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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT04026412
Other study ID # CA209-73L
Secondary ID 2019-001222-98
Status Active, not recruiting
Phase Phase 3
First received
Last updated
Start date October 8, 2019
Est. completion date December 3, 2026

Study information

Verified date January 2024
Source Bristol-Myers Squibb
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The primary purpose of the study is to compare the effectiveness of nivolumab plus concurrent chemoradiotherapy (CCRT) followed by nivolumab plus ipilimumab vs CCRT followed by durvalumab in participants with untreated Locally Advanced Non-small Cell Lung Cancer (LA NSCLC).


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 888
Est. completion date December 3, 2026
Est. primary completion date July 7, 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Eastern Cooperative Oncology Group (ECOG) performance status =1 - Locally advanced stage IIIA, IIIB, or IIIC (T1-2 N2-3 M0, T3 N1-3 M0, or T4 N0-3 M0) pathologically-confirmed NSCLC, according to 8th TNM classification. Participants who are not planned for potential curative surgical resection are eligible. - Newly diagnosed and treatment-naïve, with no prior local or systemic anticancer therapy given as primary therapy for locally advanced disease Exclusion Criteria: - Any condition including medical, emotional, psychiatric, or logistical that, in the opinion of the Investigator would preclude the participant from adhering to the protocol or would increase the risk associated with study participation - Active infection requiring systemic therapy within 14 days prior to randomization - History of organ or tissue transplant that requires systemic use of immune suppressive agents - Prior thoracic radiotherapy Other protocol-defined inclusion/exclusion criteria apply

Study Design


Related Conditions & MeSH terms


Intervention

Biological:
nivolumab
Specified dose on specified days
ipilimumab
Specified dose on specified days
durvalumab
Specified dose on specified days

Locations

Country Name City State
Argentina Local Institution - 0043 Buenos Aires Distrito Federal
Argentina Local Institution - 0042 Caba Distrito Federal
Argentina Local Institution - 0044 Caba Buenos Aires
Argentina Local Institution - 0045 Río Cuarto Cordoba
Australia Local Institution - 0028 Adelaide South Australia
Australia Local Institution - 0224 Ballarat Central Victoria
Australia Local Institution - 0031 Darlinghurst New South Wales
Australia Local Institution - 0134 Gosford New South Wales
Australia Local Institution - 0029 Greenslopes Queensland
Australia Local Institution - 0033 Kingswood New South Wales
Australia Local Institution Melbourne Victoria
Australia Local Institution - 0052 Melbourne Victoria
Australia Local Institution - 0030 Murdoch Western Australia
Belgium Local Institution - 0003 Bruxelles
Belgium Local Institution - 0001 Gent
Belgium Local Institution - 0004 Liege
Belgium Local Institution - 0002 Yvoir
Brazil Local Institution - 0036 Barretos SAO Paulo
Brazil Local Institution - 0037 Blumenau Santa Catarina
Brazil Local Institution - 0234 Ijui RIO Grande DO SUL
Brazil Local Institution - 0038 Ipatinga Minas Gerais
Brazil Local Institution - 0034 Porto Alegre RIO Grande DO SUL
Brazil Local Institution - 0035 Rio de Janeiro
Canada Local Institution - 0237 Chicoutimi Quebec
Canada Local Institution - 0127 Kingston Ontario
Canada Local Institution - 0078 Oshawa Ontario
Canada Local Institution - 0126 Quebec
Canada Local Institution - 0070 Rimouski Quebec
Canada Local Institution - 0092 Trois-Rivieres Quebec
Chile Local Institution - 0041 Santiago Metropolitana
Chile Local Institution - 0040 Vina del Mar Valparaiso
China Local Institution - 0146 Beijing BEI
China Local Institution - 0170 Changchun Jilin
China Local Institution - 0183 Changchun Jilin
China Local Institution - 0154 Changsha Hunan
China Local Institution - 0186 Chengdu Sichuan
China Local Institution - 0189 Chengdu Sichuan
China Local Institution - 0149 Chongqing Chongqing
China Local Institution - 0179 Fuzhou Fujian
China Local Institution - 0180 Gongzhuling Jilin
China Local Institution - 0192 Guiyang Guizhou
China Local Institution - 0140 Hangzhou Zhejiang
China Local Institution - 0147 Hankou Hubei
China Local Institution - 0138 Jinan Shandong
China Local Institution - 0184 Linhai Zhejiang
China Local Institution - 0178 Nanchang Jiangxi
China Local Institution - 0139 Nanjing Jiangsu
China Local Institution - 0145 Shanghai Shanghai
China Local Institution - 0148 Wuhan Hubei
China Local Institution - 0150 Wuhan Hubei
China Local Institution - 0164 Xiamen Fujian
France Local Institution - 0086 Bordeaux
France Local Institution - 0087 Dijon
France Local Institution - 0081 Lyon
France Local Institution - 0082 Montpellier
France Local Institution - 0084 Nantes
France Local Institution - 0091 Paris
France Local Institution - 0227 Paris
France Local Institution - 0090 Paris Cedex 14
France Local Institution - 0083 Paris Cedex 5
France Local Institution - 0089 Tours Cedex 09
Germany Local Institution - 0060 Berlin
Germany Local Institution - 0063 Essen
Germany Local Institution - 0076 Grosshansdorf
Germany Local Institution - 0101 Hamm
Germany Local Institution - 0073 Heidelberg
Germany Local Institution - 0061 Immenhausen
Germany Local Institution - 0062 Kempten
Germany Local Institution - 0075 Loewenstein
Germany Local Institution - 0109 Mainz
Germany Local Institution - 0072 Stuttgart
Greece Local Institution - 0135 Athens
Greece Local Institution - 0161 Athens
Greece Local Institution - 0136 Larissa
Greece Local Institution - 0162 N.Kifissia
Ireland Local Institution - 0023 Dublin
Ireland Local Institution - 0024 Dublin 8 Dublin
Italy Local Institution - 0068 Brescia
Italy Aou Policlinico V. Emanuele Di Catania Catania
Italy Azienda Ospedaliero-Universitaria Mater Domini Catanzaro
Italy Ospedale San Luca Lucca
Italy Istituto Europeo di Oncologia IRCCS Milano
Italy ASST di Monza - Azienda Ospedaliera San Gerardo Monza
Italy Azienda Ospedaliera Di Perugia Perugia
Japan Local Institution - 0199 Bunkyo-ku Tokyo
Japan Local Institution - 0200 Chuo-ku Tokyo
Japan Local Institution - 0212 Fukuoka-shi Fukuoka
Japan Local Institution - 0198 Hidaka-shi Saitama
Japan Local Institution - 0203 Kanazawa-shi Ishikawa
Japan Local Institution - 0174 Kitaadachi-gun Saitama
Japan Local Institution - 0206 Kobe Hyogo
Japan Local Institution - 0211 Kurume-shi Fukuoka
Japan Local Institution - 0204 Nagoya Aichi
Japan Local Institution - 0202 Niigata-shi Niigata
Japan Local Institution - 0205 Osaka-shi Osaka
Japan Local Institution - 0210 Osakasayama Osaka
Japan Local Institution - 0197 Ota Gunma
Japan Local Institution - 0195 Sapporo-shi Hokkaido
Japan Local Institution - 0196 Sendai-shi Miyagi
Japan Local Institution - 0232 Ube Yamaguchi
Japan Local Institution - 0175 Wakayama-shi Wakayama
Japan Local Institution - 0217 Yokohama Kanagawa
Japan Local Institution - 0201 Yokohama-Shi Kanagawa
Japan Local Institution - 0216 Yokohama-shi Kanagawa
Korea, Republic of Local Institution - 0167 Cheongju-si, Chungcheonbuk-do,
Korea, Republic of Local Institution - 0152 Seoul
Korea, Republic of Local Institution - 0168 Seoul
Mexico Local Institution - 0015 Culiacan Sinaloa
Mexico Local Institution - 0067 Df Distrito Federal
Mexico Local Institution - 0080 Guadalajara Jalisco
Mexico Local Institution - 0027 La Paz BAJA Californa SUR
Mexico Local Institution - 0014 Monterrey Nuevo LEON
Netherlands Local Institution - 0006 Amsterdam
Netherlands Local Institution - 0025 Arnhem
Netherlands Local Institution - 0240 Leiden
Netherlands Local Institution - 0005 Maastrict
Netherlands Local Institution - 0026 Veldhoven
Poland Local Institution - 0107 Bydgoszcz
Poland Local Institution - 0102 Gdansk
Poland Local Institution - 0104 Krakow
Poland Local Institution - 0235 Tomaszow Mazowiecki
Puerto Rico Local Institution - 0120 Hato Rey
Puerto Rico GCM Medical Group, PSC - Hato Rey Site San Juan
Romania Local Institution - 0018 Bucharest
Romania Local Institution - 0222 Bucuresti
Romania Local Institution - 0019 Cluj-Napoca
Romania Local Institution - 0020 Constanta
Romania Local Institution - 0017 Craiova
Romania Local Institution - 0021 Floresti/ Cluj
Russian Federation Local Institution Moscow
Russian Federation Local Institution Moscow
Russian Federation Local Institution Moscow
Russian Federation Local Institution St. Petersburg
Singapore Local Institution - 0171 Singapore
Spain Local Institution - 0106 Barcelona
Spain Local Institution - 0099 Hospitalet de Llobregat
Spain Local Institution - 0095 Madrid
Spain Local Institution - 0096 Madrid
Spain Local Institution - 0098 Pamplona
Spain Local Institution - 0105 Santiago de Compostela
Spain Local Institution - 0097 Sevilla
Spain Local Institution - 0100 Zaragoza
Sweden Local Institution - 0065 Goteborg Vastra Gotalands Lan
Sweden Local Institution - 0064 Stockholm
Switzerland Local Institution - 0057 Basel
Switzerland Local Institution - 0058 Lausanne
Switzerland Local Institution - 0059 St.Gallen
Switzerland Local Institution - 0056 Zuerich
Taiwan Local Institution - 0208 KaohsiungCity
Taiwan Local Institution - 0214 New Taipei City
Taiwan Local Institution - 0209 Tainan
Taiwan Local Institution - 0143 Taipei
Taiwan Local Institution - 0213 Taipei
Taiwan Local Institution - 0133 Taipei City
United Kingdom Local Institution - 0054 Aberdeen
United Kingdom Local Institution - 0007 Bebington
United Kingdom Local Institution - 0009 Hull
United Kingdom Local Institution - 0010 Poole Dorset
United Kingdom Local Institution - 0012 Swansea Glamorgan
United States Local Institution - 0125 Atlanta Georgia
United States Local Institution - 0165 Augusta Georgia
United States Local Institution - 0191 Austin Texas
United States Local Institution - 0108 Bethesda Maryland
United States Local Institution - 0079 Bryan Texas
United States Local Institution - 0071 Burlington Vermont
United States Local Institution - 0077 Charleston South Carolina
United States Local Institution - 0053 Cincinnati Ohio
United States Local Institution - 0131 Cincinnati Ohio
United States Local Institution - 0188 Cincinnati Ohio
United States Local Institution - 0047 Cleveland Ohio
United States Local Institution - 0112 Cleveland Ohio
United States Local Institution - 0124 Cleveland Ohio
United States Local Institution - 0130 Dallas Texas
United States Local Institution - 0218 Edgewood Kentucky
United States Local Institution - 0233 Jacksonville Florida
United States Local Institution - 0119 La Jolla California
United States Local Institution - 0129 Lone Tree Colorado
United States Local Institution - 0219 Orlando Florida
United States Local Institution - 0039 Pensacola Florida
United States Local Institution - 0166 San Francisco California
United States Local Institution - 0207 San Francisco California
United States Local Institution - 0116 Traverse City Michigan
United States Local Institution - 0123 Youngstown Ohio

Sponsors (1)

Lead Sponsor Collaborator
Bristol-Myers Squibb

Countries where clinical trial is conducted

United States,  Argentina,  Australia,  Belgium,  Brazil,  Canada,  Chile,  China,  France,  Germany,  Greece,  Ireland,  Italy,  Japan,  Korea, Republic of,  Mexico,  Netherlands,  Poland,  Puerto Rico,  Romania,  Russian Federation,  Singapore,  Spain,  Sweden,  Switzerland,  Taiwan,  United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Progression-free survival (PFS) by RECIST 1.1 per Blinded Independent Central Review (BICR) for Arm A vs Arm C Up to 7 years
Secondary Overall Survival (OS) for Arm A vs Arm C Up to 7 years
Secondary PFS by RECIST 1.1 per BICR for Arm B vs Arm C Up to 7 years
Secondary OS for Arm B vs Arm C Up to 7 years
Secondary PFS by RECIST 1.1 per BICR for Arm A vs Arm B Up to 7 years
Secondary OS for Arm A vs Arm B Up to 7 years
Secondary Objective Response Rate (ORR) by RECIST 1.1 per BICR Up to 7 years
Secondary Duration of Response (DoR) by RECIST 1.1 per BICR Up to 7 years
Secondary Time to Response (TTR) by RECIST 1.1 per BICR Up to 7 years
Secondary PFS by RECIST 1.1 per Investigator assessment Up to 7 years
Secondary ORR by RECIST 1.1 per Investigator assessment Up to 7 years
Secondary DoR by RECIST 1.1 per Investigator assessment Up to 7 years
Secondary TTR by RECIST 1.1 per Investigator assessment Up to 7 years
Secondary Time to Death or Distant Metastases (TTDM) by RECIST 1.1 per Investigator assessment Up to 7 years
Secondary Incidence of Adverse Events (AEs) Up to 7 years
Secondary Incidence of Serious Adverse Events (SAEs) Up to 7 years
Secondary Incidence of select AEs Up to 7 years
Secondary Proportion of participants without symptom deterioration based on NSCLC-SAQ Non-Small Cell Lung Cancer-Symptom Assessment Questionnaire (NSCLC-SAQ) Up to 7 years
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