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Clinical Trial Active — Not Recruiting Phase II NCT04920708

Fulvestrant, Ipatasertib and CDK4/6 Inhibition in Metastatic ER+/HER2- Breast Cancer Patients Without ctDNA Suppression

Fulvestrant, Ipatasertib and CDK4/6 Inhibition in Metastatic ER+/HER2- Breast Cancer Patients Without ctDNA Suppression — Active Not Recruiting • Phase II • Oncology • NCT04920708.

📅 14 Apr 2026 ⏱ 1 min read
Active — Not Recruiting
Check the registry for current status and eligibility criteria.
Status
Active — Not Recruiting
Phase
Phase II
NCT ID
NCT04920708
Start
2022-12-28
Completion
2027-06
ClinicaliQ Trial Snapshot
  • Fulvestrant, Ipatasertib and CDK4/6 Inhibition in Metastatic ER+/HER2- Breast Cancer Patients Without ctDNA Suppression — Active Not Recruiting • Phase II • Oncology • NCT04920708.
  • FAIM Trial Summary.
  • Adding ipatasertib to fulvestrant and palbociclib may improve survival in advanced hormone-receptor positive breast cancer patients without early treatment response.

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What This Trial Is Studying

Analysis of circulating tumour DNA (ctDNA) found in a patient's peripheral blood can identify cancer progression and predict a patient's response to therapy. By using ctDNA analysis and imaging techniques, the FAIM trial aims to determine whether the addition of the experimental drug ipatasertib to a standard combination of the hormone treatment fulvestrant and the targeted agent palbociclib increases progression free survival (PFS) for patients with hormone-receptor positive and human epidermal growth factor receptor 2 negative (HR+/HER2-) breast cancer. Conditions: Metastatic Breast Cancer, ER+ Breast Cancer, Advanced Breast Cancer Interventions:…

Full Trial Details
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Eligibility criteria, protocol, and results when available
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