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Advanced Neuroendocrine Tumors of Pancreatic OriginPhase 3RADIANT-3NCT00510068

Efficacy and Safety of Everolimus (RAD001) Compared to Placebo in Patients With Advanced Neuroendocrine Tumors

A Phase 3 study testing Everolimus in people with Advanced Neuroendocrine Tumors of Pancreatic Origin, run by Novartis Pharmaceuticals at 82 sites in 18 countries.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

Trial summary

The purpose of this study was to evaluate progression free survival in those participants assigned everolimus 10 mg/day plus Best Supportive Care versus those assigned to placebo plus Best Supportive Care in Advanced Neuroendocrine Tumors of pancreatic origin. Read more about this study

Who is it for?
Ages 18 years and older
What is being tested?
Everolimus
Type of treatment
Pill or oral medicine
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
410 participants
Where
82 sitesin 18 countries
Study dates
Jul 2007to Mar 2014
Phase
Phase 3
Are there results?
Yes, posted in the registrySummary in the doctors' view

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Patients must have advanced (unresectable or metastatic) biopsy-proven pancreatic NET
  • Measurable disease by radiologic assessment
  • Adequate blood work
  • Performance Status 0-2 : Ability to be out of bed most of the time
  • Adult male or female patients ≥ 18 years of age
  • Women of childbearing potential must have a negative serum pregnancy test
  • Written informed consent from patients must be obtained in accordance to local guidelines

Who cannot join

  • Patients with severe kind of (poorly differentiated neuroendocrine carcinoma, high-grade neuroendocrine carcinoma, adenocarcinoid, goblet cell carcinoid and small cell carcinoma) cancer are not eligible
  • Other chemotherapy, immunotherapy or radiotherapy within 4 weeks prior to starting this trial
  • Hepatic artery procedure called embolization within the last 6 months (1 month if there are other sites of measurable disease), or cryoablation/ radiofrequency ablation of hepatic metastasis within 2 months of enrollment
  • Prior therapy with the same kind of medication (mTOR inhibitors: sirolimus, temsirolimus, everolimus).
  • Uncontrolled diabetes mellitus Patients who have any severe and/or uncontrolled medical conditions such as:
  • Patients receiving chronic treatment with corticosteroids or another immunosuppressive agent
Show all 9Show fewer
  • Patients with a known history of HIV seropositivity
  • No other prior or concurrent cancer at the time enrolling to this trial
  • Other protocol defined inclusion/ exclusion criteria applied

Trial locations and contacts

82 sites in 18 countries.

82 sites in 18 countries

United States24 sites
  • Pacific Cancer Medical Center, Inc.

    Anaheim, California, 92801

  • St. Luke's Hospital and Health Network St. Luke's Cancer Network

    Bethlehem, Pennsylvania

  • Boston Medical Center BMC

    Boston, Massachusetts, 02118

  • Levine Cancer Institute

    Charlotte, North Carolina, 28203

  • Ohio State Comprehensive Cancer Center/James Cancer Hospital Dept. of OHSU Medical Center

    Columbus, Ohio, 43210

  • Kaiser Permanente Northwest Franklin Medical Offices

    Denver, Colorado

  • Wayne State University/Karmanos Cancer Institute Dept.of KarmanosCancerInst (4)

    Detroit, Michigan, 48201

  • The Center for Cancer and Blood Disorders

    Fort Worth, Texas, 76104

  • University of Texas/MD Anderson Cancer Center Dept of MD Anderson CancerCent

    Houston, Texas, 77030-4009

  • Indiana University Health Goshen Center for Cancer Dept. of Indiana Univ. Cancer

    Indianapolis, Indiana, 46202

  • University of Iowa Medical Center Dept. of Iowa Medical Center

    Iowa City, Iowa, 52242

  • Littleton Regional Hospital Dept. of Hematology/Oncology

    Littleton, New Hampshire, 03561

  • Cedars Sinai Medical Center SC-2

    Los Angeles, California, 90048

  • University of California at Los Angeles UCLA (3)

    Los Angeles, California, 90095

  • University of Louisville / James Graham Brown Cancer Center SC

    Louisville, Kentucky, 40202

  • University of South Alabama / Mitchell Cancer Institute Deptof Mitchell Cancer Inst(2)

    Mobile, Alabama, 36688

  • LSU HEALTH SCIENCES CENTER/ LSU SCHOOL OF MEDICINE Dept. of Neuroendocrine Clinic

    New Orleans, Louisiana, 70115

  • Columbia University Medical Center- New York Presbyterian Dept. of Columbia Med. Center

    New York, New York, 10032

  • Fox Chase Cancer Center

    Philadelphia, Pennsylvania, 19111-2497

  • University of Pittsburgh Medical Center Hillman Cancer Center

    Pittsburgh, Pennsylvania, 15213

  • Oregon Health & Science University Dept. of OHSU (3)

    Portland, Oregon, 97239

  • Mayo Clinic - Rochester

    Rochester, Minnesota, 55905

  • University of California San Francisco Dept. of UCSF Comp. Cancer

    San Francisco, California, 94143-0128

  • H. Lee Moffitt Cancer Center & Research Institute Malignant Hematology Clinic

    Tampa, Florida, 33612

Other trials in United States

France13 sites
  • Novartis Investigative Site

    Besançon, 25030

  • Novartis Investigative Site

    Clichy, 92110

  • Novartis Investigative Site

    Dijon, 21079

  • Novartis Investigative Site

    Lille, 59020

  • Novartis Investigative Site

    Lyon, 69437

  • Novartis Investigative Site

    Marseille, 13385

  • Novartis Investigative Site

    Montpellier, 34298

  • Novartis Investigative Site

    Paris, 75015

  • Novartis Investigative Site

    Paris, 75651

  • Novartis Investigative Site

    Reims, 51092

  • Novartis Investigative Site

    Strasbourg, France, 67098

  • Novartis Investigative Site

    Toulouse, 31054

  • Novartis Investigative Site

    Villejuif, 94805

Other trials in France

Italy6 sites
  • Novartis Investigative Site

    Bologna, BO, 40138

  • Novartis Investigative Site

    Milan, MI, 20132

  • Novartis Investigative Site

    Milan, MI, 20141

  • Novartis Investigative Site

    Milan, MI, 20162

  • Novartis Investigative Site

    Modena, MO, 41100

  • Novartis Investigative Site

    Pisa, PI, 56124

Other trials in Italy

Canada5 sites
  • Novartis Investigative Site

    Calgary, Alberta, T2N 4N2

  • Novartis Investigative Site

    Edmonton, Alberta, T6G 1Z2

  • Novartis Investigative Site

    London, Ontario, N6A 4L6

  • Novartis Investigative Site

    Montreal, Quebec, H1T 2M4

  • Novartis Investigative Site

    Montreal, Quebec, H3A 1A1

Other trials in Canada

Germany5 sites
  • Novartis Investigative Site

    Bad Berka, 99438

  • Novartis Investigative Site

    Berlin, 13353

  • Novartis Investigative Site

    Mainz, Germany, 55131

  • Novartis Investigative Site

    Marburg, 35033

  • Novartis Investigative Site

    München, 81377

Other trials in Germany

South Korea4 sites
  • Novartis Investigative Site

    Seoul, Korea, 110 744

  • Novartis Investigative Site

    Seoul, Korea, 120-752

  • Novartis Investigative Site

    Seoul, Korea, 135-710

  • Novartis Investigative Site

    Seoul, 738-736

Other trials in South Korea

Taiwan4 sites
  • Novartis Investigative Site

    Kaohsiung City, 807

  • Novartis Investigative Site

    Lin-Ko, 33305

  • Novartis Investigative Site

    Taipei, Taiwan, 10002

  • Novartis Investigative Site

    Taipei, Taiwan, ROC, 112

Other trials in Taiwan

United Kingdom4 sites
  • Novartis Investigative Site

    Glasgow, G12 0YN

  • Novartis Investigative Site

    London, EC1A 7BE

  • Novartis Investigative Site

    London, SE5 9RS

  • Novartis Investigative Site

    Withington, Greater Manchester, M20 4BX

Other trials in United Kingdom

Belgium3 sites
  • Novartis Investigative Site

    Brussels, 1070

  • Novartis Investigative Site

    Brussels, 1200

  • Novartis Investigative Site

    Leuven, 3000

Other trials in Belgium

Japan3 sites
  • Novartis Investigative Site

    Chuo-ku, Tokyo

  • Novartis Investigative Site

    Fukuoka, Fukuoka, 812-8582

  • Novartis Investigative Site

    Kashiwa, Chiba

Other trials in Japan

Greece2 sites
  • Novartis Investigative Site

    Athens, GR, 115 27

  • Novartis Investigative Site

    Athens, GR-115 22

Other trials in Greece

Spain2 sites
  • Novartis Investigative Site

    Barcelona, Catalonia, 08035

  • Novartis Investigative Site

    L'Hospitalet de Llobregat, Catalonia, 08907

Other trials in Spain

Thailand2 sites
  • Novartis Investigative Site

    Bangkok, 10400

  • Novartis Investigative Site

    Songkhla, 90110

Other trials in Thailand

Brazil1 site
  • Novartis Investigative Site

    Fortaleza, Ceará, 60430-370

Other trials in Brazil

Netherlands1 site
  • Novartis Investigative Site

    Groningen, 9713 GZ

Other trials in Netherlands

Slovakia1 site
  • Novartis Investigative Site

    Martin, Slovak Republic, 036 59

Other trials in Slovakia

Sweden1 site
  • Novartis Investigative Site

    Uppsala, SE-751 85

Other trials in Sweden

Switzerland1 site
  • Novartis Investigative Site

    Zurich, Switzerland, 8091

Other trials in Switzerland

About this study

Official title: A Randomized Double-blind Phase III Study of RAD001 10 mg/d Plus Best Supportive Care Versus Placebo Plus Best Supportive Care in the Treatment of Patients With Advanced Pancreatic Neuroendocrine Tumor (NET)

The purpose of this study was to evaluate progression free survival in those participants assigned everolimus 10 mg/day plus Best Supportive Care versus those assigned to placebo plus Best Supportive Care in Advanced Neuroendocrine Tumors of pancreatic origin.

Being tested
Everolimus, Everolimus Placebo
Keywords
Phase III, Advanced Neuroendocrine Tumor in adults, RAD001, NET, everolimus, mTOr, islet cell, neuroendocrine

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • EverolimusDrug

    Also called RAD001

    A 10-mg dose of everolimus was given by continuous oral daily dosing of two 5-mg tablets.

  • Everolimus PlaceboDrug

    a 10-mg dose of matching placebo to Everolimus was given by continuous oral daily dosing of two 5-mg tablets.

Study groups in NCT00510068
Study groupRoleWhat they receive
Everolimus 10 mg/dayExperimentalParticipants received 10 mg per day of Everolimus plus best supportive care. Patients received their first dose of everolimus at Visit 2 (Cycle 1 Day 1).
Receives: Drug: Everolimus
PlaceboPlacebo comparatorParticipants received matching placebo to everolimus daily plus best supportive care. Patients received their first dose of matching placebo at Visit 2 (Cycle 1 Day 1).
Receives: Drug: Everolimus Placebo

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Time to Progression Free Survival (PFS) Based as Per Investigator Using Kaplan-Meier Methodology

    Progression of disease is defined as the time from study start to the date of first documented progression of disease or death due to any cause. Progression of disease is defined by RECIST criteria: Progression = 20% increase in the sum of the longest diameter of all target lesions, from the smallest sum of longest diameter of all target lesions recorded at or after baseline; or a new lesion; or progression of non-target lesions.

    Measured: Time from randomisation to dates of disease progression, death from any cause or last tumor assessment, reported between day of first patient randomised, 17 August 2007, until cut-off date 28 February 2010

Secondary outcomes (17)
  1. Percentage of Participants With Objective Response Rate ( CR {Complete Response} OR PR {Partial Response})

    Objective Response defined by RECIST criteria: Partial response (PR) must have ≥ 30% decrease in the sum of the longest diameter of all target lesions, from the baseline sum. Complete response (CR) must have disappearance of all target and non-target lesions. For CR or PR, tumor measurements must be confirmed by 2nd assessments within 4 weeks . Progression = 20% increase in the sum of the longest diameter of all target lesions, from the smallest sum of longest diameter of all target lesions recorded at or after baseline; or a new lesion; or progression of non-target lesions

    Measured: Time from randomisation to dates of disease progression, death from any cause or last tumor assessment, reported between day of first patient randomised, 17 August 2007, until cut-off date 28 February 2010

  2. Overall Survival

    Overall survival (OS) was defined as the time from date of randomization to the date of death due to any cause. Analyses were performed using all deaths in the FAS population regardless of whether they were observed during the double-blind treatment period, the open-label treatment period, the post-treatment evaluations, or the survival follow-up period.

    Measured: Baseline, to death- no time limit

  3. Progression Free Survival According to Ki-67 Levels Categorized as: Less Than or Equal to 2%, > 2% to Less Than or Equal to 5% and > 5%

    The level of Ki 67 expression for evaluable tumor samples were analyzed towards progression free survival (PFS) as per local investigator assessment. The Ki-67 protein is a cellular marker for proliferation. It is strictly associated with cell proliferation. During interphase, the Ki-67 antigen can be exclusively detected within the cell nucleus, whereas in mitosis most of the protein is relocated to the surface of the chromosomes. Baseline Ki 67 levels were categorized as: less than or equal to 2%, > 2% to less than or equal to 5% and > 5%.

    Measured: Time from randomisation to dates of disease progression, death from any cause or last tumor assessment, reported between day of first patient randomised, 17 August 2007, until cut-off date 28 February 2010

  4. Progression Free Survival According to Chromogramin A Tumor Marker (CgA) Baseline Level and According to CgA Early Response

    Baseline levels of serum CgA SE were characterized towards progression free survival (PFS) as per local investigator assessment, relative to the upper limited of normal (ULN). CgA levels exceeding 2 x ULN were considered to be 'Elevated' otherwise considered as "Non-elevated". An 'early response' (applicable to only those patients with elevated levels at baseline) was defined as a decrease of greater than or equal to 30% from baseline to Cycle 2 Day 1 or normalization by Cycle 2 Day 1. CgA is widely expressed in well-differentiated pancreatic NET. CgA is present in the secretory granules of neuroendocrine cells. Pancreatic NET patients often present with elevated circulating levels of CgA in their blood. Baseline levels of these biomarkers are considered as prognostic factors.

    Measured: Time from randomisation to dates of disease progression, death from any cause or last tumor assessment, reported between day of first patient randomised, 17 August 2007, until cut-off date 28 February 2010

  5. Progression Free Survival According to Neuron Specific Enolase Tumor Marker (NSE) Baseline Level and According to NSE Early Response

    Baseline levels of serum NSE were characterized towards PFS as per local investigator assessment, relative to the upper limited of normal (ULN). NSE levels exceeding ULN were considered to be 'Elevated' otherwise considered as "Non-elevated". An 'early response' (applicable to only those patients with elevated levels at baseline) was defined as a decrease of greater than or equal to 30% from baseline to Cycle 2 Day 1 or normalization by Cycle 2 Day 1. NSE is widely expressed in well-differentiated pancreatic NET. NSE is usually expressed in the cytoplasm. Pancreatic NET patients often present with elevated circulating levels of NSE in their blood. Baseline levels of these biomarkers are considered as prognostic factors.

    Measured: Time from randomisation to dates of disease progression, death from any cause or last tumor assessment, reported between day of first patient randomised, 17 August 2007, until cut-off date 28 February 2010

  6. Number of Participants With Adverse Events (AEs), Serious Adverse Events (SAEs)

    Adverse events are defined as any unfavorable and unintended diagnosis, symptom, sign (including an abnormal laboratory finding), syndrome or disease which either occurs during study, having been absent at baseline, or, if present at baseline, appears to worsen. Serious adverse events are any untoward medical occurrences that result in death, are life threatening, require (or prolong) hospitalization, cause persistent or significant disability/incapacity, result in congenital anomalies or birth defects, or are other conditions which in judgment of investigators represent significant hazards.

    Measured: on or after the start of double-blind study medication until no later than 28 days after double-blind study medication discontinuation

  7. Number of Participants With Adverse Events (AEs), Serious Adverse Events (SAEs) (Open-label Period)

    Adverse events are defined as any unfavorable and unintended diagnosis, symptom, sign (including an abnormal laboratory finding), syndrome or disease which either occurs during study, having been absent at baseline, or, if present at baseline, appears to worsen. Serious adverse events are any untoward medical occurrences that result in death, are life threatening, require (or prolong) hospitalization, cause persistent or significant disability/incapacity, result in congenital anomalies or birth defects, or are other conditions which in judgment of investigators represent significant hazards.

    Measured: on or after the start of open-label study medication until no later than 28 days after open-label study medication discontinuation

  8. Evaluation of Pharmacokinetics (PK) Parameter: AUC0-t Last

    The PK parameters for a full PK profile at steady-state were determined in blood using non compartmental methods. This PK parameter is area under the concentration-time curve from time zero to the time of the last quantifiable concentration (AUC0-t last).

    Measured: Day 1 of every cycle (28 days/cycle) throughout the study

  9. Evaluation of Pharmacokinetics (PK) Parameters: Cmax, Cmin

    The PK parameters for a full PK profile at steady-state were determined in blood using non compartmental methods. The PK parameter: maximum (peak) drug concentration (Cmax) and minimum (trough) drug concentration (Cmin).

    Measured: Day 1 of every cycle (28 days/cycle) throughout the study

  10. Evaluation of Pharmacokinetics (PK) Parameter: CL/F

    The PK parameters for a full PK profile at steady-state were determined in blood using non compartmental methods. The PK parameter clearance of distribution expressed as a function of bioavailability (CL/F).

    Measured: Day 1 of every cycle (28 days/cycle) throughout the study

  11. Evaluation of Pharmacokinetics (PK) Parameter: Tmax -Time to Maximum (Peak) Drug Concentration

    The PK parameters for a full PK profile at steady-state were determined in blood using non compartmental methods. Values for tmax where summarized in median (range).

    Measured: Day 1 of every cycle (28 days/cycle) throughout the study

  12. Analysis of Time to Definitive Deterioration of WHO Performance Status Using Kaplan-Meier

    Time to definitive worsening is defined as a definitive increase in performance status from a baseline of 0 or 1 to WHO >= 2, or from a baseline value of 2 to WHO >= 3. If no earlier deterioration, patients were censored at the end of follow-up or at the start of further antineoplastic therapy. Rates of patients with no deterioration at 3 and 6 months were computed using Kaplan-meier method. Grade 0: Able to carry out all activity without restriction; Grade 1: Restricted in physically strenuous activity but ambulatory \& able to do light work; Grade 2: Ambulatory \& capable of all self-care but unable to carry out any work. Up \& about more than 50% of waking hours; Grade 3: Capable of only limited self-care, confined to bed or chair more than 50% of waking hours; Grade 4: Completely disabled \& cannot carry on any self-care; totally confined to bed or chair.

    Measured: 3 months, 6 months

  13. Plasma Angiogenesis Marker: Basic Fibroblast Growth Factor (bFGF)

    This biomarker is related to angiogenesis pathway, was analyzed to determine the effects of everolimus on plasma antiangiogenic molecules.

    Measured: Baseline, Cycle 2 Day 1, Cycle 3 Day 1, Cycle 4 Day 1

  14. Plasma Angiogenesis Marker: Placental Growth Factor (PLGF)

    This biomarker is related to angiogenesis pathway, was analyzed to determine the effects of everolimus on plasma antiangiogenic molecules.

    Measured: Baseline, Cycle 2 Day 1, Cycle 3 Day 1, Cycle 4 Day 1

  15. Plasma Angiogenesis Marker: Soluble Vascular Endothelial Growth Factor Receptor 1 (sVEGFR1)

    This biomarker is related to angiogenesis pathway, was analyzed to determine the effects of everolimus on plasma antiangiogenic molecules.

    Measured: Baseline, Cycle 2 Day 1, Cycle 3 Day 1, Cycle 4 Day 1

  16. Plasma Angiogenesis Marker: Soluble Vascular Endothelial Growth Factor Receptor 2 (sVEGFR2)

    This biomarker is related to angiogenesis pathway, was analyzed to determine the effects of everolimus on plasma antiangiogenic molecules.

    Measured: Baseline, Cycle 2 Day 1, Cycle 3 Day 1, Cycle 4 Day 1

  17. Plasma Angiogenesis Marker: Vascular Endothelial Growth Factor (VEGF)

    This biomarker is related to angiogenesis pathway, was analyzed to determine the effects of everolimus on plasma antiangiogenic molecules.

    Measured: Baseline, Cycle 2 Day 1, Cycle 3 Day 1, Cycle 4 Day 1

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted1 Aug 2007 (estimated)
  2. Study startJul 2007
  3. Primary completionFeb 2010
  4. Study completionMar 2014

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Quadruple blind
Who is masked
Participant, Care provider, Investigator, Outcomes assessor
Enrolment
410 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT00510068
Sponsor's protocol ID
CRAD001C2324
Other IDs
2006-006819-75
Acronym
RADIANT-3
Status last verified
Jun 2015
First submitted
31 Jul 2007
Last updated
1 Jul 2015
Data monitoring committee
Yes

Publications

  • Chan DL, Yao JC, Carnaghi C, Buzzoni R, Herbst F, Ridolfi A, Strosberg J, Kulke MH, Pavel M, Singh S. Markers of Systemic Inflammation in Neuroendocrine Tumors: A Pooled Analysis of the RADIANT-3 and RADIANT-4 Studies. Pancreas. 2021 Feb 1;50(2):130-137. doi: 10.1097/MPA.0000000000001745.

    PubMed 33560090
  • Yao JC, Voi M, Lincy J, Pavel M. Reply to V. Amoroso et al. J Clin Oncol. 2017 May 1;35(13):1488-1489. doi: 10.1200/JCO.2017.71.3875. Epub 2017 Jan 23. No abstract available.

    PubMed 28113028
  • Yao JC, Pavel M, Lombard-Bohas C, Van Cutsem E, Voi M, Brandt U, He W, Chen D, Capdevila J, de Vries EGE, Tomassetti P, Hobday T, Pommier R, Oberg K. Everolimus for the Treatment of Advanced Pancreatic Neuroendocrine Tumors: Overall Survival and Circulating Biomarkers From the Randomized, Phase III RADIANT-3 Study. J Clin Oncol. 2016 Nov 10;34(32):3906-3913. doi: 10.1200/JCO.2016.68.0702. Epub 2016 Sep 30.

    PubMed 27621394
  • Lombard-Bohas C, Yao JC, Hobday T, Van Cutsem E, Wolin EM, Panneerselvam A, Stergiopoulos S, Shah MH, Capdevila J, Pommier R. Impact of prior chemotherapy use on the efficacy of everolimus in patients with advanced pancreatic neuroendocrine tumors: a subgroup analysis of the phase III RADIANT-3 trial. Pancreas. 2015 Mar;44(2):181-9. doi: 10.1097/MPA.0000000000000262.

    PubMed 25479584
  • Yao JC, Shah MH, Ito T, Bohas CL, Wolin EM, Van Cutsem E, Hobday TJ, Okusaka T, Capdevila J, de Vries EG, Tomassetti P, Pavel ME, Hoosen S, Haas T, Lincy J, Lebwohl D, Oberg K; RAD001 in Advanced Neuroendocrine Tumors, Third Trial (RADIANT-3) Study Group. Everolimus for advanced pancreatic neuroendocrine tumors. N Engl J Med. 2011 Feb 10;364(6):514-23. doi: 10.1056/NEJMoa1009290.

    PubMed 21306238

Questions about this trial

What is this clinical trial studying?

A Phase 3 study testing Everolimus in people with Advanced Neuroendocrine Tumors of Pancreatic Origin, run by Novartis Pharmaceuticals at 82 sites in 18 countries.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 7 inclusion and 9 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 1 Jul 2015. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 82 sites in United States, France, Italy, Canada, Germany and 13 more countries. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

Yes. Results are posted in the registry (first posted 15 Dec 2011). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Time to Progression Free Survival (PFS) Based as Per Investigator Using Kaplan-Meier Methodology (time frame: Time from randomisation to dates of disease progression, death from any cause or last tumor assessment, reported between day of first patient randomised, 17 August 2007, until cut-off date 28 February 2010). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT00510068, which also lists 5 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 1 Jul 2015.

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