I am currently in a clinical trial for a new MM drug. IT IS VERY PROMISING, ALMOST AS GOOD AS C-T. the drug company pays the cost of the drug and the cancer center study team pays good for gas and toll money for each study trip. I'm 1 of 20 on pittsburgh in this study, but I can tell you IT IS VERY VERY PROMISING and is being called a life changer for millions of MM patients. The drug is Talquatemab.

Hi James,
Appreciate your input, have heard about this drug, wishing you the very best and may it help many of us in the future!
Please keep posting in 1 or 2 mos as to how you feel
Mag

We cannot participate because we live in Canada. I think it is a great program

I signed up, but not sure I can be in the study because I'm hoping I'm in remission. I definitely think its a great thing. They will be doing genetics testing on our myeloma and we can get copies of the report. Its supposed to help our doctors decide which treatment is best. My doctor signed the consent and sent it in. But they want you to have active myeloma, so they have enough myeloma cells in yyour blood sample to test. Can't do it if you live in Hawaii, Alaska or New York.

I'm a little bit skeptical of it am not comfortable giving out too much of my stats etc.