Ventoxen contains Venetoclax, a small molecule that selectively inhibits BCL-2, a protein that prevents cell death (apoptosis) and is commonly overexpressed in CLL cells. This overexpression supports cancer cell survival and contributes to drug resistance. Venetoclax binds to BCL-2, releasing pro-apoptotic proteins like BIM, which leads to mitochondrial disruption and activation of enzymes that cause cell death. Preclinical studies confirm its effectiveness in destroying BCL-2–dependent tumor cells.
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Ventoxen, when used alongside Rituximab, is prescribed for adults with chronic lymphocytic leukemia (CLL) who have previously undergone at least one line of therapy.
As a standalone treatment, Ventoxen is indicated for:
Adults with CLL and a 17p deletion or TP53 mutation who are either not suitable candidates for or have not responded to B-cell receptor pathway inhibitors.
Adults without the 17p deletion or TP53 mutation who have not responded to both chemoimmunotherapy and a B-cell receptor pathway inhibitor.
Treatment starts with a low dose of 20 mg once daily for 7 days. The dose is gradually increased over 5 weeks to a maintenance dose of 400 mg daily to reduce tumor burden and lower the risk of tumor lysis syndrome (TLS).
With Rituximab: After completing the titration phase, continue with 400 mg of Ventoxen once daily. Begin Rituximab after 7 days of maintenance dosing. Ventoxen should be continued for 24 months starting from Day 1 of Rituximab treatment.
Monotherapy: After reaching 400 mg once daily, continue treatment until the disease progresses or the medication is no longer tolerated.
Elderly (65+ years): No dose adjustment needed.
Renal impairment: Mild to moderate cases do not need adjustment. Severe impairment or dialysis: safety not established; use only if the benefit outweighs the risk.
Hepatic impairment:
Mild to moderate: No adjustment needed.
Severe: Reduce dose by at least 50% and monitor closely.
Pediatrics: Safety and effectiveness not established for those under 18.
Allergy to Venetoclax or any of its components
Concomitant use with strong CYP3A inhibitors during titration
Use of St. John’s wort products
Common side effects (≥20%): neutropenia, diarrhea, upper respiratory infections, nausea, anemia, fatigue
Serious adverse events (≥2%): pneumonia, febrile neutropenia, tumor lysis syndrome
Store below 30°C, protected from light and moisture. Keep out of children’s reach.
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