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A Study of BL-M14D1 in Combination With Atezolizumab in Patients With Extensive-stage Small Cell Lung Cancer

24 augustus 2026 bijgewerkt door: Sichuan Baili Pharmaceutical Co., Ltd.

A Phase II Clinical Study to Evaluate the Efficacy and Safety of BL-M14D1 for Injection in Combination With Atezolizumab in Patients With Extensive-stage Small Cell Lung Cancer

This Phase II study is a clinical study exploring the efficacy and safety of BL-M14D1 in combination with Atezolizumab in patients with extensive-stage small cell lung cancer.

Studie Overzicht

Studietype

Ingrijpend

Inschrijving (Geschat)

36

Fase

  • Fase 2

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studiecontact

Studie Locaties

    • Shanghai Municipality
      • Shanghai, Shanghai Municipality, China
        • Werving
        • Shanghai East Hospital
        • Contact:
          • Caicun Zhou

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

  • Volwassen
  • Oudere volwassene

Accepteert gezonde vrijwilligers

Nee

Beschrijving

Inclusion Criteria:

  1. Voluntarily sign the informed consent form and comply with the protocol requirements;
  2. No gender restriction;
  3. Age: ≥18 years;
  4. Expected survival time ≥3 months;
  5. Histopathologically and/or cytologically confirmed extensive-stage small cell lung cancer that is incurable or for which there is currently no standard treatment;
  6. Agree to provide archived tumor tissue specimens from the primary or metastatic lesion 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;
  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 (LVEF) ≥50%;
  11. Organ function levels must meet the required criteria;
  12. Urine protein ≤1+ or ≤1000 mg/24h;
  13. For premenopausal women with childbearing potential, a pregnancy test must be performed within 7 days before the start of treatment. Serum pregnancy testing must rule out pregnancy, and the patient must not be breastfeeding. All enrolled trial participants (regardless of gender) should take adequate barrier contraceptive measures throughout the entire treatment period and for 7 months after the end of treatment.

Exclusion Criteria:

  1. Use of chemotherapy, biological therapy, immunotherapy, etc., within 4 weeks or 5 half-lives before the first dose;
  2. Previous treatment with ADC drugs using topoisomerase I inhibitors as toxins;
  3. Small cell carcinoma with non-small cell carcinoma components indicated by pathology must be excluded;
  4. Use of immunomodulatory drugs within 2 weeks before the first dose of the study;
  5. Receiving long-term systemic corticosteroid therapy at a dose >10 mg/day of prednisone or equivalent before the first dose;
  6. History of severe cardiovascular or cerebrovascular diseases;
  7. Prolonged QTc interval, complete left bundle branch block, etc.;
  8. Active autoimmune diseases and inflammatory diseases;
  9. Diagnosis of another malignancy within 5 years before the first dose;
  10. Hypertension poorly controlled by two antihypertensive drugs;
  11. Patients with poorly controlled blood glucose;
  12. History of ILD/interstitial pneumonia treated with corticosteroids, etc.;
  13. Concomitant pulmonary diseases leading to clinically severe impairment of respiratory function;
  14. Presence of massive serous cavity effusion, or serous cavity effusion with symptoms, etc.;
  15. Imaging findings indicating that the tumor has invaded or encased major blood vessels in the chest, neck, pharynx, etc.;
  16. Any thrombotic event within 6 months before randomization;
  17. Patients with active central nervous system metastases;
  18. History of allergy to recombinant humanized antibodies or chimeric human-mouse antibodies, or allergy to any excipient components of the investigational drug, etc.;
  19. Previous organ transplantation or allogeneic hematopoietic stem cell transplantation;
  20. Cumulative anthracycline dose >360 mg/m² during prior (neo)adjuvant anthracycline therapy;
  21. Positive for human immunodeficiency virus antibody, active tuberculosis, active hepatitis B virus infection, or active hepatitis C virus infection;
  22. Active infections requiring systemic treatment, or occurrence of severe infection within 4 weeks before informed consent;
  23. Receipt of other unapproved clinical study drugs or treatments within 4 weeks before the first dose;
  24. Pregnant or breastfeeding women;
  25. History of severe neurological or psychiatric disorders;
  26. Presence of serious non-healing wounds, ulcers, or fractures within 4 weeks before signing informed consent;
  27. Clinically significant bleeding or obvious bleeding tendency within 4 weeks before signing informed consent;
  28. History of intestinal obstruction, inflammatory bowel disease, extensive bowel resection, or presence of Crohn's disease, ulcerative colitis, or chronic diarrhea;
  29. Trial participants who plan to receive or have received live vaccines within 28 days before the first dose;
  30. Other conditions deemed by the investigator to be unsuitable for participation in this clinical trial.

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Behandeling
  • Toewijzing: NVT
  • Interventioneel model: Opdracht voor een enkele groep
  • Masker: Geen (open label)

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: BL-M14D1+ Atezolizumab
Participants receive BL-M14D1+ Atezolizumab 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.
Toediening via intraveneuze infusie gedurende een cyclus van 3 weken.
Administration by intravenous infusion for a cycle of 3 weeks.

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Objective Response Rate (ORR)
Tijdsspanne: Up to approximately 12 months
ORR is defined as the percentage of participants, who has a CR (disappearance of all target lesions) or PR (at least a 30% decrease in the sum of diameters of target lesions). The percentage of participants who experiences a confirmed CR or PR is according to RECIST 1.1.
Up to approximately 12 months
Treatment-Emergent Adverse Event (TEAE)
Tijdsspanne: Up to approximately 12 months
TEAE is defined as any unfavorable and unintended change in the structure, function, or chemistry of the body temporally emerging, or any worsening (i.e., any clinically significant adverse change in frequency and/or intensity) of a pre-existing condition during the treatment of BL-M14D1 . The type, frequency and severity of TEAE will be evaluated during the treatment of BL-M14D1.
Up to approximately 12 months

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Progression-free survival (PFS)
Tijdsspanne: Up to approximately 12 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 12 months
Disease Control Rate (DCR)
Tijdsspanne: Up to approximately 12 months
The DCR is defined as the percentage of participants who has a CR, PR, or Stable Disease (SD: neither sufficient shrinkage to qualify for PR nor sufficient increase to qualify for progressive disease [PD: at least a 20% increase in the sum of diameters of target lesions and an absolute increase of at least 5 mm. The appearance of one or more new lesions is also considered PD]).
Up to approximately 12 months
Duration of Response (DOR)
Tijdsspanne: Up to approximately 12 months
The DOR for a responder is defined as the time from the participant's initial objective response to the first date of either disease progression or death, whichever occurs first.
Up to approximately 12 months
Overall Survival (OS)
Tijdsspanne: Up to approximately 12 months
Overall survival (OS) is defined as the time between the day the subject is randomized and the subject's death.
Up to approximately 12 months
Cmax
Tijdsspanne: Up to approximately 12 months
Maximum serum concentration (Cmax) of BL-M14D1 will be investigated.
Up to approximately 12 months
Tmax
Tijdsspanne: Up to approximately 12 months
Time to maximum serum concentration (Tmax) of BL-M14D1 will be investigated.
Up to approximately 12 months
Ctrough
Tijdsspanne: Up to approximately 12 months
Ctrough is defined as the lowest serum concentration of BL-M14D1 prior to the next dose will be administered.
Up to approximately 12 months
ADA (anti-drug antibody)
Tijdsspanne: Up to approximately 12 months
Frequency of anti-BL-M14D1 antibody (ADA) will be investigated.
Up to approximately 12 months

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Werkelijk)

9 juli 2026

Primaire voltooiing (Geschat)

1 december 2027

Studie voltooiing (Geschat)

1 december 2027

Studieregistratiedata

Eerst ingediend

12 juni 2026

Eerst ingediend dat voldeed aan de QC-criteria

12 juni 2026

Eerst geplaatst (Werkelijk)

17 juni 2026

Updates van studierecords

Laatste update geplaatst (Werkelijk)

25 augustus 2026

Laatste update ingediend die voldeed aan QC-criteria

24 augustus 2026

Laatst geverifieerd

1 augustus 2026

Meer informatie

Termen gerelateerd aan deze studie

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Nee

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

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