
Release date: 2026-01-28 17:43:47 Article From: Lucius Laos Recommended: 10
Remission is the primary treatment goal for acute myeloid leukemia (AML) and acute lymphoblastic leukemia (ALL).
Approximately one in five patients achieve complete remission plus complete remission with partial hematologic recovery (CR + CRh) with Revuforj.
In clinical trials, 21% of patients (22 out of 104) achieved complete remission (CR) or complete remission with partial hematologic recovery (CRh).
Among the 22 patients who achieved CR + CRh:
Some patients responded as early as one month after treatment initiation.
Half of the patients achieved remission within the first 2 months of treatment (the median time to CR + CRh was 1.9 months; range: 0.9 to 5.6 months), and half had a remission duration of more than 6.4 months.
Before administration, must inform your healthcare provider of all your health conditions if you have the following:
A history of any cardiac disease, including long QT syndrome.
Been advised of low blood potassium or magnesium levels.
Are pregnant or planning to become pregnant.
Are breastfeeding or planning to breastfeed.
Revuforj may cause fetal harm. For females of reproductive potential, healthcare providers will perform a pregnancy test within 7 days prior to the initiation of Revuforj treatment. If you become pregnant or suspect pregnancy during Revuforj treatment, inform your healthcare provider immediately.
Females of reproductive potential should use effective contraceptive measures during Revuforj treatment and for 4 months after the last dose.
Males with female partners of reproductive potential should also use effective contraceptive measures during Revuforj treatment and for 4 months after the last dose.
Consult your healthcare provider to select a suitable contraceptive method for this period.
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: