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Duvyzat(Givinostat)

Names
吉维司他
Indicatons
Male patients aged 6 years and older with genetically confirmed DMD.
Price:
Manufacturer:
ITALFARMACO SPA
Dosage form:
SUSPENSION
Validity period:

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.

Duvyzat(Givinostat) Instructions:Uses,Dosage, Side Effects

DUVYZAT (givinostat) is a histone deacetylase inhibitor approved for treating Duchenne muscular dystrophy (DMD) in patients aged 6 years and older. It modulates gene expression, potentially slowing disease progression by reducing muscle degeneration. The drug is administered orally as a weight-based suspension twice daily with food. Key safety considerations include monitoring for thrombocytopenia, hypertriglyceridemia, and QTc prolongation.  

Clinical trials demonstrated efficacy in delaying functional decline, with a 1.78-second improvement in 4-stair climb time versus placebo over 18 months. Common adverse reactions include diarrhea, abdominal pain, and hematological changes. DUVYZAT requires rigorous adherence to dosing guidelines and regular laboratory monitoring to mitigate risks.

Generic name
Duvyzat(Givinostat)
English name
Givinostat
Alternative Names
吉维司他
Drug prices
Indications

DUVYZAT is indicated for the treatment of Duchenne muscular dystrophy (DMD) in patients 6 years of age and older.

Therapeutic Target
Histone deacetylase (HDAC) inhibitor. The precise mechanism by which DUVYZAT exerts its effect in patients with DMD is unknown.
Active Ingredients
Givinostat hydrochloride monohydrate
Dosage Form
SUSPENSION
Specifications
8.86 mg/mL*140 mL/box
Dosage and Administration

The recommended dosage of DUVYZAT is based on body weight and administered orally twice daily with food:

10 kg to less than 20 kg: 22.2 mg (2.5 mL) twice daily;

20 kg to less than 40 kg: 31 mg (3.5 mL) twice daily;

40 kg to less than 60 kg: 44.3 mg (5 mL) twice daily;

60 kg or more: 53.2 mg (6 mL) twice daily.

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