🇮🇪Ireland
16°C Partly Cloudy · Dublin
Live Updates
--:--:-- IST
Writer Login
Latest
Clinical Trials in China / NCT06024031
Active, not recruiting Phase 2

NAC for Promoting Hematopoietic Recovery in Patients With Acute Myeloid Leukemia After Chemotherapy

NCT06024031 · tracked via the Priya Life Science China tracker
Sponsor
Peking University People's Hospital
Phase
Phase 2
Started
2023-09-10
Last updated
2024-11-07

Condition(s) studied

Acute Myeloid Leukemia

Investigational drug(s) / intervention(s)

N-acetyl-L-cysteine

N-acetyl-L-cysteine: N-acetyl-L-cysteine (Yiweishi) capsules (Guangdong Renrenkang Pharmaceutical Industry) will be given orally 400mg three times a day from day 1 to day 28 after chemotherapy. In case of drug allergy such as nausea, vomiting, rash and bronchospasm, and disease relapse, to discontinue the drug immediately.

Study summary

This is a prospective single-arm clinical study to evaluate the role of NAC after chemotherapy among patients with AML can promote hematopoietic recovery and does not affect the remission rate of the leukemia.

Eligibility

Sex
ALL
Min age
18 Years
Max age
60 Years
Healthy volunteers
No
Inclusion Criteria: 1. Newly diagnosed AML (except AML-M3) 2. Low-, intermediate risk AML (according to 2022 ELN) 3. Aged 18-60 4. No severe organ injury 1) Creatinine \< 1.5mg/dl 2) Hemobilirubin ≤ 1.5 X ULN 3) AST and ALT ≤ 3.0 X ULN 4) Cardiac ejection index ≥ 50% 5. No uncontrolled active infections 6. Sign informed consent form, have the ability to comply with study and follow-up procedures Exclusion Criteria: 1. Hypersensitivity to NAC 2. History of bronchial asthma

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Yuan Kong Beijing Beijing Municipality

More Peking University People's Hospital trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06024031 on ClinicalTrials.gov ↗ ← All trials in China