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
Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/ct2/show/NCT00065468




Registration number
NCT00065468
Ethics application status
Date submitted
24/07/2003
Date registered
25/07/2003
Date last updated
25/10/2012

Titles & IDs
Public title
Study Evaluating Interferon And CCI-779 In Advanced Renal Cell Carcinoma
Scientific title
A Phase 3, Three-Arm, Randomized, Open-Label Study Of Interferon Alfa Alone, CCI-779 Alone, And The Combination Of Interferon Alfa And CCI-779 In First-Line Poor-Prognosis Subjects With Advanced Renal Cell Carcinoma.
Secondary ID [1] 0 0
3066K1-304
Universal Trial Number (UTN)
Trial acronym
ARCC
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Carcinoma, Renal Cell 0 0
Kidney Neoplasms 0 0
Condition category
Condition code
Cancer 0 0 0 0
Non melanoma skin cancer
Cancer 0 0 0 0
Kidney

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Treatment: Drugs - Interferon Alfa
Treatment: Drugs - CCI-779
Treatment: Drugs - Interferon Alfa and CCI-779

Active Comparator: A -

Experimental: B -

Experimental: C -


Treatment: Drugs: Interferon Alfa
Interferon alfa (Roferon) 3 MU given Sub Cutaneously three time /week for the first week, 9 MU given Sub Cutaneously three time /week for the second week, 18 MU given Sub Cutaneously three time /week thereafter.

Treatment: Drugs: CCI-779
25 mg of CCI-779 given Intra Venously once per week

Treatment: Drugs: Interferon Alfa and CCI-779
15 mg of CCI-779 given Intra Venously once per week; 6 MU of IFN alfa (Roferon) given Sub Cutaneously three time /week

Intervention code [1] 0 0
Treatment: Drugs
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Overall Survival (OS)
Timepoint [1] 0 0
Baseline up to Month 80
Secondary outcome [1] 0 0
Progression-Free Survival (PFS)
Timepoint [1] 0 0
Baseline, monthly until tumor progression or death (up to Month 80)
Secondary outcome [2] 0 0
Percentage of Participants With Objective Response
Timepoint [2] 0 0
Baseline, every 2 months until tumor progression or death (up to Month 80)
Secondary outcome [3] 0 0
Percentage of Participants With Clinical Benefit
Timepoint [3] 0 0
Baseline, every 2 months until tumor progression or death (up to Month 80)
Secondary outcome [4] 0 0
Duration of Response (DR)
Timepoint [4] 0 0
Baseline, every month until tumor progression or death (up to Month 80)
Secondary outcome [5] 0 0
Time to Treatment Failure (TTF)
Timepoint [5] 0 0
Baseline, every month until tumor progression or death (up to Month 80)
Secondary outcome [6] 0 0
Quality-adjusted Time Without Symptoms or Toxicity (Q-TWiST)
Timepoint [6] 0 0
Baseline to Month 80
Secondary outcome [7] 0 0
European Quality of Life Health Questionnaire (EQ-5D) - Index Score
Timepoint [7] 0 0
Baseline

Eligibility
Key inclusion criteria
- This study will be conducted in subjects with histologically confirmed, advanced
(stage IV or recurrent disease) RCC who have not received prior systemic therapy for
their disease,
Minimum age
18 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
- Subjects with central nervous system (CNS) metastases

- Prior anticancer therapy for RCC

- Prior investigational therapy/agents within 4 weeks of randomization

Study design
Purpose of the study
Treatment
Allocation to intervention
Randomised controlled 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 3
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
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
Sample size
Target
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
NSW,SA,VIC
Recruitment hospital [1] 0 0
Pfizer Investigational Site - Kogarah
Recruitment hospital [2] 0 0
Pfizer Investigational Site - Newcastle
Recruitment hospital [3] 0 0
Pfizer Investigational Site - Westmead
Recruitment hospital [4] 0 0
Pfizer Investigational Site - Adelaide
Recruitment hospital [5] 0 0
Pfizer Investigational Site - Footscray
Recruitment hospital [6] 0 0
Pfizer Investigational Site - Heidelberg
Recruitment hospital [7] 0 0
Pfizer Investigational Site - Melbourne
Recruitment postcode(s) [1] 0 0
2217 - Kogarah
Recruitment postcode(s) [2] 0 0
- Newcastle
Recruitment postcode(s) [3] 0 0
2145 - Westmead
Recruitment postcode(s) [4] 0 0
5000 - Adelaide
Recruitment postcode(s) [5] 0 0
3012 - Footscray
Recruitment postcode(s) [6] 0 0
3084 - Heidelberg
Recruitment postcode(s) [7] 0 0
3050 - Melbourne
Recruitment outside Australia
Country [1] 0 0
United States of America
State/province [1] 0 0
Arkansas
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
Connecticut
Country [4] 0 0
United States of America
State/province [4] 0 0
Florida
Country [5] 0 0
United States of America
State/province [5] 0 0
Illinois
Country [6] 0 0
United States of America
State/province [6] 0 0
Indiana
Country [7] 0 0
United States of America
State/province [7] 0 0
Kansas
Country [8] 0 0
United States of America
State/province [8] 0 0
Kentucky
Country [9] 0 0
United States of America
State/province [9] 0 0
Louisiana
Country [10] 0 0
United States of America
State/province [10] 0 0
Maryland
Country [11] 0 0
United States of America
State/province [11] 0 0
Massachusetts
Country [12] 0 0
United States of America
State/province [12] 0 0
Michigan
Country [13] 0 0
United States of America
State/province [13] 0 0
Missouri
Country [14] 0 0
United States of America
State/province [14] 0 0
Montana
Country [15] 0 0
United States of America
State/province [15] 0 0
New Hampshire
Country [16] 0 0
United States of America
State/province [16] 0 0
New Jersey
Country [17] 0 0
United States of America
State/province [17] 0 0
New York
Country [18] 0 0
United States of America
State/province [18] 0 0
North Carolina
Country [19] 0 0
United States of America
State/province [19] 0 0
Ohio
Country [20] 0 0
United States of America
State/province [20] 0 0
Oklahoma
Country [21] 0 0
United States of America
State/province [21] 0 0
Oregon
Country [22] 0 0
United States of America
State/province [22] 0 0
Pennsylvania
Country [23] 0 0
United States of America
State/province [23] 0 0
South Carolina
Country [24] 0 0
United States of America
State/province [24] 0 0
Tennessee
Country [25] 0 0
United States of America
State/province [25] 0 0
Texas
Country [26] 0 0
United States of America
State/province [26] 0 0
Utah
Country [27] 0 0
United States of America
State/province [27] 0 0
Virginia
Country [28] 0 0
United States of America
State/province [28] 0 0
Washington
Country [29] 0 0
Argentina
State/province [29] 0 0
Aires
Country [30] 0 0
Argentina
State/province [30] 0 0
Tucuman
Country [31] 0 0
Argentina
State/province [31] 0 0
Buenos Aires
Country [32] 0 0
Argentina
State/province [32] 0 0
Cordoba
Country [33] 0 0
Argentina
State/province [33] 0 0
Mendoza
Country [34] 0 0
Argentina
State/province [34] 0 0
Quilmes
Country [35] 0 0
Canada
State/province [35] 0 0
Alberta
Country [36] 0 0
Canada
State/province [36] 0 0
British Columbia
Country [37] 0 0
Canada
State/province [37] 0 0
Manitoba
Country [38] 0 0
Canada
State/province [38] 0 0
Nova Scotia
Country [39] 0 0
Canada
State/province [39] 0 0
Ontario
Country [40] 0 0
Canada
State/province [40] 0 0
Quebec
Country [41] 0 0
Canada
State/province [41] 0 0
Hamilton, Ontario
Country [42] 0 0
Czech Republic
State/province [42] 0 0
Brno
Country [43] 0 0
Czech Republic
State/province [43] 0 0
Prague 5
Country [44] 0 0
Former Serbia and Montenegro
State/province [44] 0 0
Novi Sad
Country [45] 0 0
Germany
State/province [45] 0 0
NRW
Country [46] 0 0
Germany
State/province [46] 0 0
RP
Country [47] 0 0
Greece
State/province [47] 0 0
Creete
Country [48] 0 0
Greece
State/province [48] 0 0
Patra
Country [49] 0 0
Hungary
State/province [49] 0 0
Budapest
Country [50] 0 0
Italy
State/province [50] 0 0
RM
Country [51] 0 0
Italy
State/province [51] 0 0
Foggia
Country [52] 0 0
Italy
State/province [52] 0 0
Milano
Country [53] 0 0
Latvia
State/province [53] 0 0
Daugavpils
Country [54] 0 0
Latvia
State/province [54] 0 0
Riga
Country [55] 0 0
Lithuania
State/province [55] 0 0
Vilnius
Country [56] 0 0
Mexico
State/province [56] 0 0
Nuevo Leon
Country [57] 0 0
Mexico
State/province [57] 0 0
Leon Guanajuato
Country [58] 0 0
Netherlands
State/province [58] 0 0
GA
Country [59] 0 0
Netherlands
State/province [59] 0 0
Amsterdam
Country [60] 0 0
Netherlands
State/province [60] 0 0
Enschede
Country [61] 0 0
Poland
State/province [61] 0 0
Bytom
Country [62] 0 0
Poland
State/province [62] 0 0
Lodz
Country [63] 0 0
Poland
State/province [63] 0 0
Lublin
Country [64] 0 0
Poland
State/province [64] 0 0
Olsztyn
Country [65] 0 0
Poland
State/province [65] 0 0
Opole
Country [66] 0 0
Poland
State/province [66] 0 0
Poznan
Country [67] 0 0
Poland
State/province [67] 0 0
Siedlce
Country [68] 0 0
Poland
State/province [68] 0 0
Warszawa
Country [69] 0 0
Russian Federation
State/province [69] 0 0
Barnaul
Country [70] 0 0
Russian Federation
State/province [70] 0 0
Kemerovo
Country [71] 0 0
Russian Federation
State/province [71] 0 0
Moscow
Country [72] 0 0
Russian Federation
State/province [72] 0 0
Obninsk
Country [73] 0 0
Russian Federation
State/province [73] 0 0
Saint Petersburg
Country [74] 0 0
Russian Federation
State/province [74] 0 0
St Petersburg
Country [75] 0 0
Russian Federation
State/province [75] 0 0
Ufa
Country [76] 0 0
Serbia
State/province [76] 0 0
Belgrade
Country [77] 0 0
Slovakia
State/province [77] 0 0
Banska Bystrica
Country [78] 0 0
Slovakia
State/province [78] 0 0
Bratislava
Country [79] 0 0
Slovakia
State/province [79] 0 0
Martin
Country [80] 0 0
Slovakia
State/province [80] 0 0
Zlina
Country [81] 0 0
South Africa
State/province [81] 0 0
Eastern Cape
Country [82] 0 0
South Africa
State/province [82] 0 0
Gauteng
Country [83] 0 0
South Africa
State/province [83] 0 0
Cape Town
Country [84] 0 0
Spain
State/province [84] 0 0
Asturias
Country [85] 0 0
Spain
State/province [85] 0 0
Barcelona
Country [86] 0 0
Spain
State/province [86] 0 0
Madrid
Country [87] 0 0
Sweden
State/province [87] 0 0
Göteborg
Country [88] 0 0
Sweden
State/province [88] 0 0
Stockholm
Country [89] 0 0
Sweden
State/province [89] 0 0
Uppsala
Country [90] 0 0
Taiwan
State/province [90] 0 0
ROC
Country [91] 0 0
Taiwan
State/province [91] 0 0
Taichung
Country [92] 0 0
Taiwan
State/province [92] 0 0
Taipei
Country [93] 0 0
Taiwan
State/province [93] 0 0
Taoyuan
Country [94] 0 0
Turkey
State/province [94] 0 0
Istanbul
Country [95] 0 0
Turkey
State/province [95] 0 0
Izmir
Country [96] 0 0
Ukraine
State/province [96] 0 0
Dnietropetrovsk
Country [97] 0 0
Ukraine
State/province [97] 0 0
Donetsk
Country [98] 0 0
Ukraine
State/province [98] 0 0
Kharkov
Country [99] 0 0
Ukraine
State/province [99] 0 0
Kiev
Country [100] 0 0
Ukraine
State/province [100] 0 0
Lviv
Country [101] 0 0
Ukraine
State/province [101] 0 0
Zaporozhye
Country [102] 0 0
United Kingdom
State/province [102] 0 0
Lancashire
Country [103] 0 0
United Kingdom
State/province [103] 0 0
Strathclyde
Country [104] 0 0
United Kingdom
State/province [104] 0 0
Surrey
Country [105] 0 0
United Kingdom
State/province [105] 0 0
Nottingham
Country [106] 0 0
State/province [106] 0 0

Funding & Sponsors
Primary sponsor type
Commercial sector/Industry
Name
Pfizer
Address
Country

Ethics approval
Ethics application status

Summary
Brief summary
The primary objective of this study is efficacy. The primary efficacy endpoint of this study
is a comparison of the overall survival of subjects treated with CCI-779 [Temsirolimus],
administered intravenously [IV] once weekly and the combination of CCI-779, administered IV
once weekly with Interferon Alfa [IFN alfa] subcutaneously [SC] three times per week [TIW],
compared with the overall survival of subjects treated with IFN alfa (SC TIW) alone, in
poor-prognosis subjects with advanced RCC.
Trial website
https://clinicaltrials.gov/ct2/show/NCT00065468
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
Pfizer CT.gov Call Center
Address 0 0
Pfizer
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



Summary Results

For IPD and results data, please see https://clinicaltrials.gov/ct2/show/NCT00065468