Clinical Trial

Trial Protocol ID USOR 25238: 1L mPDAC

Trial Description

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 Adenocarcinoma Cancer (MAPKeeper 301)

MOA: Atebimetinib (IMM-1 104) is a deep cyclic dual inhibitor of MEK1 and MEK2

Key Eligibility:

  • Subjects’ initial diagnosis of metastatic pancreatic adenocarcinoma
    must have occurred ≤12 weeks prior to screening
  • Subjects has ≥1 lesion measurable by CT/MRI
  • Subjects with only localized disease are excluded
  • Subjects with squamous, adenosquamous, neuroendocrine, or
    acinar pancreatic carcinoma are excluded
  • Subjects that have received prior treatment for disease, except for
    palliative radiation or stent placement, are excluded
  • Subjects that have received prior adjuvant therapy for disease are
    excluded, unless ≥6 months have passed since the last dose and
    there are no ongoing treatment-related toxicities.
    • Prior neoadjuvant therapy is permitted

Contact us regarding Clinical Trials at MOHRSCH@usoncology.com or call us at 877-664-7724

Investigator

  • Photo of Mohit Narang, MD Mohit Narang, MD

ClinicalTrials.gov NCT ID

  • NCT07562152