Please note that the copy function is not enabled for this field.
If you wish to
modify
existing outcomes, please copy and paste the current outcome text into the Update field.
LOGIN
CREATE ACCOUNT
LOGIN
CREATE ACCOUNT
MY TRIALS
REGISTER TRIAL
FAQs
HINTS AND TIPS
DEFINITIONS
Trial Review
The ANZCTR website will be unavailable from 1pm until 3pm (AEDT) on Wednesday the 30th of October for website maintenance. Please be sure to log out of the system in order to avoid any loss of data.
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 endorsed by the ANZCTR. Before participating in a study, talk to your health care provider and refer to this
information for consumers
Download to PDF
Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT00256711
Registration number
NCT00256711
Ethics application status
Date submitted
20/11/2005
Date registered
22/11/2005
Date last updated
23/04/2009
Titles & IDs
Public title
Phase II Iressa Versus Vinorelbine (INVITE)
Query!
Scientific title
A Randomised, Open Label, Parallel Group, Multi-Centre, Phase II Study of Progression Free Survival Comparing ZD1839 (IRESSA™) (250 MG Tablet) Versus Vinorelbine (30 MG/M2 Infusion) in Chemonaive, Elderly Patients With Locally Advanced (Stage IIIB) or Metastatic (Stage IV) NSCLC
Query!
Secondary ID [1]
0
0
INVITE
Query!
Secondary ID [2]
0
0
D791AC00001
Query!
Universal Trial Number (UTN)
Query!
Trial acronym
Query!
Linked study record
Query!
Health condition
Health condition(s) or problem(s) studied:
Non-Small-Cell Lung Carcinoma
0
0
Query!
Condition category
Condition code
Cancer
0
0
0
0
Query!
Lung - Non small cell
Query!
Intervention/exposure
Study type
Interventional
Query!
Description of intervention(s) / exposure
Query!
Comparator / control treatment
Query!
Control group
Query!
Outcomes
Primary outcome [1]
0
0
To compare ZD1839 and vinorelbine in terms of progression free survival
Query!
Assessment method [1]
0
0
Query!
Timepoint [1]
0
0
Query!
Secondary outcome [1]
0
0
To compare ZD1839 and vinorelbine in terms of pulmonary symptom improvement weekly for 18 weeks.
Query!
Assessment method [1]
0
0
Query!
Timepoint [1]
0
0
Query!
Secondary outcome [2]
0
0
To compare ZD1839 and vinorelbine in terms of quality of life 3 weekly for 18 weeks then 6 weekly.
Query!
Assessment method [2]
0
0
Query!
Timepoint [2]
0
0
Query!
Secondary outcome [3]
0
0
To compare ZD1839 and vinorelbine in terms of adverse event profile continuous monitoring.
Query!
Assessment method [3]
0
0
Query!
Timepoint [3]
0
0
Query!
Secondary outcome [4]
0
0
To compare ZD1839 and vinorelbine in terms of overall objective tumour response rate (complete response and partial response) 6 weekly to progression.
Query!
Assessment method [4]
0
0
Query!
Timepoint [4]
0
0
Query!
Secondary outcome [5]
0
0
To compare ZD1839 and vinorelbine in terms of overall survival (time to death) continuous monitoring
Query!
Assessment method [5]
0
0
Query!
Timepoint [5]
0
0
Query!
Eligibility
Key inclusion criteria
* Histologically confirmed NSCLC and willing to provide paraffin embedded tumour tissue
* NSCLC - locally advanced (Stage IIIB) or metastatic (stage IV) disease, not amenable to curative surgery or radiotherapy chemonaïve, life expectancy of 12 weeks
* WHO Performance status <= 2
Query!
Minimum age
70
Years
Query!
Query!
Maximum age
No limit
Query!
Query!
Sex
Both males and females
Query!
Can healthy volunteers participate?
No
Query!
Key exclusion criteria
* Newly diagnosed CNS metastases
* Less than 4 weeks since completion of radiotherapy or persistence of any radiotherapy related toxicity.
* Hypersensitivity to ZD1839 or intravenous vinorelbine
* Prior treatment with EGFR inhibitors
* Other co-existing malignancies
* ALT/AST >2.5 x ULRR
* ANC < 2.0 x 10^9/L or platelets < 100 x 10^9/L
Query!
Study design
Purpose of the study
Treatment
Query!
Allocation to intervention
Randomised controlled trial
Query!
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Query!
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Query!
Masking / blinding
Open (masking not used)
Query!
Who is / are masked / blinded?
Query!
Query!
Query!
Query!
Intervention assignment
Parallel
Query!
Other design features
Query!
Phase
Phase 2
Query!
Type of endpoint/s
Query!
Statistical methods / analysis
Query!
Recruitment
Recruitment status
Completed
Query!
Data analysis
Query!
Reason for early stopping/withdrawal
Query!
Other reasons
Query!
Date of first participant enrolment
Anticipated
Query!
Actual
1/07/2004
Query!
Date of last participant enrolment
Anticipated
Query!
Actual
Query!
Date of last data collection
Anticipated
Query!
Actual
1/02/2006
Query!
Sample size
Target
Query!
Accrual to date
Query!
Final
Query!
Recruitment in Australia
Recruitment state(s)
NSW,QLD,WA
Query!
Recruitment hospital [1]
0
0
Research Site - St. Leonards
Query!
Recruitment hospital [2]
0
0
Research Site - Westmead
Query!
Recruitment hospital [3]
0
0
Research Site - South Brisbane
Query!
Recruitment hospital [4]
0
0
Research Site - Nedlands
Query!
Recruitment hospital [5]
0
0
Research Site - Victoria
Query!
Recruitment postcode(s) [1]
0
0
- St. Leonards
Query!
Recruitment postcode(s) [2]
0
0
- Westmead
Query!
Recruitment postcode(s) [3]
0
0
- South Brisbane
Query!
Recruitment postcode(s) [4]
0
0
- Nedlands
Query!
Recruitment postcode(s) [5]
0
0
- Victoria
Query!
Recruitment outside Australia
Country [1]
0
0
Brazil
Query!
State/province [1]
0
0
CE
Query!
Country [2]
0
0
Brazil
Query!
State/province [2]
0
0
GO
Query!
Country [3]
0
0
Brazil
Query!
State/province [3]
0
0
RJ
Query!
Country [4]
0
0
Brazil
Query!
State/province [4]
0
0
SP
Query!
Country [5]
0
0
Czech Republic
Query!
State/province [5]
0
0
CZ
Query!
Country [6]
0
0
Czech Republic
Query!
State/province [6]
0
0
Hradec Kralove
Query!
Country [7]
0
0
Czech Republic
Query!
State/province [7]
0
0
Kutná Hora
Query!
Country [8]
0
0
Czech Republic
Query!
State/province [8]
0
0
Olomouc
Query!
Country [9]
0
0
Czech Republic
Query!
State/province [9]
0
0
Ostrava - Poruba
Query!
Country [10]
0
0
Czech Republic
Query!
State/province [10]
0
0
Ostrava
Query!
Country [11]
0
0
Czech Republic
Query!
State/province [11]
0
0
Plzen
Query!
Country [12]
0
0
France
Query!
State/province [12]
0
0
Marseille Cedex 09
Query!
Country [13]
0
0
France
Query!
State/province [13]
0
0
Montpellier Cedex 5
Query!
Country [14]
0
0
France
Query!
State/province [14]
0
0
Montpellier Cedex
Query!
Country [15]
0
0
France
Query!
State/province [15]
0
0
Pierre Benite Cedex
Query!
Country [16]
0
0
France
Query!
State/province [16]
0
0
Vesoul Cedex
Query!
Country [17]
0
0
Germany
Query!
State/province [17]
0
0
Baden-Württemberg
Query!
Country [18]
0
0
Germany
Query!
State/province [18]
0
0
Bayern
Query!
Country [19]
0
0
Germany
Query!
State/province [19]
0
0
Sachsen-Anhalt
Query!
Country [20]
0
0
Germany
Query!
State/province [20]
0
0
Schleswig-Holstein
Query!
Country [21]
0
0
Germany
Query!
State/province [21]
0
0
Berlin
Query!
Country [22]
0
0
Germany
Query!
State/province [22]
0
0
Großhansdorf
Query!
Country [23]
0
0
Germany
Query!
State/province [23]
0
0
Halle
Query!
Country [24]
0
0
Germany
Query!
State/province [24]
0
0
Hamburg
Query!
Country [25]
0
0
Germany
Query!
State/province [25]
0
0
Mainz
Query!
Country [26]
0
0
Italy
Query!
State/province [26]
0
0
Ancona
Query!
Country [27]
0
0
Italy
Query!
State/province [27]
0
0
BG
Query!
Country [28]
0
0
Italy
Query!
State/province [28]
0
0
BO
Query!
Country [29]
0
0
Italy
Query!
State/province [29]
0
0
CT
Query!
Country [30]
0
0
Italy
Query!
State/province [30]
0
0
MI
Query!
Country [31]
0
0
Italy
Query!
State/province [31]
0
0
MO
Query!
Country [32]
0
0
Italy
Query!
State/province [32]
0
0
PR
Query!
Country [33]
0
0
Italy
Query!
State/province [33]
0
0
TO
Query!
Country [34]
0
0
Italy
Query!
State/province [34]
0
0
Napoli
Query!
Country [35]
0
0
Korea, Republic of
Query!
State/province [35]
0
0
Seoul
Query!
Country [36]
0
0
South Africa
Query!
State/province [36]
0
0
Cape Town
Query!
Country [37]
0
0
South Africa
Query!
State/province [37]
0
0
Durban
Query!
Country [38]
0
0
Taiwan
Query!
State/province [38]
0
0
Taichung
Query!
Country [39]
0
0
Taiwan
Query!
State/province [39]
0
0
Taipei
Query!
Country [40]
0
0
United Kingdom
Query!
State/province [40]
0
0
Cambrideshire
Query!
Country [41]
0
0
United Kingdom
Query!
State/province [41]
0
0
West Midlands
Query!
Country [42]
0
0
United Kingdom
Query!
State/province [42]
0
0
Aberdeen
Query!
Country [43]
0
0
United Kingdom
Query!
State/province [43]
0
0
Dundee
Query!
Country [44]
0
0
United Kingdom
Query!
State/province [44]
0
0
Glasgow
Query!
Country [45]
0
0
United Kingdom
Query!
State/province [45]
0
0
Nottingham
Query!
Country [46]
0
0
United Kingdom
Query!
State/province [46]
0
0
Sheffield
Query!
Funding & Sponsors
Primary sponsor type
Commercial sector/industry
Query!
Name
AstraZeneca
Query!
Address
Query!
Country
Query!
Ethics approval
Ethics application status
Query!
Summary
Brief summary
This is a randomized, open label, parallel group, multi-centre, phase II study of progression free survival, comparing oral ZD1839 (IRESSA™) (250 mg tablet once daily) to vinorelbine 30 mg/m2 infusion on days 1 and 8 of a 21-day cycle) in chemonaïve, elderly patients with locally advanced (stage IIIB) or metastatic (stage IV) non-small cell lung cancer.
Query!
Trial website
https://clinicaltrials.gov/study/NCT00256711
Query!
Trial related presentations / publications
Crino L, Cappuzzo F, Zatloukal P, Reck M, Pesek M, Thompson JC, Ford HE, Hirsch FR, Varella-Garcia M, Ghiorghiu S, Duffield EL, Armour AA, Speake G, Cullen M. Gefitinib versus vinorelbine in chemotherapy-naive elderly patients with advanced non-small-cell lung cancer (INVITE): a randomized, phase II study. J Clin Oncol. 2008 Sep 10;26(26):4253-60. doi: 10.1200/JCO.2007.15.0672.
Query!
Public notes
Query!
Contacts
Principal investigator
Name
0
0
AstraZeneca Iressa Medical Science Director, MD
Query!
Address
0
0
AstraZeneca
Query!
Country
0
0
Query!
Phone
0
0
Query!
Fax
0
0
Query!
Email
0
0
Query!
Contact person for public queries
Name
0
0
Query!
Address
0
0
Query!
Country
0
0
Query!
Phone
0
0
Query!
Fax
0
0
Query!
Email
0
0
Query!
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 not provided in
https://clinicaltrials.gov/study/NCT00256711
Download to PDF