Status:

UNKNOWN

Study to Evaluate the Safety, Tolerance, Pharmacokinetics and Preliminary Efficacy of IBI346#CIBI346Y002#

Lead Sponsor:

Chunrui Li

Collaborating Sponsors:

Innovent Biologics (Suzhou) Co. Ltd.

Conditions:

Relapsed/Refractory Multiple Myeloma

Eligibility:

All Genders

18+ years

Phase:

PHASE1

Brief Summary

An open label, single-arm clinical study evaluating the safety and efficacy of IBI346 infusion in relapsed/refractory multiple myeloma

Eligibility Criteria

Inclusion

  • According to the multiple myeloma diagnostic criteria of the International Myeloma Working Group (IMWG), there is the initial diagnosis of multiple myeloma.
  • Subjects must have previously received at least 3 anti-myeloma regimens. Subjects must have documented disease progression (according to IMWG criteria) during or within 12 months of completing their last anti-myeloma regimen prior to study entry; and prior regimens must have included proteasome inhibitor (PI) and immunomodulatory drug (IMiD).
  • Measurable disease as defined by the protocol
  • ECOG score is 0 or 1.
  • Expected survival time ≥12 weeks.

Exclusion

  • Patients suffering from graft-versus-host disease (GVHD) or requiring immunosuppressants drugs.
  • Patients who received autologous hematopoietic stem cell transplantation (ASCT) or prior allogeneic hematopoietic stem cell transplantation (ALLo-HSCT) within 12 weeks prior to mononuclear cell collection.
  • No unmobilized mononuclear cells can be collected for CAR T cell production.
  • Screening subjects who were receiving systemic steroids during the previous 7 days or who were determined by the investigator to require long-term systemic steroid use during treatment (except for inhaled or topical use, except at doses \< 10mg/ day).
  • Patients with a history of hypertension that cannot be controlled by medication (blood pressure ≥140/90 mmHg).

Key Trial Info

Start Date :

April 28 2022

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

February 28 2024

Estimated Enrollment :

36 Patients enrolled

Trial Details

Trial ID

NCT05266768

Start Date

April 28 2022

End Date

February 28 2024

Last Update

November 30 2022

Active Locations (1)

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Page 1 of 1 (1 locations)

1

Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology

Wuhan, Hubei, China, 430000

Study to Evaluate the Safety, Tolerance, Pharmacokinetics and Preliminary Efficacy of IBI346#CIBI346Y002# | DecenTrialz