
Release date: 2026-01-29 11:40:39 Article From: Lucius Laos Recommended: 7
Revumenib (Revuforj) is an oral, first-in-class targeted Menin protein inhibitor indicated for the treatment of relapsed or refractory acute leukemia with specific genetic abnormalities (KMT2A rearrangement or NPM1 mutation).
The effects and recommendations for concomitant use of other drugs with revumenib are as follows:
Effect: Increases the systemic exposure of revumenib, which may raise the risk of adverse reactions.
Measure: If concomitant use is necessary, the dose of revumenib should be reduced.
Effect: May decrease the systemic exposure of revumenib and increase that of its M1 metabolite, which could reduce the efficacy of revumenib or elevate the risk of QT prolongation associated with the M1 metabolite.
Measure: Concomitant use with revumenib should be avoided.
Effect: May induce QTc interval prolongation and its associated adverse reactions.
Measure: Concomitant use with revumenib should be avoided.
The above recommendations are based on the risk assessment of drug-drug interactions and are intended to ensure medication safety and efficacy.
Revumenib should be taken on an empty stomach or with a low-fat meal (containing approximately 400 calories and no more than 25% fat).
There are no known interactions between revumenib and alcohol, but heavy alcohol consumption may slow down the immune response and make it more difficult for the body to fight cancer.
More frequent electrocardiographic monitoring may be required for patients with congenital long QT syndrome, congestive heart failure, electrolyte abnormalities, or those taking known QTc interval-prolonging drugs.
Initiation of revumenib is contraindicated in patients with a QTcF > 450 milliseconds.
Correct electrolyte abnormalities, including hypokalemia and hypomagnesemia, before and during revumenib treatment.
Patients are advised to consult a doctor immediately if they experience dizziness, loss of consciousness, or signs of cardiac arrhythmia. Patients with a history of hypokalemia or hypomagnesemia should be advised of the importance of electrolyte monitoring.
On November 21, 2025, the U.S. Food and Drug Administration (FDA) approved the regimen of pembrolizu···【more】
Recommended:732025-17-12
Lung cancer is the most rapidly increasing malignant tumor with the fastest increasing morbidity and···【more】
Recommended:3692024-09-07
On December 12, 2025, the U.S. Food and Drug Administration (FDA) approved niraparib in combination ···【more】
Recommended:652025-15-12
The U.S. Food and Drug Administration (FDA) announced today that it has approved Omisirge (omidubice···【more】
Recommended:822025-10-12
On December 4, 2025, the U.S. Food and Drug Administration (FDA) approved lisocabtagene maraleucel (···【more】
Recommended:822025-08-12
On December 3, 2025, the U.S. Food and Drug Administration (FDA) granted full approval to pirtobruti···【more】
Recommended:982025-04-12
Primary analysis data from the randomized, double-blind, placebo-controlled phase III HER2CLIMB-02 s···【more】
Recommended:942025-01-12
The Cure SMA Foundation, a global leading non-profit organization dedicated to spinal muscular atrop···【more】
Recommended:952025-27-11

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: