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NCT Number: NCT07560449

QLS4131 Combination Therapy in Malignant Plasma Cell Neoplasms

The purpose of the study is to compare the efficacy of QLS4131(SC) in combination with QL2109, with or without pomalidomide or lenalidomide, and QLS4131 (SC) in combination with QL2109, and QLS4131 (SC) in combination with Pomalidomide, and QLS4131(SC) in combination with QL2109 and Lenalidomide.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Diagnosis of multiple myeloma confirmed according to the 2016 International Myeloma Working Group (IMWG) diagnostic criteria, or diagnosis of plasma cell leukemia and primary light-chain amyloidosis confirmed in accordance with relevant guidelines.;

For patients with multiple myeloma and plasma cell leukemia, measurable disease at screening is defined as meeting any one of the following:

  • Serum M-protein ≥0.5 g/dL (5 g/L);
  • Urine M-protein ≥200 mg/24 hours;
  • Serum immunoglobulin free light chain ≥10 mg/dL (100 mg/L) with an abnormal serum immunoglobulin κ/λ free light chain ratio.

For patients with light-chain amyloidosis:Measurable disease is defined as Involved serum free light chain ≥ 50 mg/L with an abnormal light chain ratio,ordifference between involved and uninvolved serum free light chains (dFLC) ≥ 50 mg/L.

Exclusion criteria

  • History of Grade 3 or higher cytokine release syndrome (CRS) associated with any T-cell redirecting therapy (e.g., CD3-redirecting technologies or CAR-T cell therapy);
  • Patients who received any of the following prior anti-tumor therapies before the first dose of investigational productt:
  • Previous treatment with BCMA/GPRC5D/CD3-targeted therapy;
  • Received any anti-tumor therapy within 4 weeks prior to the first dose, except for the following circumstances:
  • Cytotoxic therapy or small-molecule targeted therapy within 2 weeks or 5 half-lives, If the half-life is unknown, the washout period shall be 2 weeks (whichever is longer);
  • Immunomodulatory drug therapy within 7 days
  • Genetically modified adoptive cell therapy within 3 months.;
  • Traditional Chinese medicine with anti-tumor indications within 14 days.;
  • Radiotherapy within 14 days
  • Prior intolerance to Pomalidomide (applies to treatment cohorts containing Pomalidomide);
  • Prior intolerance to Lenalidomide (applies to treatment cohorts containing Lenalidomide);
  • Prior intolerance to QL2109 (applies to treatment cohorts containing QL2109).

Treatment and study plan

QLS4131

Drug

QLS4131 will be administered subcutaneously.

QL2109

Drug

QL2109 will be administered subcutaneously.

Pomalidomide

Drug

Pomalidomide will be self-administered as a single dose orally.

Lenalidomide

Drug

Lenalidomide will be self-administered as a single dose orally.

Dexamethasone

Drug

Dexamethasone will be administered orally or intravenously.

Primary outcomes

  1. DLT

    Time frame: From time of the first dose of QLS4131 to end of DLT period (28 days)

    To evaluate the tolerability and safety of subcutaneous administration of QLS4131 for Injection in combination with other agents in patients with malignant plasma cell neoplasms

  2. MTD

    Time frame: Up to 2 years

    To determine the maximum tolerated dose (MTD)

  3. ORR (Partial Response [PR] or Better)

    Time frame: Up to 2 years

    Overall response (PR or better) is defined as percentage of participants who have a PR or better per International Myeloma Working Group (IMWG) criteria.

  4. Overall Minimal Residual Disease (MRD)

    Time frame: Up to 2 years

    MRD-negative is defined as proportion of participants who achieve MRD negativity at a threshold of 10^-5 at any timepoint after the first dose of study drug and before disease progression or start of subsequent antimyeloma therapy.

Study contacts

Contact information is provided by the study sponsor or research team.

YU HU, Doctor of Medicine (MD)

CONTACT

[email protected]

027-85726387

Sponsors and collaborators

Lead sponsor

Qilu Pharmaceutical Co., Ltd.

Industry

Registry information

Official study title

A Multicenter, Open-Label Phase II Study to Evaluate QLS4131 Combination Therapy in the Treatment of Malignant Plasma Cell Neoplasms

Important dates

Study start
2026
Primary completion
2028
Study completion
2030
First posted
May 1, 2026
Registry last updated
May 1, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.