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A Study of BL-M08D1 in Combination With Immunochemotherapy in Patients With Diffuse Large B-Cell Lymphoma

8. september 2026 opdateret af: Sichuan Baili Pharmaceutical Co., Ltd.

A Phase Ib/II Clinical Study to Evaluate the Efficacy and Safety of BL-M08D1 for Injection in Combination With Immunochemotherapy in Patients With Diffuse Large B-Cell Lymphoma

This Phase Ib/II study is a clinical trial to explore the efficacy and safety of BL-M08D1 for injection in combination with immunochemotherapy in patients with diffuse large B-cell lymphoma.

Studieoversigt

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

204

Fase

  • Fase 2
  • Fase 1

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiekontakt

Studiesteder

    • Guangdong
      • Guangzhou, Guangdong, Kina
        • Sun Yat-sen University Cancer Center
        • Kontakt:
          • Qingqing Cai
    • Jiangsu
      • Suzhou, Jiangsu, Kina
        • The First Affiliated Hospital of Soochow University
        • Kontakt:
          • Depei Wu

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

  • Voksen
  • Ældre voksen

Tager imod sunde frivillige

Ingen

Beskrivelse

Inclusion Criteria:

  1. Voluntarily sign the informed consent form and comply with the protocol requirements;
  2. No gender restriction;
  3. Age ≥18 years and ≤75 years;
  4. Expected survival time ≥3 months;
  5. Patients with diffuse large B-cell lymphoma;
  6. Agree to provide archived tumor tissue specimens within 3 years or fresh tissue samples;
  7. Must have at least one measurable lesion;
  8. Eastern Cooperative Oncology Group (ECOG) performance status score ≤2;
  9. Toxicity from prior anti-tumor therapy must have recovered to ≤ Grade 1 as defined by NCI-CTCAE v6.0;
  10. No severe cardiac dysfunction, with left ventricular ejection fraction ≥50%;
  11. Organ function levels must meet the requirements;
  12. Urine protein ≤1+ or <1000 mg/24h;
  13. For premenopausal women with childbearing potential, a serum pregnancy test must be performed within 7 days before starting treatment, and the serum pregnancy test must exclude pregnancy; patients must not be breastfeeding; all enrolled trial participants must take adequate barrier contraceptive measures throughout the entire treatment period and for 6 months after treatment completion;
  14. Trial participants must be able and willing to comply with the visit schedule, treatment plan, laboratory tests, and other study-related procedures specified in the protocol.

Exclusion Criteria:

  1. Use of chemotherapy, biological therapy, immunotherapy, etc., within 4 weeks or 5 half-lives prior to the first dose;
  2. History of severe heart disease or cerebrovascular disease within 6 months before screening;
  3. Prolonged QT interval, complete left bundle branch block, third-degree atrioventricular block, or frequent and uncontrolled arrhythmias;
  4. Active autoimmune diseases and inflammatory diseases;
  5. Diagnosis of active malignancy within 5 years prior to the first dose;
  6. Unstable thrombotic events requiring therapeutic intervention within 6 months prior to the first dose;
  7. Hypertension inadequately controlled by antihypertensive medications;
  8. Trial participants with poorly controlled blood glucose;
  9. History of interstitial lung disease requiring corticosteroid therapy, or current ILD, or radiation pneumonitis of grade ≥2;
  10. Use of glucocorticoids at a dose >30 mg/day prednisone or equivalent, for purposes other than control of lymphoma symptoms;
  11. Concurrent pulmonary diseases resulting in clinically severe impairment of respiratory function;
  12. Patients with central nervous system involvement;
  13. Previous or current central nervous system disorders;
  14. Contraindications to any component of the study intervention, including but not limited to previous allergic reactions;
  15. Receipt of autologous hematopoietic stem cell transplantation or CAR-T cell therapy, etc., within 12 weeks prior to the first dose;
  16. Positive for human immunodeficiency virus antibody, active tuberculosis, active hepatitis B virus infection, or active hepatitis C virus infection;
  17. Active infection requiring systemic therapy within 4 weeks prior to the first study drug administration;
  18. Pleural, abdominal, or pelvic effusion or pericardial effusion requiring drainage and/or accompanied by symptoms within 4 weeks prior to the first study drug administration;
  19. Imaging findings indicating that the tumor has invaded or encased major blood vessels in the abdomen, chest, neck, pharynx, etc., or the pericardium or heart;
  20. Use of another investigational drug within 4 weeks or 5 half-lives prior to the first dose;
  21. Pregnant or breastfeeding women;
  22. Other conditions that, in the investigator's opinion, make the participant unsuitable for enrollment in this clinical trial.

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: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: BL-M08D1+R-GemOx or BL-M08D1+R-CHOP
Participants receive BL-M08D1+R-GemOx or BL-M08D1+R-CHOP for the first cycle (3 weeks). Participants with clinical benefit could receive additional treatment for more cycles. The administration will be terminated because of disease progression or intolerable toxicity occurring or other reasons.
Administration ved intravenøs infusion i en cyklus på 3 uger.
Administration by intravenous infusion for a cycle of 3 weeks.
Administration by intravenous infusion for a cycle of 3 weeks.
Administration by intravenous infusion for a cycle of 3 weeks.
Administration by intravenous infusion for a cycle of 3 weeks.
Administration by intravenous infusion for a cycle of 3 weeks.
Administration by intravenous infusion for a cycle of 3 weeks.
Oral administration for a cycle of 3 weeks.
Aktiv komparator: R-GemOx or R-CHOP
Participants receive R-GemOx or R-CHOP for the first cycle (3 weeks). Participants with clinical benefit could receive additional treatment for more cycles. The administration will be terminated because of disease progression or intolerable toxicity occurring or other reasons.
Administration by intravenous infusion for a cycle of 3 weeks.
Administration by intravenous infusion for a cycle of 3 weeks.
Administration by intravenous infusion for a cycle of 3 weeks.
Administration by intravenous infusion for a cycle of 3 weeks.
Administration by intravenous infusion for a cycle of 3 weeks.
Administration by intravenous infusion for a cycle of 3 weeks.
Oral administration for a cycle of 3 weeks.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Objektiv responsrate (ORR)
Tidsramme: Op til cirka 24 måneder
ORR er defineret som procentdelen af ​​deltagere, der har en CR (forsvinden af ​​alle mållæsioner) eller PR (mindst et 30 % fald i summen af ​​diametre af mållæsioner). Procentdelen af ​​deltagere, der oplever en bekræftet CR eller PR, er i henhold til RECIST 1.1.
Op til cirka 24 måneder
Recommended Phase II Dose (RP2D)
Tidsramme: Up to approximately 24 months
The RP2D is defined as the dose level chosen by the sponsor (in consultation with the investigators) for phase II study, based on safety, tolerability, efficacy, PK, and PD data collected during the dose escalation study of BL-M08D1.
Up to approximately 24 months

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Disease Control Rate (DCR)
Tidsramme: Op til cirka 24 måneder
Disease Control Rate (DCR): Procentdel af alle randomiserede forsøgspersoner, der vurderede den bedste overordnede respons (BOR) som komplet respons (CR), delvis respons (PR) og sygdomsstabilisering (SD) i henhold til RECIST 1.1-kriterier.
Op til cirka 24 måneder
Treatment-Emergent Adverse Event (TEAE)
Tidsramme: Op til cirka 24 måneder
TEAE er defineret som enhver ugunstig og utilsigtet ændring i kroppens struktur, funktion eller kemi, der midlertidigt opstår, eller enhver forværring (dvs. enhver klinisk signifikant negativ ændring i hyppighed og/eller intensitet) af en allerede eksisterende tilstand under behandlingen af BL-M08D1. Typen, hyppigheden og sværhedsgraden af ​​TEAE vil blive evalueret under behandlingen af ​​BL-M08D1.
Op til cirka 24 måneder
Responsens varighed (DOR)
Tidsramme: Op til cirka 24 måneder
Responsens varighed (DOR) er defineret som perioden fra den dato, hvor tumorrespons først registreres til den dato, hvor objektiv tumorprogression først registreres eller dødsdatoen.
Op til cirka 24 måneder
Progression-free Survival (PFS)
Tidsramme: Up to approximately 24 months
Progression-free survival (PFS) as assessed by BICR is defined as the time between the date subjects were randomized and the first observation of disease progression (based on BICR's image-based assessment) or death.
Up to approximately 24 months
Complete Remission Rate (CRR)
Tidsramme: Up to approximately 24 months
Complete Remission Rate (CRR) refers to the proportion of patients in a clinical trial who achieve a complete remission (CR) after receiving a specific treatment.
Up to approximately 24 months

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Anslået)

1. september 2026

Primær færdiggørelse (Anslået)

1. december 2028

Studieafslutning (Anslået)

1. december 2028

Datoer for studieregistrering

Først indsendt

8. september 2026

Først indsendt, der opfyldte QC-kriterier

8. september 2026

Først opslået (Faktiske)

14. september 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

14. september 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

8. september 2026

Sidst verificeret

1. september 2026

Mere information

Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .

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