- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT04617704
BCMA and CD19 Targeted Fast Dual CART for Chromosomal Abnomalities High-risk BCMA+ Multiple Myeloma
21. september 2021 opdateret af: Weijun Fu, Shanghai Changzheng Hospital
Exploratory Study to Evaluate Efficacy and Safety of GC012F Injection in Chromosomal Abnomalities High-risk BCMA+ Multiple Myeloma
This is a single arm, open label, multi-center prospective study to explory the safety and efficacy of GC012F CAR-T cells in patient diagnosed with high-risk chromosomal abnormalities BCMA+ multiple myeloma(MM).
Studieoversigt
Detaljeret beskrivelse
The main aim of this study is to determin the safety and efficacy of GC012F in cytogenetic high-risk MM.
GC012F is an autologus dual chimeric antigen receptor T-cell(CAR-T) therapy that targets B-cell maturation antigen(BCMA) and CD19.
This study comprises of a screening phase(less than or equal to 28 days prior to apheresis) followed by apheresis(will occur upon enroiiment); Treatment Phase including autologus stem cell transplant on Day-1 followed by infusion of GC012F on Day0 and then post-infusion assessments from Day1 to Day 84; and a Post-treatment Phase(Day 85 and up to end of the study).
Efficacy will be explored to assessed and safety will be closely monitored during the study.
Undersøgelsestype
Interventionel
Tilmelding (Forventet)
15
Fase
- Tidlig fase 1
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
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Shanghai
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Shanghai, Shanghai, Kina
- Shanghai Changzheng Hospital
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Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
18 år og ældre (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Alle
Beskrivelse
Inclusion Criteria:
- Diagnosis of active MM as defined by any of following: a) serum M protein more than or equal to 10g/dL; b) urine M protein more than or equal to 200mg/24 h; c) involved serum free light chain more than or equal to 100mg/dL with abnormal serum kappa lambda ratio;
- Patients with clear BCMA expression(percent of BCMA positive plasma cells more than or equal to 20%) detected by flow cytometry;
- High-risk chromosomal abnormal defined as presence of del17p, and/or t(4;14) and/or t(14;16);
- Estimated life expectancy more than or equal to 3 months;
- Absolute neutrophil count more than or equal to 1*10^9/L;
- Platelet count more than or equal to 25*10^9/L;
- Absolute lymphocyte count more than or equal to 1*10^8/L;
- Liver, kidney and cardiopulmonary functions meet the following requirements: a) Total bilirubin less than or equal to 2*ULN(except for Gilbert Syndrome); ALT and AST less than or equal to 2.5*ULN, maintenance of kidney function not depend on dialysis; c)Corrected serum calcium less than or equal to 12.5 mg/dL or free ion calcium less than or equal to 6.5mg/dL(1.6mmol/L);
- Sufficient venous access for leukapheresis collection and no other contraindications to leukapheresis;
- Subjects and sexual partner with fertility are willing to use effective and reliable method of contraception for at least 1 year after CAR-T infusion;
- subjects must have signed writtern informed consent.
Exclusion Criteria:
- Accompanied by other unctrolled maligancies. Two exceptions to this criteria: Recepted radical therapy carcinoma without activity within 3 years before screening; fully treated skin non-melanoma;
- Any situations not benefit for subjects to accept or tolerated to planned therapy or understand informed consent; or any situation in which investigators believe that participation in this study is not in the subject's best intreat(eg., harm to health), or any situation that may prevent, limit or confuse the assessment;
- Convulsion or stoke within past 6 months;
- Any instability or systemic disease within 6 months prior to screening, including but not limited to congestive heart failure(New York heart association classification ≥ III), unstable angina, cerebrovascular accident, or transient cerebral ischemic, myocardial infarction, LEVF<50%(assessed by an echocardiogram or multi-door circuit scan);
- Patients have central nervous system(CNS) metastases or CNS involvement(including cranial neuropathies or mass lesions and leptomeningeal disease);
- Subjects with positive HBsAg or HBcAb positive and peripheal blood HBV-DNA titer is higher than the lower limit of detection of the research institution; HCV antibody positive; HIV antibody positive; syphilis primary screening antibody positive;
- Presence or suspicious of fungi, bacteria, viruses or other infections that are uncontrollable or requiring intravenous treatment;
- Activity of autoimmune disease (such as crohn's disease, rheumatoid arthritis, systemic lupus erythematosus), orhistory of autoimmune disease within the last 3 years;
- Clinical evidence of dementia or changes of mental state;
- Exist of pulmonary fibrosis;
- Allergy subjects or history of severe hypersensitivity;
- Oxgen inhalation requirement to maintain adequate oxygen saturation;
- Surgery (except for local anesthesia surgery) plan 2 weeks before apheresis, during or 2 weeks after CAR-T infusion;
- Patients who are accounted to be not appropriate for this investigator.
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: N/A
- Interventionel model: Enkelt gruppeopgave
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
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Eksperimentel: Experimental:GC012F treatment
BCMA+ cytogenetic high-risk multiple myeloma patients be treated with a single dose of GC012F cells.
Total dose of (1-5)*10^5/kg cells will be administered at Day 0
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GC012F injection is a autologous dual CAR-T targeted BCMA and CD19.
A single infusion of CAR-T cells will be administered intravenously.
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
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Incidence and severity of adverse events after GC012F injection
Tidsramme: Minimum 2 years after GC012F infusion
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Minimum 2 years after GC012F infusion
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Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Percentage of MRD negative patients after GC012F infusion
Tidsramme: Minimum 2 years after GC012F infusion
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Minimum 2 years after GC012F infusion
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ORR(PR, VGPR, CR and sCR) of patients after GC012F treatment
Tidsramme: Minimum 2 years after GC012F infusion(Day0)
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percent of subjects who achieving PR or better after GC012F infusion
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Minimum 2 years after GC012F infusion(Day0)
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Progression free survival after GC012F treatment
Tidsramme: Minimum 2 years after GC012F infusion(Day0)
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Minimum 2 years after GC012F infusion(Day0)
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Duration of response of subjects after GC012F treatment
Tidsramme: Minimum 2 years after GC012F infusion(Day0)
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Minimum 2 years after GC012F infusion(Day0)
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Overall survivalof subjects after GC012F treatment
Tidsramme: Minimum 2 years after GC012F infusion(Day0)
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Minimum 2 years after GC012F infusion(Day0)
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Cytokines in serum after GC012F infusion
Tidsramme: Minimum 24 weeks after GC012F infusion(Day0)
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Minimum 24 weeks after GC012F infusion(Day0)
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Subset of lymphocytes in blood after GC012F infusion
Tidsramme: Minimum 2 years after GC012F infusion(Day0)
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Minimum 2 years after GC012F infusion(Day0)
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Anti-GC012F antibodies in blood after GC012F infusion
Tidsramme: Minimum 2 years after GC012F infusion(Day0)
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Minimum 2 years after GC012F infusion(Day0)
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Cell counts of GC012F in blood and bone marrow(if available) after GC012F infusion
Tidsramme: Minimum 2 years after GC012F infusion(Day0)
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Minimum 2 years after GC012F infusion(Day0)
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Copies of GC012F in blood and bone marrow(if available) after GC012F infusion
Tidsramme: Minimum 2 years after GC012F infusion(Day0)
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Minimum 2 years after GC012F infusion(Day0)
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Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Samarbejdspartnere
Datoer for undersøgelser
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Studer store datoer
Studiestart (Forventet)
1. december 2021
Primær færdiggørelse (Forventet)
31. december 2021
Studieafslutning (Forventet)
1. februar 2022
Datoer for studieregistrering
Først indsendt
20. august 2020
Først indsendt, der opfyldte QC-kriterier
30. oktober 2020
Først opslået (Faktiske)
5. november 2020
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
22. september 2021
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
21. september 2021
Sidst verificeret
1. oktober 2020
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
- Hjerte-kar-sygdomme
- Karsygdomme
- Sygdomme i immunsystemet
- Neoplasmer efter histologisk type
- Neoplasmer
- Lymfoproliferative lidelser
- Immunproliferative lidelser
- Hæmatologiske sygdomme
- Hæmoragiske lidelser
- Hæmostatiske lidelser
- Paraproteinæmier
- Blodproteinforstyrrelser
- Myelomatose
- Neoplasmer, Plasmacelle
Andre undersøgelses-id-numre
- GBF003
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