A Phase I Study of SHR-3836 in Patients With Multiple Myeloma

Trial statusRecruiting
Trial phasePhase 1
Trial typeInterventional
Biological sexAll
Age18+
SponsorShanghai Hengrui Pharmaceutical Co., Ltd.

About this trial

This is a Phase I, open-label, multicenter study to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD), and preliminary efficacy of SHR-3836 in patients with multiple myeloma (MM).

Eligibility criteria

Qualifiers

Age ≥ 18 years, male or female

Expected survival ≥ 3 months

ECOG performance status 0 or 1

Diagnosed with active multiple myeloma per IMWG criteria

Disqualifiers

Diagnosis of amyloidosis, plasma cell leukemia, Waldenström's macroglobulinemia, or POEMS syndrome.

Central nervous system involvement by tumor.

History of ≥ Grade 3 CRS with prior T-cell redirecting therapy.

Requirement for dialysis or plasmapheresis within 14 days prior to study drug.

Trial design

Treatments tested in this trial

  • SHR-3836 administered as multiple doses.

Treatment groups

99 Participants
are divided into 1 treatment group