Infusion & Immune Therapies
Artesunate IV therapy
St. George Hospital offers intravenous artesunate within individually assessed cancer and chronic-infection treatment plans. The consultation establishes the intended role alongside your other care, the relevant research and the monitoring you would need.

What is artesunate?
Artesunate is a medicine derived from artemisinin. Intravenous administration delivers it directly into the circulation. It is different from an herbal tea or an over-the-counter artemisinin supplement; preparations and uses are not interchangeable.
At St. George Hospital, artesunate is available for consideration within integrative oncology and chronic-infection programmes. The recommendation depends on the specific diagnosis and the wider plan, rather than on a general claim that all infections or cancers respond in the same way.
Clinical context and research
The European Medicines Agency authorisation for Artesunate Amivas concerns the initial treatment of severe malaria. Cancer and chronic-infection uses beyond that indication require a separate assessment; malaria approval does not establish effectiveness for them.
A phase I study in advanced solid tumours investigated safety and tolerability. It reported no objective tumour responses, although some participants had stable disease. This early study does not establish a general anticancer benefit. Your physician explains the clinical rationale for any proposed use alongside your existing treatment.
From inquiry to an individual plan
Tell us your situation
Send a short inquiry. The International Office explains how to share your records securely.
Medical assessment
Your physician reviews the diagnosis, medicines, relevant tests and suitability of the proposed treatment.
Decide together
Discuss the treatment goal, alternatives, monitoring and costs before you decide.
What the assessment covers
The review considers your full medication list, blood results, liver function and previous drug reactions. Allergic reactions and blood-cell changes are among the concerns discussed. EMA product information also describes delayed breakdown of red blood cells after artesunate treatment for severe malaria; the follow-up plan needs to reflect the context of treatment.
Before deciding, ask what change the treatment is intended to achieve, how it will be assessed and which clinician will coordinate follow-up. Treatment duration and scheduling are individual and are explained during medical review.
Planning your visit
Your treatment is planned after medical assessment. The International Office can explain the next steps and help you obtain a written cost overview. Bring your current medication list and recent medical reports to the consultation.
Frequently asked questions
Is artesunate the same as taking artemisinin supplements?
No. Artesunate is a specific medicine. An intravenous preparation, an oral supplement and a herbal extract cannot be treated as equivalent products.
Does the offer mean artesunate is approved for cancer or chronic Lyme disease?
No. The cited EU authorisation is for severe malaria. Other proposed uses require an individual clinical discussion of the indication, research and alternatives.
References
- A phase I study of intravenous artesunate in patients with advanced solid tumor malignancies. Cancer Chemotherapy and Pharmacology 2018. PMID 29392450
- Artesunate Amivas: European Medicines Agency product information. Source
Send a free inquiry
The initial inquiry is free of charge. The International Office reviews your message and your case directly and gets back to you.
- Phone
- +49 8061 398-0
- Hours
- Mon–Thu 08:00–17:00, Fri 08:00–14:00 German time (CET/CEST); in the US Mon–Thu 2–11 a.m. ET, Fri 2–8 a.m. ET.
Munich Airport (MUC), about 60 minutes by car.