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87562761MMY1001 Multiple myeloma
A Phase 1, first-in-human study of JNJ-87562761 in relapsed or refractory MM
Phase
Compound
JNJ-87562761
NCT identifier
NCT06604715
Enrollment

N=~80

For more information, including
contact details, please visit
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Study overview & design

Key eligibility criteria*:

  • Relapsed or refractory MM with measurable disease
  • Prior therapy including a PI, IMiD, and anti-CD38 therapy
  • ECOG PS 0 or 1
  • No CNS or meningeal involvement
Study design
Study design

Primary outcomes:

Part 1

  • DLTs

Parts 1 and 2

  • AEs

Part 2

  • Clinically significant abnormal laboratory values

Secondary outcomes:

  • Serum concentration of JNJ-87562761
  • PK
  • ADAs to JNJ-87562761
  • ≥PR
  • ≥VGPR
  • ≥CR
  • sCR
  • TTR
  • DOR

*Not a complete list of inclusion and exclusion criteria.
ADA, antidrug antibody; AE, adverse event; CD, cluster of differentiation; CNS, central nervous system; CR, complete response; DLT, dose-limiting toxicity; DOR, duration of response; ECOG PS, Eastern Cooperative Oncology Group performance status; IMiD, immunomodulatory drug; MM, multiple myeloma; PI, proteasome inhibitor, PK, pharmacokinetics; PR, partial response; sCR, stringent complete response; TTR, time to response; VGPR, very good partial response.

Recruiting site locations
World Map
Canada, South Korea, Spain, Taiwan
Study design
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