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Набира участници NCT04165798

KEYMAKER-U01 Umbrella Master Study: Studies of Investigational Agents With Either Pembrolizumab (MK-3475) Alone or With Pembrolizumab PLUS Chemotherapy in Participants With Non-small Cell Lung Cancer (NSCLC) (MK-3475-U01/KEYMAKER-U01)

Заболявания: Carcinoma, Non-Small-Cell Lung

Спонсор: Merck Sharp & Dohme LLC

Налично на: БГ
Обобщение
This study is referred to as the "umbrella master protocol" for pembrolizumab (MK-3475) in the treatment of non-small cell lung cancer (NSCLC). This pembrolizumab NSCLC umbrella master protocol uses a platform design and consists of this master screening study and additional substudies. Each substudy will enroll a different population of NSCLC participants.
Описание
The following pembrolizumab substudies will evaluate the efficacy of different investigational agents in combination with pembrolizumab given in sequence or in combination with pembrolizumab PLUS chemotherapy: * KEYMAKER-U01 Substudy 01A: A Phase 1/2, Umbrella Study With Rolling Arms of Investigational Agents, With Pembrolizumab With or Without Chemotherapy in Treatment-Naive Participants With Stage IV Non-small Cell Lung Cancer (NSCLC) (MK-3475-01A) - NCT04165070 * KEYMAKER-U01 Substudy 2: A Phase 2, Umbrella Study with Rolling Arms of Investigational Agents in Combination with Pembrolizumab in Treatment Naïve Patients with PD-L1 Positive Advanced Non-small Cell Lung Cancer (NSCLC) (MK-3475-01B) - NCT04165083 * KEYMAKER-U01 Substudy 3: A Phase 2, Umbrella Study with Rolling Arms of Investigational Agents in Combination with Pembrolizumab in Patients with Advanced Non-small Cell Lung Cancer (NSCLC) Previously Treated with anti-PD-(L)1 Therapy (MK-3475-01C) - NCT04165096 * KEYMAKER-U01 Substudy 01E: A Phase 2 Umbrella Study With Rolling Arms of Investigational Agents With or Without Chemotherapy in Combination With Pembrolizumab in Treatment of Participants With Newly Diagnosed Resectable Stages II-IIIB (N2) Non-small Cell Lung Cancer (NSCLC) (MK-3475-01E) - NCT06788912 * KEYMAKER-U01 Substudy 01F: A Phase 1b/2 Umbrella Study With Rolling Arms of Investigational Agents for Second-line Treatment of Participants With Advanced or Metastatic Nonsquamous Non-small Cell Lung Cancer (NSCLC) With KRAS G12C Mutations (MK-3475-01F) - NCT number pending * KEYMAKER-U01 Substudy 01G: A Phase 2, Umbrella Study With Rolling Arms of Investigational Agents in Combination With Pembrolizumab With or Without Platinum-based Chemotherapy in Treatment-Naïve Participants With Stage IV Non-small Cell Lung Cancer (NSCLC) (MK-3475-01G) - NCT06731907 * KEYMAKER-U01 Substudy 01H: A Phase 2, Randomized, Umbrella Study With Rolling Arms of Investigational Agents in Participants with Previously Treated Stage IV Nonsquamous Non-small Cell Lung Cancer (NSCLC) (MK-3475-01H) - NCT06780085 * KEYMAKER-U01 Substudy 01I: A Phase 2, Randomized, Umbrella Study With Rolling Arms of Investigational Agents in Participants With Previously Treated Stage IV Squamous Non-small Cell Lung Cancer (NSCLC) (MK-3475-01I) - NCT06780098 * KEYMAKER-U01 Substudy 01J: A Randomized Phase 2 Umbrella Study With Rolling Arms of Investigational Agents for First-line Treatment of Participants With Advanced or Metastatic Nonsquamous Non-small Cell Lung Cancer (NSCLC) With KRAS G12C Mutations (MK-3475-01J) - NCT number pending
Кой може да участва
Inclusion Criteria: The main inclusion criteria include but are not limited to the following: * Has histologically- or cytologically-confirmed diagnosis of Stage IV squamous or nonsquamous NSCLC * Has measurable disease per Response Evaluation Criteria in Solid Tumors version 1.1 Exclusion Criteria: The main exclusion criteria include but are not limited to the following: * Has an active autoimmune disease that has required systemic treatment in the 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
Интервенции
Tumor Imaging
DIAGNOSTIC_TEST
Tumor Tissue Collection
PROCEDURE
Blood Sample Collection
PROCEDURE
Места на провеждане 47
Унгария (3)
Orszagos Koranyi Pulmonologiai Intezet ( Site 0060)
Budapest
COMPLETED
Petz Aladar Megyei Oktato Korhaz ( Site 0062)
Győr , Győr-Moson-Sopron
COMPLETED
Jász-Nagykun-Szolnok Vármegyei Hetényi Géza Kórház ( Site 0061)
Szolnok , Jász-Nagykun-Szolnok
COMPLETED
Израел (7)
Soroka Medical Center ( Site 0072)
Beersheba
COMPLETED
Rambam Health Care Campus-Oncology ( Site 0076)
Haifa
COMPLETED
Shaare Zedek Medical Center ( Site 0075)
Jerusalem
Study Coordinator
Meir Medical Center ( Site 0071)
Kfar Saba
COMPLETED
Rabin Medical Center ( Site 0074)
Petah Tikva
COMPLETED
Chaim Sheba Medical Center ( Site 0070)
Ramat Gan
Study Coordinator
Sourasky Medical Center ( Site 0077)
Tel Aviv
COMPLETED
Италия (3)
Azienda Ospedaliera Universitaria Careggi ( Site 0173)
Florence , Firenze
COMPLETED
IRCCS Ospedale San Raffaele ( Site 0171)
Milan
COMPLETED
Policlinico Gemelli di Roma ( Site 0174)
Roma
COMPLETED
Полша (3)
Uniwersyteckie Centrum Kliniczne-Early Clinical Trials Unit ( Site 0150)
Gdansk , Pomeranian Voivodeship
COMPLETED
Szpital Wojewódzki im. Mikoaja Kopernika w Koszalinie-Oddzial Dzienny Chemioterapii ( Site 0152)
Koszalin , West Pomeranian Voivodeship
ACTIVE_NOT_RECRUITING
Narodowy Instytut Onkologii im. Marii Sklodowskiej-Curie - P-Klinika Nowotworow Pluca i Klatki Pier ( Site 0151)
Warsaw , Masovian Voivodeship
Study Coordinator
Южна Корея (3)
Seoul National University Bundang Hospital ( Site 0081)
Seongnam-si , Kyonggi-do
COMPLETED
Severance Hospital ( Site 0080)
Seoul
COMPLETED
Samsung Medical Center ( Site 0082)
Seoul
COMPLETED
Испания (3)
Hospital Clínic de Barcelona ( Site 0092)
Barcelona
Study Coordinator
ICO L Hospitalet ( Site 0090)
L'Hospitalet de Llobregat , Barcelona
Study Coordinator
Hospital Universitario Quiron Madrid ( Site 0091)
Madrid
Study Coordinator
Taiwan (3)
Changhua Christian Hospital ( Site 0181)
Changhua
Study Coordinator
Taipei Medical University Hospital ( Site 0180)
Taipei
Study Coordinator
Chang Gung Medical Foundation-Linkou Branch ( Site 0182)
Taoyuan District
Study Coordinator
Ukraine (4)
COMMUNAL NONPROFIT ENTERPRISE CLINICAL CENTER OF ONCOLOGY, HEMATOLOGY, TRANSPLANTOLOGY AND PALLIATI ( Site 0463)
Cherkasy , Cherkasy Oblast
Study Coordinator
Communal Non-Commercial Enterprise "Prykarpatski Clinical Oncological Center" of Ivano-Frankivsk Reg ( Site 0460)
Ivano-Frankivsk , Ivano-Frankivsk Oblast
Study Coordinator
ME RIVNE REGIONAL ANTITUMOR CENTER ( Site 0461)
Rivne , Rivne Oblast
Study Coordinator
Uzhhorod Multispecialty City Clinical Hospital ( Site 0462)
Uzhhorod , Zakarpattia Oblast
Study Coordinator
САЩ (18)
MedStar Franklin Square Medical Center ( Site 0033)
Baltimore , Maryland
COMPLETED
Massachusetts General Hospital ( Site 0003)
Boston , Massachusetts
COMPLETED
Dana Farber Cancer Institute ( Site 0002)
Boston , Massachusetts
COMPLETED
Cleveland Clinic Main ( Site 0006)
Cleveland , Ohio
COMPLETED
Ohio State University Comprehensive Cancer Center ( Site 0015)
Columbus , Ohio
Study Coordinator
City of Hope ( Site 0014)
Duarte , California
COMPLETED
Sanford Fargo Medical Center ( Site 0039)
Fargo , North Dakota
Study Coordinator
Banner MD Anderson Cancer Center ( Site 0001)
Gilbert , Arizona
COMPLETED
John Theurer Cancer Center at Hackensack University Medical Center ( Site 0037)
Hackensack , New Jersey
COMPLETED
The University of Texas MD Anderson Cancer Center ( Site 0009)
Houston , Texas
Study Coordinator
Dartmouth Hitchcock Medical Center ( Site 0016)
Lebanon , New Hampshire
Study Coordinator
University of Kentucky Markey Cancer Center ( Site 0019)
Lexington , Kentucky
COMPLETED
Laura and Isaac Perlmutter Cancer Center at NYU Langone Health ( Site 0034)
New York , New York
COMPLETED
Oncology Hematology West, PC DBA Nebraska Cancer Specialists ( Site 0031)
Omaha , Nebraska
COMPLETED
Abramson Cancer Center of the University of Pennsylvania ( Site 0010)
Philadelphia , Pennsylvania
Study Coordinator
UCSF Medical Center at Mission Bay ( Site 0007)
San Francisco , California
COMPLETED
Sanford Cancer Center ( Site 0038)
Sioux Falls , South Dakota
Study Coordinator
Georgetown University ( Site 0036)
Washington D.C. , District of Columbia
COMPLETED
Технически детайли
Статус
Набира участници
Вид изследване
OBSERVATIONAL
Пол
Мъже и жени
Минимална възраст
18 Years
Здрави доброволци
Не
Начална дата
19.12.2019
Крайна дата
13.02.2032
Регистрационен номер
NCT04165798
Източник
clinicaltrials.gov
Запитване за медицински туризъм

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