Enter a search term to see results
Trilogy-3 Multiple myeloma
A Phase 2, single-arm study of ramantamig (JNJ-79635322) in relapsed or refractory MM
Phase
Compound
Ramantamig (BCMA × GPRC5D × CD3 trispecific Ab)
NCT identifier
NCT07266441
Enrollment

N=~157

For more information, including
contact details, please visit
the J&J Clinical Trial Finder
Study overview & design

Key eligibility criteria*:

  • ≥3 prior lines
  • Triple-class exposed (PI, iMiD, anti-CD38 mAb)
Study design
Study design

Primary outcomes:

  • ORR

Secondary outcomes:

  • VGPR or better
  • CR or better
  • DOR
  • PFS
  • OS
  • TTNT

*Not a complete list of inclusion and exclusion criteria.

CR, complete response; DOR, duration of response; iMiD, immunomodulatory drug; mAb, monoclonal antibody; MM, multiple myeloma; ORR, overall response rate; OS, overall survival; PFS, progression-free survival; PI, proteasome inhibitor; SC, subcutaneous; TTNT, time to next line of therapy; VGPR, very good partial response.

Recruiting site locations
World Map
Israel
Study design
Rotate device to view larger version of image
Ramantamig mechanism of action
The following is video of the proposed mechanism of action for ramantamig, an investigational product which has not been reviewed by the FDA. Correlation to clinical effect has not been established.
Ramantamig mechanism of action
0:00
Mechanism of disease in multiple myeloma
Mechanism of disease in multiple myeloma
0:00