- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT07654400
A Study of BL-M14D1 in Combination With Atezolizumab in Patients With Extensive-stage Small Cell Lung Cancer
12 giugno 2026 aggiornato da: 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.
Panoramica dello studio
Stato
Non ancora reclutamento
Intervento / Trattamento
Tipo di studio
Interventistico
Iscrizione (Stimato)
36
Fase
- Fase 2
Contatti e Sedi
Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.
Contatto studio
- Nome: Sa Xiao, PHD
- Numero di telefono: 15013238943
- Email: xiaosa@baili-pharm.com
Luoghi di studio
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Shanghai Municipality
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Shanghai, Shanghai Municipality, Cina
- Shanghai East Hospital
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Contatto:
- Caicun Zhou
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Criteri di partecipazione
I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.
Criteri di ammissibilità
Età idonea allo studio
- Adulto
- Adulto più anziano
Accetta volontari sani
No
Descrizione
Inclusion Criteria:
- Voluntarily sign the informed consent form and comply with the protocol requirements;
- No gender restriction;
- Age: ≥18 years;
- Expected survival time ≥3 months;
- Histopathologically and/or cytologically confirmed extensive-stage small cell lung cancer that is incurable or for which there is currently no standard treatment;
- Agree to provide archived tumor tissue specimens from the primary or metastatic lesion within 3 years, or fresh tissue samples;
- Must have at least one measurable lesion as defined by RECIST v1.1;
- Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1;
- Toxicities from prior anti-tumor therapy have recovered to ≤ Grade 1 as defined by NCI-CTCAE v6.0;
- No severe cardiac dysfunction, with left ventricular ejection fraction (LVEF) ≥50%;
- Organ function levels must meet the required criteria;
- Urine protein ≤1+ or ≤1000 mg/24h;
- 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:
- Use of chemotherapy, biological therapy, immunotherapy, etc., within 4 weeks or 5 half-lives before the first dose;
- Previous treatment with ADC drugs using topoisomerase I inhibitors as toxins;
- Small cell carcinoma with non-small cell carcinoma components indicated by pathology must be excluded;
- Use of immunomodulatory drugs within 2 weeks before the first dose of the study;
- Receiving long-term systemic corticosteroid therapy at a dose >10 mg/day of prednisone or equivalent before the first dose;
- History of severe cardiovascular or cerebrovascular diseases;
- Prolonged QTc interval, complete left bundle branch block, etc.;
- Active autoimmune diseases and inflammatory diseases;
- Diagnosis of another malignancy within 5 years before the first dose;
- Hypertension poorly controlled by two antihypertensive drugs;
- Patients with poorly controlled blood glucose;
- History of ILD/interstitial pneumonia treated with corticosteroids, etc.;
- Concomitant pulmonary diseases leading to clinically severe impairment of respiratory function;
- Presence of massive serous cavity effusion, or serous cavity effusion with symptoms, etc.;
- Imaging findings indicating that the tumor has invaded or encased major blood vessels in the chest, neck, pharynx, etc.;
- Any thrombotic event within 6 months before randomization;
- Patients with active central nervous system metastases;
- History of allergy to recombinant humanized antibodies or chimeric human-mouse antibodies, or allergy to any excipient components of the investigational drug, etc.;
- Previous organ transplantation or allogeneic hematopoietic stem cell transplantation;
- Cumulative anthracycline dose >360 mg/m² during prior (neo)adjuvant anthracycline therapy;
- Positive for human immunodeficiency virus antibody, active tuberculosis, active hepatitis B virus infection, or active hepatitis C virus infection;
- Active infections requiring systemic treatment, or occurrence of severe infection within 4 weeks before informed consent;
- Receipt of other unapproved clinical study drugs or treatments within 4 weeks before the first dose;
- Pregnant or breastfeeding women;
- History of severe neurological or psychiatric disorders;
- Presence of serious non-healing wounds, ulcers, or fractures within 4 weeks before signing informed consent;
- Clinically significant bleeding or obvious bleeding tendency within 4 weeks before signing informed consent;
- History of intestinal obstruction, inflammatory bowel disease, extensive bowel resection, or presence of Crohn's disease, ulcerative colitis, or chronic diarrhea;
- Trial participants who plan to receive or have received live vaccines within 28 days before the first dose;
- Other conditions deemed by the investigator to be unsuitable for participation in this clinical trial.
Piano di studio
Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: N / A
- Modello interventistico: Assegnazione di gruppo singolo
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
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Sperimentale: 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.
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Somministrazione mediante infusione endovenosa per un ciclo di 3 settimane.
Administration by intravenous infusion for a cycle of 3 weeks.
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Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Objective Response Rate (ORR)
Lasso di tempo: Up to approximately 12 months
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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.
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Up to approximately 12 months
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Treatment-Emergent Adverse Event (TEAE)
Lasso di tempo: Up to approximately 12 months
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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.
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Up to approximately 12 months
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Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Progression-free survival (PFS)
Lasso di tempo: Up to approximately 12 months
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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.
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Up to approximately 12 months
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Disease Control Rate (DCR)
Lasso di tempo: Up to approximately 12 months
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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]).
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Up to approximately 12 months
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Duration of Response (DOR)
Lasso di tempo: Up to approximately 12 months
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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.
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Up to approximately 12 months
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Overall Survival (OS)
Lasso di tempo: Up to approximately 12 months
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Overall survival (OS) is defined as the time between the day the subject is randomized and the subject's death.
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Up to approximately 12 months
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Cmax
Lasso di tempo: Up to approximately 12 months
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Maximum serum concentration (Cmax) of BL-M14D1 will be investigated.
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Up to approximately 12 months
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Tmax
Lasso di tempo: Up to approximately 12 months
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Time to maximum serum concentration (Tmax) of BL-M14D1 will be investigated.
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Up to approximately 12 months
|
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Ctrough
Lasso di tempo: Up to approximately 12 months
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Ctrough is defined as the lowest serum concentration of BL-M14D1 prior to the next dose will be administered.
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Up to approximately 12 months
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ADA (anti-drug antibody)
Lasso di tempo: Up to approximately 12 months
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Frequency of anti-BL-M14D1 antibody (ADA) will be investigated.
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Up to approximately 12 months
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Collaboratori e investigatori
Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.
Collaboratori
Studiare le date dei record
Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.
Studia le date principali
Inizio studio (Stimato)
1 luglio 2026
Completamento primario (Stimato)
1 dicembre 2027
Completamento dello studio (Stimato)
1 dicembre 2027
Date di iscrizione allo studio
Primo inviato
12 giugno 2026
Primo inviato che soddisfa i criteri di controllo qualità
12 giugno 2026
Primo Inserito (Effettivo)
17 giugno 2026
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
17 giugno 2026
Ultimo aggiornamento inviato che soddisfa i criteri QC
12 giugno 2026
Ultimo verificato
1 giugno 2026
Maggiori informazioni
Termini relativi a questo studio
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
- BL-M14D1-201
Informazioni su farmaci e dispositivi, documenti di studio
Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti
No
Studia un dispositivo regolamentato dalla FDA degli Stati Uniti
No
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .
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