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MelanomaPhase 3NCT00324155

Dacarbazine and Ipilimumab vs. Dacarbazine With Placebo in Untreated Unresectable Stage III or IV Melanoma

A Phase 3 study testing Ipilimumab and Dacarbazine in people with Melanoma, run by Bristol-Myers Squibb at 127 sites in 25 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 clinical research study is to examine the safety and effectiveness (how well the drug works) of two different treatments for patients with melanoma. One treatment is an investigational compound (a drug that is not currently approved by the United States Food and Drug Administration [FDA]), know as… Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Melanoma
What is being tested?
Ipilimumab and Dacarbazine
Type of treatment
Injection or infusion
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
681 participants
Where
127 sitesin 25 countries
Study dates
Aug 2006to Oct 2013
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

  • Informed Consent
  • Measurable Disease
  • Eastern Cooperative Oncology Group (ECOG) 0 or 1
  • Lab / imaging requirements
  • Neg for Human Immunodeficiency Virus (HIV), Hepatitis B (HepB), C
  • Men and Women > 18 years (16 were allowable)
  • Prior therapy restriction (adjuvant only)

Who cannot join

  • Pregnant / nursing
  • Inadequate contraception
  • Brain metastasis
  • Primary ocular or mucosal melanoma

Trial locations and contacts

127 sites in 25 countries.

127 sites in 25 countries

United States32 sites
  • University Of New Mexico Cancer Center

    Albuquerque, New Mexico, 87106

  • Pacific Cancer Medical Center

    Anaheim, California, 92801

  • Greater Baltimore Medical Center

    Baltimore, Maryland, 21204

  • Sinai Hospital Of Baltimore

    Baltimore, Maryland, 21215

  • St. Luke'S Hospital & Health Network

    Bethlehem, Pennsylvania, 18015

  • Dana Farber Cancer Institute

    Boston, Massachusetts, 02115

  • Blumenthal Cancer Center

    Charlotte, North Carolina, 28204

  • University Of Chicago

    Chicago, Illinois, 60637

  • Ellis Fischel Cancer Center

    Columbia, Missouri, 65203

  • Central Indiana Cancer Centers

    Fishers, Indiana, 46037

  • Saint Francis Hospital And Medical Center

    Hartford, Connecticut, 06105

  • Kentucky Cancer Clinic

    Hazard, Kentucky, 41701

  • Hutchinson Clinic, Pa

    Hutchinson, Kansas, 67502

  • Indiana University Cancer Center

    Indianapolis, Indiana, 46202

  • Cancer Specialists Of North Florida Beaches

    Jacksonville, Florida, 32256

  • Thompson Cancer Survival Center

    Knoxville, Tennessee, 37916

  • Wilshire Oncology Medical Group Inc

    La Verne, California, 91750

  • The Angeles Clinic And Research Institute

    Los Angeles, California, 90025

  • Joe Arrington Cancer Research And Treatment Center

    Lubbock, Texas, 79410

  • Lowcountry Hematology & Oncology, Pa

    Mt. Pleasant, South Carolina, 29464

  • Vanderbilt-Ingram Cancer Ctr

    Nashville, Tennessee, 37232

  • Memorial Sloan Kettering Cancer Center

    New York, New York, 10065

  • Mid-Illinois Hematology/Oncology Associates, Ltd.

    Normal, Illinois, 61761

  • Orlando Health, Inc. M.D. Anderson Cancer Center Orlando

    Orlando, Florida, 32806

  • Comprehensive Cancer Center

    Palm Springs, California, 92262

  • Oncology Specialists, Sc

    Park Ridge, Illinois, 60068

  • Hematology Oncology Associates Of The Treasure Coast

    Port Saint Lucie, Florida, 34952

  • Providence Portland Medical Center

    Portland, Oregon, 97213

  • Virginia Cancer Institute

    Richmond, Virginia, 23226

  • St Joseph Oncology Inc

    Saint Joseph, Missouri, 64507

  • Sharp Clinical Oncology Research

    San Diego, California, 92123

  • Hematology Oncology, P.C.

    Stamford, Connecticut, 06902-3628

Other trials in United States

Russia9 sites
  • Local Institution

    Moscow, 105229

  • Local Institution

    Moscow, 115478

  • Local Institution

    Murmansk, 183047

  • Local Institution

    Pyatigorsk, Stavropol Kray, 357502

  • Local Institution

    Ryazan, 390011

  • Local Institution

    Saint Petersburg, 191104

  • Local Institution

    Saint Petersburg, 198255

  • Local Institution

    Samara, 443066

  • Local Institution

    Stavropol, 355047

Other trials in Russia

France8 sites
  • Local Institution

    Bordeaux, 33075

  • Local Institution

    Brest, Cedex, 29200

  • Local Institution

    Marseille, 13009

  • Local Institution

    Nantes, Cedex 1, 44093

  • Local Institution

    Paris, 75010

  • Local Institution

    Pierre-Bénite, 69495

  • Local Institution

    Saint-Etienne, Cedex 2, 42055

  • Local Institution

    Villejuif, 94805

Other trials in France

Germany7 sites
  • Local Institution

    Berlin, 12200

  • Local Institution

    Heidelberg, 69120

  • Local Institution

    Jena, 07740

  • Local Institution

    Kiel, 24105

  • Local Institution

    Mannheim, 68167

  • Local Institution

    München, 81675

  • Local Institution

    Tübingen, 72076

Other trials in Germany

Italy7 sites
  • Local Institution

    Genova, 16128

  • Local Institution

    Milan, 20141

  • Local Institution

    Naples, 80131

  • Local Institution

    Padova, 35128

  • Local Institution

    Ragusa, 97100

  • Local Institution

    Rome, 00144

  • Local Institution

    Siena, 53100

Other trials in Italy

South Africa6 sites
  • Local Institution

    Cape Town, Western Cape, 7570

  • Local Institution

    Groenkloof, Gauteng, 0181

  • Local Institution

    Johannesburg, 2199

  • Local Institution

    Port Elizabeth, Eastern Cape, 6000

  • Local Institution

    Pretoria, Gauteng, 0041

  • Local Institution

    Saxonworld, Gauteng, 2196

Other trials in South Africa

United Kingdom6 sites
  • Local Institution

    Bristol, Avon, BS2 8ED

  • Local Institution

    Chelmsford, Essex, CM1 7ET

  • Local Institution

    Guildford, Surrey, GU2 7XX

  • Local Institution

    London, Greater London, SW3 6JJ

  • Local Institution

    Metropolitan Borough of Wirral, Merseyside, CH63 3JY

  • Local Institution

    Poole, Dorset, BH15 2JB

Other trials in United Kingdom

Argentina5 sites
  • Local Institution

    Buenos Aires, Buenos Aires, 1185

  • Local Institution

    Buenos Aires, Buenos Aires, C1408INH

  • Local Institution

    Buenos Aires, Buenos Aires, C1426ANZ

  • Local Institution

    Córdoba, Córdoba Province, X5000AAI

  • Local Institution

    Santa Fe, Santa Fe Province, S3000FFU

Other trials in Argentina

Australia5 sites
  • Local Institution

    Box Hill, Victoria, 3128

  • Local Institution

    Coffs Harbour, New South Wales, 2450

  • Local Institution

    Newcastle, New South Wales, 2300

  • Local Institution

    Port Macquarie, New South Wales, 2444

  • Local Institution

    South Brisbane, Queensland, 4101

Other trials in Australia

Poland5 sites
  • Local Institution

    Gdansk, 80-219

  • Local Institution

    Lodz, 93-509

  • Local Institution

    Lublin, 20-090

  • Local Institution

    Poznan, 61-866

  • Local Institution

    Wroclaw, 51-124

Other trials in Poland

Belgium4 sites
  • Local Institution

    Brasschaat, 2930

  • Local Institution

    Brussels, 1200

  • Local Institution

    Edegem, B-2650

  • Local Institution

    Ghent, 9000

Other trials in Belgium

Brazil4 sites
  • Local Institution

    Fortaleza, Ceará, 60430-230

  • Local Institution

    Porto Alegre, Rio Grande do Sul, 90050-170

  • Local Institution

    Porto Alegre, Rs, Rio Grande do Sul, 90610-000

  • Local Institution

    São Paulo, São Paulo, 01508-010

Other trials in Brazil

Canada4 sites
  • Local Institution

    Edmonton, Alberta, T6G 1Z2

  • Local Institution

    Montreal, Quebec, H1T 2W4

  • Local Institution

    Montreal, Quebec, H3T 1E2

  • Local Institution

    Saskatoon, Saskatchewan, S7N 4H4

Other trials in Canada

Spain4 sites
  • Local Institution

    Barcelona, 08036

  • Local Institution

    Canarias, 38320

  • Local Institution

    Valencia, 46014

  • Local Institution

    Zaragoza, 50009

Other trials in Spain

Ukraine4 sites
  • Local Institution

    Cherkassy, 18009

  • Local Institution

    Dnipro, 49044

  • Local Institution

    Lviv, 79031

  • Local Institution

    Uzhhorod, 88000

Other trials in Ukraine

Ireland3 sites
  • Local Institution

    Cork

  • Local Institution

    Dublin, Dublin 4

  • Local Institution

    Galway, Galway

Other trials in Ireland

Netherlands3 sites
  • Local Institution

    Eindhoven, 5623 EJ

  • Local Institution

    Hv Amsterdam, 1081

  • Local Institution

    Wurzburg, 97080

Other trials in Netherlands

Czechia2 sites
  • Local Institution

    Olomouc, 775 20

  • Local Institution

    Prague, 128 08

Other trials in Czechia

Israel2 sites
  • Local Institution

    Jerusalem, 91120

  • Local Institution

    Tel Aviv, 64239

Other trials in Israel

Switzerland2 sites
  • Local Institution

    Basel, CH-4031

  • Local Institution

    Geneva, 1211

Other trials in Switzerland

Austria1 site
  • Local Institution

    Vienna, 1090

Other trials in Austria

Chile1 site
  • Local Institution

    Santiago

Other trials in Chile

Hungary1 site
  • Local Institution

    Kaposyar, 7400

Other trials in Hungary

Norway1 site
  • Local Institution

    Montebello, Oslo, 0310

Other trials in Norway

Portugal1 site
  • Local Institution

    Lisbon, 1099-023

Other trials in Portugal

About this study

Official title: A Multi-center, Randomized, Double-Blind, Two-Arm, Phase III Study in Patients With Untreated Stage III (Unresectable) or IV Melanoma Receiving Dacarbazine Plus 10 mg/kg Ipilimumab (MDX-010) vs. Dacarbazine With Placebo

The purpose of this clinical research study is to examine the safety and effectiveness (how well the drug works) of two different treatments for patients with melanoma. One treatment is an investigational compound (a drug that is not currently approved by the United States Food and Drug Administration [FDA]), know as Ipilimumab (also known as MDX-010 or BMS-734016) together with an approved chemotherapy drug called Dacarbazine

Read the detailed description

For the extension phase:

Allocation: single arm study; Masking: open label; Intervention Model: Single Group

Conditions
Melanoma
Being tested
Ipilimumab, Placebo, Dacarbazine
Keywords
Stage IIIc N3 (unresectable), Stage IV melanoma
Medical subject headings
Melanoma

What participants receive

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

  • IpilimumabDrug

    Also called MDX-010, BMS-734016

    Intravenous solution; intravenous; 10mg/kg; one dose every 3 weeks for 10 weeks then one dose every 12 weeks starting at Week 24, until disease progression, unacceptable toxicity or withdrawal of consent

    In Maintenance phase: Only Ipilimumab: 10mg/kg, every 12 weeks will be continued until disease progression

  • PlaceboDrug

    Intravenous solution; intravenous; 0 mg; one dose every 3 weeks for 10 weeks then one dose every 12 weeks starting at Week 24; until disease progression, unacceptable toxicity or withdrawal of consent

  • DacarbazineDrug

    Intravenous solution; intravenous; 850 mg/m^2; one dose every 3 weeks for 22 weeks, until disease progression, unacceptable toxicity or withdrawal of consent

Study groups in NCT00324155
Study groupRoleWhat they receive
Arm A: Ipilimumab and DacarbazineExperimentalIn Maintenance phase: Ipilimumab will be continued. Dacarbazine was given up to Week 22 and is not given in the Maintenance phase
Receives: Drug: Ipilimumab; Drug: Dacarbazine
Arm B: Placebo and DacarbazineActive comparatorNot described
Receives: Drug: Placebo; Drug: Dacarbazine

What is being measured

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

  1. Overall Survival (OS)

    OS was defined as the time from the date of randomization until the date of death. Analysis of OS was to be done once 416 deaths had occurred (primary endpoint). However, analysis occurred at 414 deaths (February 7, 2011), due to operational timing of the study. Median number of months of OS and associated confidence interval calculated using the method of Brookmeyer and Crowley.

    Measured: Date of randomization to 37 months through 5-year follow-up and up to approximately 76 months

Secondary outcomes (12)
  1. Survival Rate at 1 Year, 18 Months, 2 Years, and 3 Years

    The survival rate (percentage of participants alive) was defined as the probability that a participant is alive at 1 year (or 18 months, 2 years, or 3 years) following randomization and was estimated via the Kaplan-Meier method.

    Measured: Date of randomization to 3 years following randomization

  2. Disease Control Rate (DCR)

    DCR=number whose best overall response (BOR) was partial response (PR), complete response (CR) or stable disease (SD), divided by all randomized participants (unevaluable participants included). Independent review committee assessment. BOR=date of first dose to last tumor assessment prior to subsequent cancer therapy (including tumor resection, excluding palliative local radiotherapy). Modified World Health Organization criteria: CR=disappearance of all lesions; no evidence of progressive disease (PD); PR=50% or more decrease in the sum of products of the longest diameter and greatest perpendicular diameter of all index lesions compared with baseline; SD=neither sufficient decrease to qualify for PR nor sufficient increase to qualify for PD; PD=at least 25% increase in sum of products of all index lesions and/or appearance of any new lesions; nonindex lesions: appearance of any new lesions and/or unequivocal progression of nonindex lesions.

    Measured: First dose to last tumor assessment prior to subsequent therapy at data cutoff for Primary Endpoint (approximately 5 years)

  3. Median Number of Months of Progression-free Survival (PFS)

    PFS=time between randomization and date of progression or death, whichever occurs first. Participants who died without reported prior progression were considered to have progressed on date of death. For those alive and not progressed, PFS was censored on date of last evaluable tumor assessment (TA). Those who have not died and have no recorded postbaseline TA were censored at randomization. Those who died without any recorded postbaseline TA were considered to have progressed on date of death. Evaluation was conducted by both investigator and an independent review committee (IRC), who assessed radiologic imaging studies, photographs of skin lesions, and clinical data. Progressive disease defined using modified criteria of the World Health Organization: demonstration of at least a 25% increase in the sum of products of all index lesions or the appearance of any new lesions. For nonindex lesions: appearance of any new lesions or unequivocal progression of nonindex lesions.

    Measured: Randomization to date of progression or death to approximately 5 years

  4. Progression-free Survival (PFS) Rate Truncated at Week 12

    PFS rate=probability patient was progression-free at Day 78, calculated as total patients receiving treatment and with an overall response of stable disease (SD), partial response (PR), or complete response (CR) at Week 12, divided by total patients. For those alive and not progressed at or before Week 12, PFS censored on date of last evaluable tumor assessment (TA) at or before Week 12. Those with an assessment of PD prior to Week 12 and subsequent assessment of SD, PR, or CR at Week 12 were called progression-free at Week 12. Those with no recorded postbaseline TA dated on or before Day 109, and who had not died on or before Day 109, were censored at randomization. PD=at least 25% increase in sum of products of all index lesions or appearance of any new lesions. Both an investigator and independent review committee (IRC) assessed radiologic imaging studies, photographs of skin lesions, and clinical data. IRC assessment was considered primary over that of the investigators.

    Measured: Day 78

  5. Best Overall Response Rate (BORR)

    BORR=number with Best Overall Response (BOR) of complete response (CR) or partial response (PR), divided by total number of randomized patients. BOR=date of first dose to the last tumor assessment prior to subsequent cancer therapy (including tumor resection surgery but excluding palliative local radiotherapy for bone lesions). Independent review committee assessment. Modified criteria of the World Health Organization (mWHO): CR=disappearance of all lesions; no evidence of progressive disease; PR=50% or greater decrease in the sum of products of the longest diameter and greatest perpendicular diameter of all index lesions compared with baseline. Immune-related (ir) response criteria (irRC) assess tumor response in patients on immunotherapy: irCR=disappearance of all lesions in 2 consecutive observations at least 4 weeks apart; irPR=50% or greater decrease in total measureable tumor burden compared with peak in 2 observations at least 4 weeks apart.

    Measured: First dose to last tumor assessment at data cutoff for primary endpoint (approximately 5 years)

  6. Duration of Response (DOR): Randomized Participants With Response of Complete Response (CR) or Partial Response (PR)

    DOR defined in those with Best Overall Response (BOR)=CR or PR per independent review committee (IRC) as time between date of response of confirmed CR or PR, whichever occurred first, and date of PD or death. If PR assessed before CR, DOR confirmed at earlier time-point showing PR. Modified criteria of the World Health Organization (mWHO): CR=disappearance of all lesions;no evidence of PD; PR=50% or greater decrease in the sum of products of longest and greatest perpendicular diameters (SPD) of all index lesions compared with baseline. PD=an increase of 25% or greater in SPD of index lesions compared with the smallest recorded sum, or appearance of 1 or more new lesions. Immune-related response criteria (irRC): SD=50% decrease in total measurable tumor burden compared with peak cannot be established nor 25% increase compared with nadir, in absence of unequivocal progression of nonindex lesions. Unconfirmed immune-related (ir) CR, irPR, or irPD=irSD.

    Measured: Day of CR or PR to day of PD or death up to data cutoff for primary endpoint (approximately 5 years)

  7. Time to Response: All Randomized Participants With Response to Treatment

    Time to response was defined as the time between the first dose of study therapy and the date when measurement criteria were met for Best Overall Response (BOR) of partial response (PR) or complete response (CR), whichever occurred first, per independent review committee. Note that if an overall response of PR occurred before confirmation of CR, the time to response endpoint was not determined by the time that the BOR of CR was shown but rather by the earlier time point showing PR. Modified criteria of the World Health Organization: CR=disappearance of all lesions; no evidence of progressive disease (PD); PR=50% or more decrease in the sum of products of the longest and greatest perpendicular diameters (SPD) of all index lesions compared with baseline; PD=an increase of 25% or greater in the SPD of index lesions compared with the smallest recorded sum, or the appearance of 1 or more new lesions.

    Measured: First dose to date of BOR up to data cutoff for primary endpoint (approximately 5 years)

  8. Duration of Stable Disease (SD): Randomized Participants With Stable Disease

    Duration of SD was defined in those whose Best Overall Response (BOR) was SD, per independent review committee (IRC) as the time between Week 12 and date of progressive disease (PD) or death , whichever occurs first. For those who underwent tumor resection following Week 12 but prior to PD, duration of SD was censored on date of last evaluable tumor assessment (TA) prior to resection. For those with BOR of SD at Week 12, date of PD was used in analysis of duration of SD. For those with BOR=SD who have not subsequently progressed and who remain alive, duration of SD censored on date of last evaluable TA. Modified criteria of the World Health Organization (mWHO): SD=insufficient decrease to qualify for partial response or sufficient increase to qualify for PD; PD=an increase of 25% or more in sum of products of longest diameter and greatest perpendicular diameter of index lesions compared with smallest recorded sum, or appearance of 1 or more new lesions.

    Measured: Week 12 to date of disease progression or death up to data cutoff for primary endpoint (approximately 5 years)

  9. Percentage of Participants With Brain Metastasis-Free Survival at Time of Data Cutoff

    Brain metastasis-free survival was defined as the time from randomization to the date of progression with a new lesion located in the brain. New brain lesions prior to Week 12 constituted a progression event (unlike main progression-free survival analysis). A participant who dies without documentation of a brain lesion was considered to have progressed with brain metastasis on the date of death. Participants who are free of brain metastasis were censored on the date of their last tumor assessment. An independent review committee evaluated images of participants with clinical symptoms to determine the number of those free of brain metastasis. The brain metastasis-free status was reported as a percent of participants (n/N), where n= participants with metastasis-free brains at data cutoff for the Primary Endpoint and N= randomized participants. A 2-sided Clopper and Pearson confidence interval was performed.

    Measured: Date of randomization up to data cutoff for primary endpoint (approximately 5 years)

  10. Number of Participants With Adverse Events (AEs), Drug-related AEs, AEs Leading to Discontinuation, Serious Adverse Events (SAEs), Drug-related SAEs, Drug-related Hypersensitivity, Immune-related AEs/SAEs, and Inflammatory AEs/SAEs

    AE=any new undesirable symptom, sign, clinically significant laboratory abnormality, or medical condition occurring after starting study treatment, even if the event was not considered to be drug-related. SAE=a medical event that at any dose results in death, persistent or significant disability/incapacity, or drug dependency/abuse; is life-threatening, an important medical event, or a congenital anomaly/birth defect; or requires or prolongs hospitalization. Treatment-related=having certain, probable, possible, or missing relationship to study drug. Grade (Gr) 1=Mild, Gr 2=Moderate, Gr 3=Severe, Gr 4= Potentially Life-threatening or disabling. Randomization=Day 1; start of treatment (first dose)=Week 1. Summarization time frame is from first dose to 70 days after last dose of study at time of 414 deaths.

    Measured: Week 1 (First Dose) to 70 days after last dose of study up to data cutoff for primary endpoint (approximately 5 years)

  11. Number of Participants With Grade 2-3 and Grade 3-4 Immune-related Adverse Events (irAEs) With Resolution Resolved

    irAEs included the categories: gastrointestinal (GI), diarrhea, liver, endocrine, and skin. Grade 2=moderate adverse events (AEs); minimal, local, or noninvasive intervention indicated. Grade 3=severe AEs, medically significant but not immediately life-threatening. Grade 4=life-threatening consequences; urgent intervention indicated. Resolution is defined as improvement to Grade 1 or less or to the Grade at baseline (prior to treatment).

    Measured: Week 1 (first dose) to 70 days after last dose up to data cutoff for primary endpoint (approximately 5 years)

  12. Time to Resolution of Grade 2-3, Grade 3-4 Immune-related Adverse Events (irAEs)

    irAEs included the categories: gastrointestinal (GI), diarrhea, liver, endocrine, and skin. Grade 2=Moderate adverse events (AEs); minimal, local or noninvasive intervention indicated. Grade 3=severe AEs, medically significant but not immediately life-threatening. Grade 4=life-threatening consequences; urgent intervention indicated. Time to resolution is defined as improvement to Grade 1 or less or to the Grade at baseline (prior to treatment).

    Measured: Week 1 (first dose) to 70 days after last dose up to database lock for primary endpoint (approximately 5 years)

Timeline

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

  1. First posted10 May 2006 (estimated)
  2. Study startAug 2006
  3. Primary completionJan 2011
  4. Study completionOct 2013

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
Double blind
Who is masked
Participant, Investigator
Enrolment
681 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT00324155
Sponsor's protocol ID
CA184-024
Status last verified
Oct 2014
First submitted
8 May 2006
Last updated
3 Nov 2014
Data monitoring committee
Yes

Publications

  • Maio M, Grob JJ, Aamdal S, Bondarenko I, Robert C, Thomas L, Garbe C, Chiarion-Sileni V, Testori A, Chen TT, Tschaika M, Wolchok JD. Five-year survival rates for treatment-naive patients with advanced melanoma who received ipilimumab plus dacarbazine in a phase III trial. J Clin Oncol. 2015 Apr 1;33(10):1191-6. doi: 10.1200/JCO.2014.56.6018. Epub 2015 Feb 23.

    PubMed 25713437
  • Schadendorf D, Hodi FS, Robert C, Weber JS, Margolin K, Hamid O, Patt D, Chen TT, Berman DM, Wolchok JD. Pooled Analysis of Long-Term Survival Data From Phase II and Phase III Trials of Ipilimumab in Unresectable or Metastatic Melanoma. J Clin Oncol. 2015 Jun 10;33(17):1889-94. doi: 10.1200/JCO.2014.56.2736. Epub 2015 Feb 9.

    PubMed 25667295
  • Robert C, Thomas L, Bondarenko I, O'Day S, Weber J, Garbe C, Lebbe C, Baurain JF, Testori A, Grob JJ, Davidson N, Richards J, Maio M, Hauschild A, Miller WH Jr, Gascon P, Lotem M, Harmankaya K, Ibrahim R, Francis S, Chen TT, Humphrey R, Hoos A, Wolchok JD. Ipilimumab plus dacarbazine for previously untreated metastatic melanoma. N Engl J Med. 2011 Jun 30;364(26):2517-26. doi: 10.1056/NEJMoa1104621. Epub 2011 Jun 5.

    PubMed 21639810

Questions about this trial

What is this clinical trial studying?

A Phase 3 study testing Ipilimumab and Dacarbazine in people with Melanoma, run by Bristol-Myers Squibb at 127 sites in 25 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 4 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 3 Nov 2014. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 127 sites in United States, Russia, France, Germany, Italy and 20 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. 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 10 Mar 2014). 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?

Overall Survival (OS) (time frame: Date of randomization to 37 months through 5-year follow-up and up to approximately 76 months). 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 NCT00324155, which also lists 3 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 3 Nov 2014.

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