ComboMATCH-EAY191-N5 (HER2-Positive Cancers) - Clinical Trial

What is the Purpose of this Study?

We are doing this study to find out if neratinib combined with palbociclib is better than neratinib alone when it comes to treating HER2-positive tumors.

What is the Condition Being Studied?

HER2-Positive Cancers

Who Can Participate in the Study?

Adults ages 18+ who:

  • Are part of the ComboMATCH Master Registration Trial EAY191
  • Have a type of solid tumor (not breast cancer) that has too much of a protein called HER2
  • Have had their disease return after treatment or have disease that did not respond to treatment

For more information about this study, please contact the study team at nick.jeffries@duke.edu.

Age Group
Adults

What is Involved?

If you choose to join this study, you will be randomly assigned (like a coin flip) to 1 of 2 groups:

Group One

If you are in this group, you will get the study drugs neratinib and palbociclib. You will get neratinib as pills you take by mouth once every day, and palbociclib as pills you take by mouth every day for 21 days, followed by 7 days off.

You will start this study regimen taking neratinib alone. Over the first two weeks of treatment, you will gradually increase the dose you take. On week three, you will start taking the full dose of neratinib and you will also start taking palbociclib on the schedule described above. You will take neratinib and palbociclib for as long you as you and th study doctor believe that your are benefitting.

Group Two

If you are in this group, you will get the study drug neratinib. You will get this drug as a pill you take by mouth once every day. Every 28 days of this treatment is called a cycle. Over the first two weeks of treatment, you will gradually increase the dose you take.

Study Details

Full Title
EAY191-N5: A Randomized Trial of Neratinib, A Pan-ERBB Inhibitor, Alone or in Combination with Palbociclib, a CDK4/6 Inhibitor, in Patients with HER2+ Gynecologic Cancers and Other Solid Tumors: A ComboMATCH Treatment Trial
Principal Investigator
Gynecologic Oncologist
Protocol Number
IRB: PRO00115696
NCT: NCT06126276
Phase
Phase II
ClinicalTrials.gov
Enrollment Status
Open for Enrollment