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

8. september 2026 oppdatert av: 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.

Studieoversikt

Studietype

Intervensjonell

Registrering (Antatt)

204

Fase

  • Fase 2
  • Fase 1

Kontakter og plasseringer

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

Studiekontakt

Studiesteder

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

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:

  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

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

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: 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.
Administrering ved intravenøs infusjon i en syklus på 3 uker.
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.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Objektiv responsrate (ORR)
Tidsramme: Opptil ca 24 måneder
ORR er definert som prosentandelen av deltakerne som har en CR (forsvinning av alle mållesjoner) eller PR (minst 30 % reduksjon i summen av diametre av mållesjoner). Andelen deltakere som opplever bekreftet CR eller PR er i henhold til RECIST 1.1.
Opptil ca 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
Tiltaksbeskrivelse
Tidsramme
Disease Control Rate (DCR)
Tidsramme: Opptil ca 24 måneder
Disease Control Rate (DCR): Prosentandel av alle randomiserte forsøkspersoner som vurderte den beste totale responsen (BOR) som fullstendig respons (CR), delvis respons (PR) og sykdomsstabilisering (SD) i henhold til RECIST 1.1-kriterier.
Opptil ca 24 måneder
Treatment-Emergent Adverse Event (TEAE)
Tidsramme: Opptil ca 24 måneder
TEAE er definert som enhver ugunstig og utilsiktet endring i kroppens struktur, funksjon eller kjemi som oppstår midlertidig, eller enhver forverring (dvs. enhver klinisk signifikant negativ endring i frekvens og/eller intensitet) av en eksisterende tilstand under behandlingen av BL-M08D1. Type, frekvens og alvorlighetsgrad av TEAE vil bli evaluert under behandlingen av BL-M08D1.
Opptil ca 24 måneder
Responsens varighet (DOR)
Tidsramme: Opptil omtrent 24 måneder
Responsens varighet (DOR) er definert som perioden fra datoen da tumorrespons først blir registrert til datoen når objektiv tumorprogresjon først blir registrert eller dødsdatoen.
Opptil omtrent 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

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. september 2026

Primær fullføring (Antatt)

1. desember 2028

Studiet fullført (Antatt)

1. desember 2028

Datoer for studieregistrering

Først innsendt

8. september 2026

Først innsendt som oppfylte QC-kriteriene

8. september 2026

Først lagt ut (Faktiske)

14. september 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

14. september 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

8. september 2026

Sist bekreftet

1. september 2026

Mer informasjon

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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