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QLS4131 Combination Therapy in Malignant Plasma Cell Neoplasms

27. april 2026 oppdatert av: Qilu Pharmaceutical Co., Ltd.

A Multicenter, Open-Label Phase II Study to Evaluate QLS4131 Combination Therapy in the Treatment of 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.

Studieoversikt

Studietype

Intervensjonell

Registrering (Antatt)

162

Fase

  • Fase 2

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

  • Navn: YU HU, Doctor of Medicine (MD)
  • Telefonnummer: 027-85726387
  • E-post: dr_huyu@126.com

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Voksen
  • Eldre voksen

Tar imot friske frivillige

Nei

Beskrivelse

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:

    1. Previous treatment with BCMA/GPRC5D/CD3-targeted therapy;
    2. 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).

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: Ikke-randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: QLS4131(SC) in combination with QL2109, with or without Pomalidomide or Lenalidomide
Participants will receive QLS4131 and QL2109 as SC injections; Pomalidomide/ Lenalidomide will be self-administered as a single dose orally; dexamethasone may be given orally or intravenously as a pretreatment medication and study drug.
Deksametason vil bli administrert oralt eller intravenøst.
QLS4131 will be administered subcutaneously.
QL2109 will be administered subcutaneously.
Pomalidomide will be self-administered as a single dose orally.
Lenalidomide will be self-administered as a single dose orally.
Eksperimentell: QLS4131(SC) in combination with QL2109
Participants will receive QLS4131 and QL2109 as SC injections; dexamethasone may be given orally or intravenously as a pretreatment medication and study drug.
Deksametason vil bli administrert oralt eller intravenøst.
QLS4131 will be administered subcutaneously.
QL2109 will be administered subcutaneously.
Eksperimentell: QLS4131(SC) in combination with Pomalidomide
Participants will receive QLS4131 as SC injections; Pomalidomide will be self-administered as a single dose orally; dexamethasone may be given orally or intravenously as a pretreatment medication and study drug.
Deksametason vil bli administrert oralt eller intravenøst.
QLS4131 will be administered subcutaneously.
Pomalidomide will be self-administered as a single dose orally.
Eksperimentell: QLS4131(SC) in combination with QL2109 for injection and Lenalidomide
Participants will receive QLS4131 and QL2109 as SC injections; Lenalidomide will be self-administered as a single dose orally; dexamethasone may be given orally or intravenously as a pretreatment medication and study drug.
Deksametason vil bli administrert oralt eller intravenøst.
QLS4131 will be administered subcutaneously.
QL2109 will be administered subcutaneously.
Lenalidomide will be self-administered as a single dose orally.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
DLT
Tidsramme: 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
From time of the first dose of QLS4131 to end of DLT period (28 days)
MTD
Tidsramme: Up to 2 years
To determine the maximum tolerated dose (MTD)
Up to 2 years
ORR (Partial Response [PR] or Better)
Tidsramme: 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.
Up to 2 years
Overall Minimal Residual Disease (MRD)
Tidsramme: 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.
Up to 2 years

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Antatt)

1. juni 2026

Primær fullføring (Antatt)

1. juni 2028

Studiet fullført (Antatt)

1. juni 2030

Datoer for studieregistrering

Først innsendt

21. april 2026

Først innsendt som oppfylte QC-kriteriene

27. april 2026

Først lagt ut (Faktiske)

1. mai 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

1. mai 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

27. april 2026

Sist bekreftet

1. april 2026

Mer informasjon

Begreper knyttet til denne studien

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

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