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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/study/NCT01378975




Registration number
NCT01378975
Ethics application status
Date submitted
21/06/2011
Date registered
23/06/2011
Date last updated
1/08/2016

Titles & IDs
Public title
A Study of Vemurafenib in Metastatic Melanoma Participants With Brain Metastases
Scientific title
An Open-label, Single-arm, Phase II, Multicenter Study, to Evaluate the Efficacy of Vemurafenib in Metastatic Melanoma Patients With Brain Metastases
Secondary ID [1] 0 0
MO25743
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Malignant Melanoma 0 0
Condition category
Condition code
Cancer 0 0 0 0
Malignant melanoma
Cancer 0 0 0 0
Brain

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

Experimental: Cohort 1: Previously Untreated Participants - Participants who had not received previous treatment for brain metastases \[i.e., had never received brain stereotactic radiotherapy (SRT), whole-brain radiotherapy (WBRT), surgery, or any other treatment for their brain metastases\] received Vemurafenib 960 milligram (mg) tablet orally, twice daily (BID) from Day 1 until development of progressive disease within the brain or outside of the brain (whichever occurred first), unacceptable toxicity, consent withdrawal, protocol violation endangering participant's safety, death, reasons deemed by the investigator, or study termination by the Sponsor.

Experimental: Cohort 2: Previously treated Participants - Participants who were previously treated with brain SRT, WBRT, or surgery for their brain metastases and have progressed following this treatment, received Vemurafenib 960 milligram (mg) tablet orally, BID from Day 1 until development of progressive disease within the brain or outside of the brain (whichever occurred first), unacceptable toxicity, consent withdrawal, protocol violation endangering participant's safety, death, reasons deemed by the investigator, or study termination by the Sponsor.


Treatment: Drugs: Vemurafenib
960 mg oral doses twice daily until disease progression, unacceptable toxicity or consent withdrawal.
Intervention code [1] 0 0
Treatment: Drugs
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Best Overall Response Rate (BORR) Within Brain of Previously Untreated Participants (Assessed by Independent Review Committee [IRC] Using Modified Response Evaluation Criteria in Solid Tumors [RECIST])
Timepoint [1] 0 0
Baseline up to the disease progression or death from any cause (approximately 4 years)
Secondary outcome [1] 0 0
Best Overall Response Rate (BORR) in the Brain of Participants With Previously Treated or Untreated Brain Metastases as Assessed by the IRC Using RECIST v1.1
Timepoint [1] 0 0
Baseline up to the disease progression or death from any cause (approximately 4 years)
Secondary outcome [2] 0 0
Best Overall Response Rate (BORR) in the Brain of Participants With Previously Treated Brain Metastases as Assessed by the IRC Using RECIST v1.1
Timepoint [2] 0 0
Baseline up to the disease progression or death from any cause (approximately 4 years)
Secondary outcome [3] 0 0
Best Overall Response Rate Outside the Brain (Assessed by IRC)
Timepoint [3] 0 0
Baseline up to the disease progression or death from any cause (approximately 4 years)
Secondary outcome [4] 0 0
Duration of Response (DOR) (Assessed by Investigator and IRC)
Timepoint [4] 0 0
Date of the earliest qualifying response until the earliest date of PD or death from any cause (approximately up to 4 years)
Secondary outcome [5] 0 0
Progression-Free Survival (PFS) Based on Overall Tumor Response (Assessed by Investigator)
Timepoint [5] 0 0
Baseline up to the disease progression or death from any cause (approximately 4 years)
Secondary outcome [6] 0 0
Progression-Free Survival (PFS) Based on Tumor Assessment Within Brain Only (Assessed by Investigator )
Timepoint [6] 0 0
Baseline up to the disease progression or death from any cause (approximately 4 years)
Secondary outcome [7] 0 0
Time to Development of New Brain Metastases in Responders
Timepoint [7] 0 0
Date of first treatment and the earliest date of documentation of new brain lesions (approximately up to 4 years)
Secondary outcome [8] 0 0
Overall Survival
Timepoint [8] 0 0
Baseline up to the disease progression or death from any cause (approximately 4 years)
Secondary outcome [9] 0 0
Best Overall Response Rate (BORR) Within the Brain and Outside Brain (Assessed by Investigator)
Timepoint [9] 0 0
Baseline up to the disease progression or death from any cause (approximately 4 years)
Secondary outcome [10] 0 0
Best Overall Response Rate (BORR) Within the Brain and Outside Brain (Not Necessarily Follows the RECIST Criteria - as Assessed by Investigator)
Timepoint [10] 0 0
Baseline up to the disease progression or death from any cause (approximately 4 years)
Secondary outcome [11] 0 0
Percentage of Participants With Adverse Events (AE)
Timepoint [11] 0 0
From signing of informed consent form up to 28 days after the last dose of study drug (approximately up to 4 years)

Eligibility
Key inclusion criteria
* Adult participants, >/= 18 years of age
* Histologically confirmed metastatic melanoma (Stage IV, American Joint Committee on Cancer) with BRAF V600 mutation (cobas 4800 BRAF V600 Mutation Test)
* Measurable brain metastases, defined as lesions that were accurately measured in at least one dimension (longest diameter to be recorded) as =0.5 cm in the brain MRI with contrast, treated or untreated
* Participants may or may not have received prior systemic therapy for metastatic melanoma and either a) have received no prior treatment for brain metastases or b) have received prior treatment for brain metastases and have progressed
* Participants may or may not have symptoms related to their brain metastases
* Eastern Cooperative Oncology Group (ECOG) performance status 0-1
* Participants must have recovered from all side effects of their most recent systemic or local treatment for metastatic melanoma
Minimum age
18 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
* Increasing corticosteroid dose during the 7 days prior to first dose of study drug
* Leptomeningeal involvement in participants with no prior treatment for brain metastases
* Previous malignancy requiring active treatment within the past 2 years, except for treated and controlled basal or squamous cell carcinoma of the skin, or carcinoma in-situ of the cervix
* Concurrent administration of any anticancer therapies other than those administered in the study
* Treatment with any cytotoxic, investigational drug or targeted therapy 4 weeks prior to first dose of study drug. Radiation therapy =1 week prior to first administration of vemurafenib; and stereotactic radiotherapy =1 day prior to prior to first administration of vemurafenib
* Prior treatment with BRAF or MEK inhibitors
* Clinically significant cardiovascular disease or event within the 6 months prior to first dose of study drug

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
Parallel
Other design features
Phase
Phase 2
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
1/07/2011
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
1/07/2015
Sample size
Target
Accrual to date
Final
146
Recruitment in Australia
Recruitment state(s)
NSW,VIC
Recruitment hospital [1] 0 0
- Wentworthville
Recruitment hospital [2] 0 0
- Melbourne
Recruitment postcode(s) [1] 0 0
2145 - Wentworthville
Recruitment postcode(s) [2] 0 0
3002 - Melbourne
Recruitment outside Australia
Country [1] 0 0
United States of America
State/province [1] 0 0
California
Country [2] 0 0
United States of America
State/province [2] 0 0
Colorado
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
Massachusetts
Country [5] 0 0
United States of America
State/province [5] 0 0
Michigan
Country [6] 0 0
United States of America
State/province [6] 0 0
Minnesota
Country [7] 0 0
United States of America
State/province [7] 0 0
Missouri
Country [8] 0 0
United States of America
State/province [8] 0 0
North Carolina
Country [9] 0 0
United States of America
State/province [9] 0 0
Texas
Country [10] 0 0
United States of America
State/province [10] 0 0
Washington
Country [11] 0 0
Canada
State/province [11] 0 0
Ontario
Country [12] 0 0
France
State/province [12] 0 0
Bordeaux
Country [13] 0 0
France
State/province [13] 0 0
Nice
Country [14] 0 0
France
State/province [14] 0 0
Paris
Country [15] 0 0
Germany
State/province [15] 0 0
Essen
Country [16] 0 0
Germany
State/province [16] 0 0
Frankfurt
Country [17] 0 0
Germany
State/province [17] 0 0
Kiel
Country [18] 0 0
Germany
State/province [18] 0 0
Mannheim
Country [19] 0 0
Germany
State/province [19] 0 0
Münster
Country [20] 0 0
Germany
State/province [20] 0 0
Tübingen
Country [21] 0 0
Israel
State/province [21] 0 0
Tel-Hashomer
Country [22] 0 0
Italy
State/province [22] 0 0
Lombardia
Country [23] 0 0
Italy
State/province [23] 0 0
Toscana
Country [24] 0 0
Netherlands
State/province [24] 0 0
Amsterdam
Country [25] 0 0
Netherlands
State/province [25] 0 0
Groningen
Country [26] 0 0
Spain
State/province [26] 0 0
Navarra
Country [27] 0 0
Spain
State/province [27] 0 0
Barcelona
Country [28] 0 0
Spain
State/province [28] 0 0
Madrid
Country [29] 0 0
United Kingdom
State/province [29] 0 0
Northwood

Funding & Sponsors
Primary sponsor type
Commercial sector/industry
Name
Hoffmann-La Roche
Address
Country

Ethics approval
Ethics application status

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

Contacts
Principal investigator
Name 0 0
Clinical Trials
Address 0 0
Hoffmann-La Roche
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/NCT01378975