
Release date: 2026-01-04 11:00:37 Article From: Lucius Laos Recommended: 115
Ivosidenib has interactions with a variety of drugs, which may affect its efficacy or increase the risk of adverse reactions. Close monitoring and dosage adjustment are required when used in combination.
The three categories of common interactions listed below are only partial representative examples. In actual clinical medication, the patient’s complete medication history shall be comprehensively taken into consideration.
Ivosidenib, a kinase inhibitor that prolongs the QT interval (highest risk), may enhance the QT interval-prolonging effect of amiodarone.
Management Recommendations: Consider alternative drug combinations. If co-administration is unavoidable, monitor for QT interval prolongation and ventricular arrhythmias. Patients with other risk factors for QT interval prolongation may be at higher risk. Consider adjusting the treatment regimen.
Ivosidenib, a drug that prolongs the QT interval (highest risk), may enhance the QT interval-prolonging effect of amisulpride.
Management Recommendations: Consider alternative drug combinations. Patients with other risk factors (e.g., advanced age, female gender, bradycardia, hypokalemia, hypomagnesemia, heart disease, and higher plasma drug concentrations) may be at an increased risk of such toxicities. Consider adjusting the treatment regimen.
Ivosidenib, a drug that prolongs the QT interval (highest risk), may enhance the QT interval-prolonging effect of azithromycin (systemic administration).
Management Recommendations: Consider alternative drug combinations. Patients with other risk factors (e.g., advanced age, female gender, bradycardia, hypokalemia, hypomagnesemia, heart disease, and higher plasma drug concentrations) may be at an increased risk of such toxicities. Consider adjusting the treatment regimen.
For more information about the use of Tibsovo (Ivosidenib), please refer to the package insert or consult your doctor or pharmacist.
Ivosidenib is a prescription drug. Treatment should be initiated and supervised by a physician experienced in cancer therapy.
This product is available as tablets for oral administration.
For the treatment of acute myeloid leukemia (AML): The recommended dosage is once daily, in combination with azacitidine. Administer consecutively for seven days at the start of each 28-day treatment cycle (also referred to as a "course of treatment"). Treatment should continue as long as clinical benefit is observed or the patient can tolerate the medication.
For the treatment of cholangiocarcinoma: The recommended dosage is once daily. Treatment should continue until disease progression or unacceptable toxicity occurs.
Some patients with AML or cholangiocarcinoma have mutations in the gene encoding the IDH1 protein. This mutation leads to abnormal protein function, resulting in the overproduction of a substance called 2-hydroxyglutarate (2-HG). Elevated 2-HG levels induce cellular changes that may contribute to cancer development.
The active ingredient in Tibsovo (Ivosidenib) blocks the activity of the mutated IDH1 protein, thereby reducing 2-HG production. This, in turn, slows down the growth and spread of cancer cells.
On November 21, 2025, the U.S. Food and Drug Administration (FDA) approved the regimen of pembrolizu···【more】
Recommended:2622025-17-12
Lung cancer is the most rapidly increasing malignant tumor with the fastest increasing morbidity and···【more】
Recommended:4832024-09-07
On December 12, 2025, the U.S. Food and Drug Administration (FDA) approved niraparib in combination ···【more】
Recommended:2672025-15-12
The U.S. Food and Drug Administration (FDA) announced today that it has approved Omisirge (omidubice···【more】
Recommended:2772025-10-12
On December 4, 2025, the U.S. Food and Drug Administration (FDA) approved lisocabtagene maraleucel (···【more】
Recommended:2582025-08-12
On December 3, 2025, the U.S. Food and Drug Administration (FDA) granted full approval to pirtobruti···【more】
Recommended:3032025-04-12
Primary analysis data from the randomized, double-blind, placebo-controlled phase III HER2CLIMB-02 s···【more】
Recommended:2652025-01-12
The Cure SMA Foundation, a global leading non-profit organization dedicated to spinal muscular atrop···【more】
Recommended:2442025-27-11

Lucius Pharmaceutical Co., Ltd., was established in 2020 in Vientiane, the capital of Laos. It aims to offer safe, effective, and affordable medicines globally. With a factory spanning 25,000 square meters, the company manufactures 200+ generic drugs in diverse therapeutic fields.
Address:No.26 Thongmang village, Xaythany district, Vientiane Capital, Laos
E-mail:laoslucius@gmail.com
Whatsapp: