Belzutifan(Welireg)
Acetylcysteine Injection, FLUIMUCIL, Acetylcysteine InjectionAcetylcysteine Injection, FLUIMUCIL, Acetylcysteine InjectionAcetylcysteine Injection, FLUIMUCIL, Acetylcysteine Injection
Reference price:
Manufacturer:
MSD
Formulation:
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.

Welireg(Belzutifan) Instructions:Uses,Dosage, Side Effects

WELIREG, with the active pharmaceutical ingredient belzutifan, is an orally administered medication available as 40 mg film-coated tablets. Chemically, belzutifan is 3-[[(1S,2S,3R)-2,3-Difluoro-2,3-dihydro-1-hydroxy-7-(methylsulfonyl)-1H-inden-4-yl]oxy]-5-fluorobenzonitrile. It is designed for therapeutic use in adult patients with specific oncological conditions, including tumors associated with von Hippel-Lindau disease and certain types of advanced kidney cancer.

The therapeutic effect of belzutifan is derived from its activity as an inhibitor of hypoxia-inducible factor 2 alpha (HIF-2αα). HIF-2αα is a key transcription factor that plays a significant role in the body's oxygen-sensing mechanisms by modulating genes involved in adaptation to hypoxic (low oxygen) conditions. By targeting and inhibiting HIF-2αα, WELIREG interferes with cellular pathways that contribute to the growth and progression of certain cancers.

Generic name

Belzutifan(Welireg)
English name
Belzutifan
Alternative Names
Welireg
Drug prices
Indications

1. Von Hippel-Lindau (VHL) disease: For the treatment of adult patients with von Hippel-Lindau (VHL) disease who require therapy for associated renal cell carcinoma (RCC), central nervous system (CNS) hemangioblastomas, or pancreatic neuroendocrine tumors (pNET), not requiring immediate surgery. 

2. Advanced Renal Cell Carcinoma (RCC): For the treatment of adult patients with advanced renal cell carcinoma (RCC) with a clear cell component following a programmed death receptor-1 (PD-1) or programmed death-ligand 1 (PD-L1) inhibitor and a vascular endothelial growth factor tyrosine kinase inhibitor (VEGF-TKI).

Therapeutic Target
Hypoxia-inducible factor 2 alpha (HIF-2 α α).
Active Ingredients
Belzutifan
Dosage form
TABLET
specifications
40mg*90 tablets/bottle
Description
Belzutifan is an inhibitor of hypoxia-inducible factor-2αα (HIF-2αα). The chemical name is 3-[[(1S,2S,3R)-2,3-Difluoro-2,3-dihydro-1-hydroxy-7-(methylsulfonyl)-1H-inden-4-yl]oxy]-5-fluorobenzonitrile. The molecular formula is C1717H1212F33NO44S, and the molecular weight is 383.34 Daltons. Belzutifan is a white to light brown powder. It is soluble in acetonitrile, dimethoxyethane, and acetone; sparingly soluble in ethyl acetate; very slightly soluble in isopropanol and toluene; and insoluble in water. WELIREG tablets are supplied as blue, film-coated tablets for oral use containing 40 mg of belzutifan and the following inactive ingredients: croscarmellose sodium, hypromellose acetate succinate, magnesium stearate, mannitol, microcrystalline cellulose, and silicon dioxide. The film coating contains FD&C Blue aluminum lake, polyethylene glycol, polyvinyl alcohol, talc, and titanium dioxide.
Dosage and Administration

The recommended dosage of WELIREG is 120 mg administered orally once daily until disease progression or unacceptable toxicity. It should be taken at the same time each day and may be taken with or without food.

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