene

Country where clinical trial is conducted

United States, 

References & Publications (6)

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

Outcome

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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