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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01511913
Other study ID # CA184-143
Secondary ID ENCEPP/SDPP/2723
Status Completed
Phase
First received
Last updated
Start date June 3, 2012
Est. completion date December 12, 2019

Study information

Verified date December 2021
Source Bristol-Myers Squibb
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to examine the safety of Ipilimumab and patterns of use in the treatment of unresectable or metastatic melanoma in the post-approval setting


Description:

Time Perspective: this study does have a retrospective component involving a subset of patients


Recruitment information / eligibility

Status Completed
Enrollment 1411
Est. completion date December 12, 2019
Est. primary completion date March 30, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility For more information regarding BMS clinical trial participation, please visit www.BMSStudyConnect.com. Inclusion Criteria: - Diagnosis of unresectable or metastatic melanoma - Age of 18 years or older at time of entry into the study - Patients who have initiated treatment for unresectable or metastatic melanoma at medical practice (e.g. community-based, office-based, hospital-based, academic setting)within 21 days before informed consent for this study OR in the case where treatment has not yet been initiated, documentation that the treatment strategy was determined before informed consent for this study, and treatment must be initiated within 28 days after informed consent - Ipilimumab-treated patients must be receiving treatment for the indication(s) approved in their country of residence or where they are receiving treatment Exclusion Criteria: - Current or pending participation in a clinical trial examining therapy for the treatment of any cancer (including unresectable or metastatic melanoma) - Current use of therapy to treat a primary cancer other than melanoma

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Argentina Local Institution Caba
Argentina Local Institution Caba
Argentina Local Institution Caba
Argentina Local Institution Cordoba
Argentina Local Institution Rosario- Santa Fe
Argentina Local Institution Tucuman
Australia Local Institution Adelaide South Australia
Australia Local Institution Bedford Park South Australia
Australia Local Institution Cairns Queensland
Australia Local Institution Canberra Australian Capital Territory
Australia Local Institution Corrimal New South Wales
Australia Local Institution Douglas Queensland
Australia Local Institution Frankston Victoria
Australia Local Institution Greenslopes Queensland
Australia Local Institution Kurralta Park South Australia
Australia Local Institution Lismore New South Wales
Australia Local Institution Malvern Victoria
Australia Local Institution Port Macquarie New South Wales
Australia Local Institution Tamworth New South Wales
Australia Local Institution Tweeds Head New South Wales
Australia Local Institution Wagga Wagga New South Wales
Australia Local Institution Waratah New South Wales
Austria Local Institution Feldkirch
Austria Local Institution Graz
Austria Local Institution Linz
Austria Local Institution Salzburg
Austria Local Institution St Poelten
Austria Local Institution Vienna
Belgium Local Institution Brasschaat
Belgium Local Institution Brussels
Belgium Local Institution Edegem
Belgium Local Institution Haint Saint Paul
Belgium Local Institution Hasselt
Belgium Local Institution Kortrijk
Belgium Local Institution Leuven
Canada Local Institution London Ontario
Canada Local Institution Mississauga Ontario
Canada Local Institution Moncton New Brunswick
Canada Local Institution Quebec
Canada Local Institution Québec
Canada Local Institution Saskatoon Saskatchewan
Canada Local Institution Windsor Ontario
France Local Institution Bayonne
France Local Institution Besancon
France Local Institution Boulogne
France Local Institution Boulogne sur Mer
France Local Institution Brest Cedex
France Local Institution Clermont Ferrand Cédex 1
France Local Institution Dijon
France Local Institution Grenoble Cédex
France Local Institution Lille Cedex
France Local Institution Limoges Cedex
France Local Institution Montauban
France Local Institution Mougins
France Local Institution Nouvelle Caledonie
France Local Institution Paris Cedex 10
France Local Institution Pierre Bénite
France Local Institution Quimper
France Local Institution Quimper Cedex
France Local Institution Soissons cedex
France Local Institution Strasbourg Cedex
France Local Institution Vandoeuvre Les Nancy
Germany Local Institution Augsburg
Germany Local Institution Bochum
Germany Local Institution Buxtehude
Germany Local Institution Chemnitz
Germany Local Institution Darmstadt
Germany Local Institution Dessau-Roblau
Germany Local Institution Dortmund
Germany Local Institution Dresden
Germany Local Institution Düsseldorf
Germany Local Institution Frankfurt
Germany Local Institution Gera
Germany Local Institution Halle/Saale
Germany Local Institution Hamburg
Germany Local Institution Hamburg
Germany Local Institution Hamburg
Germany Local Institution Hannover
Germany Local Institution Jena
Germany Local Institution Koblenz
Germany Local Institution Lüdenscheid
Germany Local Institution Magdeburg
Germany Local Institution Mainz
Germany Local Institution Mannheim
Germany Local Institution Marburg
Germany Local Institution Münster
Germany Local Institution Plauen
Germany Local Institution Quedlinburg
Germany Local Institution Recklinghausen
Germany Local Institution Rostock
Germany Local Institution Schwäbisch Hall
Germany Local Institution Stuttgart
Germany Local Institution Tübingen
Germany Local Institution Würzburg
Greece Local Institutio Alexandroupolis
Greece Local Institution Athens
Greece Local Institution Athens
Greece Local Institution Cholargos Athens
Greece Local institution Goudi Athens
Greece Local Institution Heraklion Crete
Greece Local Institution Mezourlo
Greece Local Institution Neas Efkarpia Thessaloniki
Greece Local Institution Neo Faliro
Greece Local Institution Neo Faliro Athens
Ireland Local Institution Cork
Ireland Local Institution Dublin
Ireland Local Institution Galway
Ireland Local Institution Tullamore
Ireland Local Institution Wilton Cork
Israel Local Institution Haifa
Israel Local Institution Tel Aviv
Israel Local Institution Tel Hashomer
Poland Local Institution Bydgoszcz
Poland Local Institution Lódz
Poland Local Institution Warszawa
Poland Local Institution Wroclaw
Spain Local Institution Barcelona
Spain Local Institution Donostia
Spain Local Institution Las Palmas de Gran Canaria
Spain Local Institution Madrid
Spain Local Institution Madrid
Spain Local Institution Madrid
Spain Local Institution Madrid
Spain Local Institution Palma
Spain Local Institution Palma de Mallorca
Spain Local Institution Pamplona
Spain Local Institution Santa Cruz de Tenerife
Spain Local Institution Santander
Spain Local Institution Santiago De Compostela; A Coruña
Spain Local Institution Sevilla
Spain Local Institution Sta Cruz de Tenerife
Spain Local Institution Terrassa
Spain Local Institution Valladolid
Spain Local Institution Zaragoza
Switzerland Local Institution Baden
Switzerland Local Institution Lugano
Switzerland Local Institution Zurich
Switzerland Local Institution Zürich
United Kingdom Local Institution Belfast Ireland
United Kingdom Local Institution Birmingham
United Kingdom Local Institution Bristol
United Kingdom Local Institution Cardiff South Glamorgan
United Kingdom Local Institution Chelmsford, Essex Essex
United Kingdom Local Institution Exeter
United Kingdom Local Institution Hull
United Kingdom Local Institution Leeds
United Kingdom Local Institution Lincoln
United Kingdom Local Institution London
United Kingdom Local Institution London
United Kingdom Local Institution London
United Kingdom Local Institution London England
United Kingdom Local Institution Oxfordshire
United Kingdom Local Institution Plymouth
United Kingdom Local Institution Poole
United Kingdom Local Institution Preston
United Kingdom Local Institution Rhyl Denbigshire
United Kingdom Local Institution Southend Essex
United Kingdom Local Institution Staffordshire
United Kingdom Local Institution Taunton, Somerset
United Kingdom Local Institution Truro, Cornwall
United Kingdom Local Institution Wirral
United Kingdom Local Institution Wolverhampton
United Kingdom Local Institution Yeovil, Somerset
United States Local Institution Canton Ohio
United States Local Institution Chicago Illinois
United States Local Institution Columbus Ohio
United States Mid Ohio Onc/Hem, Inc Columbus Ohio
United States Local Institution Denver Colorado
United States Local Institution Detroit Michigan
United States Local Institution Encinitas California
United States Local Institution Everett Washington
United States Local Institution Gilbert Arizona
United States Local Institution Hattiesburg Mississippi
United States Local Institution Hot Springs Arkansas
United States Local Institution Knoxville Tennessee
United States Local Institution La Jolla California
United States Local Institution Lakeland Florida
United States Local Institution Lincoln Nebraska
United States Local Institution Long Beach California
United States Local Institution Los Angeles California
United States Local Institution Miami Beach Florida
United States Local Institution Middletown Ohio
United States Local Institution Morristown New Jersey
United States Local Institution Niles Illinois
United States Local Institution Orange Park Florida
United States Local Institution Portland Oregon
United States Local Institution Washington District of Columbia

Sponsors (1)

Lead Sponsor Collaborator
Bristol-Myers Squibb

Countries where clinical trial is conducted

United States,  Argentina,  Australia,  Austria,  Belgium,  Canada,  France,  Germany,  Greece,  Ireland,  Israel,  Poland,  Spain,  Switzerland,  United Kingdom, 

References & Publications (2)

Dalle S, Mortier L, Corrie P, Lotem M, Board R, Arance AM, Meiss F, Terheyden P, Gutzmer R, Buysse B, Oh K, Brokaw J, Le TK, Mathias SD, Scotto J, Lord-Bessen J, Moshyk A, Kotapati S, Middleton MR. Long-term real-world experience with ipilimumab and non-i — View Citation

Middleton MR, Dalle S, Claveau J, Mut P, Hallmeyer S, Plantin P, Highley M, Kotapati S, Le TK, Brokaw J, Abernethy AP. Real-world treatment practice in patients with advanced melanoma in the era before ipilimumab: results from the IMAGE study. Cancer Med. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Incidence and severity of adverse reactions in patients treated with Ipilimumab in the post-approval setting Every 12 months up to 5 years
Primary Incidence rate with person-year-exposure and frequency estimate of adverse events/serious adverse events Every 12 months up to 5 years
Primary Frequency at which immunosuppressive therapy was administered to patients to manage treatment-related adverse events associated with Ipilimumab Every 12 months up to 5 years
Primary Patterns of disease monitoring as observed in a real-world setting To evaluate patterns of care, descriptive statistics will describe treatment, dosing, regimen, indication, treatment rationales, management of treatment-related adverse events, reasons for treatment termination Every 12 months up to 5 years
Secondary Quality of life (QoL), impact on work productivity, and overall satisfaction among patients receiving any therapy for unresectable or metastatic melanoma Every 12 months up to 5 years
Secondary Resource utilization associated with advanced melanoma treatment Descriptive statistics will be reported for healthcare utilization (inpatient, outpatient, emergency department and other ancillary services) and imputed costs Every 12 months up to 5 years
Secondary Overall survival (OS) in patients receiving Ipilimumab or other therapies for unresectable or metastatic melanoma Every 12 months up to 5 years
See also
  Status Clinical Trial Phase
Terminated NCT05050006 - ITIL-168 in Advanced Melanoma Phase 2