Pembrolizumab/Vibostolimab Coformulation (MK-7684A) or Pembrolizumab/Vibostolimab Coformulation Plus Docetaxel Versus Docetaxel for Metastatic Non Small Cell Lung Cancer (NSCLC) With Progressive Disease After Platinum Doublet Chemotherapy and Immunotherapy (MK-7684A-002, KEYVIBE-002)

NCT ID: NCT04725188

Last Updated: 2025-08-15

Study Results

Results available

Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.

View full results

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

PHASE2

Total Enrollment

255 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-04-20

Study Completion Date

2024-10-17

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The main purpose of this study is to compare pembrolizumab/vibostolimab coformulation (MK-7684A) plus docetaxel or pembrolizumab/vibostolimab coformulation to normal saline placebo plus docetaxel. Participants with metastatic non-small cell lung cancer (NSCLC) and progressive disease (PD) after platinum doublet chemotherapy and treatment with one prior anti- programmed cell death 1 (PD-1)/ programmed cell death ligand 1(PD-L1) monoclonal antibody (mAb). MK-7684A is a coformulation product of pembrolizumab/vibostolimab. The dual primary hypotheses of the study are pembrolizumab/vibostolimab coformulation plus docetaxel and pembrolizumab/vibostolimab coformulation is superior to normal saline placebo plus docetaxel with respect to progression free survival (PFS) per Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST 1.1) by blinded independent central review (BICR).

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Participants may receive additional 17 cycles of pembrolizumab/vibostolimab (each cycle length = 21 days) for an additional 1 year of treatment as second course phase at investigator's discretion.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Metastatic Non Small Cell Lung Cancer

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Investigators
Arm 1 and Arm 3: Double-blind with in-house blinding Arm 2: Unblinded Open-label

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Arm 1: Pembrolizumab/Vibostolimab coformulation + Docetaxel

Participants receive pembrolizumab/vibostolimab (coformulation of 200 mg pembrolizumab and 200 mg vibostolimab) via intravenous (IV) infusion once every 3 weeks (Q3W) for up to 35 cycles up to approximately 2 years plus docetaxel 75 mg/m\^2 via IV infusion Q3W. Each cycle will be 21 days.

Group Type EXPERIMENTAL

Pembrolizumab/Vibostolimab coformulation

Intervention Type BIOLOGICAL

Pembrolizumab 200 mg + vibostolimab 200 mg/20 mL vial IV infusion Q3W up to approximately 2 years.

Docetaxel

Intervention Type DRUG

Docetaxel 75 mg\^m2 IV infusion Q3W until discontinuation due to progressive disease or unacceptable toxicity. Docetaxel will serve as part of an experimental treatment in Arm 1, and as an active comparator in Arm 3.

Arm 2: Pembrolizumab/Vibostolimab coformulation

Participants receive pembrolizumab/vibostolimab (coformulation of 200 mg pembrolizumab and 200 mg vibostolimab) via IV infusion Q3W for up to 35 cycles up to approximately 2 years. Each cycle will be 21 days.

Group Type EXPERIMENTAL

Pembrolizumab/Vibostolimab coformulation

Intervention Type BIOLOGICAL

Pembrolizumab 200 mg + vibostolimab 200 mg/20 mL vial IV infusion Q3W up to approximately 2 years.

Arm 3: Placebo + Docetaxel

Participants receive normal saline placebo via IV infusion Q3W for up to 35 cycles up to approximately 2 years plus docetaxel 75 mg/m\^2 IV infusion Q3W. Each cycle will be 21 days.

Group Type ACTIVE_COMPARATOR

Docetaxel

Intervention Type DRUG

Docetaxel 75 mg\^m2 IV infusion Q3W until discontinuation due to progressive disease or unacceptable toxicity. Docetaxel will serve as part of an experimental treatment in Arm 1, and as an active comparator in Arm 3.

Placebo

Intervention Type DRUG

Normal saline IV infusion Q3W up to approximately 2 years

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Pembrolizumab/Vibostolimab coformulation

Pembrolizumab 200 mg + vibostolimab 200 mg/20 mL vial IV infusion Q3W up to approximately 2 years.

Intervention Type BIOLOGICAL

Docetaxel

Docetaxel 75 mg\^m2 IV infusion Q3W until discontinuation due to progressive disease or unacceptable toxicity. Docetaxel will serve as part of an experimental treatment in Arm 1, and as an active comparator in Arm 3.

Intervention Type DRUG

Placebo

Normal saline IV infusion Q3W up to approximately 2 years

Intervention Type DRUG

Other Intervention Names

Discover alternative or legacy names that may be used to describe the listed interventions across different sources.

MK-7684A Taxotere

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Has a histologically or cytologically confirmed diagnosis of metastatic non-small cell lung cancer (NSCLC)
* Has confirmation that epidermal growth factor receptor (EGFR), anaplastic lymphoma kinase (ALK), or reactive oxygen species (ROS) 1 directed therapy is not indicated as primary therapy
* Has progressive disease (PD) on treatment with one prior anti-programmed cell death 1 (PD-1)/ programmed cell death ligand 1 (PD-L1) monoclonal antibody (mAb) administered either as monotherapy or in combination with other checkpoint inhibitors or other therapies

* Retreatment with the same anti-PD-L1/PD-L1 mAb is acceptable in the overall course of treatment
* Has PD as determined by the investigator after platinum doublet chemotherapy for metastatic disease
* Has measurable disease defined as at least 1 measurable lesion by computed tomography (CT) or magnetic resonance imaging (MRI), based on Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST 1.1)
* Has provided tumor tissue for PD-L1 biomarker analysis from an archival sample or newly obtained core or excisional biopsy of a tumor lesion not previously irradiated
* Has a life expectancy of at least 3 months
* Has an Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 to 1 assessed within 7 days prior to randomization
* Male participants randomized to docetaxel are eligible to participant if they agree to refrain from donating sperm, and either 1) be abstinent from heterosexual intercourse; or 2) must agree to follow contraceptive guidance as per study protocol unless confirmed to be azoospermic during the intervention period and for at least 180 days after the last dose of docetaxel
* Female participants must be not pregnant, not breastfeeding, and not be a woman of child-bearing potential (WOCBP). A WOCBP is eligible is she agrees to either use contraception, or be abstinent from heterosexual intercourse during the intervention period and for ≥120 days after the last dose of study intervention. If a WOCBP is randomized to docetaxel, she agrees not to donate eggs and either uses contraception or be abstinent from heterosexual intercourse during the treatment period and for ≥180 days after the last dose of docetaxel
* Has adequate organ function

Exclusion Criteria

* Has known active or untreated central nervous system (CNS) metastases and/or carcinomatous meningitis
* Has a known history of an additional malignancy, except if the participant has undergone potentially curative therapy with no evidence of that disease recurrence for at least 3 years since initiation of that therapy
* Has received docetaxel as monotherapy or in combination with other therapies
* Has received previous treatment with another agent targeting the T-cell immunoreceptor with immunoglobulin \[Ig\] and immunoreceptor tyrosine-based inhibitory motif \[ITIM\] domains (TIGIT) pathway
* Has received radiotherapy within 2 weeks of start of study intervention. One week washout is permitted for palliative radiation to non-CNS disease
* Has received a live or live-attenuated vaccine within 30 days before the first dose of study intervention
* Is currently participating in or has participated in a study of an investigational agent or has used an investigational device within 4 weeks before the first dose of study intervention
* Has severe hypersensitivity (≥Grade 3) to docetaxel or pembrolizumab/vibostolimab coformulation and/or any of its excipients
* Has an active autoimmune disease that has required systemic treatment in past 2 years
* Has a diagnosis of immunodeficiency or is receiving chronic systemic steroid therapy or any other form of immunosuppressive therapy within 7 days before the first dose of study intervention
* Has interstitial lung disease, or history of pneumonitis requiring steroids for treatment
* Has known history of active human immunodeficiency virus (HIV), Hepatitis B or Hepatitis C
* Has had an allogenic tissue/solid organ transplant
* Has a known psychiatric or substance abuse disorder that would interfere with the participant's ability to cooperate with the requirements of the study
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Merck Sharp & Dohme LLC

INDUSTRY

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Medical Director

Role: STUDY_DIRECTOR

Merck Sharp & Dohme LLC

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Cedars-Sinai Medical Center ( Site 2522)

Los Angeles, California, United States

Site Status

Illinois Cancer Care ( Site 2534)

Peoria, Illinois, United States

Site Status

Baptist Health Lexington-Research ( Site 2502)

Lexington, Kentucky, United States

Site Status

University of Maryland ( Site 2528)

Baltimore, Maryland, United States

Site Status

Hattiesburg Clinic Hematology/Oncology ( Site 2511)

Hattiesburg, Mississippi, United States

Site Status

Mercy Research - Cancer and Hematology Center ( Site 2535)

Springfield, Missouri, United States

Site Status

Mercy Research - David C. Pratt Cancer Center ( Site 2532)

St Louis, Missouri, United States

Site Status

Montefiore- Einstein Center for Cancer Care-Oncology ( Site 2509)

The Bronx, New York, United States

Site Status

University of Cincinnati Medical Center-University of Cincinnati Cancer Center ( Site 2526)

Cincinnati, Ohio, United States

Site Status

St Francis Cancer Center-Research Office ( Site 2531)

Greenville, South Carolina, United States

Site Status

Centro de Oncología e Investigación de Buenos Aires ( Site 0008)

Berazategui, Buenos Aires, Argentina

Site Status

Hospital Privado de Comunidad ( Site 0004)

Mar del Plata, Buenos Aires, Argentina

Site Status

Instituto de Investigaciones Clínicas Mar del Plata ( Site 0002)

Mar del Plata, Buenos Aires, Argentina

Site Status

Instituto de Oncología de Rosario ( Site 0003)

Rosario, Santa Fe Province, Argentina

Site Status

Hospital Privado Universitario de Córdoba ( Site 0001)

Córdoba, , Argentina

Site Status

Fundación CORI para la Investigación y Prevención del Cáncer ( Site 0005)

La Rioja, , Argentina

Site Status

Canberra Hospital ( Site 0104)

Canberra, Australian Capital Territory, Australia

Site Status

Gold Coast University Hospital-Clinical Trials Service ( Site 0106)

Southport, Queensland, Australia

Site Status

Fiona Stanley Hospital-Medical Oncology ( Site 0102)

Murdoch, Western Australia, Australia

Site Status

Medizinische Universität Graz ( Site 0201)

Graz, Styria, Austria

Site Status

Ordensklinikum Linz GmbH Elisabethinen-Department of Pneumology ( Site 0203)

Linz, Upper Austria, Austria

Site Status

Klinik Floridsdorf-Abteilung für Innere Medizin und Pneumologie ( Site 0204)

Vienna, , Austria

Site Status

AZ Sint-Maarten, Campus Leopoldstraat 2 ( Site 0333)

Mechelen, Antwerpen, Belgium

Site Status

UZ Brussel ( Site 0336)

Brussels, Bruxelles-Capitale, Region de, Belgium

Site Status

Grand Hôpital de Charleroi-Oncology & Hematology ( Site 0337)

Charleroi, Hainaut, Belgium

Site Status

Jessa Ziekenhuis-Pulmonology & Thoracic Oncology ( Site 0338)

Hasselt, Limburg, Belgium

Site Status

AZ Nikolaas ( Site 0334)

Sint-Niklaas, Oost-Vlaanderen, Belgium

Site Status

Hospital Nossa Senhora da Conceição ( Site 0403)

Porto Alegre, Rio Grande do Sul, Brazil

Site Status

ICESP - INSTITUTO DO CÂNCER DO ESTADO DE SÃO PAULO-Pesquisa Clinica ( Site 0400)

São Paulo, São Paulo, Brazil

Site Status

Centro de Tratamento de Tumores Botafogo - CTTB-Pesquisa Clínica ( Site 0402)

Rio de Janeiro, , Brazil

Site Status

Hospital Paulistano ( Site 0406)

São Paulo, , Brazil

Site Status

Rigshospitalet ( Site 0702)

Copenhagen, Capital Region, Denmark

Site Status

Odense Universitetshospital ( Site 0700)

Odense, Region Syddanmark, Denmark

Site Status

Sygehus Soenderjylland-Kraeftambulatoriet ( Site 0705)

Sønderborg, Region Syddanmark, Denmark

Site Status

Oulun yliopistollinen sairaala ( Site 0902)

Oulu, North Ostrobothnia, Finland

Site Status

Tampereen yliopistollinen sairaala-Oncology ( Site 0906)

Tampere, Pirkanmaa, Finland

Site Status

Vaasan Keskussairaala ( Site 0903)

Vaasa, Pohjanmaa, Finland

Site Status

Turku University Hospital-The Department of Pulmonary Medicine ( Site 0905)

Turku, Southwest Finland, Finland

Site Status

Nouvel Hôpital Civil (NHC) ( Site 1000)

Strasbourg, Alsace, France

Site Status

Institut Bergonié - Centre Régional de Lutte Contre Le Cance-Medical Oncology ( Site 1009)

Bordeaux, Aquitaine, France

Site Status

Centre Hospitalier Universitaire de Caen - Hôpital Côte de Nacre ( Site 1006)

Caen, Calvados, France

Site Status

CHU de Toulouse - Hopital Larrey-service de pneumologie ( Site 1008)

Toulouse, Haute-Garonne, France

Site Status

Clinique Ambroise Paré ( Site 1007)

Beuvry, Pas-de-Calais, France

Site Status

Centre Hospitalier du Mans ( Site 1002)

Le Mans, Sarthe, France

Site Status

Gustave Roussy ( Site 1005)

Villejuif, Val-de-Marne, France

Site Status

HIA Sainte Anne ( Site 1003)

Toulon, Var, France

Site Status

Centre Hospitalier d'Avignon-Service d'Oncologie médicale et d'hématologie clinique ( Site 1004)

Avignon, Vaucluse, France

Site Status

Onkologie Ravensburg ( Site 1104)

Ravensburg, Baden-Wurttemberg, Germany

Site Status

Klinikverbund Allgaeu gGmbH ( Site 1109)

Immenstadt im Allgäu, Bavaria, Germany

Site Status

Helios Dr. Horst Schmidt Kliniken ( Site 1108)

Wiesbaden, Hesse, Germany

Site Status

Universitätsklinikum Bonn ( Site 1111)

Bonn, North Rhine-Westphalia, Germany

Site Status

Helios Klinikum Emil von Behring Berlin-Zehlendorf ( Site 1106)

Berlin, , Germany

Site Status

Soroka Medical Center ( Site 1202)

Beersheba, , Israel

Site Status

Rambam Health Care Campus-Oncology ( Site 1203)

Haifa, , Israel

Site Status

Shaare Zedek Medical Center-Oncology ( Site 1206)

Jerusalem, , Israel

Site Status

Sourasky Medical Center ( Site 1205)

Tel Aviv, , Israel

Site Status

Azienda Ospedaliera S. Giovanni Addolorata-Oncologia Medica ( Site 1307)

Rome, Lazio, Italy

Site Status

Azienda Ospedaliera Dei Colli-U.O.C Pneumologia Oncologica DH PNL ONC ( Site 1308)

Naples, Napoli, Italy

Site Status

CRO-IRCCS-medical oncology ( Site 1304)

Aviano, Pordenone, Italy

Site Status

Azienda Sanitaria Ospedaliera S Luigi Gonzaga-Oncologia Polmonare ( Site 1300)

Orbassano, Torino, Italy

Site Status

Azienda Ospedaliera Universitaria Careggi-SOD ONCOLOGIA MEDICA ( Site 1306)

Florence, Tuscany, Italy

Site Status

Ospedale San Raffaele-Oncologia Medica ( Site 1305)

Milan, , Italy

Site Status

Istituto Europeo di Oncologia IRCCS-Divisione di Oncologia Toracica ( Site 1301)

Milan, , Italy

Site Status

Fondazione Policlinico Universitario Agostino Gemelli-Medical Oncology ( Site 1303)

Roma, , Italy

Site Status

Hospital Sultan Ismail ( Site 1503)

Johor Bahru, Johor, Malaysia

Site Status

University Malaya Medical Centre ( Site 1501)

Lembah Pantai, Kuala Lumpur, Malaysia

Site Status

Hospital Tengku Ampuan Afzan ( Site 1500)

Kuantan, Pahang, Malaysia

Site Status

Beacon Hospital Sdn Bhd ( Site 1504)

Petaling Jaya, Selangor, Malaysia

Site Status

Przychodnia Lekarska KOMED ( Site 1704)

Konin, Greater Poland Voivodeship, Poland

Site Status

Narodowy Instytut Onkologii im. Marii Sklodowskiej-Curie - P-Klinika Nowotworow Pluca i Klatki Pier

Warsaw, Masovian Voivodeship, Poland

Site Status

Saint Petersburg State University-Clinic of advanced medical technologies n. a. Nicolay I. Pirogov (

Saint Petersburg, Leningradskaya Oblast', Russia

Site Status

Saint-Petersburg City Clinical Oncology Dispensary-Department of chemotherapy ( Site 1911)

Saint Petersburg, Leningradskaya Oblast', Russia

Site Status

Moscow Clinical Research Center-Chemotherapy department ( Site 1910)

Moscow, Moscow, Russia

Site Status

Central Clinical Hospital of the Presidential Administrative Department ( Site 1902)

Moscow, Moscow, Russia

Site Status

Hadassah Medical-Oncology department ( Site 1912)

Moscow, Moscow Oblast, Russia

Site Status

Nizhegorodsky Regional Oncology Dispensary, Branch #2-chemotherapy ( Site 1909)

Nizhny Novgorod, Nizhny Novgorod Oblast, Russia

Site Status

Budgetary Healthcare Institution of Omsk Region Clinical Oncology Dispensary ( Site 1908)

Omsk, Omsk Oblast, Russia

Site Status

GBUZ LOKB-Oncology department #1 ( Site 1905)

Saint Petersburg, Sankt-Peterburg, Russia

Site Status

N.N.Petrov Research Institute of Oncology-Department of Chemotherapy and Innovative Technologies ( S

Saint Petersburg, Sankt-Peterburg, Russia

Site Status

Seoul National University Bundang Hospital ( Site 2003)

Seongnam, Kyonggi-do, South Korea

Site Status

The Catholic University Of Korea St. Vincent's Hospital-Medical Oncology ( Site 2005)

Suwon, Kyonggi-do, South Korea

Site Status

Chungbuk National University Hospital-Internal medicine ( Site 2004)

Cheongju-si, North Chungcheong, South Korea

Site Status

Asan Medical Center-Oncology ( Site 2000)

Songpagu, Seoul, South Korea

Site Status

HOSPITAL CLÍNIC DE BARCELONA-ICHMO- Clinic Institut of Haematological and Oncological diseases ( Sit

Barcelona, Catalonia, Spain

Site Status

Hospital de la Santa Creu i Sant Pau-Oncología Médica ( Site 2102)

Barcelona, Catalonia, Spain

Site Status

HOSPITAL GENERAL UNIVERSITARIO GREGORIO MARAÑON-ONCOLOGY ( Site 2101)

Madrid, , Spain

Site Status

Hospital Universitario Virgen de Valme-Departamento de Oncologia ( Site 2103)

Seville, , Spain

Site Status

Ospedale Regionale Bellinzona e Valli ( Site 2203)

Bellinzona, Canton Ticino, Switzerland

Site Status

Chang Gung Memorial Hospital at Kaohsiung ( Site 2303)

Kaohsiung Niao Sung Dist, Kaohsiung, Taiwan

Site Status

Taichung Veterans General Hospital-Chest ( Site 2307)

Taichung, , Taiwan

Site Status

NATIONAL CHENG-KUNG UNI. HOSP.-clinical trial center ( Site 2302)

Tainan City, , Taiwan

Site Status

National Taiwan University Hospital-Oncology ( Site 2304)

Taipei, , Taiwan

Site Status

Mackay Memorial Hospital-Chest Medicine ( Site 2305)

Taipei, , Taiwan

Site Status

Chulalongkorn University ( Site 2403)

Bangkok, Bangkok, Thailand

Site Status

Faculty of Medicine Siriraj Hospital ( Site 2400)

Bangkok, Bangkok, Thailand

Site Status

Countries

Review the countries where the study has at least one active or historical site.

United States Argentina Australia Austria Belgium Brazil Denmark Finland France Germany Israel Italy Malaysia Poland Russia South Korea Spain Switzerland Taiwan Thailand

Provided Documents

Download supplemental materials such as informed consent forms, study protocols, or participant manuals.

Document Type: Study Protocol and Statistical Analysis Plan

View Document

Related Links

Access external resources that provide additional context or updates about the study.

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

MK-7684A-002

Identifier Type: OTHER

Identifier Source: secondary_id

KEYVIBE-002

Identifier Type: OTHER

Identifier Source: secondary_id

2022-501252-28-00

Identifier Type: REGISTRY

Identifier Source: secondary_id

U1111-1275-8661

Identifier Type: REGISTRY

Identifier Source: secondary_id

2020-004034-38

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id

7684A-002

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.