Study of Pembrolizumab With Concurrent Chemoradiation Therapy Followed by Pembrolizumab With or Without Olaparib in Stage III Non-Small Cell Lung Cancer (NSCLC) (MK-7339-012/KEYLYNK-012)

NCT ID: NCT04380636

Last Updated: 2025-08-17

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

ACTIVE_NOT_RECRUITING

Clinical Phase

PHASE3

Total Enrollment

870 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-07-06

Study Completion Date

2027-02-15

Brief Summary

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The purpose of this study is to assess the efficacy and safety of pembrolizumab in combination with concurrent chemoradiation therapy followed by either pembrolizumab with olaparib placebo (Arm 1) or with olaparib (Arm 2) compared to concurrent chemoradiation therapy followed by durvalumab (Arm 3) in participants with unresectable, locally advanced NSCLC. Arms 1 and 2 will be studied in a double-blind design and Arm 3 will be open-label. The primary hypotheses are:

1. Pembrolizumab with concurrent chemoradiation therapy followed by pembrolizumab with olaparib is superior to concurrent chemoradiation therapy followed by durvalumab with respect to progression-free survival (PFS) and overall survival (OS)
2. Pembrolizumab with concurrent chemoradiation therapy followed by pembrolizumab is superior to concurrent chemoradiation therapy followed by durvalumab with respect to PFS and OS

Detailed Description

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Conditions

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Lung Neoplasms Carcinoma, Non-Small-Cell Lung

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

TRIPLE

Participants Investigators Outcome Assessors

Study Groups

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pembrolizumab+chemoradiation→pembrolizumab+olaparib placebo

Participants will receive pembrolizumab 200 mg intravenously (IV) every 3 weeks (Q3W) in combination with 3 cycles of the investigator's choice of platinum doublet chemotherapy and concurrent standard thoracic radiotherapy (60 Gray (Gy) over 6 weeks) followed by pembrolizumab plus olaparib placebo twice a day (BID) for approximately 1 year.

Group Type EXPERIMENTAL

Pembrolizumab

Intervention Type BIOLOGICAL

intravenous (IV) infusion

Placebo for olaparib

Intervention Type DRUG

oral tablets

Etoposide

Intervention Type DRUG

IV infusion

Carboplatin

Intervention Type DRUG

IV infusion

Cisplatin

Intervention Type DRUG

IV infusion

Paclitaxel

Intervention Type DRUG

IV infusion

Pemetrexed

Intervention Type DRUG

IV infusion

Thoracic Radiotherapy

Intervention Type RADIATION

external beam radiation

pembrolizumab+chemoradiation→pembrolizumab+olaparib

Participants will receive pembrolizumab 200 mg IV Q3W in combination with 3 cycles of the investigator's choice of platinum doublet chemotherapy and concurrent standard thoracic radiotherapy (60 Gy over 6 weeks) followed by pembrolizumab plus olaparib 300 mg BID for approximately 1 year.

Group Type EXPERIMENTAL

Pembrolizumab

Intervention Type BIOLOGICAL

intravenous (IV) infusion

Olaparib

Intervention Type DRUG

oral tablets

Etoposide

Intervention Type DRUG

IV infusion

Carboplatin

Intervention Type DRUG

IV infusion

Cisplatin

Intervention Type DRUG

IV infusion

Paclitaxel

Intervention Type DRUG

IV infusion

Pemetrexed

Intervention Type DRUG

IV infusion

Thoracic Radiotherapy

Intervention Type RADIATION

external beam radiation

chemoradiation→durvalumab

Participants will receive 3 cycles of the investigator's choice of platinum doublet chemotherapy with concurrent standard thoracic radiotherapy (60 Gy over 6 weeks) followed by durvalumab 10 mg/kg every 2 weeks (Q2W) for approximately 1 year.

Group Type ACTIVE_COMPARATOR

Etoposide

Intervention Type DRUG

IV infusion

Carboplatin

Intervention Type DRUG

IV infusion

Cisplatin

Intervention Type DRUG

IV infusion

Paclitaxel

Intervention Type DRUG

IV infusion

Pemetrexed

Intervention Type DRUG

IV infusion

Thoracic Radiotherapy

Intervention Type RADIATION

external beam radiation

Durvalumab

Intervention Type DRUG

IV infusion

Interventions

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Pembrolizumab

intravenous (IV) infusion

Intervention Type BIOLOGICAL

Olaparib

oral tablets

Intervention Type DRUG

Placebo for olaparib

oral tablets

Intervention Type DRUG

Etoposide

IV infusion

Intervention Type DRUG

Carboplatin

IV infusion

Intervention Type DRUG

Cisplatin

IV infusion

Intervention Type DRUG

Paclitaxel

IV infusion

Intervention Type DRUG

Pemetrexed

IV infusion

Intervention Type DRUG

Thoracic Radiotherapy

external beam radiation

Intervention Type RADIATION

Durvalumab

IV infusion

Intervention Type DRUG

Other Intervention Names

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KEYTRUDA® MK-3475 LYNPARZA® MK-7339 AZD2281 KU-0059436 VEPESID® PARAPLATIN® PLATINOL® TAXOL® ALIMTA® IMFINZI®

Eligibility Criteria

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Inclusion Criteria

* Has pathologically (histologically or cytologically) confirmed diagnosis of NSCLC
* Has Stage IIIA, IIIB, or IIIC NSCLC by American Joint Committee on Cancer Version 8
* Is unable to undergo surgery with curative intent for Stage III NSCLC
* Has no evidence of metastatic disease indicating Stage IV NSCLC
* Has measurable disease as defined by RECIST 1.1
* Has not received prior treatment (chemotherapy, targeted therapy or radiotherapy) for Stage III NSCLC; participants who have received neoadjuvant and/or adjuvant therapy for early stage disease are not eligible
* Has provided a tumor tissue sample (tissue biopsy \[core, incisional, or excisional\])
* Has an Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 or 1 assessed within 7 days prior to the first administration of study intervention
* Has a life expectancy of at least 6 months
* A male participant must agree to use contraception and refrain from donating sperm during the intervention period and for at least the time needed to eliminate each study intervention after the last dose of study intervention unless confirmed to be azoospermic (vasectomized or secondary to medical cause). The length of time required to continue contraception for each study intervention is as follows: Olaparib, platinum doublet, and radiotherapy: 90 days
* A female participant is eligible to participate if she is not pregnant, not breastfeeding, and agrees to use contraception and refrain from donating eggs (ova, oocytes) to others or freeze/store for her own use for the purpose of reproduction during the treatment period and for at least the time needed to eliminate each study intervention after the last dose of study intervention and agrees to abstain from breastfeeding during the study intervention period and for at least 120 days after the last dose of study intervention. The length of time required to continue contraception for each study intervention is as follows: Pembrolizumab: 120 days; Olaparib, platinum doublet, and radiotherapy: 180 days
* Has a negative highly sensitive pregnancy test (\[urine or serum\] as required by local regulations) within 24 hours for urine or within 72 hours for serum before the first dose of study intervention. If a urine test cannot be confirmed as negative (e.g., an ambiguous result), a serum pregnancy test is required. In such cases, the participant must be excluded from participation if the serum pregnancy result is positive.
* Has had her medical history, menstrual history, and recent sexual activity reviewed by the investigator to decrease the risk for inclusion of a woman with an early undetected pregnancy.
* Has adequate pulmonary function tests
* Has adequate organ function
* Has provided written informed consent

Exclusion Criteria

* Has small cell lung cancer or a mixed tumor with presence of small cell elements
* Has myelodysplastic syndrome (MDS)/acute myeloid leukemia (AML) or has features suggestive of MDS/AML
* Has had documented weight loss \>10% (from baseline) in the preceding 3 months
* Has received prior radiotherapy to the thorax, including radiotherapy to the esophagus, mediastinum, or for breast cancer
* Has received prior therapy with an anti-programmed cell death 1 (ant-PD-1), anti-programmed cell death ligand 1 (anti-PD-L1), or anti- programmed cell death ligand 2 (anti-PD-L2) agent or with an agent directed to another stimulatory or co-inhibitory T-cell receptor
* Has received prior therapy with olaparib or with any other polyadenosine 5'diphosphoribose (polyADP ribose) polymerization (PARP) inhibitor
* Has had major surgery \<4 weeks prior to the first dose of study treatment (except for placement of vascular access)
* Is expected to require any other form of antineoplastic therapy, while on study
* Has received a live or live attenuated vaccine within 30 days before the first dose of study intervention; administration of killed vaccines is allowed
* Has received colony-stimulating factors (e.g., granulocyte colony-stimulating factor \[GCSF\], granulocyte-macrophage colony-stimulating factor \[GM-CSF\] or recombinant erythropoietin) within 28 days prior to the first dose of study treatment
* Is currently receiving either strong (phenobarbital, enzalutamide, phenytoin, rifampicin, rifabutin, rifapentine, carbamazepine, nevirapine and St John's Wort) or moderate (e.g. bosentan, efavirenz, modafinil) inducers of CYP3A4 that cannot be discontinued for the duration of the study
* Is currently receiving either strong (eg, itraconazole, telithromycin, clarithromycin, protease inhibitors boosted with ritonavir or cobicistat, indinavir, saquinavir, nelfinavir, boceprevir, telaprevir) or moderate (eg. ciprofloxacin, erythromycin, diltiazem, fluconazole, verapamil) inhibitors of cytochrome P450 (CYP)3A4 that cannot be discontinued for the duration of the study
* Is unable to interrupt aspirin or other nonsteroidal anti-inflammatory drugs (NSAIDs), other than an aspirin dose ≤1.3 grams per day, for at least 2 days before, during, and for at least 2 days after administration of pemetrexed
* Is unable/unwilling to take folic acid, vitamin B12, and dexamethasone during administration of pemetrexed
* Has received an investigational agent or has used an investigational device within 4 weeks prior to study treatment
* The presence of uncontrolled, potentially reversible cardiac conditions, as judged by the investigator or has congenital long QT syndrome
* Has a diagnosis of immunodeficiency or is receiving chronic systemic steroid therapy or any other form of immunosuppressive therapy within 7 days prior the first dose of study intervention
* Has a known additional malignancy that is progressing or has required active treatment within the past 5 years with the exception of basal cell carcinoma of the skin, squamous cell carcinoma of the skin, superficial bladder cancer, or carcinoma in situ (excluding carcinoma-in situ-of the bladder) that have undergone potentially curative therapy
* Has severe hypersensitivity (≥Grade 3) to study intervention and/or any of its excipients
* Has an active autoimmune disease that has required systemic treatment in past 2 years
* Has a history of (noninfectious) pneumonitis/interstitial lung disease that required steroids or has current pneumonitis/interstitial lung disease
* Has an active infection requiring systemic therapy
* Has a known history of human immunodeficiency virus (HIV) infection
* Has a known history of Hepatitis B or known active Hepatitis C virus infection
* Has active tuberculosis (TB; Mycobacterium tuberculosis) and is receiving treatment
* Has a history or current evidence of any condition, therapy, laboratory abnormality or other circumstance that might confound the results of the study, or interfere with the participant's participation for the full duration of the study, such that it is not in the best interest of the participant to participate, in the opinion of the treating investigator
* Is considered a poor medical risk due to a serious, uncontrolled medical disorder or nonmalignant systemic disease in the opinion of the treating investigator
* Has a known psychiatric or substance abuse disorder that would interfere with the participant's ability to cooperate with the requirements of the study
* Is unable to swallow orally administered medication or has a gastrointestinal disorder affecting absorption
* Has had an allogenic tissue/solid organ transplant
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Merck Sharp & Dohme LLC

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Medical Director

Role: STUDY_DIRECTOR

Merck Sharp & Dohme LLC

Locations

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University of South Alabama, Mitchell Cancer Institute ( Site 0003)

Mobile, Alabama, United States

Site Status

St. Bernards Medical Center ( Site 0089)

Jonesboro, Arkansas, United States

Site Status

St Joseph Heritage Healthcare-Oncology ( Site 0088)

Fullerton, California, United States

Site Status

Long Beach Memorial Medical Center ( Site 0006)

Long Beach, California, United States

Site Status

UCLA Hematology/Oncology - Santa Monica ( Site 0013)

Los Angeles, California, United States

Site Status

St. Joseph Heritage Healthcare Local Lab ( Site 0011)

Santa Rosa, California, United States

Site Status

Torrance Memorial Physician Network / Cancer Center ( Site 0093)

Torrance, California, United States

Site Status

Memorial Regional Hospital-Memorial Cancer Institute ( Site 0095)

Hollywood, Florida, United States

Site Status

Miami VA Healthcare System ( Site 0024)

Miami, Florida, United States

Site Status

Mid Florida Hematology and Oncology Center ( Site 0022)

Orange City, Florida, United States

Site Status

Orlando Health, UF Health Cancer Center Inc ( Site 0092)

Orlando, Florida, United States

Site Status

Fort Wayne Medical Oncology and Hematology ( Site 0094)

Fort Wayne, Indiana, United States

Site Status

Parkview Research Center ( Site 0032)

Fort Wayne, Indiana, United States

Site Status

Franciscan Health Lafayette East ( Site 0031)

Lafayette, Indiana, United States

Site Status

University of Kentucky ( Site 0096)

Lexington, Kentucky, United States

Site Status

Norton Brownsboro Hospital-Norton Cancer Institute - Brownsboro ( Site 0035)

Louisville, Kentucky, United States

Site Status

Pikeville Medical Center ( Site 0036)

Pikeville, Kentucky, United States

Site Status

Massachusetts General Hospital ( Site 0038)

Boston, Massachusetts, United States

Site Status

Henry Ford Hospital ( Site 0045)

Detroit, Michigan, United States

Site Status

VA St. Louis Health Care System ( Site 0047)

St Louis, Missouri, United States

Site Status

Washington University Siteman Cancer Center ( Site 0046)

St Louis, Missouri, United States

Site Status

CHI Health St. Francis ( Site 0053)

Grand Island, Nebraska, United States

Site Status

Rutgers Cancer Institute of New Jersey ( Site 0054)

New Brunswick, New Jersey, United States

Site Status

Valley Health Systems - Ridgewood Campus ( Site 0056)

Paramus, New Jersey, United States

Site Status

Montefiore Einstein Center ( Site 0083)

The Bronx, New York, United States

Site Status

Novant Health Presbyterian ( Site 0081)

Charlotte, North Carolina, United States

Site Status

Duke University Medical Center ( Site 0050)

Durham, North Carolina, United States

Site Status

Piedmont Hematology-Oncology Associates ( Site 0080)

Winston-Salem, North Carolina, United States

Site Status

The Lindner Center for Research and Education at The Christ Hospital ( Site 0060)

Cincinnati, Ohio, United States

Site Status

Fox Chase Cancer Center ( Site 0063)

Philadelphia, Pennsylvania, United States

Site Status

Sanford Cancer Center Oncology Clinic ( Site 0066)

Sioux Falls, South Dakota, United States

Site Status

Veterans Affairs Puget Sound Health Care System [Seattle, WA] ( Site 0075)

Seattle, Washington, United States

Site Status

Cancer Care Northwest ( Site 0074)

Spokane Valley, Washington, United States

Site Status

Clinica Adventista Belgrano-Oncology ( Site 4002)

Caba., Buenos Aires, Argentina

Site Status

Instituto Médico Río Cuarto ( Site 4003)

Río Cuarto, Córdoba Province, Argentina

Site Status

Queen Elizabeth II Health Sciences Centre ( Site 0100)

Halifax, Nova Scotia, Canada

Site Status

Centre Hospitalier de l Universite de Montreal - CHUM ( Site 0102)

Montreal, Quebec, Canada

Site Status

CIUSSS Ouest de l Ile - St-Mary s Hospital ( Site 0108)

Montreal, Quebec, Canada

Site Status

McGill University Health Center - Research Institute ( Site 0114)

Montreal, Quebec, Canada

Site Status

Centre intégré de cancérologie du CHU de Québec Université Laval, Hôpital de l'Enfant-Jésus ( Site 0110)

Québec, Quebec, Canada

Site Status

OrlandiOncologia ( Site 0201)

Providencia, Region M. de Santiago, Chile

Site Status

Bradfordhill ( Site 0200)

Santiago, Region M. de Santiago, Chile

Site Status

Centro Investigación del Cáncer James Lind ( Site 0202)

Temuco, Región de la Araucanía, Chile

Site Status

Oncocentro ( Site 0203)

Viña del Mar, Región de Valparaíso, Chile

Site Status

Bradford Hill Norte ( Site 0204)

Antofagasta, , Chile

Site Status

Peking Union Medical College Hospital ( Site 3201)

Beijing, Beijing Municipality, China

Site Status

Cancer Hospital Chinese Academy of Medical Sciences ( Site 3213)

Beijing, Beijing Municipality, China

Site Status

Beijing Cancer Hospital ( Site 3212)

Beijing, Beijing Municipality, China

Site Status

Beijing Cancer Hospital ( Site 3224)

Beijing, Beijing Municipality, China

Site Status

Daping Hospital,Third Military Medical University ( Site 3235)

Chongqing, Chongqing Municipality, China

Site Status

Fujian Provincial Cancer Hospital ( Site 3226)

Fuzhou, Fujian, China

Site Status

The First Affiliated Hospital of Xiamen University ( Site 3219)

Xiamen, Fujian, China

Site Status

Peking University Shenzhen Hospital ( Site 3216)

Shenzhen, Guangdong, China

Site Status

Cancer Hospital Chinese Academy Of Medical Sciences. Shenzhen Center ( Site 3200)

Shenzhen, Guangdong, China

Site Status

Henan Cancer Hospital ( Site 3205)

Zhengzhou, Henan, China

Site Status

Wuhan Union Hospital Cancer Center ( Site 3222)

Wuhan, Hubei, China

Site Status

Hubei Cancer Hospital ( Site 3218)

Wuhan, Hubei, China

Site Status

Xiangya Hospital of Central South University ( Site 3637)

Changsha, Hunan, China

Site Status

Second Xiangya Hospital of Central-South University ( Site 3227)

Changsha, Hunan, China

Site Status

Hunan Cancer Hospital ( Site 3225)

Changsha, Hunan, China

Site Status

Hunan Cancer Hospital ( Site 3238)

Changsha, Hunan, China

Site Status

Jiangsu Cancer Hospital ( Site 3234)

Nanjing, Jiangsu, China

Site Status

The Second Affiliated Hospital of Nanchang University ( Site 3206)

Nanchang, Jiangxi, China

Site Status

Jilin Cancer Hospital ( Site 3230)

Changchun, Jilin, China

Site Status

Shanghai Chest Hospital ( Site 3207)

Shanghai, Shanghai Municipality, China

Site Status

Zhongshan Hospital Fudan University ( Site 3220)

Shanghai, Shanghai Municipality, China

Site Status

Shanghai Pulmonary Hospital ( Site 3203)

Shanghai, Shanghai Municipality, China

Site Status

West China Hospital of Sichuan University ( Site 3202)

Chengdu, Sichuan, China

Site Status

Tianjin Medical University Cancer Institute & Hospital ( Site 3204)

Tianjin, Tianjin Municipality, China

Site Status

The 1st Affil Hosp of College of Medicine, Zhejiang Univ ( Site 3232)

Hangzhou, Zhejiang, China

Site Status

Masarykuv onkologicky ustav ( Site 2206)

Brno, Brno-mesto, Czechia

Site Status

Fakultni nemocnice Ostrava ( Site 2201)

Ostrava, Ostrava Mesto, Czechia

Site Status

Fakultni nemocnice Kralovske Vinohrady-Radioterapeuticka a onkologicka klinika ( Site 2200)

Prague, Praha 10, Czechia

Site Status

Fakultni nemocnice v Motole ( Site 2210)

Prague, Praha 5, Czechia

Site Status

Nemocnice Na Plesi s.r.o. ( Site 2202)

Nová Ves pod Pleší, Pribram, Czechia

Site Status

Krajska nemocnice Liberec, a.s. ( Site 2209)

Liberec, , Czechia

Site Status

Vseobecna fakultni nemocnice v Praze ( Site 2208)

Prague, , Czechia

Site Status

Nemocnice Na Bulovce ( Site 2205)

Prague, , Czechia

Site Status

North Estonia Medical Centre Foundation ( Site 1601)

Tallinn, Harju, Estonia

Site Status

Tartu University Hospital ( Site 1600)

Tartu, Tartu, Estonia

Site Status

Clinique Clairval ( Site 0802)

Marseille, Bouches-du-Rhone, France

Site Status

C.H.R.U. de Brest - Hopital Cavale Blanche ( Site 0806)

Brest, Brittany Region, France

Site Status

Centre Hospitalier Annecy Genevois ( Site 0811)

Epagny Metz Tessy, Haute-Savoie, France

Site Status

Clinique Teissier Groupe ( Site 0808)

Valenciennes, Nord, France

Site Status

Hopital Avicenne ( Site 0803)

Bobigny, Seine-Saint-Denis, France

Site Status

Clinique de l'Europe-Service de pneumologie ( Site 0816)

Amiens, Somme, France

Site Status

H.I.A. Sainte-Anne ( Site 0815)

Toulon, Var, France

Site Status

CHD Vendee ( Site 0807)

La Roche-sur-Yon, Vendee, France

Site Status

Universitätsmedizin Göttingen - Georg-August-Universität ( Site 0917)

Göttingen, Lower Saxony, Germany

Site Status

Johannes Wesling Klinikum Minden ( Site 0908)

Minden, North Rhine-Westphalia, Germany

Site Status

GEHO Muenster ( Site 0910)

Münster, North Rhine-Westphalia, Germany

Site Status

Johanna Etienne Hospital-Klinik für Onkologie ( Site 0916)

Neuss, North Rhine-Westphalia, Germany

Site Status

LungenClinic Grosshansdorf GmbH ( Site 0901)

Großhansdorf, Schleswig-Holstein, Germany

Site Status

Zentralklinik Bad Berka GmbH ( Site 0905)

Bad Berka, Thuringia, Germany

Site Status

Universitaetsklinikum Jena ( Site 0911)

Jena, Thuringia, Germany

Site Status

Charite-Universitaetsmedizin Berlin Campus Virchow-Klinikum ( Site 0900)

Berlin, , Germany

Site Status

Katholisches Marienkrankenhaus gGmbH ( Site 0902)

Hamburg, , Germany

Site Status

Bekes Megyei Kozponti Korhaz - Pandy Kalman Tagkorhaza ( Site 2303)

Gyula, Bekes County, Hungary

Site Status

Bacs-Kiskun Megyei Korhaz-Onkoradiologiai Kozpont ( Site 2302)

Kecskemét, Bács-Kiskun county, Hungary

Site Status

Petz Aladar Megyei Oktato Korhaz ( Site 2306)

Győr, Győr-Moson-Sopron, Hungary

Site Status

Orszagos Koranyi Pulmonologiai Intezet ( Site 2305)

Budapest, , Hungary

Site Status

Országos Korányi Pulmonológiai Intézet-VI. Tüdöbelosztály és Bronchológia ( Site 2309)

Budapest, , Hungary

Site Status

Azienda Ospedaliera Umberto I- Torrette ( Site 1009)

Torrette, Ancona, Italy

Site Status

Policlinico Agostino Gemelli ( Site 1002)

Rome, Lazio, Italy

Site Status

Istituto Clinico Humanitas Research Hospital ( Site 1000)

Rozzano, Lombardy, Italy

Site Status

Azienda Ospedaliero Universitaria Careggi ( Site 1001)

Florence, , Italy

Site Status

Azienda Ospedaliera Vito Fazzi ( Site 1003)

Lecce, , Italy

Site Status

Fondazione IRCCS Istituto Nazionale dei Tumori di Milano ( Site 1008)

Milan, , Italy

Site Status

Policlinico di Modena ( Site 1007)

Modena, , Italy

Site Status

A.O.U. Santa Maria della Misericordia di Udine ( Site 1004)

Udine, , Italy

Site Status

Kurume University Hospital ( Site 3112)

Kurume, Fukuoka, Japan

Site Status

Kobe Minimally Invasive Cancer Center ( Site 3100)

Kobe, Hyōgo, Japan

Site Status

Kanagawa Cancer Center ( Site 3101)

Yokohama, Kanagawa, Japan

Site Status

Kansai Medical University Hospital ( Site 3103)

Hirakata, Osaka, Japan

Site Status

Osaka Medical and Pharmaceutical University Hospital ( Site 3110)

Takatsuki, Osaka, Japan

Site Status

National Hospital Organization Kyushu Cancer Center ( Site 3104)

Fukuoka, , Japan

Site Status

Niigata Cancer Center Hospital ( Site 3109)

Niigata, , Japan

Site Status

Osaka International Cancer Institute ( Site 3106)

Osaka, , Japan

Site Status

Juntendo University Hospital ( Site 3111)

Tokyo, , Japan

Site Status

Tokyo Metropolitan Komagome Hospital ( Site 3108)

Tokyo, , Japan

Site Status

Cancer Institute Hospital of JFCR ( Site 3107)

Tokyo, , Japan

Site Status

Showa Medical University Hospital ( Site 3105)

Tokyo, , Japan

Site Status

Pauls Stradins Clinical University Hospital ( Site 1501)

Riga, , Latvia

Site Status

Riga East Clinical University Hospital ( Site 1500)

Riga, , Latvia

Site Status

Hospital of Lithuanian University of Health Sciences Kauno klinikos-Pulmonology ( Site 4201)

Kaunas, Kaunas County, Lithuania

Site Status

National Cancer Institute-Department of Thoracic Surgery and Oncology ( Site 4200)

Vilnius, Vilniaus Miestas, Lithuania

Site Status

Hospital Civil de Guadalajara Fray Antonio Alcalde ( Site 0500)

Guadalajara, Jalisco, Mexico

Site Status

Hospital Universitario "Dr. Jose Eleuterio Gonzalez" ( Site 0508)

Monterrey, Nuevo León, Mexico

Site Status

CLIMERS Clinical Medical Research ( Site 0506)

Orizaba, Veracruz, Mexico

Site Status

Instituto Nacional de Cancerologia ( Site 0502)

Tlalpan, , Mexico

Site Status

Akershus Universitetssykehus HF ( Site 1106)

Lorenskog, Akershus, Norway

Site Status

Vestre Viken HF Drammen Sykehus ( Site 1101)

Drammen, Buskerud, Norway

Site Status

Helse Stavanger HF Stavanger Universitetssjukehus ( Site 1103)

Stavanger, Rogaland, Norway

Site Status

Oslo Universitetssykehus HF. Ulleval ( Site 1100)

Oslo, , Norway

Site Status

Sykehuset Oestfold ( Site 1107)

Grålum, Østfold fylke, Norway

Site Status

Hospital Nacional Carlos Alberto Seguin Escobedo ESSALUD ( Site 0604)

Arequipa, Ariqipa, Peru

Site Status

Detecta Clínica ( Site 0607)

Surquillo, Muni Metro de Lima, Peru

Site Status

IPOR Instituto Peruano de Oncología & Radioterapia ( Site 0606)

Lima, , Peru

Site Status

Oncosalud ( Site 0605)

Lima, , Peru

Site Status

Clinica San Gabriel ( Site 0601)

Lima, , Peru

Site Status

Hospital Nacional Cayetano Heredia ( Site 0602)

Lima, , Peru

Site Status

Mazowiecki Szpital Wojewódzki w Siedlcach-Siedleckie Centrum Onkologii ( Site 2404)

Siedlce, Masovian Voivodeship, Poland

Site Status

Narodowy Instytut Onkologii im. Marii Sklodowskiej-Curie - Panstwowy Instytut Badawczy w Warszawie ( Site 2402)

Warsaw, Masovian Voivodeship, Poland

Site Status

Szpital Morski im. PCK. Szpitale Pomorskie Sp. Z o.o ( Site 2400)

Gdynia, Pomeranian Voivodeship, Poland

Site Status

SPZOZ MSWIA z Warminsko-Mazurskim Centrum Onkologii w Olsztynie ( Site 2401)

Olsztyn, Warmian-Masurian Voivodeship, Poland

Site Status

MEMORIAL HEALTHCARE INTERNATIONAL S.R.L. ( Site 2500)

Bucharest, București, Romania

Site Status

Gral Medical SRL-Medical Oncology ( Site 2511)

Bucharest, București, Romania

Site Status

Spitalul Universitar de Urgenta Bucuresti ( Site 2508)

Bucharest, București, Romania

Site Status

Institutul Oncologic Prof.Dr. Ion Chiricuta Cluj-Napoca ( Site 2506)

Cluj-Napoca, Cluj, Romania

Site Status

S.C. Radiotherapy Center Cluj S.R.L ( Site 2503)

Comuna Floresti, Cluj, Romania

Site Status

Centrul de Oncologie Sfantul Nectarie-Medical ( Site 2510)

Craiova, Dolj, Romania

Site Status

Radiology Therapeutic Center-Oncology ( Site 2502)

Otopeni, Ilfov, Romania

Site Status

S C Oncocenter Oncologie Clinica S R L-Medical Oncology ( Site 2509)

Timișoara, Timiș County, Romania

Site Status

Policlinica Oncomed SRL ( Site 2504)

Timișoara, Timiș County, Romania

Site Status

Spitalul Clinic Judetean De Urgenta Constanta ( Site 2501)

Constanța, , Romania

Site Status

Institutul Regional de Oncologie Iasi ( Site 2505)

Iași, , Romania

Site Status

Chelyabinsk Regional Clinical Oncological Dispensary ( Site 1913)

Chelyabinsk, Chelyabinsk Oblast, Russia

Site Status

MSROI named after P.A. Hertsen branch of FSBI NMRC Radiology ( Site 1903)

Moscow, Moscow, Russia

Site Status

Nizhniy Novgorod Region Oncology Dispensary ( Site 1914)

Nizhny Novgorod, Nizhny Novgorod Oblast, Russia

Site Status

Medical institute named after Berezin Sergey ( Site 1906)

Saint Petersburg, Sankt-Peterburg, Russia

Site Status

Scientific Research Oncology Institute n.a. N.N.Petrov ( Site 1905)

Saint Petersburg, Sankt-Peterburg, Russia

Site Status

Sverdlovsk Regional Oncology Hospital ( Site 1909)

Yekaterinburg, Sverdlovsk Oblast, Russia

Site Status

Republican Clinical Oncology Dispensary of Tatarstan MoH named after professor M.Z. Sigal ( Site 1911)

Kazan', Tatarstan, Respublika, Russia

Site Status

Yaroslavl Regional SBIH Clinical Oncology Hospital ( Site 1910)

Yaroslavl, Yaroslavl Oblast, Russia

Site Status

National Cancer Center ( Site 2800)

Goyang-si, Kyonggi-do, South Korea

Site Status

Seoul National University Bundang Hospital ( Site 2801)

Seongnam-si, Kyonggi-do, South Korea

Site Status

The Catholic University of Korea St. Vincent s Hospital ( Site 2805)

Suwon, Kyonggi-do, South Korea

Site Status

Ajou University Hospital ( Site 2803)

Suwon, Kyonggi-do, South Korea

Site Status

Gyeongsang National University Hospital ( Site 2804)

Jinju, Kyongsangnam-do, South Korea

Site Status

Chungbuk National University Hospital ( Site 2802)

Cheongju-si, North Chungcheong, South Korea

Site Status

Keimyung University Dongsan Hospital CRC room 1 ( Site 2807)

Daegu, Taegu-Kwangyokshi, South Korea

Site Status

Kangbuk Samsung Hospital ( Site 2806)

Seoul, , South Korea

Site Status

Severance Hospital Yonsei University Health System ( Site 2808)

Seoul, , South Korea

Site Status

Hospital Universitario Puerta de Hierro (Majadahonda) ( Site 1202)

Majadahonda, Madrid, Spain

Site Status

Hospital Universitario Quiron Madrid ( Site 1200)

Pozuelo de Alarcón, Madrid, Spain

Site Status

H.R.U Malaga - Hospital General ( Site 1206)

Málaga, Malaga, Spain

Site Status

H.U. Vall de Hebron ( Site 1201)

Barcelona, , Spain

Site Status

Hospital Clinic de Barcelona ( Site 1204)

Barcelona, , Spain

Site Status

Hospital Universitario Virgen Macarena ( Site 1205)

Seville, , Spain

Site Status

Hospital Universitario La Fe ( Site 1203)

Valencia, , Spain

Site Status

Chulalongkorn University ( Site 3003)

Bangkok, Bangkok, Thailand

Site Status

Ramathibodi Hospital. ( Site 3000)

Bangkok, Bangkok, Thailand

Site Status

Chiang Mai University Maharaj Nakorn Chiang Mai Hospital ( Site 3001)

Chiang Mai, , Thailand

Site Status

Srinagarind Hospital. Khon Kaen University ( Site 3002)

Khon Kaen, , Thailand

Site Status

Ankara Bilkent Sehir Hastanesi ( Site 2002)

Ankara, Adana, Turkey (Türkiye)

Site Status

Memorial Ankara Hastanesi ( Site 2006)

Ankara, , Turkey (Türkiye)

Site Status

Istanbul Uni. Cerrahpasa Tip Fakultesi ( Site 2000)

Istanbul, , Turkey (Türkiye)

Site Status

Medipol Universite Hastanesi ( Site 2003)

Istanbul, , Turkey (Türkiye)

Site Status

Göztepe Prof. Dr. Süleyman Yalçın Şehir Hastanesi-oncology ( Site 2001)

Istanbul, , Turkey (Türkiye)

Site Status

Ege University Medical Faculty ( Site 2005)

Izmir, , Turkey (Türkiye)

Site Status

Medical center Medikal Plaza of Ecodnipro LLC ( Site 2107)

Dnipro, Dnipropetrovsk Oblast, Ukraine

Site Status

SOGrigoriev Inst for Med Radiolgy and Oncology of NAMS of Ukraine-Clinical oncology and hematology ( Site 2110)

Kharkiv, Kharkivs’ka Oblast’, Ukraine

Site Status

Communal nonprofit enterprise "Kherson Regional Oncology Dispensary" of Kherson Regional Council ( Site 2109)

Antonivka Village, Kherson Oblast, Ukraine

Site Status

LLC Ukrainian Center of Tomotherapy ( Site 2105)

Kropyvnytskyi, Kirovohrad Oblast, Ukraine

Site Status

Medical Center of Yuriy Spizhenko LLC.-Clinical Trial ( Site 2104)

Kapitanivka Village, Kyivska Oblast, Ukraine

Site Status

SNPE National Cancer Institute ( Site 2101)

Kyiv, Kyivska Oblast, Ukraine

Site Status

Medical Center Verum ( Site 2106)

Kyiv, Kyivska Oblast, Ukraine

Site Status

Kyiv City Clinical Oncology Center ( Site 2100)

Kyiv, , Ukraine

Site Status

Weston Park Hospital ( Site 1406)

Sheffield, Derbyshire, United Kingdom

Site Status

Guys and St Thomas NHS Foundation Trust ( Site 1410)

London, London, City of, United Kingdom

Site Status

University College Hospital NHS Foundation Trust ( Site 1403)

London-Camden, London, City of, United Kingdom

Site Status

Royal Marsden Hospital (Sutton) ( Site 1407)

London, Surrey, United Kingdom

Site Status

Southampton General Hospital ( Site 1400)

Southampton, Worcestershire, United Kingdom

Site Status

Leeds Teaching Hospitals NHS Trust ( Site 1401)

Leeds, , United Kingdom

Site Status

Christie NHS Foundation Trust ( Site 1409)

Manchester, , United Kingdom

Site Status

Countries

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United States Argentina Canada Chile China Czechia Estonia France Germany Hungary Italy Japan Latvia Lithuania Mexico Norway Peru Poland Romania Russia South Korea Spain Thailand Turkey (Türkiye) Ukraine United Kingdom

References

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Jabbour SK, Cho BC, Bria E, Kato T, Bhosle J, Gainor JF, Reguart N, Wang L, Morgensztern D, Shentu Y, Kim SJ, Souza F, Reck M. Rationale and Design of the Phase III KEYLYNK-012 Study of Pembrolizumab and Concurrent Chemoradiotherapy Followed by Pembrolizumab With or Without Olaparib for Stage III Non-Small-Cell Lung Cancer. Clin Lung Cancer. 2022 Sep;23(6):e342-e346. doi: 10.1016/j.cllc.2022.04.003. Epub 2022 Apr 29.

Reference Type DERIVED
PMID: 35618629 (View on PubMed)

Related Links

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Other Identifiers

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MK-7339-012

Identifier Type: OTHER

Identifier Source: secondary_id

KEYLYNK-012

Identifier Type: OTHER

Identifier Source: secondary_id

205352

Identifier Type: REGISTRY

Identifier Source: secondary_id

2023-503591-25-00

Identifier Type: REGISTRY

Identifier Source: secondary_id

U1111-1287-5477

Identifier Type: REGISTRY

Identifier Source: secondary_id

2019-003237-41

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id

7339-012

Identifier Type: -

Identifier Source: org_study_id

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