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A Study of BL-B01D1 in Combination With Osimertinib as Perioperative Therapy in Patients With EGFR-mutated Resectable Non-small Cell Lung Cancer(PANKU-Lung09)

12. juni 2026 opdateret af: Sichuan Baili Pharmaceutical Co., Ltd.

A Phase II/III Randomized Controlled Clinical Study of BL-B01D1 in Combination With Osimertinib as Perioperative Therapy in Patients With EGFR-mutated Resectable Non-small Cell Lung Cancer(PANKU-Lung09)

This trial is a registrational Phase II/III, randomized, open-label, multicenter study to evaluate the efficacy and safety of BL-B01D1 in combination with osimertinib in resectable EGFR-mutant non-small cell lung cancer.

Studieoversigt

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

90

Fase

  • Fase 2
  • Fase 3

Kontakter og lokationer

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

Studiekontakt

Studiesteder

    • Shanghai Municipality
      • Shanghai, Shanghai Municipality, Kina
        • Shanghai Pulmonary Hospital
        • Kontakt:
          • Peng Zhang
      • Shanghai, Shanghai Municipality, Kina
        • Shanghai East Hospital
        • Kontakt:
          • Caicun Zhou

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 informed consent and agree to comply with the protocol requirements;
  2. Aged ≥18 years and ≤75 years, regardless of gender;
  3. Expected survival time ≥3 months;
  4. Patients with non-small cell lung cancer;
  5. One of the EGFR sensitive mutation types detected in the tumor tissue;
  6. Agree to provide archived primary tumor tissue specimens obtained within 12 months or fresh tissue samples;
  7. Undergo pulmonary function testing within 28 days prior to the first dose;
  8. ECOG performance status score of 0 or 1;
  9. No severe cardiac dysfunction;
  10. Organ function levels must meet the required criteria;
  11. Urine protein ≤1+ or <1000 mg/24h;
  12. For premenopausal women of 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 lactating; all enrolled trial participants must use adequate barrier contraceptive measures throughout the entire treatment period and for 7 months after the end of treatment.

Exclusion Criteria:

  1. SCLC, mixed SCLC and NSCLC, or other non-NSCLC pathological types;
  2. Trial participants who subsequently receive only segmentectomy or wedge resection;
  3. Trial participants deemed surgically inoperable by the study center's surgical evaluation;
  4. Undergoing major surgery within 4 weeks prior to the first dose, among others;
  5. Previous receipt of systemic anti-tumor therapy for non-small cell lung cancer other than that for this study, among others;
  6. Receiving long-term systemic corticosteroid therapy with prednisone >10 mg/day within 2 weeks prior to randomization, among others;
  7. History of severe heart disease or cerebrovascular disease;
  8. Prolonged QTc interval, complete left bundle branch block, etc.;
  9. Any thrombotic event within 6 months prior to screening;
  10. Trial participants with known or suspected interstitial lung disease, among others;
  11. Diagnosis of active malignant tumors within 5 years prior to study randomization;
  12. Hypertension inadequately controlled by two antihypertensive medications;
  13. Trial participants with poorly controlled blood glucose;
  14. Severe infection occurring within 4 weeks prior to study randomization, among others;
  15. Presence of large serous cavity effusion, or serous cavity effusion with symptoms, etc.;
  16. Imaging findings indicating tumor invasion or encasement of the abdomen, chest, etc.;
  17. Severe non-healing wounds, ulcers, or fractures within 4 weeks prior to signing informed consent;
  18. Trial participants with clinically significant bleeding or obvious bleeding tendency within 4 weeks prior to signing informed consent;
  19. Inflammatory bowel disease, history of extensive bowel resection, history of immune-related enteritis, etc.;
  20. History of allergy to the investigational drug, etc.;
  21. History of solid organ transplantation, autologous or allogeneic stem cell transplantation;
  22. Positive for human immunodeficiency virus antibodies, active hepatitis B virus infection, or hepatitis C virus infection;
  23. History of severe neurological or psychiatric disorders;
  24. Trial participants planning to receive or having received live vaccines within 28 days prior to study randomization;
  25. Other conditions deemed by the investigator as unsuitable for participation in this clinical trial due to complications or other circumstances.

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-B01D1+Osimertinib
Participants receive BL-B01D1+Osimertinib in 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.
Andre navne:
  • BMS-986507
  • Iza-Bren
  • Izalontamab Brengitecan
Oral administration for a cycle of 3 weeks.
Aktiv komparator: Osimertinib
Participants receive Osimertinib in 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.
Oral administration for a cycle of 3 weeks.
Aktiv komparator: Carboplatin + Pemetrexed or Cisplatin + Pemetrexed
Participants receive Carboplatin + Pemetrexed or Cisplatin + Pemetrexed in 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 ved intravenøs infusion i en cyklus på 3 uger.
Administration ved intravenøs infusion i en cyklus på 3 uger.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Major Pathological Response (MPR)
Tidsramme: Up to approximately 24 months
MPR is defined as the presence of viable tumor tissue ≤10% in the surgical specimen at the time of tumor resection.
Up to approximately 24 months

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Behandling 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-B01D1. Typen, hyppigheden og sværhedsgraden af ​​TEAE vil blive evalueret under behandlingen af ​​BL-B01D1.
Op til cirka 24 måneder
Anti-lægemiddel antistof (ADA)
Tidsramme: Op til cirka 24 måneder
Hyppigheden af ​​anti-BL-B01D1 antistof (ADA) vil blive undersøgt.
Op til cirka 24 måneder
Samlet overlevelse (OS)
Tidsramme: Op til cirka 24 måneder
Den samlede overlevelse (OS) er defineret som tiden mellem den dag, hvor forsøgspersonen randomiseres, og forsøgspersonens død.
Op til cirka 24 måneder
Pathologic complete response (pCR)
Tidsramme: Up to approximately 24 months
pCR is defined as the absence of any residual tumor (lesions) in the primary tumor upon surgical resection.
Up to approximately 24 months
Event-Free Survival (EFS)
Tidsramme: Up to approximately 24 months
EFS is defined as the time from randomization to the occurrence of any of the following events, whichever occurs first.
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. juni 2026

Primær færdiggørelse (Anslået)

1. december 2032

Studieafslutning (Anslået)

1. december 2032

Datoer for studieregistrering

Først indsendt

8. juni 2026

Først indsendt, der opfyldte QC-kriterier

8. juni 2026

Først opslået (Faktiske)

11. juni 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

15. juni 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

12. juni 2026

Sidst verificeret

1. juni 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 .

Kliniske forsøg med Ikke-småcellet lungekræft

Kliniske forsøg med BL-B01D1

Abonner