Trial intelligence / Profile preview

BCD-248 in Relapsed/Refractory Multiple Myeloma

NCT06668792Phase 2

Key facts

Status
Recruiting
Start
Dec 2024
Primary completion
Feb 2026
Countries
1
Sponsor
BIOCAD
Modality
Prophylactic Vaccines, Bispecific Antibodies, Therapeutic Vaccines
Drugs
BCD-248
Conditions
multiple myeloma (MM)
01

Overview

Phase 2, open-label, single-arm trial of BCD-248 in multiple myeloma (MM), sponsored by BIOCAD. Primary endpoint: Overall Response Rate at 24 weeks. Started Dec 2024; status: recruiting.

02

Design

1 arm
Study design
Non-randomizedOpen-labelSingle group
  • BCD-248

    Experimental arm receiving BCD-248

03

Who it enrols

Patients aged 18+ with relapsed/refractory multiple myeloma who have received at least 2 prior lines of therapy (including PI, IMiD, anti-CD38) and have not received prior anti-BCMA or anti-CD3 therapy.

04

Endpoints

Primary

  • Overall Response Rate

Secondary

  • Progression-Free Survival

  • Complete Response Rate

  • Minimal Residual Disease Negativity Rate

  • Duration of Response

  • Time to Progression

  • Time to Response

  • Overall Survival

  • Incidence and Characteristics of Adverse Events

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