- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT07753226
A Study of SI-B036 in Patients With Locally Advanced or Metastatic Breast Cancer and Other Solid Tumors
8. september 2026 oppdatert av: Sichuan Baili Pharmaceutical Co., Ltd.
A Phase I Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetic Characteristics and Preliminary Efficacy of SI-B036 Bispecific Antibody Injection in Patients With Locally Advanced or Metastatic Breast Cancer and Other Solid Tumors
This study is an open-label, multicenter, dose-escalation and expansion, non-randomized Phase I clinical study evaluating the safety, tolerability, pharmacokinetic characteristics and preliminary efficacy of SI-B036 bispecific antibody injection in patients with locally advanced or metastatic breast cancer and other solid tumors.
Studieoversikt
Detaljert beskrivelse
The study consists of two phases: a dose-escalation phase (Phase Ia) and an expansion phase (Phase Ib).
Studietype
Intervensjonell
Registrering (Antatt)
39
Fase
- Fase 1
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiekontakt
- Navn: Sa Xiao, PHD
- Telefonnummer: +8615013238943
- E-post: xiaosa@baili-pharm.com
Studiesteder
-
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Beijing Municipality
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Beijing, Beijing Municipality, Kina
- Rekruttering
- Cancer Hospital Chinese Academy of Medical Sciences
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Ta kontakt med:
- Binghe Xu
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-
Deltakelseskriterier
Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
- Voksen
- Eldre voksen
Tar imot friske frivillige
Nei
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 breast cancer and other solid tumors;
- Agree to provide archived tumor tissue specimens from the primary or metastatic site within 2 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 score of 0 or 1;
- Toxicity from prior antitumor therapy must 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 required criteria;
- 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 a negative serum pregnancy result, and they must be non-lactating; all enrolled patients (both males and females) must adopt adequate barrier contraceptive measures throughout the entire treatment period and for 6 months after treatment completion;
- The trial participant must be able and willing to comply with the protocol-specified visits, treatment plan, laboratory tests, and other study-related procedures.
Exclusion Criteria:
- Use of chemotherapy, biotherapy, immunotherapy, or similar treatments within 4 weeks or 5 half-lives prior to the first dose;
- Receipt of immunosuppressive drug therapy within 2 weeks 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;
- Prior experience of ≥ Grade 3 toxicity related to anti-angiogenic therapy during previous anti-angiogenic treatment;
- Diagnosis of another solid tumor within 5 years prior to the first dose;
- Unstable thrombotic events requiring therapeutic intervention within 6 months prior to the first dose;
- Poorly controlled hypertension;
- Diabetes mellitus with poor glycemic control;
- History of interstitial lung disease (ILD) requiring steroid therapy, or current ILD, or ≥ Grade 2 radiation pneumonitis;
- Concurrent pulmonary disease resulting in severe impairment of respiratory function;
- Active central nervous system metastases;
- History of allergy to recombinant humanized antibodies or human-mouse chimeric antibodies, or allergy to any excipient component of SI-B036;
- Prior organ transplantation or allogeneic hematopoietic stem cell transplantation;
- Positive for human immunodeficiency virus antibodies, active tuberculosis, active hepatitis B virus infection, or active hepatitis C virus infection;
- Active infection requiring systemic therapy within 4 weeks prior to the first dose of the study drug;
- Presence of pleural, abdominal, or pelvic effusion, or pericardial effusion requiring drainage and/or accompanied by symptoms within 4 weeks prior to the first dose of the study drug;
- Imaging findings suggesting tumor invasion or encasement of major thoracic blood vessels, pericardium, or heart;
- Trial participants with clinically significant bleeding or obvious bleeding tendency within 4 weeks prior to screening;
- History of fistula, gastrointestinal perforation, or intra-abdominal abscess within 6 months prior to the first dose;
- 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 participant unsuitable for participation in this clinical trial.
Studieplan
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: N/A
- Intervensjonsmodell: Enkeltgruppeoppdrag
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
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Eksperimentell: SI-B036
Participants receive SI-B036 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 by intravenous infusion for a cycle of 3 weeks.
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Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
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Fase Ia: Dosebegrensende toksisitet (DLT)
Tidsramme: Inntil 21 dager etter første dose
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DLT vurderes i henhold til NCI-CTCAE v5.0 i løpet av den første syklusen og definert som forekomst av noen av toksisitetene i DLT-definisjonen dersom etterforskeren vurderer det som mulig, sannsynlig eller definitivt relatert til studiemedikamentadministrasjon.
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Inntil 21 dager etter første dose
|
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Fase Ia: Maksimal tolerert dose (MTD)
Tidsramme: Inntil 21 dager etter første dose
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MTD er definert som det høyeste dosenivået der ikke mer enn 1 av 6 deltakere opplevde en DLT i løpet av den første syklusen.
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Inntil 21 dager etter første dose
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Phase Ib: 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 SI-B036.
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Up to approximately 24 months
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Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
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AUC0-t
Tidsramme: Opptil ca 24 måneder
|
AUC0-t er definert som areal under serumkonsentrasjon-tid-kurven fra tid 0 til tidspunktet for siste målbare konsentrasjon.
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Opptil ca 24 måneder
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Objektiv responsrate (ORR)
Tidsramme: Opptil ca 24 måneder
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Objektiv responsrate (ORR) er definert som antall CR og PR i behandlings- og kontrollgruppene delt på antallet av den gruppen i hele analysesettet (FAS).
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Opptil ca 24 måneder
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Disease Control Rate (DCR)
Tidsramme: Opptil ca 24 måneder
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Disease Control Rate (DCR): Prosentandel av alle randomiserte forsøkspersoner som vurderte den beste totale responsen (BOR) som fullstendig respons (CR), delvis respons (PR) og sykdomsstabilisering (SD) i henhold til RECIST 1.1-kriterier.
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Opptil ca 24 måneder
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Responsens varighet (DOR)
Tidsramme: Opptil omtrent 24 måneder
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Responsens varighet (DOR) er definert som perioden fra datoen da tumorrespons først blir registrert til datoen når objektiv tumorprogresjon først blir registrert eller dødsdatoen.
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Opptil omtrent 24 måneder
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Treatment-Emergent Adverse Event (TEAE)
Tidsramme: Up to approximately 24 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 SI-B036.
The type, frequency and severity of TEAE will be evaluated during the treatment of SI-B036.
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Up to approximately 24 months
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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-SI-B036 antibody (ADA) will be investigated.
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Up to approximately 24 months
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Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Samarbeidspartnere
Studierekorddatoer
Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.
Studer hoveddatoer
Studiestart (Faktiske)
18. august 2026
Primær fullføring (Antatt)
1. desember 2028
Studiet fullført (Antatt)
1. desember 2028
Datoer for studieregistrering
Først innsendt
4. august 2026
Først innsendt som oppfylte QC-kriteriene
4. august 2026
Først lagt ut (Faktiske)
7. august 2026
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
10. september 2026
Siste oppdatering sendt inn som oppfylte QC-kriteriene
8. september 2026
Sist bekreftet
1. september 2026
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- SI-B036-103
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Nei
Studerer et amerikansk FDA-regulert enhetsprodukt
Nei
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