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NCT07490613

An Open-label, Multicenter, Phase I Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Efficacy of SHR-3836 in Patients With Multiple Myeloma

Recruiting now Phase 1 Last updated 2 June 2026
What this trial tests

Phase 1 trial testing SHR-3836 administered as multiple doses. in Multiple Myeloma in 99 participants. Currently enrolling.

Timeline
2 June 2026
Primary endpoint
1 April 2028
1 April 2029

Quick facts

Lead sponsorShanghai Hengrui Pharmaceutical Co., Ltd.
PhasePhase 1
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationna
Designsequential
Maskingnone
Primary purposetreatment
Enrollment99
Start date2 June 2026
Primary completion1 April 2028
Estimated completion1 April 2029
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Shanghai Hengrui Pharmaceutical Co., Ltd. — full company profile →

Who can join

18 and older, any sex, with Multiple Myeloma. Patients with the condition only — healthy volunteers not accepted.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

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).

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Multiple Myeloma

Currently open trials in the same condition.

Other Shanghai Hengrui Pharmaceutical Co., Ltd. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07490613.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing