I’m starting new treatment in October. Teclistamab and immunoglobulin infusion. Just want to know what I’m in for. Side effects?
I was a participant in a Teclisimab trial through Atrium/Levine Center for Hematology, etc. I took TEC every two weeks via infusion from April 1 through June 2026. According to my physician, Dr. Barry Paul, all my light chains are now "invisible", meaning I no longer have symptoms of Amyloidosis. Of course, it is never gone unfortunately.
TEC kills your immune system, so during the time I was taking it, I caught colds and coughed a lot. I also got UTIs - once to the extent that I was hospitalized for a week when I was in sepsis. In June, they started infusing me with IVIG (hope that is the right order of the letters) to rebuild my immune system. I continue to get a 3-hour infusion each month and will through the end of the year. Feeling much stronger now.
Best of luck.
Starting a new treatment can feel both hopeful and nerve-wracking — totally understandable to want to know what's ahead!
Teclistamab is a newer bispecific antibody treatment being explored for amyloidosis. While specific community experiences with Teclistamab aren't widely documented yet, the immunoglobulin infusion Show Full Answer