Product image of LuciElace 345 mg (Elacestrant) 345mg supplied by GNH India

LuciElace 345 mg

Active Ingredient:
Elacestrant
Brand:
LuciElace 345 mg

LuciElace 345 mg (Elacestrant) 345mg

Elacestrant, the active ingredient in LuciElace 345 mg, is a selective estrogen receptor degrader (SERD) presented as a 345 mg tablet for oral use. It is indicated for the treatment of estrogen receptor-positive, HER2-negative advanced or metastatic breast cancer in postmenopausal women or adult men who have experienced disease progression following at least one line of endocrine therapy.

GNH India supplies LuciElace 345 mg as a licensed, GDP-compliant international pharmaceutical supplier serving oncology centres worldwide.

Strength

345mg

Pack Size

30s

Manufacturer / TM Owner

Lucius Pharmaceuticals

1
Pack/s
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Indications & Clinical Uses

LuciElace 345 mg is a hormone therapy used to treat estrogen receptor-positive breast cancer. It is specifically indicated for patients with advanced or metastatic breast cancer who have experienced disease progression after previous endocrine therapy.

  • Estrogen receptor-positive breast cancer: Treats advanced or metastatic breast cancer in postmenopausal women or adult men with ESR1 mutations.
  • HER2-negative breast cancer: Effective in patients whose cancer does not express the HER2 protein.
  • ESR1-mutated breast cancer: Targets cancer with specific mutations in the estrogen receptor gene.

How It Works

  • Elacestrant works by binding to estrogen receptors and promoting their degradation. This action inhibits the growth of estrogen-driven tumors by preventing estrogen from stimulating cancer cell proliferation. It is particularly effective in patients with ESR1 mutations, which are common in advanced breast cancer.

Side Effects

LuciElace 345 mg may cause various side effects, ranging from common to serious.

Common Side Effects

  • Nausea: Feeling sick to the stomach.
  • Fatigue: A feeling of tiredness or weakness.
  • Vomiting: Expelling stomach contents through the mouth.
  • Decreased appetite: A reduced desire to eat.
  • Constipation: Difficulty passing stools.
  • Hair loss: Thinning or loss of hair.
  • Diarrhea: Frequent, loose, or watery bowel movements.
  • Headache: Pain in the head.

Serious or Rare Side Effects

  • Liver toxicity: Damage to the liver, which can cause jaundice or abnormal liver function tests.
  • Bone fractures: Increased risk of bone breaks due to the medication's effects on bone density.
  • Allergic reactions: Severe allergic responses, including rash, itching, or difficulty breathing.

Precautions & Warnings

LuciElace 345 mg should be used with caution and under medical supervision. Important precautions include:

  • Pregnancy: Avoid use during pregnancy due to potential harm to the fetus.
  • Breastfeeding: Do not use while breastfeeding.
  • Hepatic impairment: Adjust dosage for patients with moderate hepatic impairment.
  • Drug interactions: Avoid concurrent use with strong CYP3A inducers or inhibitors.
  • Monitoring: Regularly monitor liver function and bone health during treatment.
  • Storage: Store at 20℃ to 25℃: Keep in a dry place and out of reach of children.

Avoid Interactions

LuciElace 345 mg may interact with other medications, which can affect its efficacy or increase the risk of side effects.

Major Interactions (Avoid)

  • Strong CYP3A inducers: Such as rifampin, which can decrease elacestrant levels.
  • Strong CYP3A inhibitors: Such as ketoconazole, which can increase elacestrant levels.
  • Hormonal therapies: Other estrogen receptor modulators or antagonists.

Moderate Interactions (Monitor Closely)

  • Moderate CYP3A inducers: Such as efavirenz, which may reduce elacestrant effectiveness.
  • Moderate CYP3A inhibitors: Such as fluconazole, which may increase elacestrant levels.
  • Herbal products: Such as St. John's Wort, which can affect drug metabolism.

Frequently Asked Questions

LuciElace 345 mg is used to treat estrogen receptor-positive, HER2-negative advanced or metastatic breast cancer in postmenopausal women or adult men who have experienced disease progression following at least one line of endocrine therapy. It is specifically indicated for patients with ESR1 mutations.

Elacestrant works by binding to estrogen receptors and promoting their degradation. This action inhibits the growth of estrogen-driven tumors by preventing estrogen from stimulating cancer cell proliferation. It is particularly effective in patients with ESR1 mutations, which are common in advanced breast cancer.

The recommended dosage of LuciElace 345 mg is one 345 mg tablet taken orally once daily with food. The prescriber will determine the appropriate dosage based on the patient's condition and response to treatment.

LuciElace 345 mg should not be used during pregnancy or breastfeeding. It is important to use effective birth control during treatment and for one week after the final dose. If pregnancy occurs during treatment, consult your doctor immediately.

To order LuciElace 345 mg from GNH India, submit an enquiry on the product page at gnhindia.com with the required quantity. GNH India supplies hospitals, pharmacies, and procurement teams across international markets. The team will ask you to confirm your trade or institutional credentials and will reply with pricing, availability, shipping, and the necessary import paperwork.

LuciElace 345 mg is a selective estrogen receptor degrader (SERD) specifically designed to treat estrogen receptor-positive, HER2-negative advanced or metastatic breast cancer with ESR1 mutations. It differs from other hormone therapies by targeting the estrogen receptor directly, leading to its degradation and inhibiting tumor growth.

LuciElace 345 mg should be stored at 20℃ to 25℃ in a dry place and kept out of reach of children. The tablets should be swallowed whole with water and not chewed, crushed, or split. If a dose is missed for more than 6 hours or vomiting occurs, skip the dose and take the next dose the following day at its regularly scheduled time.

The most serious risks associated with LuciElace 345 mg include liver toxicity, bone fractures, and severe allergic reactions. Regular monitoring of liver function and bone health is recommended during treatment. Patients should report any unusual symptoms to their doctor immediately.

LuciElace 345 mg should not be used by pregnant women, breastfeeding mothers, or individuals with severe hepatic impairment. It is also not recommended for patients who are allergic to elacestrant or any of the ingredients in the tablet. Always consult your doctor before starting any new medication.

LuciElace 345 mg may interact with other medications, particularly strong CYP3A inducers or inhibitors. It is important to inform your doctor about all prescription and nonprescription medications, vitamins, nutritional supplements, and herbal products you are taking before starting LuciElace 345 mg.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

References

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