Clin2
NCT06607757Possibly a fitRecruiting

Capivasertib plus fulvestrant for high-risk lobular breast cancer

CCCA Assessed by Ki67 Drop Below <2.7% From Baseline

Treatments studied

Part of Cancer clinical trials.

This trial tests adding capivasertib to fulvestrant for women with a certain type of breast cancer (invasive lobular carcinoma) that is hormone-receptor positive and has a high risk of coming back. The treatment is given before surgery to see if it works better than fulvestrant alone.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 2
Enrollment
120 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You are a postmenopausal woman aged 18 or older.
  • You have been diagnosed with invasive lobular breast cancer (confirmed by a central lab) that has not been treated yet.
  • Your cancer is hormone-receptor positive (at least 10% cells positive) and HER2-negative.
  • Your cancer is high-risk, meaning it is either at least 2 cm in size or has spread to lymph nodes (confirmed by imaging or biopsy).
  • You have not had any prior treatment for this breast cancer (including hormone therapy, chemotherapy, or targeted therapy).
  • Your overall health is good (ECOG score 0 or 1) and your heart, blood, and organ function are within study limits.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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