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Trial record 42 of 48 for:    Dovitinib

Bioavailability and Food Effect Study of TKI258 (CSF Capsules vs. FMI Capsules)in Adult Patients With Advanced Solid Tumors

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT01030055
Recruitment Status : Completed
First Posted : December 11, 2009
Last Update Posted : December 13, 2013
Information provided by (Responsible Party):
Novartis ( Novartis Pharmaceuticals )

Brief Summary:
This study will evaluate the relative bioavailability of 2 oral formulations of TKI258, and the effect of food on the bioavailability of TKI258, in adult patients with advanced solid tumor

Condition or disease Intervention/treatment Phase
Neoplasms Cancer Tumors Drug: TKI258 (dovitinib) Phase 1

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 60 participants
Allocation: Non-Randomized
Intervention Model: Crossover Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: A Randomized, Open-label, Multi-center, Phase I, Crossover Study to Assess the Relative Bioavailability of 2 Oral Formulations of TKI258, and the Effect of Food on the Bioavailability of TKI258, in Patients With Advanced Solid Tumors
Study Start Date : February 2010
Actual Primary Completion Date : June 2012
Actual Study Completion Date : June 2012

Arm Intervention/treatment
Experimental: TKI258 - bioavailability Drug: TKI258 (dovitinib)
bioavailability (anhydrate capsules) food (monohydrae capsules)
Other Name: dovitinib

Experimental: TKI258 - food Drug: TKI258 (dovitinib)
bioavailability (anhydrate capsules) food (monohydrae capsules)
Other Name: dovitinib

Primary Outcome Measures :
  1. Determine the relative bioavailability of the final market image form of TKI258 (monohydrate capsules) as compared to the clinical service form of TKI258 (anhydrate capsules) [ Time Frame: 9 days ]
  2. Determine the effect of food on the bioavailability of TKI258 [ Time Frame: 22 days ]

Secondary Outcome Measures :
  1. Characterize the safety and tolerability of TKI258, including acute and chronic toxicities [ Time Frame: Up to 28 days after the last dose of study drug ]
  2. Evaluate preliminary evidence of anti-tumor activity of TKI258 in patients with advanced solid tumors. [ Time Frame: Every 8 weeks until progression of disease ]

Information from the National Library of Medicine

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

Inclusion Criteria:

  • Patients with an advanced solid tumor, except breast cancer,which has progressed despite standard therapy, or for which no standard therapy exists
  • World Health Organization (WHO) performance status ≤ 2
  • Patient must meet protocol-specified laboratory values

Exclusion Criteria:

  • Patients with brain cancer
  • Patients who have concurrent severe and/or uncontrolled medical conditions which could compromise participation in the study
  • Patients who have not recovered from previous anti-cancer therapies
  • Female patients who are pregnant, breast feeding, or not willing to use an effective method of birth control

Other protocol-defined inclusion/exclusion criteria may apply

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 identifier (NCT number): NCT01030055

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United States, California
City of Hope National Medical Center
Duarte, California, United States, 91010
University of California at Los Angeles
Los Angeles, California, United States, 90095
United States, North Carolina
Duke University Medical Center Cancer Dept
Durham, North Carolina, United States, 27710
United States, Utah
University of Utah / Huntsman Cancer Institute
Salt Lake City, Utah, United States, 84112
Sponsors and Collaborators
Novartis Pharmaceuticals
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Study Director: Novartis Pharmaceuticals Novartis Pharmaceuticals

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Responsible Party: Novartis Pharmaceuticals Identifier: NCT01030055     History of Changes
Other Study ID Numbers: CTKI258A2112
First Posted: December 11, 2009    Key Record Dates
Last Update Posted: December 13, 2013
Last Verified: December 2013

Keywords provided by Novartis ( Novartis Pharmaceuticals ):
Administration, oral
CHIR 258
TKI 258