A Study of BL-M08D in Patients With Locally Advanced or Metastatic Digestive Tract Tumors and Other Solid Tumors
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
Studieoversigt
Status
Status
Betingelser
Betingelser
Intervention / Behandling
Intervention / Behandling
Undersøgelsestype
Undersøgelsestype
Tilmelding (Anslået)
Tilmelding
Fase
Fase
- Fase 2
- Fase 1
Kontakter og lokationer
Studiekontakt
Studiekontakt
- Navn: Sa Xiao, PHD
- Telefonnummer: +8615013238943
- E-mail: xiaosa@baili-pharm.com
Studiesteder
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Beijing Municipality
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Beijing, Beijing Municipality, Kina
- Cancer Hospital Chinese Academy of Medical Sciences
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Kontakt:
- Jing Huang
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Deltagelseskriterier
Berettigelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Beskrivelse
Inclusion Criteria:
- Voluntarily sign the informed consent form and comply with the protocol requirements;
- No gender restriction;
- Age: ≥18 years and ≤75 years;
- Expected survival time ≥3 months;
- Locally advanced or metastatic gastrointestinal tumors and other solid tumors;
- Agree to provide archival tumor tissue specimens from the primary or metastatic site 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, with no deterioration within 2 weeks prior to the first dose;
- 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 ≥50%;
- Organ function levels must meet the requirements;
- Coagulation function: international normalized ratio ≤1.5, and activated partial thromboplastin time ≤1.5 × upper limit of normal;
- Urine protein ≤1+ or ≤1000 mg/24 h;
- 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;
- 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:
- Use of chemotherapy, biological therapy, immunotherapy, etc., within 4 weeks or 5 half-lives prior to the first dose;
- History of severe cardiac or cerebrovascular disease;
- Prolonged QTc interval, complete left bundle branch block, third-degree atrioventricular block, or frequent and uncontrolled arrhythmias;
- Active autoimmune diseases and inflammatory diseases;
- Diagnosis of another malignant tumor within 5 years prior to the first dose;
- Unstable thrombotic events requiring therapeutic intervention within 6 months prior to the first dose;
- Hypertension inadequately controlled by antihypertensive medication;
- Poorly controlled blood glucose;
- History of interstitial lung disease requiring hormone therapy, or current ILD, or radiation pneumonitis of Grade ≥2;
- Severe impairment of respiratory function;
- Active central nervous system metastases;
- Previous or concurrent central nervous system disorders;
- History of allergy to recombinant humanized antibodies or human-mouse chimeric antibodies, or allergy to any excipient component of BL-M08D1;
- Previous organ transplantation or allogeneic hematopoietic stem cell transplantation;
- Positive for human immunodeficiency virus antibody, active tuberculosis, active hepatitis B virus infection, or active hepatitis C virus infection;
- Active infection requiring systemic treatment within 4 weeks prior to the first study drug administration;
- Pleural, abdominal, or pericardial effusion requiring drainage and/or accompanied by symptoms within 4 weeks prior to the first study drug administration;
- Imaging findings indicating tumor invasion or encasement of abdominal, thoracic, cervical, or other regions;
- Use of another investigational drug within 4 weeks or 5 half-lives prior to the first dose;
- Pregnant or breastfeeding women;
- Other conditions deemed by the investigator to make the patient unsuitable for participation in this clinical trial.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: N/A
- Interventionel model: Enkelt gruppeopgave
- Maskning: Ingen (Åben etiket)
Antal våben
Våben og indgreb
Deltagergruppe / ArmDeltagergruppe / Arm |
Intervention / BehandlingIntervention / Behandling |
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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.
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Administration ved intravenøs infusion i en cyklus på 3 uger.
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Hvad måler undersøgelsen?
Primære resultatmål
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Objektiv responsrate (ORR)
Tidsramme: Op til cirka 24 måneder
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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.
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Op til cirka 24 måneder
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Recommended Phase II Dose (RP2D)
Tidsramme: Up to approximately 24 months
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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.
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Up to approximately 24 months
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Sekundære resultatmål
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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AUC0-t
Tidsramme: Op til cirka 24 måneder
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AUC0-t er defineret som areal under serumkoncentration-tid-kurven fra tidspunkt 0 til tidspunktet for den sidste målelige koncentration.
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Op til cirka 24 måneder
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Disease Control Rate (DCR)
Tidsramme: Op til cirka 24 måneder
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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.
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Op til cirka 24 måneder
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Treatment-Emergent Adverse Event (TEAE)
Tidsramme: Op til cirka 24 måneder
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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.
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Op til cirka 24 måneder
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Responsens varighed (DOR)
Tidsramme: Op til cirka 24 måneder
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Responsens varighed (DOR) er defineret som perioden fra den dato, hvor tumorrespons først registreres til den dato, hvor objektiv tumorprogression først registreres eller dødsdatoen.
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Op til cirka 24 måneder
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Cmax
Tidsramme: Up to approximately 24 months
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Cmax is defined as the maximum observed drug concentration in plasma after administration.
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Up to approximately 24 months
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Tmax
Tidsramme: Up to approximately 24 months
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Tmax is defined as the time required to reach the maximum drug concentration in plasma following drug administration.
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Up to approximately 24 months
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T1/2
Tidsramme: Up to approximately 24 months
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T1/2 is defined as the time required for the plasma concentration of a drug to decrease by 50% during the elimination phase.
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Up to approximately 24 months
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CL (Clearance)
Tidsramme: Up to approximately 24 months
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Clearance (CL) is the volume of plasma from which a drug is completely removed per unit time.
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Up to approximately 24 months
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Ctrough
Tidsramme: Up to approximately 24 months
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Ctrough is defined as the lowest serum concentration prior to the next dose will be administered.
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Up to approximately 24 months
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Progression-free Survival (PFS)
Tidsramme: Up to approximately 24 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 24 months
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Anti-drug Antibody (ADA)
Tidsramme: Up to approximately 24 months
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Frequency of anti-BL-M08D1 antibody (ADA) will be investigated.
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Up to approximately 24 months
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Samarbejdspartnere og efterforskere
Sponsor
Sponsor
Samarbejdspartnere
Samarbejdspartnere
Datoer for undersøgelser
Studer store datoer
Studiestart (Anslået)
Studiestart
Primær færdiggørelse (Anslået)
Primær færdiggørelse
Studieafslutning (Anslået)
Studieafslutning
Datoer for studieregistrering
Først indsendt
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Først opslået
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering sendt
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
Andre undersøgelses-id-numre
- BL-M08D1-202
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
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