Polimod Oral Uses, Dosage, Side Effects and more
Polimod Oral is a synthetic dipeptide with immunomodulatory properties.
Polimod Oral modulates the immune system to induce an immune response against bacterial or viral pathogens
Trade Name | Polimod Oral |
Generic | Pidotimod |
Pidotimod Other Names | Pidotimod |
Weight | 400mg |
Type | Liquid |
Formula | C9H12N2O4S |
Weight | Average: 244.27 Monoisotopic: 244.051778048 |
Groups | Experimental |
Therapeutic Class | |
Manufacturer | Ajanta Pharma Ltd |
Available Country | India |
Last Updated: | January 7, 2025 at 1:49 am |
Uses
Polimod Oral is a synthetic agent with immunomodulatory properties used in patients with documented cell-mediated immunosuppression to stimulate their immunity during lung and urinary tract infections.
For use as immunostimulant therapy for treatment of cell-mediated immunosuppression with respiratory or urinary infections .
Polimod Oral is also used to associated treatment for these conditions: Recurrent Upper Respiratory Tract Infection, Immunostimulation
How Polimod Oral works
Polimod Oral inhibits tumor necrosis factor α (TNF-α) induced increases in extracellular signal-related kinase (ERK) phosphorylation . It also increases nuclear factor κB (NFκB) expression and translocation to the nucleus. It is these to modulatory effects on ERK and NFκB signalling which are thought to produce the increase in toll-like receptor expression seen with pidotimod. Polimod Oral increase maturation of dendritic cells responsible for presenting antigens to naive Th-cells . It also appears to result in a greater population these cells diiferentiating to Th1 cells which are believed to mediate the immune response to pathogens like bacteria and viruses . Lastly, pidotimod appears to increase antigen-specific antibody titer and cytotoxic response with antigen exposure . The precise mechanism and timeline of events leading to these effects is unknown.
Elimination Route
Bioavailability of 45% .
Half Life
Half life of 4 h .
Elimination Route
95% of intravenous dose is eliminated in the urine as the parent compound .