- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT07591090
A Phase II Study of AK146D1 Combined With AK112 in Advanced Breast Cancer
21. juli 2026 oppdatert av: Akeso
A Phase II Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Anti-tumor Efficacy of AK146D1 Combined With AK112 in Patients With Advanced Breast Cancer
This is a Phase II clinical study aimed at evaluating the safety, tolerability, antitumor efficacy, PK and immunogenicity of AK146D1 combined with AK112 in advanced breast cancer.
Studieoversikt
Status
Rekruttering
Forhold
Intervensjon / Behandling
Studietype
Intervensjonell
Registrering (Antatt)
200
Fase
- Fase 2
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiekontakt
- Navn: Ting Liu
- Telefonnummer: +86(0760)8987 3999
- E-post: clinicaltrials@akesobio.com
Studer Kontakt Backup
- Navn: Zhimin Shao, Study Principal Investigator
Studiesteder
-
-
Shanghai Municipality
-
Shanghai, Shanghai Municipality, Kina
- Rekruttering
- Fudan University Shanghai Cancer Center
-
Ta kontakt med:
- Zhimin Shao
- Telefonnummer: +86 021-64175590
- E-post: szmgcp2016@163.com
-
-
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:
- Be able to understand and voluntarily sign the written informed consent form.
- Aged of ≥ 18 years and ≤75 years.
- ECOG PS 0 or 1.
- The expected lifespan is ≥3 months.
- Patients with histologically confirmed locally advanced, recurrent, or metastatic breast cancer who are not eligible for curative surgical resection; and who have histologically or cytologically confirmed HER2-negative disease.
- At least one measurable lesion according to RECIST v1.1. Patients with only bone lesions or cutaneous lesions are not ineligible for enrollment.
- Have sufficient organ function.
- Females patients must not be pregnant at screening or have evidence of non-childbearing potential. Agree to use medically accepted methods of contraception.
Exclusion Criteria:
- Patients had breast cancer amenable to curative treatment at study enrollment.
- Concurrent other histopathological types confirmed by tumor histology or cytology.
- Having other active malignancies within 3 years.
- Currently participating in another interventional clinical study.
- Presence of active metastases to the central nervous system. For patients with asymptomatic brain metastasis or stable symptoms after treatment can be included.
- Prior treatment with any therapy targeting Trop-2 or Nectin-4, or any chemotherapy agent targeting topoisomerase I.
- Receipt of systemic anti-tumor therapy (including chemotherapy, immunotherapy, biological agents, etc.) within 4 weeks prior to the first dose.
- Toxicity of previous antineoplastic therapy has not resolved to NCI CTCAE 6.0 grade 1 or lower.
- Patients with clinically significant cardiovascular or cerebrovascular diseases or risks.
- Patients with active autoimmune diseases requiring systemic treatment within 2 years.
- Receipt of systemic anti-infective therapy within 2 weeks prior to the first dose.
- Known to be positive for HIV and other infections.
- Previous history of severe hypersensitivity reactions.
- Live attenuated vaccines were received within 4 weeks.
- Patients with a history of mental illness and incapacitated or limited capacity.
- Any disease or condition that, in the opinion of the investigator, would compromise patient safety or interfere with study assessments.
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: Ikke-randomisert
- Intervensjonsmodell: Sekvensiell tildeling
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Eksperimentell: Arm A
Participants in this group will receive AK146D1 combined with AK112 as i.v.
infusion.
|
AK146D1 for injection is an anti-Trop2/Nectin4 bispecific antibody-drug conjugate.
AK112 Injection is a PD-1/VEGF bispecific antibody.
|
|
Eksperimentell: Arm B
Participants in this group will receive AK146D1 as i.v.
infusion.
|
AK146D1 for injection is an anti-Trop2/Nectin4 bispecific antibody-drug conjugate.
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Antall deltakere med bivirkninger (AES)
Tidsramme: Fra tidspunktet for signering av informert samtykkeskjema gjennom 30 dager (for AES) eller 90 dager (for SAE) etter den siste dosen av studiemedisinen.
|
AE -er refererer til enhver uhyggelig medisinsk forekomst eller forverring av eksisterende medisinske hendelser etter at deltakerne har signert ICF -ene, enten de anses som relatert til studiebehandlingen.
|
Fra tidspunktet for signering av informert samtykkeskjema gjennom 30 dager (for AES) eller 90 dager (for SAE) etter den siste dosen av studiemedisinen.
|
|
Number of participants with dose limiting toxicities (DLTs)
Tidsramme: During the first 3 weeks of treatment in Safety Run-in Phase.
|
DLTs are defined as toxicities that meet pre-defined severity criteria, and assessed as having a suspected relationship to study drug.
|
During the first 3 weeks of treatment in Safety Run-in Phase.
|
|
Objective Response Rate (ORR) assessed by investigator per RECIST v1.1
Tidsramme: Up to approximately 2 years.
|
ORR is the proportion of participants with complete response(CR) or partial response(PR) , assessed based on RECIST v1.1.
|
Up to approximately 2 years.
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Progression Free Survival (PFS) assessed by investigator per RECIST v1.1
Tidsramme: Up to approximately 2 years.
|
PFS is defined as the time from the start of treatment until the first documentation of disease progression (based on RECIST Version 1.1) or death due to any cause, whichever occurs first.
|
Up to approximately 2 years.
|
|
Disease Control Rate (DCR) assessed per RECIST v1.1
Tidsramme: Up to approximately 2 years.
|
DCR is defined as the proportion of participants with CR, PR, or SD, assessed based on RECIST v1.1.
|
Up to approximately 2 years.
|
|
Duration of response (DoR) assessed by the investigator per RECIST v1.1
Tidsramme: Up to approximately 2 years.
|
DoR is defined as the duration from the first documentation of objective response to the first documented disease progression (based on RECIST Version 1.1) or death due to any cause, whichever occurs first.
|
Up to approximately 2 years.
|
|
Time to response (TTR) assessed by the investigator per RECIST v1.1
Tidsramme: Up to approximately 2 years.
|
TTR is defined as the time to objective response based on RECIST v1.1.
|
Up to approximately 2 years.
|
|
Overall survival (OS)
Tidsramme: Up to approximately 2 years.
|
OS is defined as the time from the first dose to death from any cause.
|
Up to approximately 2 years.
|
|
Serum PK concentration of AK146D1 and AK112
Tidsramme: From pre-dose to the end of the last dose, an average of 6 months.
|
Serum PK concentration of AK146D1 and AK112 in participants after administration.
|
From pre-dose to the end of the last dose, an average of 6 months.
|
|
Anti-drug antibodies (ADA)
Tidsramme: From pre-dose to 30 days post end of treatment.
|
The number and percentage of participants with detectable anti-drug antibodies (ADA)
|
From pre-dose to 30 days post end of treatment.
|
Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Sponsor
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)
17. juli 2026
Primær fullføring (Antatt)
1. september 2027
Studiet fullført (Antatt)
4. februar 2029
Datoer for studieregistrering
Først innsendt
9. mai 2026
Først innsendt som oppfylte QC-kriteriene
9. mai 2026
Først lagt ut (Faktiske)
15. mai 2026
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
22. juli 2026
Siste oppdatering sendt inn som oppfylte QC-kriteriene
21. juli 2026
Sist bekreftet
1. juli 2026
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- AK146D1-202
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Nei
Studerer et amerikansk FDA-regulert enhetsprodukt
Nei
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