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Efficacy and Safety of Utidelone Capsule and Utidelone Injection in Patients With HER-2 Negative Advanced Breast Cancer

29. juni 2026 oppdatert av: Beijing Biostar Pharmaceuticals Co., Ltd.

A Randomized,Controlled Phase III Study on Efficacy and Safety of Utidelone Capsule and Utidelone Injection in Patients With HER-2 Negative Advanced Breast Cancer

This study is a randomized controlled study.The primary objective is to evaluate the Progression-Free Survival(PFS) of Utidelone Capsule combined with Capecitabine compared with Utidelone Injection combined with Capecitabine in patients with HER-2 negative advanced breast cancer.

Studieoversikt

Studietype

Intervensjonell

Registrering (Antatt)

308

Fase

  • Fase 3

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

Studiesteder

      • Beijing, Kina
        • Cancer Hospital Chinese Academy of Medical Sciences
        • Ta kontakt med:
          • Binghe Xu

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:

  1. Patients who have fully understood the objectives, content, process of the study and possible adverse events, voluntarily serves as a subject and signs the informed consent form.
  2. Subjects aged ≥18 and ≤75.
  3. Male or female subjects with ECOG performance status scored 0-1.
  4. Patients who were diagnosed with HER-2 negative advanced breast cancer by histopathology.
  5. Patients with locally advanced,recurrent,or metastatic breast cancer.
  6. Patients who had received chemotherapy regimens, including at least one taxanes or anthracyclines.
  7. Patients with hormone receptor positive should have disease progression after endocrine therapy.
  8. At least one measurable lesion present according to RECIST 1.1 criteria.
  9. Expected survival time ≥ 12 weeks
  10. Baseline routine blood tests is normal.
  11. Liver and kidney function test results are normal.
  12. Fertile males and females of childbearing potential must agree to use effective contraception (so do their partners, using hormonal or barrier contraception, or abstinence) during the study and within at least 6 months after the last dose. The blood or urine pregnancy test for female patients of childbearing potential prior to enrollment must be negative.

Exclusion Criteria:

  1. Patients who have received non-investigational anti-tumor therapies within 4 weeks prior to study drug administration.
  2. Patients who have used Capecitabine or Utidelone within 6 months prior to randomization.
  3. Patients with breast cancer with CNS metastases leptomeningeal metastases.
  4. Patients with uncontrollable bone metastases,existing or recent risk of fracture, recent need for surgery or local radiotherapy, or other critical conditions.
  5. Patients with uncontrollable pleural effusion,pericardial effusion or ascites requiring repeated drainage(once a month or more)
  6. Patients with serious cardiovascular disease.
  7. Patients with mental illnesses which are hard to control, patients who lack legal capacity or have limited legal capacity.
  8. Patients with gastrointestinal disorders affecting oral administration.
  9. Patients with active infections and need systemic therapy currently.
  10. Patients with peripheral neuropathy grade≥2 during randomization.
  11. Patients with toxicity grade ≥2 which caused by prior anti-tumor therapy.(NCI-CTCAE 5.0,except for what is considered no safety risk such as alopecia by investigator.)
  12. Patients who have received any major surgery(except for diagnostic procedures such as biopsy),or have sustained major trauma within 4 weeks to randomization;or is expected to undergo major surgery during the treatment.
  13. Patients who have received radiotherapy within 2 weeks to randomization.
  14. Patients who have received interventional therapy in another clinical trail or have received other investigational treatments.
  15. Patients with other malignant tumor within 5 years to randomization excluding curatively treated cervical carcinoma in situ, cutaneous basal cell carcinoma or squamous cell carcinoma, and papillary thyroid carcinoma.
  16. Patients with allergy of caster oil:patients with previous fluorouracil medication history with severe allergy or known dihydropyrimidine dehydrogenase (DPD) deficiency;
  17. Pregnant or lactating patients.
  18. Patients who, in the opinion of the investigator, are not suitable to participate in this study.

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: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: Utidelone Capsule combined with Capecitabine
Utidelone Capsule: 60 mg/m2/d, administered once a day orally continuously for 5 days from day 1 to day 5, with a treatment cycle of 21 days.
Capecitabine: 1000mg/m2, twice a day continuously for 14 days from day 1 to day 14, with a 21 day treatment cycle.
Aktiv komparator: Utidelone Injection combined with Capecitabine
Capecitabine: 1000mg/m2, twice a day continuously for 14 days from day 1 to day 14, with a 21 day treatment cycle.
Utidelone Injection:30 mg/m2/d, administered once a day intravenously, continuously for 5 days from day 1 to day 5, with a treatment cycle of 21 days.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Progression-Free Survival
Tidsramme: 6 weeks
To evaluate the Progression-Free Survival (PFS) of Utidelone capsules combined with Capecitabine compared with Utidelone Injection combined with Capecitabine
6 weeks

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Behandlingsrelatert bivirkning-TRAE
Tidsramme: 12 måneder
Antall deltakere med behandlingsrelaterte bivirkninger som vurdert av CTCAE v5.0
12 måneder
Objective Response Rate
Tidsramme: 6 weeks
The percentage of patients who have a partial response or complete response to the treatment.
6 weeks
Disease Control Rate
Tidsramme: 6 weeks
The proportion of patients who achieve a complete response , partial response , or stable disease as their best overall response.
6 weeks
Duration of Response
Tidsramme: 6 weeks
The time from the first documented objective response to the first documented disease progression or death from any cause, whichever occurs first.
6 weeks
Time to Treatment Failure
Tidsramme: 3 weeks
The time from randomization to discontinuation of treatment due to any cause
3 weeks
Median treatment cycle
Tidsramme: 12 months
Median number of actual treatment cycles completed by patients
12 months

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

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 (Antatt)

1. august 2026

Primær fullføring (Antatt)

1. mars 2028

Studiet fullført (Antatt)

1. mars 2029

Datoer for studieregistrering

Først innsendt

29. juni 2026

Først innsendt som oppfylte QC-kriteriene

29. juni 2026

Først lagt ut (Faktiske)

6. juli 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

6. juli 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

29. juni 2026

Sist bekreftet

1. juni 2026

Mer informasjon

Begreper knyttet til denne studien

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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