Clinical Trial

Safety and Effectiveness Study of Pre-operative Artesunate in Stage II/ III Colorectal Cancer

Study acronym: NeoART-M
Not Yet Recruiting Phase 2
View on ClinicalTrials.gov →
Summary
TThis study evaluates the safety and effectiveness of pre-operative artesunate, given orally once a day for 14 days prior to surgery, in patients with Stage II/III colorectal cancer. Artesunate is an established antimalarial drug with an excellent safety profile. It is well tolerated, affordable, and widely available. Several laboratory studies and one small pilot clinical study in patients with colorectal cancer have shown that artesunate can reduce the proliferation and growth of cancer cells. One hundred patients diagnosed with Stage II/III operable colorectal cancer will be randomly allocated to receive oral artesunate 200 mg daily or a matching placebo for 14 days prior to surgery. Patients will then be followed closely for 5 years to determine whether pre-operative artesunate reduces the risk of cancer recurrence after surgery.
Trial Details
NCT Number NCT07095309
Lead Sponsor Metanoic Health Ltd.
Collaborators: Clinical Research Malaysia
Conditions Stage II/III Colon Cancer, Bowel Cancer
Enrollment 120 participants
Start Date 2025-08-15
Primary Completion 2032-08-30 (estimated)
Study Completion 2033-07-31 (estimated)
Updated on ClinicalTrials.gov 2025-07-31