Actively Recruiting

Phase 1
Age: 18Years +
All Genders
NCT06604715

A Study of JNJ-87562761 in Participants With Relapsed or Refractory Multiple Myeloma

Led by Janssen Research & Development, LLC · Updated on 2026-05-08

80

Participants Needed

15

Research Sites

151 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The purpose of this study is to determine the recommended phase 2 dose(s) (RP2D\[s\]) of JNJ-87562761 in Part 1 (dose escalation), and to determine the safety and tolerability at RP2D in Part 2 (dose expansion) in participants with multiple myeloma (MM) whose disease has come back after treatment (relapsed) or hasn't responded to treatment (refractory).

CONDITIONS

Official Title

A Study of JNJ-87562761 in Participants With Relapsed or Refractory Multiple Myeloma

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 years or older
  • Diagnosis of relapsed or refractory multiple myeloma with measurable disease defined by specific levels of serum or urine M-protein or abnormal free light chain levels
  • Prior treatment including a proteasome inhibitor, immunomodulatory agent, and anti-CD38 therapy
  • ECOG performance status of 0 or 1
  • Estimated glomerular filtration rate (eGFR) greater than 30 mL/min/1.73 m²
  • Agreement to avoid breastfeeding, pregnancy, gamete donation, and to use an external condom during treatment and for 6 months after last dose
Not Eligible

You will not qualify if you...

  • Active plasma cell leukemia, Waldenström's macroglobulinemia, POEMS syndrome, or immunoglobulin light chain amyloidosis
  • Prior allogeneic transplant within 6 months or autologous transplant within 12 weeks before study treatment
  • Receipt of live attenuated vaccine within 4 weeks before first dose
  • CNS involvement or meningeal involvement of multiple myeloma
  • Unresolved non-hematologic toxicity greater than Grade 1 from prior anticancer therapy (except alopecia, tissue fibrosis, or mild peripheral neuropathy)
  • High cumulative corticosteroid dose (≥140 mg prednisone equivalent) within 14 days before treatment
  • Recent antitumor therapies within specified timeframes before first dose, including targeted therapy, monoclonal antibodies, chemotherapy, and radiotherapy
  • Pulmonary compromise requiring supplemental oxygen
  • Active infections such as HIV with detectable viral load or low CD4 count, active hepatitis B or C, or serious uncontrolled infections
  • Active autoimmune disease requiring systemic immunosuppressive therapy within 6 months before treatment
  • Certain cardiac conditions including recent myocardial infarction and severe congestive heart failure

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 15 locations

1

Princess Margaret Hospital

Toronto, Ontario, Canada, M5G 2M9

Actively Recruiting

2

Jewish General Hospital

Montreal, Quebec, Canada, H3T 1E2

Actively Recruiting

3

Seoul National University Hospital

Seoul, South Korea, 03080

Actively Recruiting

4

Asan Medical Center

Seoul, South Korea, 05505

Actively Recruiting

5

Samsung Medical Center

Seoul, South Korea, 06351

Actively Recruiting

6

The Catholic University of Korea Seoul St Marys Hospital

Seoul, South Korea, 137 701

Actively Recruiting

7

Hosp. Univ. Germans Trias I Pujol

Badalona, Spain, 08916

Actively Recruiting

8

Hosp Clinic de Barcelona

Barcelona, Spain, 08036

Actively Recruiting

9

Hosp Univ Fund Jimenez Diaz

Madrid, Spain, 28040

Actively Recruiting

10

Clinica Univ. de Navarra

Pamplona, Spain, 31008

Actively Recruiting

11

Hosp Clinico Univ de Salamanca

Salamanca, Spain, 37007

Actively Recruiting

12

Kaohsiung Chang Gung Memorial Hospital

Kaohsiung City, Taiwan, 833

Actively Recruiting

13

China Medical University Hospital

Taichung, Taiwan, 404

Actively Recruiting

14

National Cheng Kung University Hospital

Tainan, Taiwan, 70403

Actively Recruiting

15

National Taiwan University Hospital

Taipei, Taiwan, 100225

Actively Recruiting

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Research Team

S

Study Contact

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SEQUENTIAL

Primary Purpose

TREATMENT

Number of Arms

1

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