Overview of Cycloferon
| Property | Description |
|---|---|
| Active ingredient | Meglumine Acridоnacetate |
| Forms | Tablets (enteric-coated), Injection Solution, Liniment |
| Pharmacological class | Low Molecular Weight Interferon Inducer |
| Common use | Immune modulation, Antiviral support |
| Origin | Synthetic (derived from acridone acetic acid) |
Pharmacological Class and Available Forms
Cycloferon is a synthetic medicinal product defined by its sole active ingredient, Meglumine Acridоnacetate, a compound which is a low-molecular-weight salt of 10-carboxymethyl-9-acridanone (Cridanimod) and N-methylglucamine. The medicine is primarily classified as a low molecular weight interferon inducer and an immunomodulatory drug, meaning it promotes the body's own defense mechanisms, rather than acting as a direct external inhibitor.
To facilitate various applications, Cycloferon is available in several dosage forms: enteric-coated tablets for oral intake, an injection solution for intramuscular or intravenous route of administration, and a liniment for topical use. This broad range allows for both systemic and localized approaches.
General Mechanism and Purpose
The general purpose of Cycloferon is etiotropic, a term indicating its action is directed at supporting the body in addressing the underlying cause, especially where enhanced immune system activity is beneficial. The core mechanism involves acting as a powerful trigger for host cells to rapidly produce and release their own endogenous interferons—the body's natural antiviral proteins. Meglumine Acridоnacetate functions as a rapid inducer of these key proteins, leading to a prompt increase in their levels. This indicates the medicine's role is to stimulate the body's natural defensive proteins to quickly establish an antiviral state, thereby enhancing the immune system's general resistance to a wide spectrum of viral challenges.
