
Release date: 2026-01-13 17:00:53 Article From: Lucius Laos Recommended: 83
Capivasertib in combination with fulvestrant can be used as a second-line or third-line treatment regimen for patients with metastatic breast cancer who are hormone receptor-positive, human epidermal growth factor receptor 2-negative, and harbor PIK3CA/AKT1 gene mutations or PTEN gene inactivation.
Capivasertib in combination with fulvestrant (Faslodex) is indicated for the treatment of adult patients with locally advanced or metastatic breast cancer who are hormone receptor-positive, human epidermal growth factor receptor 2-negative, and have at least one PIK3CA/AKT1/PTEN gene mutation confirmed by an FDA-approved test. This indication applies to patients whose disease has progressed after receiving at least one endocrine-based therapy in the metastatic setting, or who have experienced recurrence within 12 months or later after completion of adjuvant therapy.
Store this medication in its original packaging container, tightly close the bottle cap, and keep it out of the reach of children. Store at room temperature, away from excessive heat and moisture (do not store in the bathroom).
Keep all medications out of sight and reach of children, as many containers are not child-resistant. Always lock the safety cap. Store medications in a secure location that is both inaccessible and invisible to them.
Dispose of unused medications in a manner that is inaccessible to pets, children, and other individuals. Do not flush this medication down the toilet. Utilize a medication take-back program. Consult your pharmacist for information on medication take-back programs available in your community.
1. Keep all appointments with your doctor and laboratory. Your doctor will order certain laboratory tests before and during your treatment to monitor your body’s response to capivasertib.
2. Your doctor will order a laboratory test before you start treatment to determine if your cancer is suitable for treatment with capivasertib.
3. Do not share this medication with others. If you have any questions about prescription refills, consult your pharmacist.
4. Maintain a written list of all prescription and over-the-counter medications, vitamins, minerals, and dietary supplements you are taking. Bring this list with you every time you visit your doctor or are admitted to the hospital. You should carry this list with you at all times for emergencies.
On November 21, 2025, the U.S. Food and Drug Administration (FDA) approved the regimen of pembrolizu···【more】
Recommended:2622025-17-12
Lung cancer is the most rapidly increasing malignant tumor with the fastest increasing morbidity and···【more】
Recommended:4832024-09-07
On December 12, 2025, the U.S. Food and Drug Administration (FDA) approved niraparib in combination ···【more】
Recommended:2672025-15-12
The U.S. Food and Drug Administration (FDA) announced today that it has approved Omisirge (omidubice···【more】
Recommended:2772025-10-12
On December 4, 2025, the U.S. Food and Drug Administration (FDA) approved lisocabtagene maraleucel (···【more】
Recommended:2582025-08-12
On December 3, 2025, the U.S. Food and Drug Administration (FDA) granted full approval to pirtobruti···【more】
Recommended:3032025-04-12
Primary analysis data from the randomized, double-blind, placebo-controlled phase III HER2CLIMB-02 s···【more】
Recommended:2652025-01-12
The Cure SMA Foundation, a global leading non-profit organization dedicated to spinal muscular atrop···【more】
Recommended:2442025-27-11

Lucius Pharmaceutical Co., Ltd., was established in 2020 in Vientiane, the capital of Laos. It aims to offer safe, effective, and affordable medicines globally. With a factory spanning 25,000 square meters, the company manufactures 200+ generic drugs in diverse therapeutic fields.
Address:No.26 Thongmang village, Xaythany district, Vientiane Capital, Laos
E-mail:laoslucius@gmail.com
Whatsapp: