Checkmate CMP-001
REGISTER
The information on this site is not intended or implied to be a substitute for professional medical advice, diagnosis or treatment. Content within the patient forum is user-generated and has not been reviewed by medical professionals. Other sections of the Melanoma Research Foundation website include information that has been reviewed by medical professionals as appropriate. All medical decisions should be made in consultation with your doctor or other qualified medical professional.

Checkmate CMP-001

› Forums › General Melanoma Community › Checkmate CMP-001

  • Post
    • August 2, 2017 at 9:13 pm
    Enid Weiss
    Participant

    I am going to start the Checkmate CMP-001 clinical trial in about two weeks. I am curious to know if anyone else on this board is participating in this trial as well, and has any thoughts/comments/feelings about it.  Thanks!

Viewing 0 reply threads
  • Replies
      • August 2, 2017 at 9:51 pm
      ed williams
      Participant

      Hi Enid, I just took a look at some of the clinical trial data and it looks interesting!! CMP-001 has been used on about 700 humans in prior attempts to find a patient population so that is good from a risk stand point. I didn't find any specific mouse data but they said it improved Pembro when combined in mouse models. It look like they are recruiting 60 people for phase 1/2 trial so it might be hard to find any one else that has tried this in melanoma!!! Here are two links that I found that might be of some interest to you. Best Wishes!!!Ed http://ascopubs.org/doi/abs/10.1200/JCO.2016.34.15_suppl.TPS9593  http://adisinsight.springer.com/drugs/800020832

        • August 3, 2017 at 12:43 am
        Enid Weiss
        Participant

        Thanks so much, Ed!

         

Viewing 0 reply threads
  • You must be logged in to reply to this topic.
About the MRF Patient Forum

The MRF Patient Forum is the oldest and largest online community of people affected by melanoma. It is designed to provide peer support and information to caregivers, patients, family and friends. There is no better place to discuss different parts of your journey with this cancer and find the friends and support resources to make that journey more bearable.

The information on the forum is open and accessible to everyone. To add a new topic or to post a reply, you must be a registered user. Please note that you will be able to post both topics and replies anonymously even though you are logged in. All posts must abide by MRF posting policies.