A Study to Learn About the Study Medicine PF-07220060 Together With Letrozole Compared to Letrozole Alone in Women Post Menopause
第2相
完了
NCT06465368
| 対象疾患 | Breast Cancer |
|---|
| 相 | 第2相 |
|---|
| スポンサー | Pfizer |
|---|
| ステータス | 完了 |
|---|
| 参加者数 | 121 名 |
|---|
| 介入(薬剤) | PF-07220060, letrozole |
|---|
| 開始日 | 2024年7月11日 |
|---|
| 完了日 | 2025年7月10日 |
|---|
| 結果公開日 | 2026年7月15日 |
|---|
概要
The purpose of this study is to learn about the effects of the study medicine PF-07220060 plus letrozole, compared with the effects of taking letrozole alone without PF-07220060 for treatment of breast cancer. This study is seeking for participants who are: * women of age 18 years and older post menopause (either naturally or surgically). * confirmed to have Hormone receptor (HR) positive, Human epidermal growth factor receptor 2 (HER2) negative breast cancer. HER2 negative describes cells that have a small amount or none of a protein called HER2 on their surface. In normal cells, HER2 helps control cell growth. Cancer cells that are HER2 negative may grow more slowly and are less likely to recur (come back) or spread to other parts of the body than cancer cells that have a large amount of HER2 on their surface. * not been treated for their cancer before this study. Participants will be randomly assigned (like flipping a coin) to receive the treatment (PF-07220060 plus letrozole) or letrozole alone. Both PF-07220060 and letrozole are taken by mouth. PF-07220060 will be taken twice a day for 14 days. Letrozole will be taken once a day for 14 days. Participants will have a screening
Percentage of Participants With Complete Cell Cycle Arrest (CCCA) at Day 14
Day 14 · Percentage of participants
| PF-07220060 + Letrozole | 88.2 Percentage of participants |
|---|
| Letrozole Alone | 17.9 Percentage of participants |
|---|
BENITIONS で見る
ClinicalTrials.gov の原文を見る
すべての治験
このページは ClinicalTrials.gov の公開データをまとめたものです。医学的助言ではなく、投資助言でもありません。必ず専門医にご相談ください。