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Atebimetinib + GnP as a First Line Treatment in Patients With Metastatic Pancreatic Adenocarcinoma

RecruitingPhase 3

A Phase 3 Randomized, Open-Label Study of Atebimetinib in Combination With the Modified Gemcitabine and Nab-Paclitaxel Regimen Versus the Standard Gemcitabine and Nab-Paclitaxel Regimen for the Treatment of Patients With Metastatic Pancreatic Ductal Pancreatic Adenocarcinoma Cancer (MAPKeeper 301)

Who can join

Ages 18 and older · All sexes

Full eligibility criteria
Inclusion Criteria:

* Must be ≥18 years of age
* Must have confirmed diagnosis according to AJCC staging as follows:

  * Metastatic pancreatic adenocarcinoma within 12 weeks prior to screening
* Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
* Participants must be treatment naive as follows:

  * First-line PDAC participants will have received no previous systemic anti-cancer therapy
* Must have evidence of measurable disease (at least one target lesion) per RECIST v1.1 criteria
* Adequate organ function, hepatic function, coagulation studies and protocol determined clinical laboratory values

Exclusion Criteria:

* Inability to swallow oral medications
* Participant has squamous, adenosquamous, neuroendocrine (carcinoid, islet cell) or acinar pancreatic carcinoma
* Participants with only locally advanced disease
* Symptomatic, untreated, or actively progressing known central nervous system (CNS) metastases

About the study

The purpose of this study is to evaluate the safety and efficacy of atebimetinib in combination with modified GnP compared with SOC GnP alone.

What is being tested

Sponsor: Immuneering Corporation · Participants: 510 · Started: Jun 5, 2026

Contact the study team

Official record on ClinicalTrials.gov — NCT07562152

Locations in the U.S.

AlabamaClearview Cancer Institute, Huntsville
ArizonaCity of Hope, Phoenix
CaliforniaCity of Hope, Duarte
University of California San Diego, San Diego
ColoradoPoudre Valley Health Care, Inc, Fort Collins
Rocky Mountain Cancer Centers, Lone Tree
DelawareMedical Oncology Hematology Consultants, Newark
FloridaHematology Oncology Associates of the Treasure Coast, Port Saint Lucie
Florida Cancer Specialists - South, Sarasota
Florida Cancer Specialists - North, St. Petersburg
Florida Cancer Specialists - East, West Palm Beach
GeorgiaPiedmont Cancer Institute, Atlanta
Piedmont Healthcare, Atlanta
IllinoisIllinois Cancer Specialists, Arlington Heights
City of Hope, Chicago
OSF Medical Center, Peoria
KansasUniversity of Kansas Cancer Center, Fairway
MarylandMaryland Oncology, Columbia
MissouriMissouri Cancer Associates, Columbia
NevadaComprehensive Cancer Centers, Las Vegas
New JerseyRegional Cancer Care, Belleville
New YorkMemorial Sloan Kettering Cancer Center, New York
NYU Langone Health, New York
North CarolinaFirstHealth of the Carolinas, Pinehurst
OhioTaylor Cancer Research Center, Maumee
OregonWillamette Valley Cancer Institute, Eugene
Oregon Health and Science University, Portland
PennsylvaniaThomas Jefferson University, Philadelphia
South DakotaAvera Cancer Institute Research, Sioux Falls
TennesseeWest Cancer Center, Germantown
Sarah Cannon Research Institute, Nashville
Tennessee Oncology, Nashville
TexasTexas Oncology - West Texas, Abilene
Texas Oncology - Austin, Austin
Texas Oncology - San Antonio, San Antonio
Texas Oncology Gulf Coast, Webster
VirginiaBlue Ridge Cancer Care, Blacksburg
Virginia Cancer Specialists, Fairfax
WashingtonUniversity of Washington Fred Hutchinson Cancer Center, Seattle
Northwest Cancer Specialists, Vancouver
WisconsinUniversity of Wisconsin Carbone Cancer Center, Madison

Conditions

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