Supportan Drink: safety and potential benefits for cancer patients on therapy
Official title: Evaluation of Safety and Efficacy of Supportan® Drink
Run by Fresenius Kabi Taiwan Ltd. · NCT06902402 · Data updated 2026-11-12
This trial tests whether Supportan Drink is safe and helpful for people with cancer who are receiving chemotherapy, radiotherapy, immunotherapy, or targeted therapy.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 135 (estimated) |
| Sponsor | Fresenius Kabi Taiwan Ltd. Industry-sponsored |
| Drugs / interventions | chemotherapy, immunotherapy |
| Locations | 1 site (Keelung, Taiwan) |
| Status | Recruiting |
| Started | April 8, 2025 |
| Main results expected | December 31, 2027 |
| Study ends | December 31, 2027 |
| Registry record updated | October 1, 2026 |
| Trial ID | NCT06902402 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Patients actively receiving chemotherapy, radiotherapy, immunotherapy, or targeted therapy.
✕Probably not a fit
Patients with certain liver, kidney, or heart conditions or those deemed unsuitable by the investigator may not benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This interventional study investigates the safety and potential benefits of Supportan Drink in cancer patients who are undergoing various cancer therapies. Eligible participants are those actively receiving treatment, while those with liver, kidney, or heart disease may be excluded at the investigator’s discretion. The study is sponsored by Fresenius Kabi Taiwan Ltd. and is located at Keelung Chang Gung Memorial Hospital’s Lover’s Lake branch in Keelung, Taiwan. Details on dosing, duration, and specific outcomes are not provided in the available information.
Why it matters
Potential benefit: If successful, the drink could offer a safe supportive option to help patients during cancer therapy.
How similar studies have gone: Safe and supportive nutrition products have been studied in cancer care, but details for Supportan Drink are not provided here.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: 1\. Patients receiving chemotherapy and/or radiotherapy, or immunotherapy, or targeted therapy; Exclusion Criteria: 1\. Patient with documented diagnosis of liver, kidney or heart disease in the hospital's electronic medical record (EMR); severity of disease evaluated by Investigator as not being suitable to participate in this study;
Where it's running
-
Keelung Chang Gung Memorial Hospital-Lover's lake branch
Keelung, Taiwan, Taiwan Recruiting
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Adequacy of Middle Molecules Clearance in Haemodiafiltration and its Relation to Patient Outcomes
This study looks at whether higher convective volumes in haemodiafiltration and different dialysate sodium levels affect toxin clearance, patient-reported outcomes, and nutritional status in adults with end-stage kidney disease.
-
Child Growth Improvement program for stunting risk kids
This study tests a community-based nutrition program with screening, education, supplementation, and follow-up to help 1–5 year-olds at risk of stunting.
-
Using REMS ultrasound to check bone density in children and teens with conditions that lower bone strength
This project will test whether REMS, a radiation-free ultrasound method, can measure bone mineral density in children and adolescents aged 5–18 who have conditions that weaken their bones.
-
Screening for Malnutrition and Sarcopenia in Outpatients
This project will screen adult outpatients (18+) in hospital clinics in Turkey to see how common the risk of malnutrition and sarcopenia is.
-
Optimizing Cancer Treatment with EPA-enriched Nutrition for Malnutrition
This trial tests whether EPA-enriched nutrition helps undernourished adults with stage III–IV lung or colorectal cancer who are starting or receiving systemic cancer therapy.
-
Goat milk–derived formula versus undiluted goat milk for infants who cannot be exclusively breastfed: growth and gut health
This study will test whether a goat milk–derived formula is safe and supports similar growth and gut health for 8–10 week old infants who cannot be exclusively breastfed, compared with undiluted goat milk or breast milk.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.