A Clinical Study of SHR-5421 in Patients With Multiple Myeloma

Sponsor
Suzhou Suncadia Biopharmaceuticals Co., Ltd.
Study ID
NCT07652281
Phase
PHASE1
Status
Recruiting
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Conditions

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • SHR-5421 for Injection — DRUG
    SHR-5421 for injection.

Study Details

This is a Phase I, open-label, multicenter study to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD), and preliminary efficacy of SHR-5421 in patients with multiple myeloma (MM).

Key Dates

First listed
Jun 17, 2026
Start date
Jul 23, 2026
Status verified
Jun 2026
Primary completion
Apr 30, 2028
Completion
Apr 30, 2029

Study Design

Enrollment
97 participants (estimated)
Allocation
NA
Intervention model
SEQUENTIAL
Primary purpose
TREATMENT

Arms

  • Experimental: SHR-5421 Group
    SHR-5421 administered as multiple doses.

Primary Outcome Measure

Determination of Phase II Dose (RP2D) of SHR-5421 [ Time Frame: 24 months. ]

Central Contacts

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