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Elacestrant(Orserdu)

Names
Orserdu,Elacestrant,艾拉司群,依拉司群
Indicatons
Advanced or metastatic breast cancer that is ER-positive, HER2-negative, and has ESR1 mutations.
Price:
Manufacturer:
Stemline
Dosage form:
TABLET
Validity period:
24 months

Reminder: The outer packaging is for reference only, please purchase and use under the guidance of a pharmacist. For read by medical and pharmaceutical professionals only.

Orserdu(Elacestrant) Instructions:Uses,Dosage, Side Effects

ORSERDU™ (Elacestrant) is a targeted therapy designed for the treatment of ER-positive, HER2-negative, ESR1-mutated advanced or metastatic breast cancer. This medication works by inhibiting the estrogen receptor, which is a key driver of cancer cell growth. It is particularly useful for patients who have not responded well to previous endocrine therapies. The drug is available in oral tablet form and is typically administered once daily with food.

ORSERDU™ has been approved for use in postmenopausal women and adult men. However, careful monitoring is required during treatment due to potential side effects such as liver toxicity and dyslipidemia. It is essential to assess liver function regularly and to adjust doses based on the severity of side effects or drug interactions.

Generic name
Elacestrant(Orserdu)
English name
Elacestrant
Alternative Names
Orserdu,Elacestrant,艾拉司群,依拉司群
Drug prices
Indications

Treatment of postmenopausal women or adult men with estrogen receptor (ER)-positive, HER2-negative, ESR1-mutated advanced or metastatic breast cancer following disease progression after ≥1 line of endocrine therapy.

Therapeutic Target
Estrogen receptor-alpha (ERα). Elacestrant binds to ERα, induces receptor degradation via the proteasomal pathway, and inhibits estrogen-dependent tumor proliferation.
Active Ingredients
Elacestrant hydrochloride (equivalent to 345 mg or 86 mg elacestrant free base per tablet).
Dosage Form
TABLET
Specifications
345mg*30tablets/bottle
Dosage and Administration

Recommended dose: 345 mg orally once daily with food.

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