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CancerNCT06902402

Evaluation of Safety and Efficacy of Supportan® Drink

A study testing Supportan® Drink in people with Cancer and Malnutrition (Calorie), run by Fresenius Kabi Taiwan Ltd. at 1 site in Taiwan.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

The goal of this clinical trial is to demonstrate safety and efficacy of Supportan® Drink Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Cancer, Malnutrition (Calorie)
What is being tested?
Supportan® Drink
Could I receive a placebo?
No, everyone receives an active treatment
How many people
135 participants
Where
1 siteTaiwan
Study dates
8 Apr 2025to 31 Dec 2027
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • 1. Patients receiving chemotherapy and/or radiotherapy, or immunotherapy, or targeted therapy;

Who cannot join

  • 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;

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Taiwan1 site, 1 recruiting
  • Keelung Chang Gung Memorial Hospital-Lover's lake branch

    Keelung, Taiwan, 204201

    Pei-Hung Dr. Chang, ph555chang@cgmh.org.tw

    Recruiting

Other trials in Taiwan

About this study

The goal of this clinical trial is to demonstrate safety and efficacy of Supportan® Drink

Being tested
Supportan® Drink
Medical subject headings
Neoplasms, Malnutrition

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Supportan® DrinkDietary supplement

    flavour

Study groups in NCT06902402
Study groupRoleWhat they receive
Supportan® DrinkExperimentalNot described
Receives: Dietary Supplement: Supportan® Drink

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change in body weight from Baseline to end of treatment at Week 4 (Week 4 -Baseline)

    Measured: 4 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted30 Mar 2025
  2. Study start8 Apr 2025
  3. Primary completion31 Dec 2027 (estimated)
  4. Study completion31 Dec 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
135 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06902402
Sponsor's protocol ID
Supp-015-CEN
Status last verified
Sep 2026
First submitted
12 Mar 2025
Last updated
1 Oct 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing Supportan® Drink in people with Cancer and Malnutrition (Calorie), run by Fresenius Kabi Taiwan Ltd. at 1 site in Taiwan.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 1 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Taiwan. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Each site lists its own contact: choose the nearest one under Trial locations. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in body weight from Baseline to end of treatment at Week 4 (Week 4 -Baseline) (time frame: 4 weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 1 Oct 2026.

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