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Recruiting Phase 2 NCT03899155

Pan Tumor Rollover Study

Phase 2 – studying effectiveness and dosage
Conditions: Cancer

Sponsor: Bristol-Myers Squibb

trial.available_in: БГ
Overview
Main Objective of this study is to examine long-term safety of nivolumab monotherapy including combinations and other cancer therapies in various tumor types.
Who can participate
Inclusion Criteria * Signed Written Informed Consent. * Eligible to receive continued study treatment per the Parent Study, including treatment beyond progression per investigator assessment in the Parent Study. * On treatment hold in the Parent Study following long-lasting response or are eligible for treatment rechallenge as defined in the Parent Study. * WOCBP and male participants who are sexually active must agree to follow instructions for method(s) of contraception as described below and included in the ICF. Exclusion Criteria * Participant is not eligible for study treatment per the Parent Study eligibility criteria. * Participants not receiving clinical benefit as assessed by the Investigator. * Any clinical adverse event (AE), laboratory abnormality, or intercurrent illness which, in the opinion of the Investigator, indicates that participation in the study is not in the best interest of the participant. * Other protocol-defined Inclusion/Exclusion Criteria apply
Locations 34
Argentina (1)
Local Institution - 0199
Berazategui , Buenos Aires
COMPLETED
Australia (1)
Local Institution - 0045
Coffs Harbour , New South Wales
COMPLETED
Belgium (1)
Local Institution - 0329
Brussels
WITHDRAWN
Brazil (1)
Local Institution - 0260
Belo Horizonte , Minas Gerais
COMPLETED
Canada (1)
Cross Cancer Institute
Edmonton , Alberta
Quincy Chu, Site 0111
Chile (1)
Local Institution - 0363
Temuco , Araucania
COMPLETED
China (1)
Local Institution - 0169
Hefei , Anhui
WITHDRAWN
Czech Republic (1)
Local Institution - 0371
Brno
WITHDRAWN
Denmark (1)
Local Institution
Odense C
WITHDRAWN
Finland (1)
Local Institution
Helsinki
WITHDRAWN
France (1)
Local Institution - 0006
Bordeaux , Gironde
COMPLETED
Greece (1)
Alexandra Hospital
Athens , Attica
Michail Liontos, Site 0381
Hong Kong (1)
Queen Mary Hospital
Hong Kong
Thomas Yau, Site 0339
Hungary (1)
Local Institution - 0290
Gyöngyössolymos , Heves County
COMPLETED
Ireland (1)
Local Institution - 0227
Dublin
WITHDRAWN
Israel (1)
Local Institution - 0190
Haifa
COMPLETED
Italy (1)
IRCCS - Istituto Scientifico Romagnolo per lo Studio dei Tumori - Dino Amadori - Srl
Meldola , Fc
Angelo Delmonte, Site 0361
Japan (1)
Local Institution - 0242
Hirosaki-shi , Aomori
COMPLETED
Mexico (1)
Local Institution - 0152
León , Guanajuato
WITHDRAWN
Netherlands (1)
Local Institution - 0335
Amsterdam , North Holland
WITHDRAWN
New Zealand (1)
Auckland City Hospital
Auckland
Edward Gane, Site 0370
Norway (1)
Local Institution - 0213
Bergen
COMPLETED
Peru (1)
Local Institution - 0179
Santiago de Surco , Lima region
COMPLETED
Poland (1)
Centrum Onkologii im. Prof. Franciszka Lukaszczyka
Bydgoszcz , Kuyavian-Pomeranian Voivodeship
Bogdan Zurawski, Site 0358
Puerto Rico (1)
FDI Clinical Research
San Juan , PR
Mirelis Acosta-Rivera, Site 0334
Romania (1)
Onco Clinic Consult SA
Craiova , Dolj
Patricia Visan, Site 0378
Russia (1)
Local Institution - 0257
Krasnodar , Krasnodarskiy Kray
WITHDRAWN
South Korea (1)
Local Institution - 0389
Seongnam-si , Gyeonggi-do
WITHDRAWN
Spain (1)
Local Institution - 0047
Donostia / San Sebastian , Guipuzcoa
COMPLETED
Sweden (1)
Local Institution
Gothenburg
WITHDRAWN
Taiwan (1)
Taichung Veterans General Hospital
Taichung
Teng-Yu Lee, Site 0388
Turkey (1)
Local Institution - 0330
Ankara
WITHDRAWN
United Kingdom (1)
Local Institution - 0141
London , Greater London
COMPLETED
United States (1)
Local Institution - 0220
Huntsville , Alabama
COMPLETED
Technical details
Status
Recruiting
Phase
Phase 2
Study type
INTERVENTIONAL
Sex
Male and female
Minimum age
18 Years
Healthy volunteers
No
Start date
09.08.2019
Completion date
25.08.2029
Registry ID
NCT03899155
Source
anzctr
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Information is automatically extracted from ClinicalTrials.gov. Consult your doctor before taking action.