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

Part of paid clinical trials in Gilbert, Arizona.

Sponsor
Merck Sharp & Dohme LLC
Study ID
NCT06623422
Phase
PHASE3
Status
Recruiting

Conditions

  • Carcinoma, Non-Small-Cell Lung

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Pembrolizumab — BIOLOGICAL
    IV Infusion
  • Cisplatin — DRUG
    IV infusion
  • Carboplatin — DRUG
    IV infusion
  • Pemetrexed — DRUG
    IV infusion
  • Gemcitabine — DRUG
    IV infusion
  • Paclitaxel — DRUG
    IV infusion
  • Intismeran autogene — BIOLOGICAL
    IM injection
  • Placebo — OTHER
    IM injection

Study Details

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).

Key Dates

Start date
Oct 21, 2024
Status verified
May 2026
Primary completion
May 16, 2033
Completion
Jan 26, 2038

Study Design

Enrollment
680 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Experimental: Pembrolizumab + Intismeran autogene
    For neoadjuvant treatment, participants will receive pembrolizumab 200 mg via intravenous (IV) infusion every 3-week cycle for up to 4 cycles PLUS background chemotherapy via IV infusion (cisplatin 75 mg/m\^2 or carboplatin area under the curve \[AUC\] 5 or 6 mg/mL/min, pemetrexed 500 mg/m\^2, gemcitabine 1000 mg/m\^2, paclitaxel 175 mg/m\^2 or 200 mg/m\^2 given at a dose and combination per investigator's choice) every 3-week cycle for up to 4 cycles (total neoadjuvant treatment duration of up to \~12 weeks). After surgical resection, for adjuvant treatment, participants will receive pembrolizumab 400 mg via IV infusion every 6-week cycle for up to 7 cycles PLUS intismeran autogene 1 mg via intramuscular (IM) injection every 3 weeks for up to 9 doses (total adjuvant treatment duration of up to \~42 weeks).
  • Active Comparator: Pembrolizumab + Placebo
    For neoadjuvant treatment, participants will receive pembrolizumab 200 mg via IV infusion every 3-week cycle for up to 4 cycles PLUS background chemotherapy via IV infusion (cisplatin 75 mg/m\^2 or carboplatin AUC 5 or 6 mg/mL/min, pemetrexed 500 mg/m\^2, gemcitabine 1000 mg/m\^2, paclitaxel 175 mg/m\^2 or 200 mg/m\^2 given at a dose and combination per investigator's choice) every 3-week cycle for up to 4 cycles (total neoadjuvant treatment duration of up to \~12 weeks). After surgical resection, for adjuvant treatment, participants will receive pembrolizumab 400 mg via IV infusion every 6-week cycle for up to 7 cycles PLUS matching placebo via IM injection every 3 weeks for up to 9 doses (total adjuvant treatment duration of up to \~42 weeks).

Primary Outcome Measure

Disease-Free Survival (DFS) [ Time Frame: Up to ~97 months ]

Central Contacts

Locations (48)

FacilityCityStateZIPSite coordinators
Banner MD Anderson Cancer Center ( Site 0181)GilbertArizona85234
Study Coordinator
480-256-6444
The University of Arizona Cancer Center - North Campus ( Site 0163)TucsonArizona85719
Study Coordinator
520-694-2873
Providence St. Jude Medical Center ( Site 0106)FullertonCalifornia92835
Study Coordinator
714-446-5900
VA Long Beach Healthcare System ( Site 0199)Long BeachCalifornia90822
Study Coordinator
562-826-8000
USC Norris Comprehensive Cancer Center ( Site 0205)Los AngelesCalifornia90033
Study Coordinator
323-865-3000
UCSF Medical Center at Mission Bay ( Site 0178)San FranciscoCalifornia94158
Study Coordinator
877-827-3222
University of Colorado Anschutz Medical Campus ( Site 0151)AuroraColorado80045
Study Coordinator
303-724-9690
UCHealth Memorial Hospital Central ( Site 0125)Colorado SpringsColorado80909
Study Coordinator
719-365-5000
Banner MD Anderson Cancer Center at North Colorado Medical Center ( Site 0207)GreeleyColorado80631
Study Coordinator
970-810-3894
Centura Health - St. Anthony North Health Campus ( Site 0189)WestminsterColorado80023
Study Coordinator
720-627-4840
Yale University School of Medicine ( Site 0201)New HavenConnecticut06510
Study Coordinator
203-785-7564
Eastern CT Hematology & Oncology Associates ( Site 0202)NorwichConnecticut06360
Study Coordinator
860-886-8362
The Oncology Institute of Hope and Innovation - Fort Lauderdale ( Site 0156)Fort LauderdaleFlorida33316
Study Coordinator
954-771-0692
Miami Cancer Institute at Baptist Health, Inc. ( Site 0214)MiamiFlorida33176
Study Coordinator
786-596-2000
Beacon Cancer Care ( Site 0127)Post FallsIdaho83854
Study Coordinator
208-755-2804
The University of Chicago Medical Center ( Site 0118)ChicagoIllinois60637
Study Coordinator
773-702-2984
Maryland Oncology Hematology (MOH) ( Site 8102)RockvilleMaryland20850
Study Coordinator
570-808-4772
Dana Farber Cancer Hospital ( Site 0155)BostonMassachusetts02215
Study Coordinator
617-632-3000
Massachusetts General Hospital ( Site 0136)BostonMassachusetts02114
Study Coordinator
617-724-4000
Ellis Fischel Cancer Center ( Site 0133)ColumbiaMissouri65212-
Lake Regional Hospital-Cancer Center ( Site 0123)Osage BeachMissouri65065-
Roswell Park Cancer Institute ( Site 0184)BuffaloNew York14263
Study Coordinator
716-845-3167
Hematology-Oncology Associates of CNY ( Site 0164)East SyracuseNew York13057
Study Coordinator
315-472-7504
Icahn School of Medicine at Mount Sinai ( Site 0116)New YorkNew York10029
Study Coordinator
212-523-5559
Memorial Sloan Kettering Cancer Center ( Site 0137)New YorkNew York10065
Study Coordinator
212-639-2000
The Blavatnik Family- Chelsea Medical Center at Mount Sinai ( Site 0216)New YorkNew York10011
Study Coordinator
202-207-2510
SUNY Upstate Cancer Center ( Site 0140)SyracuseNew York13210
Study Coordinator
315-464-8237
Montefiore Medical Center ( Site 0160)The BronxNew York10461
Study Coordinator
718-405-8404
Westchester Medical Center ( Site 0196)ValhallaNew York10595
Study Coordinator
914-493-7000
Novant Health Weisiger Cancer Insititute ( Site 0266)CharlotteNorth Carolina28204
Study Coordinator
980-302-6000
Novant Health Forsyth Medical Center ( Site 0166)Winston-SalemNorth Carolina27103
Study Coordinator
336-718-5000
University of Cincinnati Medical Center ( Site 0119)CincinnatiOhio45219
Study Coordinator
513-558-2119
St. Lukes Hospital and Health Network ( Site 0186)BethlehemPennsylvania18015
Study Coordinator
484-526-7952
Thompson Cancer Survival Center ( Site 0168)KnoxvilleTennessee37916
Study Coordinator
865-331-1720
Elliston Place Medical Oncology & Hematology ( Site 0215)NashvilleTennessee37203
Study Coordinator
615-961-9469
Texas Oncology - DFW ( Site 8103)DallasTexas75246
Study Coordinator
214-370-1987
UT Southwestern Medical Center ( Site 0190)DallasTexas75390
Study Coordinator
903-592-6152
Houston Methodist Cancer Center ( Site 0191)HoustonTexas77030
Study Coordinator
713-363-8890
MD Anderson Cancer Center ( Site 0150)HoustonTexas77030
Study Coordinator
713-792-6363
Memorial Hermann Cancer Center ( Site 0172)HoustonTexas77030
Study Coordinator
713-704-3961
Michael E. DeBakey VA Medical Center ( Site 0197)HoustonTexas77030
Study Coordinator
713-873-200
O'Quinn Medical Tower at McNair Campus ( Site 0131)HoustonTexas77030
Study Coordinator
832-957-6500
The University of Texas Health Science Center at Tyler dba UT Health East Texas HOPE Cancer Center ( Site 0148)TylerTexas75701
Study Coordinator
903-592-6152
Virginia Cancer Specialists ( Site 0167)FairfaxVirginia22031
Study Coordinator
571-350-8400
Virginia Oncology Associates (VOA) ( Site 8101)NorfolkVirginia23502
Study Coordinator
757-466-8683
VCU Health Adult Outpatient Pavillion ( Site 0193)RichmondVirginia23219
Study Coordinator
804-828-7999
Swedish Cancer Institute ( Site 0143)SeattleWashington98104
Study Coordinator
855-922-6237
Virginia Mason Franciscan Health - St. Michael Cancer Center ( Site 0192)SilverdaleWashington98383
Study Coordinator
564-240-3100

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