Trial Review

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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/study/NCT00741260




Registration number
NCT00741260
Ethics application status
Date submitted
22/08/2008
Date registered
26/08/2008
Date last updated
5/09/2018

Titles & IDs
Public title
Study Evaluating The Combination Of Neratinib And Capecitabine In Solid Tumors And Breast Cancer
Scientific title
A Phase 1/2, Open-Label Study Of Neratinib (HKI-272) In Combination With Capecitabine In Subjects With Solid Tumors And ErbB-2 Positive Metastatic Or Locally Advanced Breast Cancer
Secondary ID [1] 0 0
3144A1-2206 / B1891017
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Breast Cancer 0 0
Condition category
Condition code
Cancer 0 0 0 0
Breast

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Treatment: Drugs - Neratinib
Treatment: Drugs - Capecitabine

Experimental: Neratinib and Capecitabine (Dose Level 1) - Neratinib 160 mg and Capecitabine 1500 mg/m\^2

Experimental: Neratinib and Capecitabine (Dose Group 2) - Neratinib 240 mg and Capecitabine 1500 mg/m\^2

Experimental: Neratinib and Capecitabine (Dose Group 3) - Neratinib 240 mg and Capecitabine 2000 mg/m\^2

Experimental: Neratinib and Capecitabine (Dose Group 4) - Neratinib 200 mg and Capecitabine 2000 mg/m\^2

Experimental: Neratinib and Capecitabine (Dose Group 5) - Neratinib 160 mg and Capecitabine 2000 mg/m\^2

Experimental: Neratinib and Capecitabine MTD (Dose Group 6) - Neratinib and Capecitabine Maximum Tolerated Dose without prior lapatinib

Experimental: Neratinib and Capecitabine MTD (Dose Group 7) - Neratinib and Capecitabine Maximum Tolerated Dose with prior lapatinib


Treatment: Drugs: Neratinib
Neratinib orally once daily continually

Treatment: Drugs: Capecitabine
Capecitabine orally on days 1-14 of each 21 day cycle
Intervention code [1] 0 0
Treatment: Drugs
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Number of Participants With Dose Limiting Toxicities
Timepoint [1] 0 0
From first dose date to day 21
Primary outcome [2] 0 0
Maximum Tolerated Dose (MTD) of Neratinib
Timepoint [2] 0 0
From first dose date to day 21.
Primary outcome [3] 0 0
Maximum Tolerated Dose (MTD) of Capecitabine
Timepoint [3] 0 0
From first dose date to day 21.
Secondary outcome [1] 0 0
Overall Response Rate
Timepoint [1] 0 0
From first dose date to progression or last tumor assessment, up to three years.
Secondary outcome [2] 0 0
Clinical Benefit Rate
Timepoint [2] 0 0
From first dose date to progression or last tumor assessment, up to three years.
Secondary outcome [3] 0 0
Duration of Response
Timepoint [3] 0 0
From start date of response to first PD/death, up to three years.

Eligibility
Key inclusion criteria
INCLUSION CRITERIA

PART 1:

* confirmed pathologic diagnosis of a solid tumor not curable with available therapies for which neratinib plus capecitabine is a reasonable treatment option.

PART 2:

* confirmed histologically and/or cytologically confirmed diagnosis of breast cancer, metastatic or locally advanced.
* erbB-2 gene amplified tumor (FISH or CISH) or erbB-2 overexpression (IHC 3+, or IHC2+ with FISH or CISH confirmation), based on local testing, or based on centralized FISH testing prior to day 1.
* disease progression on or following at least 1 prior trastuzumab containing treatment regimen (at least 6 weeks) for metastatic or locally advanced disease. (Prior adjuvant trastuzumab is allowed but not required). A 2 week period is required between the last dose of trastuzumab treatment and first dose of the test article.
* Prior treatment with a taxane in the neoadjuvant, adjuvant, locally advanced, and/or metastatic disease treatment setting.

PARTS 1 and 2:

* At least 1 measurable lesion as defined by RECIST criteria.
* LVEF within institutional range of normal as measured by multi-gated acquisition (MUGA) or echocardiogram (ECHO).

EXCLUSION CRITERIA

PART 2:

* prior treatment with capecitabine, lapatinib (20 subjects with prior lapatinib exposure will be enrolled) or any erbB-2 targeted agents except trastuzumab. Treatment with erbB-2 targeted therapy must exceed 2 weeks (14 days) in order to be exclusionary.
* prior treatment with anthracyclines with a cumulative dose of doxorubicin of greater than 400 mg/m², epirubicin dose of greater than 800 mg/m², or the equivalent dose for other anthracyclines.

PARTS 1 and 2:

* Subjects with bone as the only site of disease.
* Active uncontrolled or symptomatic central nervous system (CNS) metastases, as indicated by clinical symptoms, cerebral edema, and/or progressive growth. Subjects with a history of CNS metastases or cord compression are allowable if they have been considered definitively treated and are off anticonvulsants and steroids for at least 4 weeks before the first dose of test article.
* Any other cancer within 5 years prior to screening with the exception of adequately treated cervical carcinoma in situ, or adequately treated basal or squamous cell carcinoma of the skin.
Minimum age
18 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria

Study design
Purpose of the study
Treatment
Allocation to intervention
Non-randomised trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Open (masking not used)
Who is / are masked / blinded?



Intervention assignment
Other
Other design features
Phase
Phase 1
Type of endpoint/s
Statistical methods / analysis

Recruitment
Recruitment status
Completed
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
9/12/2008
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
1/06/2018
Sample size
Target
Accrual to date
Final
105
Recruitment in Australia
Recruitment state(s)
QLD,VIC
Recruitment hospital [1] 0 0
Mater Private Centre for HOCA - South Brisbane
Recruitment hospital [2] 0 0
Border Medical Oncology - Wodonga
Recruitment postcode(s) [1] 0 0
4101 - South Brisbane
Recruitment postcode(s) [2] 0 0
3690 - Wodonga
Recruitment outside Australia
Country [1] 0 0
United States of America
State/province [1] 0 0
Alabama
Country [2] 0 0
United States of America
State/province [2] 0 0
California
Country [3] 0 0
United States of America
State/province [3] 0 0
Florida
Country [4] 0 0
United States of America
State/province [4] 0 0
Idaho
Country [5] 0 0
United States of America
State/province [5] 0 0
Indiana
Country [6] 0 0
United States of America
State/province [6] 0 0
Missouri
Country [7] 0 0
United States of America
State/province [7] 0 0
New York
Country [8] 0 0
United States of America
State/province [8] 0 0
Ohio
Country [9] 0 0
United States of America
State/province [9] 0 0
Pennsylvania
Country [10] 0 0
United States of America
State/province [10] 0 0
Texas
Country [11] 0 0
Brazil
State/province [11] 0 0
RS - Brazil
Country [12] 0 0
Brazil
State/province [12] 0 0
RS
Country [13] 0 0
China
State/province [13] 0 0
Beijing
Country [14] 0 0
China
State/province [14] 0 0
Jiangsu
Country [15] 0 0
Croatia
State/province [15] 0 0
Zagreb
Country [16] 0 0
Hong Kong
State/province [16] 0 0
Hong Kong
Country [17] 0 0
Hungary
State/province [17] 0 0
Budapest
Country [18] 0 0
Hungary
State/province [18] 0 0
Nyiregyhaza
Country [19] 0 0
Korea, Republic of
State/province [19] 0 0
Seoul
Country [20] 0 0
Russian Federation
State/province [20] 0 0
Kazan
Country [21] 0 0
Russian Federation
State/province [21] 0 0
Perm
Country [22] 0 0
Russian Federation
State/province [22] 0 0
Saint Petersburg
Country [23] 0 0
Singapore
State/province [23] 0 0
Singapore
Country [24] 0 0
Spain
State/province [24] 0 0
Barcelona
Country [25] 0 0
Spain
State/province [25] 0 0
Madrid
Country [26] 0 0
Spain
State/province [26] 0 0
Valencia

Funding & Sponsors
Primary sponsor type
Commercial sector/industry
Name
Puma Biotechnology, Inc.
Address
Country

Ethics approval
Ethics application status

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
Puma
Address 0 0
Biotechnology
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for scientific queries

No information has been provided regarding IPD availability


What supporting documents are/will be available?

No Supporting Document Provided



Results publications and other study-related documents

No documents have been uploaded by study researchers.

Results are available at https://clinicaltrials.gov/study/NCT00741260