A Phase 2 Study to Evaluate the Efficacy and Safety of Pembrolizumab Plus Investigational Agents in Combination With Etoposide and Cisplatin or Carboplatin for the First-Line Treatment of Participants With Extensive-Stage Small Cell Lung Cancer (KEYNOTE-B99)

Who is this study for? Patients with Small-Cell Lung Cancer
What treatments are being studied? Pembrolizumab+Etoposide+Cisplatin+Carboplatin
Status: Completed
Location: See all (49) locations...
Intervention Type: Biological, Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

The purpose of this study is to evaluate the use of investigational agents (MK-4830, boserolimab (MK-5890) and lenvatinib (MK-7902)) in combination with pembrolizumab (MK-3475) and etoposide/platinum chemotherapy for the first-line treatment of participants with extensive-stage small cell Lung Cancer (ES-SCLC). No formal hypothesis testing will be performed for this study.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Has histologically or cytologically confirmed diagnosis of extensive-stage small cell lung cancer (ES-SCLC) in need of first-line therapy

• Has ES-SCLC defined as Stage IV (T any, N any, M1a/b/c) by the American Joint Committee on Cancer, Eighth Edition

• Male participants are eligible to participate if they agree to the following during the intervention period and for at least the time needed to eliminate each study intervention after the last dose of study intervention. The length of time required to continue contraception for each study intervention is as follows: Lenvatinib (7 days); Etoposide, Cisplatin, or Carboplatin (180 days) and Pembrolizumab, MK-4830, or (no contraception measures); refrain from donating sperm plus either be abstinent from heterosexual intercourse as their preferred and usual lifestyle (abstinent on a long-term and persistent basis) and agree to remain abstinent or must agree to use contraception per protocol unless confirmed to be azoospermic

• A female participant is eligible to participate if she is not pregnant or breastfeeding, and at least one of the following conditions applies: Is not a woman/women of childbearing potential (WOCBP) or is a WOCBP and uses a contraceptive method that is highly effective with low user dependency or be abstinent from heterosexual intercourse as their preferred and usual lifestyle (abstinent on a long-term and persistent basis), during the intervention period and for at least the time needed to eliminate each study intervention after the last dose of study intervention and agrees not to donate eggs to others or freeze/store for her own use for the purpose of reproduction during this period. The length of time required to continue contraception for each study intervention is as follows: Lenvatinib (30 days), Etoposide, Cisplatin, or Carboplatin (180 days), and Pembrolizumab, MK-4830, or Boserolimab (120 days)

• A WOCBP must have a negative highly sensitive pregnancy test (urine or serum as required by local regulations) within 24 hours (urine test) or 72 hours (serum test) before the first dose of study intervention

• Abstains from breastfeeding during the study intervention period and for at least 120 days after study intervention

• Has measurable disease per RECIST 1.1 as assessed by local site investigator/radiology and verified by blinded independent central review (BICR)

• Submits an archival tumor tissue sample or newly obtained core, incisional, or excisional biopsy of a tumor lesion not previously irradiated where such sample exist

• Has an Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1 assessed within 7 days before randomization

• Has adequate organ function within 10 days before the first dose of study intervention

• Has adequately controlled blood pressure (BP) with or without antihypertensive medications, defined as BP ≤150/90 mm Hg with no changes in antihypertensive medications within 1 week before randomization

Locations
United States
Arizona
Banner MD Anderson Cancer Center ( Site 0102)
Gilbert
Colorado
University of Colorado Anschutz Medical Campus ( Site 0104)
Aurora
Georgia
Georgia Cancer Specialists ( Site 0106)
Atlanta
Indiana
Parkview Research Center at Parkview Regional Medical Center ( Site 0130)
Fort Wayne
Kentucky
Baptist Health Lexington-Research ( Site 0108)
Lexington
Maryland
MFSMC-HJWCI-Oncology Research ( Site 0128)
Baltimore
Nebraska
Oncology Hematology West, PC dba Nebraska Cancer Specialists ( Site 0122)
Omaha
Oncology Hematology West, PC dba Nebraska Cancer Specialists ( Site 0129)
Omaha
New York
Perlmutter Cancer Center at NYU Langone Hospital - Long Island ( Site 0114)
Mineola
Memorial Sloan Kettering Cancer Center ( Site 0115)
New York
Ohio
Cleveland Clinic-Taussig Cancer Center ( Site 0116)
Cleveland
Pennsylvania
UPMC Hillman Cancer Center ( Site 0127)
Pittsburgh
South Carolina
St Francis Cancer Center-Research Office ( Site 0117)
Greenville
Virginia
Virginia Cancer Institute ( Site 0119)
Richmond
Other Locations
Austria
Klinik Floridsdorf-Abteilung für Innere Medizin und Pneumologie ( Site 2100)
Vienna
Klinik Penzing-2. Lungenabteilung ( Site 2101)
Vienna
Canada
Hamilton Health Sciences-Juravinski Cancer Centre ( Site 2003)
Hamilton
Kingston Health Sciences Centre-Kingston General Hospital Site ( Site 2005)
Kingston
St. Marys Hospital Center ( Site 2000)
Montreal
Hungary
Országos Korányi Pulmonológiai Intézet-XIV. Tüdöbelgyógyászat ( Site 2806)
Budapest
Semmelweis University-Pulmonológiai Klinika ( Site 2802)
Budapest
Jász-Nagykun-Szolnok Megyei Hetényi Géza Kórház-Onkologiai Kozpont ( Site 2800)
Szolnok
Torokbalint Tudogyogyintezet-Onkopulmonologiai Jarobeteg Centrum ( Site 2801)
Törökbálint
Zala Megyei Szent Rafael Kórház-Pulmonológia ( Site 2805)
Zalaegerszeg
Israel
Rambam Health Care Campus-Oncology ( Site 2600)
Haifa
Shaare Zedek Medical Center ( Site 2602)
Jerusalem
Meir Medical Center ( Site 2601)
Kfar Saba
Rabin Medical Center-Oncology ( Site 2604)
Petah Tikva
Sheba Medical Center-ONCOLOGY ( Site 2603)
Ramat Gan
Italy
Istituto Europeo di Oncologia IRCCS-Divisione di Oncologia Toracica ( Site 2304)
Milan
Ospedale San Raffaele-Oncologia Medica ( Site 2303)
Milan
ospedale le scotte-U.O.C. Immunoterapia Oncologica ( Site 2300)
Siena
Poland
Samodzielny Publiczny Zespó Grulicy i Chorób Puc w Olsztynie-Oddzial Onkologii z Pododdzialem Chemi
Olsztyn
Narodowy Instytut Onkologii im. Marii Sklodowskiej-Curie - P-Klinika Nowotworow Pluca i Klatki Pier
Warsaw
Republic of Korea
Chungbuk National University Hospital ( Site 1107)
Cheongju-si
Seoul National University Bundang Hospital ( Site 1104)
Seongnam
Asan Medical Center-Department of Oncology ( Site 1103)
Seoul
Samsung Medical Center ( Site 1100)
Seoul
Seoul National University Hospital ( Site 1101)
Seoul
Severance Hospital, Yonsei University Health System-Medical oncology ( Site 1105)
Seoul
The Catholic University Of Korea St. Vincent's Hospital ( Site 1106)
Suwon
Russian Federation
Krasnoyarsk Regional Oncology Dispensary, Named after Krizhanovsky ( Site 2708)
Krasnoyarsk
GBUZ SPb CRPCstmc(o) ( Site 2705)
Saint Petersburg
N.N.Petrov Research Institute of Oncology-Department of Chemotherapy and Innovative Technologies ( S
Saint Petersburg
Scientific research institution of oncology named after N.N. Petrov-Thoracic oncology ( Site 2704)
Saint Petersburg
Spain
Hospital Universitari Vall d'Hebron-Oncology ( Site 2401)
Barcelona
Instituto Catalan de Oncologia - Hospital Duran i Reynals ( Site 2403)
L'hospitalet De Llobregat
Hospital Insular de Gran Canaria ( Site 2402)
Las Palmas De Gran Canaria
Switzerland
Cantonal Hospital St.Gallen-Oncology & Hematology ( Site 2502)
Sankt Gallen
Time Frame
Start Date: 2021-07-15
Completion Date: 2025-06-23
Participants
Target number of participants: 126
Treatments
Experimental: Pembrolizumab + MK-4830 + Chemotherapy
Participants receive pembrolizumab 200 mg IV infusion on Day 1 of each cycle (cycle length = 3 weeks) every 3 weeks (Q3W) up to 35 administrations (up to approximately 2 years) or until disease progression (PD) or discontinuation, MK-4830 800 mg IV infusion on Day 1 of each cycle Q3W, up to 35 administrations (up to approximately 2 years) or until PD or discontinuation; etoposide 100 mg/m\^2 on Days 1, 2, 3 of each cycle for up to 4 cycles (up to approximately 12 weeks) and cisplatin 75 mg/m\^2 or carboplatin AUC 5 mg/ml/min IV, Day 1 of each cycle Q3W up to 4 cycles (up to approximately 12 weeks) or until PD or discontinuation.
Experimental: Pembrolizumab + Boserolimab + Chemotherapy
Participants receive pembrolizumab 200 mg IV infusion on Day 1 of each cycle Q3W up to 35 administrations (up to approximately 2 years) or until PD or discontinuation, boserolimab 30 mg IV infusion on Day 1 of each cycle (cycle length = 6 weeks) every 6 weeks (Q6W), up to 18 administrations (up to approximately 2 years) or until PD or discontinuation; etoposide 100 mg/m\^2 on Days 1, 2, 3 of each cycle for up to 4 cycles (up to approximately 12 weeks) and cisplatin 75 mg/m\^2 or carboplatin AUC 5 mg/ml/min IV, Day 1 of each cycle Q3W up to 4 cycles (up to approximately 12 weeks) or until PD or discontinuation.
Experimental: Pembrolizumab + Lenvatinib + Chemotherapy
Participants receive pembrolizumab 200 mg IV infusion on Day 1 of each 3 week cycle (Q3W) up to 35 administrations (up to approximately 2 years) or until PD or discontinuation, lenvatinib 8 mg once daily (QD) orally up to Cycles 1-4 cycles and up to 20 mg QD orally for Cycles 5-31 or until PD or discontinuation; etoposide 100 mg/m\^2 on Days 1, 2, 3 of each cycle for up to 4 cycles (up to approximately 12 weeks) and cisplatin 75 mg/m\^2 or carboplatin AUC 5 mg/ml/min IV, Day 1 of each cycle Q3W up to 4 cycles (up to approximately 12 weeks) or until PD or discontinuation.
Sponsors
Leads: Merck Sharp & Dohme LLC

This content was sourced from clinicaltrials.gov