Product/Composition:- | Everolimus tablets |
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Strength:- | 0.75 mg, 1.25 mg, 2.5 mg, 5 mg, 7.5 mg, 10 mg |
Form:- | Tablet |
Reference Brands:- | Zortress, Afinitor(US & EU) |
MOQ | As per the manufacturer batch size |
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Everolimus inhibits mTOR, blocking cell growth, proliferation, and survival. It effectively treats cancers, such as neuroendocrine tumors, breast cancer, and renal cell carcinoma, and prevents organ rejection in transplants. Benefits include targeted therapy, improved progression-free survival, and manageable side effects, supporting long-term disease management.
Everolimus tablets, marketed as Afinitor and Zortress, are approved in the US by the FDA and in the EU via EMA for various indications including cancer and transplant rejection. Regulatory approval requires a comprehensive dossier containing clinical trial data, manufacturing details, safety, efficacy, and pharmacovigilance strategies. In the US, FDA review involves stringent evaluation of clinical and quality data, while the EMA ensures compliance with regional standards. For guidance on dossier preparation, regulatory pathways, and market accession, visit PharmaTradz. Ensuring thorough regulatory compliance is critical for the safe, effective, and timely approval of everolimus tablets worldwide, supporting optimal patient outcomes in oncology and transplantation.