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A Study of BL-M08D in Patients With Locally Advanced or Metastatic Digestive Tract Tumors and Other Solid Tumors

25. august 2026 opdateret af: Sichuan Baili Pharmaceutical Co., Ltd.

A Phase Ib/II Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetic Characteristics and Preliminary Efficacy of BL-M08D1 for Injection in Patients With Locally Advanced or Metastatic Digestive Tract Tumors and Other Solid Tumors

This Phase Ib/II study is a clinical trial exploring the efficacy and safety of BL-M08D1 for injection in patients with locally advanced or metastatic digestive tract tumors and other solid tumors.

Studieoversigt

Status

Ikke rekrutterer endnu

Betingelser

Intervention / Behandling

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

60

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

    • Beijing Municipality
      • Beijing, Beijing Municipality, Kina
        • Cancer Hospital Chinese Academy of Medical Sciences
        • Kontakt:
          • Jing Huang

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. Locally advanced or metastatic gastrointestinal tumors and other solid tumors;
  6. Agree to provide archival tumor tissue specimens from the primary or metastatic site within 3 years, or fresh tissue samples;
  7. Must have at least one measurable lesion as defined by RECIST v1.1;
  8. Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1, with no deterioration within 2 weeks prior to the first dose;
  9. Toxicities from prior anti-tumor therapy 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. Coagulation function: international normalized ratio ≤1.5, and activated partial thromboplastin time ≤1.5 × upper limit of normal;
  13. Urine protein ≤1+ or ≤1000 mg/24 h;
  14. For premenopausal women of childbearing potential, a pregnancy test must be performed within 7 days before starting treatment, with serum pregnancy results being negative, and they must be non-lactating; all enrolled patients (regardless of male or female) must adopt adequate barrier contraceptive measures throughout the entire treatment period and for 6 months after the completion of treatment;
  15. The trial participant is capable 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 cardiac or cerebrovascular disease;
  3. Prolonged QTc 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 another malignant tumor 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 medication;
  8. Poorly controlled blood glucose;
  9. History of interstitial lung disease requiring hormone therapy, or current ILD, or radiation pneumonitis of Grade ≥2;
  10. Severe impairment of respiratory function;
  11. Active central nervous system metastases;
  12. Previous or concurrent central nervous system disorders;
  13. History of allergy to recombinant humanized antibodies or human-mouse chimeric antibodies, or allergy to any excipient component of BL-M08D1;
  14. Previous organ transplantation or allogeneic hematopoietic stem cell transplantation;
  15. Positive for human immunodeficiency virus antibody, active tuberculosis, active hepatitis B virus infection, or active hepatitis C virus infection;
  16. Active infection requiring systemic treatment within 4 weeks prior to the first study drug administration;
  17. Pleural, abdominal, or pericardial effusion requiring drainage and/or accompanied by symptoms within 4 weeks prior to the first study drug administration;
  18. Imaging findings indicating tumor invasion or encasement of abdominal, thoracic, cervical, or other regions;
  19. Use of another investigational drug within 4 weeks or 5 half-lives prior to the first dose;
  20. Pregnant or breastfeeding women;
  21. Other conditions deemed by the investigator to make the patient unsuitable for participation 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: N/A
  • Interventionel model: Enkelt gruppeopgave
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: BL-M08D1
Participants receive BL-M08D1 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.

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
AUC0-t
Tidsramme: Op til cirka 24 måneder
AUC0-t er defineret som areal under serumkoncentration-tid-kurven fra tidspunkt 0 til tidspunktet for den sidste målelige koncentration.
Op til cirka 24 måneder
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
Cmax
Tidsramme: Up to approximately 24 months
Cmax is defined as the maximum observed drug concentration in plasma after administration.
Up to approximately 24 months
Tmax
Tidsramme: Up to approximately 24 months
Tmax is defined as the time required to reach the maximum drug concentration in plasma following drug administration.
Up to approximately 24 months
T1/2
Tidsramme: Up to approximately 24 months
T1/2 is defined as the time required for the plasma concentration of a drug to decrease by 50% during the elimination phase.
Up to approximately 24 months
CL (Clearance)
Tidsramme: Up to approximately 24 months
Clearance (CL) is the volume of plasma from which a drug is completely removed per unit time.
Up to approximately 24 months
Ctrough
Tidsramme: Up to approximately 24 months
Ctrough is defined as the lowest serum concentration prior to the next dose will be administered.
Up to approximately 24 months
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
Anti-drug Antibody (ADA)
Tidsramme: Up to approximately 24 months
Frequency of anti-BL-M08D1 antibody (ADA) will be investigated.
Up to approximately 24 months

Samarbejdspartnere og efterforskere

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

Sponsor

Samarbejdspartnere

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

19. august 2026

Først indsendt, der opfyldte QC-kriterier

19. august 2026

Først opslået (Faktiske)

21. august 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

27. august 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

25. august 2026

Sidst verificeret

1. august 2026

Mere information

Begreber relateret til denne undersøgelse

Andre undersøgelses-id-numre

  • BL-M08D1-202

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

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