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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02106546
Other study ID # M11-089
Secondary ID 2013-005020-42
Status Completed
Phase Phase 3
First received
Last updated
Start date April 10, 2014
Est. completion date November 20, 2019

Study information

Verified date October 2020
Source AbbVie
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the safety and efficacy of the addition of veliparib plus carboplatin and paclitaxel versus the addition of placebo plus carboplatin and paclitaxel in adults with advanced or metastatic squamous non-small cell lung cancer (NSCLC).


Recruitment information / eligibility

Status Completed
Enrollment 970
Est. completion date November 20, 2019
Est. primary completion date January 3, 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years to 99 Years
Eligibility Inclusion Criteria: 1. Life expectancy > 12 weeks 2. Subject must have cytologically or histologically confirmed squamous NSCLC. 3. Subject must have advanced or metastatic squamous NSCLC that is not amenable to surgical resection or radiation with curative intent at time of study Screening. 4. Subjects with recurrent squamous NSCLC after surgical treatment that is not amenable to surgical resection or radiation with curative intent are eligible. 5. Subject must have at least 1 unidimensional measurable NSCLC lesion on a computerized tomography (CT) scan as defined by Response Evaluation Criteria In Solid Tumors (RECIST - version 1.1). Exclusion Criteria: 1. Subject has a known hypersensitivity to paclitaxel or to other drugs formulated with polyethoxylated castor oil (Cremophor). 2. Subject has a known hypersensitivity to platinum compounds. 3. Subject has peripheral neuropathy >= grade 2. 4. Subject has non-squamous NSCLC, or a known epidermal growth factor receptor (EGFR) mutation of exon 19 deletion or L858R mutation in exon 21, or a known anaplastic lymphoma kinase (ALK) gene rearrangement. 5. Subject has received prior cytotoxic chemotherapy (including definitive chemoradiotherapy) for NSCLC, except for adjuvant or neoadjuvant therapy.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Carboplatin
Carboplatin administered intravenously over approximately 15 to 30 minutes at (AUC 6 mg/mL/min) immediately following paclitaxel infusion.
Veliparib
Capsules taken orally twice a day, 12 hours apart.
Paclitaxel
Paclitaxel administered intravenously over 3 hours at a dose of 200 mg/m².
Placebo to veliparib
Capsules taken orally twice a day, 12 hours apart.

Locations

Country Name City State
Australia Flinders Centre for Innovation /ID# 125605 Bedford Park South Australia
Australia Sunshine Coast University Hosp /ID# 125608 Birtinya Queensland
Australia The Townsville Hospital /ID# 125609 Douglas Queensland
Australia Barwon Health University Hospital Geelong /ID# 125606 Geelong Victoria
Australia Southern Medical Day Care Ctr /ID# 125604 Wollongong New South Wales
Australia The Queen Elizabeth Hospital /ID# 125607 Woodville South Australia
Austria Ordensklinikum Linz GmbH, Elisabethinen /ID# 126183 Linz
Belarus Bobruysk Interdistrict Onco. /ID# 128999 Bobruisk
Belarus Brest Regional Hospital /ID# 125955 Brest
Belarus State Institution Republican Scientific Practical Center of Oncology and Medica /ID# 125815 Lesnoy
Belarus Mogilev Reg Clin Oncology Dis /ID# 128639 Mogilev
Belarus Vitebsk Reg Clin Onc Disp /ID# 125516 Vitebsk
Brazil Fundacao Pio XII - Hospital de Cancer de Barretos /ID# 126736 Barretos Sao Paulo
Brazil Clinica de Neoplasias Litoral - Centro de Novos Tratamentos Itajai /ID# 127738 Itajai Santa Catarina
Brazil Hospital Sao Lucas da PUCRS /ID# 127737 Porto Alegre Rio Grande Do Sul
Brazil Instituto COI de Educacao e Pesquisa /ID# 127739 Rio de Janeiro
Brazil Instituto Nacional de Câncer José de Alencar Gomes da Silva (INCA) /ID# 127309 Rio de Janeiro
Brazil Fundacao Antonio Prudente - AC Camargo Cancer Center /ID# 126737 Sao Paulo
Canada University of Calgary /Id# 126326 Calgary Alberta
Canada Cross Cancer Institute /ID# 126154 Edmonton Alberta
Canada Juravinski Cancer Clinic /ID# 126153 Hamilton Ontario
Canada Victoria Hospital /ID# 126669 London Ontario
Canada McGill Univ HC /ID# 130431 Montreal Quebec
Canada The Ottawa Hospital /ID# 126522 Ottawa Ontario
Canada Iucpq-Ul /Id# 126524 Québec Quebec
Canada CSSS Alphonse-Desjardins, CHAU de Levis /ID# 126149 Quebec City Quebec
Canada Princess Margaret Cancer Centre /ID# 126155 Toronto Ontario
Croatia Klinicki bolnicki centar Osijek /ID# 132214 Osijek Osjecko-baranjska Zupanija
Croatia Opca bolnica Pula /ID# 126540 Pula
Croatia Opca bolnica Dr. Josip Bencevi /ID# 126539 Slavonski Brod
Croatia Klinika za plucne bolesti Jordanovac /ID# 126537 Zagreb Grad Zagreb
Czechia Nemocnice Kyjov, prispevkova organizace /ID# 125819 Kyjov
Czechia Nemocnice Na Plesi s.r.o. /ID# 125817 Nová Ves pod Pleší Pribram
Czechia Nemocnice Novy Jicin /ID# 125818 Nový Jicín 1
Czechia Fakultni Nemocnice Olomouc /ID# 125820 Olomouc Olomoucky Kraj
Czechia Vitkovicka nemocnice a. s. /ID# 127023 Ostrava
Denmark Herlev Hospital /ID# 125995 Herlev Hovedstaden
Denmark Odense Universitets Hospital /ID# 125996 Odense C Syddanmark
Egypt University of Alexandria /ID# 128337 Alexandria
Egypt Cairo Uni Hosp Al Kasr El Ainy /ID# 128338 Cairo
Egypt Cairo Uni Hosp Al Kasr El Ainy /ID# 128340 Cairo
Egypt Naser Institute for Res & Dev /ID# 129263 Cairo
Estonia North Estonian Medical Centre /ID# 128215 Tallinn
Estonia Tartu University Hospital /ID# 127735 Tartu
Finland Helsinki Univ Central Hospital /ID# 125897 Helsinki
Finland Vaasa Central Hospital /ID# 125896 Vaasa
France CHRU de Brest - Hopital Morvan /ID# 127903 Brest
France Centre Hosp Intercommunal de Creteil /ID# 125922 Creteil Val-de-Marne
France Centre Hospitalier Le Mans /ID# 127902 Le Mans CEDEX 9 Sarthe
France CHRU Lille - Hôpital Claude Huriez /ID# 126353 Lille CEDEX Hauts-de-France
France CHU Hopital Nord /ID# 128388 Marseille Bouches-du-Rhone
France Centre Antoine Lacassagne /ID# 126360 Nice
France Hopital Haut-Lévêque /ID# 135270 Pessac CEDEX Gironde
France Hospital Pontchaillou /ID# 126356 Rennes
France Hopital Larrey - CHU de Toulouse /ID# 128394 Toulouse
Germany Charite-Univ. Berlin, Benjamin-Franklin /ID# 125708 Berlin
Germany Lungen Clinic Grosshansdorf /ID# 126107 Grosshansdorf
Germany Klinikum Kassel /ID# 127025 Kassel
Germany Klinik Loewenstein GmbH /ID# 126191 Löwenstein
Germany Univ Johannes Gutenberg /ID# 125603 Mainz
Greece General Hospital of Chest Diseases of Athens SOTIRIA /ID# 125879 Athens
Greece Metropolitan Hospital /ID# 125878 Athens
Greece University General Hospital of Heraklion PA.G.N.I /ID# 125877 Heraklion
Greece Papageorgiou General Hospital Thessaloniki /ID# 125876 Nea Efkarpia Thessaloniki
Hungary Orszagos Koranyi Pulmonologiai Intezet /ID# 126112 Budapest XII Budapest
Hungary Debreceni Egyetem Klinikai Központ /ID# 126119 Debrecen
Hungary Veszprem Megyei Tudogyogyintez /ID# 126121 Farkasgyepu
Hungary Petz Aladar Megyei Oktato Korh /ID# 126110 Gyor
Hungary Bekes Megyei Pandy Kalman Korhaz /ID# 126117 Gyula
Hungary Matrahaza Gyogyintezet /ID# 126109 Kékesteto
Hungary CRU Hungary Egeszsegugyi és Szolgaltato Kft. /ID# 135234 Miskolc Borsod-Abauj-Zemplen
Hungary Fejer Megyei Szent Gyorgy Korh /ID# 126118 Szekesfehervar
Hungary Jasz-Nagykun-Szolnok Megyei Hetenyi Geza Korhaz /ID# 126120 Szolnok
Hungary Tudogyogyintezet Toeroekbalint /ID# 126111 Torokbalint
Ireland Cork University Hospital /ID# 126176 Cork
Ireland Beaumont Hospital /ID# 126218 Dublin
Ireland St. James's Hospital /ID# 126177 Dublin 8 Dublin
Ireland University Hospital Limerick /ID# 126175 Limerick
Ireland University Hospital Waterford /ID# 126178 Waterford
Israel Assaf Harofeh Medical Center /ID# 127076 Be'er Ya'akov
Israel Hadassah University Hospital /ID# 127077 Jerusalem
Israel Meir Medical Center /ID# 127078 Kfar Saba
Israel Sheba Medical Center /ID# 127079 Ramat Gan
Italy AO San Giuseppe Moscati /ID# 125701 Avellino
Italy Istituto Europeo di Oncologia /ID# 125702 Milan
Italy Azienda Ospedaliera San Gerardo di Monza _ Oncologia Medica /ID# 125704 Monza
Italy A.O.U. San Luigi Gonzaga /ID# 125700 Orbassano
Italy Azienda Ospedaliero Uni Parma /ID# 125703 Parma
Italy Azienda Ospedaliera-Universitaria di Perugia-Divisione di Oncologia Medica. /ID# 125699 Perugia
Italy Istituto Oncologico del Medite /ID# 132844 Viagrande
Latvia P. Stradins Clinical Univ Hosp /ID# 126322 Riga
Latvia Riga East Clinical Univ Hosp /ID# 125597 Riga
Lithuania Hospital of Lithuanian University of Health Sciences Kaunas Clinics /ID# 127176 Kovno Kaunas
Lithuania National Cancer Institute /ID# 126323 Vilnius
Mexico Centro Estatal de Cancerologia /ID# 127583 Chihuahua
Mexico Hospital Angeles Centro Medico /ID# 127620 San Luis Potosí
Mexico Cancerologia de Queretaro S.C. /ID# 125920 Santiago de Querétaro
Netherlands Vrije Universiteit Medisch Centrum /ID# 125578 Amsterdam
Netherlands Amphia Ziekenhuis /ID# 126466 Breda
Netherlands Catharina Ziekenhuis /ID# 125577 Eindhoven
Netherlands Ziekenhuis St. Jansdal /ID# 125576 Harderwijk
Netherlands Atrium-Orbis Zuyderland Medisch Centrum /ID# 125710 Heerlen
Netherlands Jeroen Bosch Ziekenhuis /ID# 125709 S Hertogenbosch
Netherlands Isala /ID# 125579 Zwolle
New Zealand Wellington Hospital (Capital and Coast District Health Board) /ID# 125755 Wellington
Norway Haukeland University Hospital /ID# 126338 Bergen Hordaland
Norway Nordland Hospital /ID# 126337 Bodø
Norway Sorlandet Sykehus HF /ID# 126341 Kristiansand
Norway Oslo Universitetssykehus, Radiumhospitalet /ID# 126335 Oslo
Norway Stavanger University Hospital /ID# 126336 Stavanger
Norway Sykehuset i Vestfold HF /ID# 126340 Tonsberg
Poland Szpital Morski im. PCK /ID# 126547 Gdynia
Poland Mrukmed. Lekarz Beata Madej Mruk i Partner /ID# 126548 Rzeszów Podkarpackie
Poland NZOZ Magodent Ctr. Med. Ostro /ID# 126545 Warsaw
Poland Mazowiecki Szpital Onkologiczn /ID# 126546 Wieliszew
Portugal CCA Braga - Hospital de Braga /ID# 125837 Braga
Portugal Ctr Hosp Univ Coimbra, EPE /ID# 125838 Coimbra
Portugal Hospital Senhora da Oliveira de Guimaraes, EPE /ID# 126761 Guimaraes Braga
Portugal Hospital Pulido Valente /ID# 125835 Lisbon
Portugal Centro Hospitalar de Sao Joao, EPE /ID# 125875 Porto
Portugal IPO Porto FG, EPE /ID# 125836 Porto
Puerto Rico VA Caribbean Healthcare System /ID# 124562 San Juan
Russian Federation Belgorod Oncology Dispensary /ID# 129899 Belgorod
Russian Federation Sverdlovsk Regional Oncology Center Dispensary /ID# 128457 Ekaterinburg Sverdlovskaya Oblast
Russian Federation State Budgetary Healthcare Institution"Irkutsk Regional Oncology Center /ID# 128460 Irkutsk
Russian Federation Federal State Budgetary Scientific Institution N.N. Blokhin Russian Cancer Resea /ID# 128458 Moscow Moskva
Russian Federation State Regional Budgetary Healthcare Institution " Murmansk Regional Oncology Dis /ID# 128461 Murmansk
Russian Federation Orenburg Regional Clinical Onc /ID# 137474 Orenburg
Russian Federation Ogarev Mordovia State Univ /ID# 127595 Saransk
Russian Federation Smolensk Regional Onc Clin Dis /ID# 127144 Smolensk
Russian Federation Cancer Research Institute Siberian Branch of the Russian Academy of Medical Scie /ID# 127143 Tomsk
Russian Federation Volgograd Regional Clinical Oncology Dispensary /ID# 126350 Volgograd Volgogradskaya Oblast
Serbia Clinical Center Serbia /ID# 128738 Belgrade Beograd
Serbia Institute for Oncology and Rad /ID# 128721 Belgrade
Serbia University Hospital Bezanijska /ID# 128761 Belgrade
Serbia Clinical Center of Nis /ID# 128735 NIS Nisavski Okrug
Serbia Institute For Pulmonary Diseas /ID# 128737 Sremska Kamenica
Slovakia Univerzitna Nemocnica Bratislava /ID# 126342 Bratislava
Slovakia MEDEON, s.r.o. /ID# 128517 Pieštany
South Africa Netcare Oncology Intervent Ctr /ID# 126100 Cape Town Western Cape
South Africa The Oncology Centre /ID# 126096 Durban Kwazulu-Natal
South Africa Cancercare Outeniqua Oncology Unit /ID# 126103 George Western Cape
South Africa Sandton Oncology Centre /ID# 126097 Johannesburg Gauteng
South Africa Wits Clinical Research Site /ID# 126101 Johannesburg Gauteng
South Africa GVI Oncology /ID# 126102 Port Elizabeth Eastern Cape
South Africa Dr Albert, Bouwer and Jordaan Incorporated /ID# 126098 Pretoria Gauteng
South Africa Mary Potter Oncology Centre /ID# 126099 Pretoria Gauteng
South Africa University of Pretoria /ID# 127297 Pretoria Gauteng
Spain Hospital Universitario Vall d'Hebron /ID# 125159 Barcelona
Spain Hospital Duran i Reynals /ID# 125161 L'Hospitalet de Llobregat Barcelona
Spain Hospital Universitario HM Sanchinarro /ID# 125162 Madrid
Spain Hospital Universitario Puerta de Hierro Majadahonda /ID# 125160 Majadahonda Madrid
Spain Hospital Universitario Virgen del Rocio /ID# 125207 Sevilla
Spain Fundacion Instituto Valenciano Oncologia IVO /ID# 125205 Valencia
Sweden Gavle Sjukhus /ID# 126444 Gavle
Sweden Sahlgrenska University Hosp /ID# 129997 Goteborg
Sweden University Hospital Linkoping /ID# 126443 Linkoping
Sweden Karolinska Univ Sjukhuset /ID# 126445 Solna
Switzerland Hirslanden Medical Center /ID# 128216 Aarau
Switzerland Inselspital, Universitaetsklinik /ID# 126347 Bern
Switzerland Kantonsspital St. Gallen /ID# 126349 St. Gallen Sankt Gallen
Switzerland Spital STS AG /ID# 126348 Thun
Turkey Akdeniz University Medical Fac /ID# 126997 Antalya
Turkey Istanbul University-Cerrahpasa, Cerrahpasa Medical Faculty /ID# 126186 Istanbul
Turkey Marmara University Medical Fac /ID# 126187 Istanbul
Turkey Dr. Suat Seren Gogus Has /ID# 126190 Izmir
Turkey Ege University Medical Faculty /ID# 126189 Izmir
Ukraine Cherkassy Regional Onc Ctr /ID# 128222 Cherkasy
Ukraine Regional Municipal Non-Profit Enterprise Bukovynian Clinical Oncology Center /ID# 128220 Chernivtsi
Ukraine Municipal Non-Profit Enterprise City Clinical Hospital No.4 of Dnipro City Counc /ID# 128217 Dnipro
Ukraine Communal non-profit enterprise Regional Center of Oncology /ID# 128221 Kharkiv Kharkivska Oblast
Ukraine Lviv Oncological Regional Therapeutical and Diagnostic Centre /ID# 128218 Lviv
Ukraine Poltava Regional Clinical Oncology Centre of Poltava Regional Council /ID# 128223 Poltava
Ukraine Municipal Non-Profit Enterprise of Sumy Regional Council Sumy Regional Clinical /ID# 128219 Sumy
United Kingdom Betsi Cadwaladr Univ Health Bo /ID# 127177 Bangor
United Kingdom North Devon District Hospital /ID# 125689 Barnstaple
United Kingdom The Royal Bournemouth Hospital /ID# 125690 Bournemouth
United Kingdom East Kent Hosp Univ NHS Trust /ID# 125698 Canterbury
United Kingdom Cheltenham General Hospital /ID# 125692 Cheltenham Gloucestershire
United Kingdom Gartnavel General Hospital /ID# 126233 Glasgow
United Kingdom James Paget University Hosp /ID# 125696 Great Yarmouth
United Kingdom Charing Cross Hospital /ID# 125688 London
United Kingdom Guy's and St Thomas' NHS Found /ID# 125694 London London, City Of
United Kingdom Maidstone Hospital /ID# 125693 Maidstone
United Kingdom The Newcastle Upon Tyne Hospitals NHS Foundation Trust Freeman Hospital /ID# 129228 Newcastle Upon Tyne
United Kingdom Norfolk and Norwich Univ Hosp /ID# 125697 Norwich Norfolk
United Kingdom The Clatterbridge Cancer Ctr /ID# 125695 Wirral
United States Illinois Cancer Specialists /ID# 127468 Arlington Heights Illinois
United States Winship Cancer Institute of Emory University /ID# 124061 Atlanta Georgia
United States VA Eastern Colorado Healthcare System /ID# 128065 Aurora Colorado
United States Texas Oncology - Austin Midtown /ID# 127477 Austin Texas
United States Texas Oncology - South Austin /ID# 127476 Austin Texas
United States St. Luke's Mountain States Tumor Institute - Boise /ID# 124059 Boise Idaho
United States University of Vermont Medical Center /ID# 128064 Burlington Vermont
United States Gabrail Cancer Center Research /ID# 127415 Canton Ohio
United States Parkland Health and Hosp Syste /ID# 128518 Dallas Texas
United States Texas Oncology- Baylor Charles A. Sammons Cancer Center /ID# 128385 Dallas Texas
United States UT Southwestern Medical Center /ID# 127876 Dallas Texas
United States Henry Ford Health System /ID# 126500 Detroit Michigan
United States NorthShore University HealthSystem - Evanston Hospital /ID# 128585 Evanston Illinois
United States Holy Cross Hospital /ID# 128074 Fort Lauderdale Florida
United States University of Florida - Archer /ID# 126476 Gainesville Florida
United States The Jones Clinic, PC /ID# 124062 Germantown Tennessee
United States Goshen Center for Cancer Care /ID# 123875 Goshen Indiana
United States Hackensack Univ Med Ctr /ID# 124057 Hackensack New Jersey
United States Ingalls Memorial Hosp /ID# 128360 Harvey Illinois
United States Appalachian Regional Healthcare, Inc (ARH) /ID# 128061 Hazard Kentucky
United States Penn State University and Milton S. Hershey Medical Center /ID# 126676 Hershey Pennsylvania
United States University of Texas MD Anderson Cancer Center /ID# 127946 Houston Texas
United States Franciscan St. Francis Health /ID# 126678 Indianapolis Indiana
United States Cancer Specialists of North Florida - Southpoint /ID# 127815 Jacksonville Florida
United States Northeast Arkansas Clinical Ch /ID# 128071 Jonesboro Arkansas
United States Sparrow Regional Cancer Center, Sparrow Health System /ID# 127156 Lansing Michigan
United States Comprehensive Cancer Ctrs Neva /ID# 127491 Las Vegas Nevada
United States Dartmouth-Hitchcock Medical Center /ID# 128075 Lebanon New Hampshire
United States Nebraska Hematology Oncology /ID# 127699 Lincoln Nebraska
United States SE Nebraska Hema/Oncology Consultants P.C.d/b/a Southeast Nebraska Cancer Center /ID# 126477 Lincoln Nebraska
United States LA Hem-Oncology Med Group /ID# 129178 Los Angeles California
United States Minnesota Oncology Hematology, PA /ID# 127473 Minneapolis Minnesota
United States Virginia Oncology Associates /ID# 127458 Norfolk Virginia
United States Texas Oncology - Paris /ID# 127484 Paris Texas
United States Northwest Cancer Specialists, P.C. /ID# 127486 Vancouver Washington
United States Northwest Cancer Specialists, P.C. /ID# 127488 Vancouver Washington
United States Texas Oncology - Waco /ID# 127459 Waco Texas
United States Midwestern Regional CTC /ID# 126124 Zion Illinois

Sponsors (1)

Lead Sponsor Collaborator
AbbVie

Countries where clinical trial is conducted

United States,  Australia,  Austria,  Belarus,  Brazil,  Canada,  Croatia,  Czechia,  Denmark,  Egypt,  Estonia,  Finland,  France,  Germany,  Greece,  Hungary,  Ireland,  Israel,  Italy,  Latvia,  Lithuania,  Mexico,  Netherlands,  New Zealand,  Norway,  Poland,  Portugal,  Puerto Rico,  Russian Federation,  Serbia,  Slovakia,  South Africa,  Spain,  Sweden,  Switzerland,  Turkey,  Ukraine,  United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Other Change in Quality of Life: European Organisation for Research and Treatment of Cancer Quality of Life Core 30 Question Questionnaire (EORTC-QLQ-C30). From Screening (prior to dosing) up to 2 years
Other Change in Quality of Life: European Organisation for Research and Treatment of Cancer Quality of Life Lung Cancer 13 Question Questionnaire (EORTC-LC13). From Screening (prior to dosing) up to 2 years
Other Change in Eastern Cooperative Oncology Group (ECOG) Performance Status From Screening (prior to dosing) up to 2 years
Other Change in Quality of Life: European Quality of Life-5 Dimensions-5 Levels Questionnaire (EQ-5D-5L) From Screening (prior to dosing) up to 2 years
Other Duration of Response The duration of overall response for a given subject will be defined as the number of days from the day the criteria are met for Complete or Partial Response (whichever is recorded first) to the date that Progressive Disease (PD) is objectively documented. From complete or partial response to disease progression (up to 3 years from randomization).
Primary Overall Survival (OS) in current smokers Time to death for a given subject will be defined as the number of days from the date that the subject was randomized to the date of the subject's death. Up to 3 years from first dose of study drug
Secondary Overall Survival (OS) in all subjects Time to death for a given subject will be defined as the number of days from the date that the subject was randomized to the date of the subject's death. Up to 3 years from first dose of study drug
Secondary Progressive-Free Survival (PFS) in current smokers and in all subjects Defined as the number of days from the date that the subject was randomized to the date the subject experiences an event of disease progression or to the date of death (all causes of mortality) if disease progression is not reached. Up to 3 years from first dose of study drug
Secondary Objective Response Rate (ORR) in current smokers and in all subjects Objective response rate is defined as the proportion of subjects with complete or partial response as determined by the investigator per RECIST (version 1.1) Up to 3 years from first dose of study drug
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