- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT07654400
A Study of BL-M14D1 in Combination With Atezolizumab in Patients With Extensive-stage Small Cell Lung Cancer
24 augusti 2026 uppdaterad av: 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.
Studieöversikt
Status
Rekrytering
Betingelser
Intervention / Behandling
Studietyp
Interventionell
Inskrivning (Beräknad)
36
Fas
- Fas 2
Kontakter och platser
Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.
Studiekontakt
- Namn: Sa Xiao, PHD
- Telefonnummer: 15013238943
- E-post: xiaosa@baili-pharm.com
Studieorter
-
-
Shanghai Municipality
-
Shanghai, Shanghai Municipality, Kina
- Rekrytering
- Shanghai East Hospital
-
Kontakt:
- Caicun Zhou
-
-
Deltagandekriterier
Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.
Urvalskriterier
Åldrar som är berättigade till studier
- Vuxen
- Äldre vuxen
Tar emot friska volontärer
Nej
Beskrivning
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.
Studieplan
Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Behandling
- Tilldelning: N/A
- Interventionsmodell: Enskild gruppuppgift
- Maskning: Ingen (Open Label)
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
|
Experimentell: 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.
|
Administrering genom intravenös infusion under en cykel på 3 veckor.
Administration by intravenous infusion for a cycle of 3 weeks.
|
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Objective Response Rate (ORR)
Tidsram: 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)
Tidsram: 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
|
Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Progression-free survival (PFS)
Tidsram: 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)
Tidsram: 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)
Tidsram: 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)
Tidsram: 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
Tidsram: Up to approximately 12 months
|
Maximum serum concentration (Cmax) of BL-M14D1 will be investigated.
|
Up to approximately 12 months
|
|
Tmax
Tidsram: Up to approximately 12 months
|
Time to maximum serum concentration (Tmax) of BL-M14D1 will be investigated.
|
Up to approximately 12 months
|
|
Ctrough
Tidsram: 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)
Tidsram: Up to approximately 12 months
|
Frequency of anti-BL-M14D1 antibody (ADA) will be investigated.
|
Up to approximately 12 months
|
Samarbetspartners och utredare
Det är här du hittar personer och organisationer som är involverade i denna studie.
Samarbetspartners
Studieavstämningsdatum
Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.
Studera stora datum
Studiestart (Faktisk)
9 juli 2026
Primärt slutförande (Beräknad)
1 december 2027
Avslutad studie (Beräknad)
1 december 2027
Studieregistreringsdatum
Först inskickad
12 juni 2026
Först inskickad som uppfyllde QC-kriterierna
12 juni 2026
Första postat (Faktisk)
17 juni 2026
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
25 augusti 2026
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
24 augusti 2026
Senast verifierad
1 augusti 2026
Mer information
Termer relaterade till denna studie
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- BL-M14D1-201
Läkemedels- och apparatinformation, studiedokument
Studerar en amerikansk FDA-reglerad läkemedelsprodukt
Nej
Studerar en amerikansk FDA-reglerad produktprodukt
Nej
Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .