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A Study of Pembrolizumab (MK-3475) With or Without Intismeran Autogene (V940) in Participants With Non-small Cell Lung Cancer (V940-009/INTerpath-009)

RecruitingPhase 3

A Phase 3 Randomized Double-blind Study of Adjuvant Pembrolizumab With or Without V940 in Participants With Resectable Stage II to IIIB (N2) NSCLC Not Achieving pCR After Receiving Neoadjuvant Pembrolizumab With Platinum-based Doublet Chemotherapy (INTerpath-009)

Who can join

Ages 18 and older · All sexes

Full eligibility criteria
Inclusion Criteria:

The main inclusion criteria include but are not limited to the following:

* Has histologically/cytologically confirmed diagnosis of previously untreated and pathologically confirmed resectable clinical Stage II, IIIA, or IIIB (N2) non-small cell lung cancer (NSCLC) \[American Joint Committee on Cancer (AJCC) 8th Edition\]
* Has an Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1 within 7 days before the first dose of study intervention
* Participants who have not achieved a pathological complete response (pCR) following completion of neoadjuvant chemotherapy and pembrolizumab followed by surgery will be eligible
* Confirmation that epidermal growth factor receptor (EGFR)-directed therapy is not indicated as primary therapy (documentation of absence of tumor-activating EGFR mutations \[eg, DEL19 or L858R\])
* Human immunodeficiency virus (HIV)-infected participants must have well controlled HIV on anti-retroviral therapy (ART)
* Participants who are hepatitis B surface antigen (HBsAg) positive are eligible if they have received hepatitis B virus (HBV) antiviral therapy for at least 4 weeks and have undetectable HBV viral load prior to randomization
* Participants with history of hepatitis C virus (HCV) infection are eligible if HCV viral load is undetectable at screening

Exclusion Criteria:

The main exclusion criteria include but are not limited to the following:

* Diagnosis of small cell lung cancer (SCLC) or, for mixed tumors, presence of small cell elements, or has a neuroendocrine tumor with large-cell components, or a sarcomatoid carcinoma, or a pancoast tumor
* Documentation by local test report indicating presence of anaplastic lymphoma kinase (ALK) gene rearrangements
* Received prior neoadjuvant therapy for their current NSCLC diagnosis
* Received prior therapy with an anti-programmed cell death 1 (PD-1), anti-programmed cell death ligand 1 (PD-L1), or anti-programmed cell-death ligand 2 (PD-L2) agent, or with an agent directed to another stimulatory or coinhibitory T-cell receptor (eg, cytotoxic T-lymphocyte-associated protein \[CTLA-4\], OX-40, CD137)
* Received prior systemic anticancer therapy including investigational agents other than what is specified in this protocol
* Received prior treatment with a cancer vaccine
* Received prior radiotherapy within 2 weeks of start of study intervention, or has radiation-related toxicities, requiring corticosteroids
* Received a live or live-attenuated vaccine within 30 days before the first dose of study intervention

About the study

The goal of this study is to learn if people who receive intismeran autogene and pembrolizumab after surgery are cancer-free longer than people who receive placebo and pembrolizumab. Researchers want to know if giving intismeran autogene and pembrolizumab after surgery can help prevent the cancer from coming back in people with non-small cell lung cancer (NSCLC) whose tumors did not respond completely to treatment before surgery (neoadjuvant treatment).

What is being tested

Sponsor: Merck Sharp & Dohme LLC · Participants: 680 · Started: Oct 21, 2024

Contact the study team

Official record on ClinicalTrials.gov — NCT06623422

Locations in the U.S.

ArizonaBanner MD Anderson Cancer Center ( Site 0181), Gilbert
The University of Arizona Cancer Center - North Campus ( Site 0163), Tucson
CaliforniaProvidence St. Jude Medical Center ( Site 0106), Fullerton
VA Long Beach Healthcare System ( Site 0199), Long Beach
UCLA Jonsson Comprehensive Cancer Center ( Site 0135), Los Angeles
USC Norris Comprehensive Cancer Center ( Site 0205), Los Angeles
UCSF Medical Center at Mission Bay ( Site 0178), San Francisco
ColoradoUniversity of Colorado Anschutz Medical Campus ( Site 0151), Aurora
UCHealth Memorial Hospital Central ( Site 0125), Colorado Springs
Banner MD Anderson Cancer Center at North Colorado Medical Center ( Site 0207), Greeley
Centura Health - St. Anthony North Health Campus ( Site 0189), Westminster
ConnecticutYale University School of Medicine ( Site 0201), New Haven
Eastern CT Hematology & Oncology Associates ( Site 0202), Norwich
FloridaThe Oncology Institute of Hope and Innovation - Fort Lauderdale ( Site 0156), Fort Lauderdale
Miami Cancer Institute at Baptist Health, Inc. ( Site 0214), Miami
IdahoBeacon Cancer Care ( Site 0127), Post Falls
IllinoisThe University of Chicago Medical Center ( Site 0118), Chicago
IndianaFranciscan Health ( Site 0219), Indianapolis
MarylandMaryland Oncology Hematology (MOH) ( Site 8102), Rockville
MassachusettsDana Farber Cancer Hospital ( Site 0155), Boston
Massachusetts General Hospital ( Site 0136), Boston
New YorkRoswell Park Cancer Institute ( Site 0184), Buffalo
Hematology-Oncology Associates of CNY ( Site 0164), East Syracuse
Icahn School of Medicine at Mount Sinai ( Site 0116), New York
Memorial Sloan Kettering Cancer Center ( Site 0137), New York
The Blavatnik Family- Chelsea Medical Center at Mount Sinai ( Site 0216), New York
SUNY Upstate Cancer Center ( Site 0140), Syracuse
Montefiore Medical Center ( Site 0160), The Bronx
Westchester Medical Center ( Site 0196), Valhalla
North CarolinaNovant Health Weisiger Cancer Insititute ( Site 0266), Charlotte
Novant Health Forsyth Medical Center ( Site 0166), Winston-Salem
OhioUniversity of Cincinnati Medical Center ( Site 0119), Cincinnati
OregonGood Samaritan Regional Medical Center-Samaritan Pastega Regional Cancer Center ( Site 0217), Corvallis
PennsylvaniaSt. Lukes Hospital and Health Network ( Site 0186), Bethlehem
TennesseeTennessee Oncology, PLLC - Chattanooga Downtown ( Site 0315), Chattanooga
Thompson Cancer Survival Center ( Site 0168), Knoxville
Elliston Place Medical Oncology & Hematology ( Site 0215), Nashville
TexasTexas Oncology - DFW ( Site 8103), Dallas
UT Southwestern Medical Center ( Site 0190), Dallas
Houston Methodist Cancer Center ( Site 0191), Houston
MD Anderson Cancer Center ( Site 0150), Houston
Memorial Hermann Cancer Center ( Site 0172), Houston
Michael E. DeBakey VA Medical Center ( Site 0197), Houston
O'Quinn Medical Tower at McNair Campus ( Site 0131), Houston
The University of Texas Health Science Center at Tyler dba UT Health East Texas HOPE Cancer Center ( Site 0148), Tyler
VirginiaVirginia Cancer Specialists ( Site 0167), Fairfax
Virginia Oncology Associates (VOA) ( Site 8101), Norfolk
VCU Health Adult Outpatient Pavillion ( Site 0193), Richmond
WashingtonSwedish Cancer Institute ( Site 0143), Seattle
St. Joseph Medical Center Hematology and Oncology - Silverdale ( Site 0192), Silverdale

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.