Compound · clinical trials

FB825 clinical trials

Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 2 trials in our China, Taiwan and USA registers that name FB825 as an intervention. Synced 9 Nov 2026

2Current trials

2Recruiting now

1Lead sponsor

3Country registers

Maintained by Sreepriya Prasannan

MSc Digital Transformation of Life Sciences (Innopharma Education / Griffith College); MSc & BSc Botany HSE Spark Ignite 2026 — Top 14 finalist

Compiled from ClinicalTrials.gov registry records · Synced 9 Nov 2026 · Editorial standards

At a glance

FB825 is named as an intervention in 2 current clinical trials in our China, Taiwan and USA registers. 2 are recruiting patients now. All registered phases are Phase 2. The lead sponsor is Oneness Biotech Co., Ltd. The most-studied condition is Atopic Dermatitis.

How FB825 works

All drug targets →

Diseases it has been tested for in clinical trials, by furthest phase

Allergic asthmaPhase 2
Atopic eczemaPhase 2

Mechanisms and diseases from ChEMBL via the Open Targets Platform (release 26.09), ChEMBL record CHEMBL4297952, CC BY-SA 3.0. The Guide to Pharmacology has no record of this medicine, so its targets rest on ChEMBL alone. Trial phases are not approvals: approved uses are shown from the regulators' own records where we hold them.

Patient leaflets for FB825

The package leaflet is the official guide for patients that comes with every medicine. These links go to the regulators that publish it.

UK
United Kingdom: Search MHRA Products
Patient information leaflets and SmPCs for UK-licensed products.
US
United States: Search DailyMed
FDA-approved labels, including patient and medication guides.

Leaflets differ between brands and countries; always read the one that comes with your own medicine. This is regulatory information, not medical advice.

Trials by status

Recruiting2100%

Trials by phase

Phase 22100%

Clinical trials of FB825

2 trials

Study	Phase	Status	Lead sponsor	Registers
Evaluate the Efficacy and Safety of FB825 in Adult With Allergic Asthma NCT05008965 · ClinicalTrials.gov ↗ · Allergic Asthma	Phase 2	Recruiting	Oneness Biotech Co., Ltd	China, Taiwan
Evaluate Efficacy and Safety of Repeat Subcutaneous Doses of FB825 in Adults With Moderate-to-Severe Atopic Dermatitis NCT06397911 · Atopic Dermatitis	Phase 2	Recruiting	Oneness Biotech Co., Ltd	USA, China, Taiwan

Registers list studies that are recruiting, about to open, active but closed to enrolment, or enrolling by invitation. The UK and USA registers cover industry-sponsored studies only. Trial titles and statuses are copied from the registry as published.

Conditions studied with FB825

2 conditions

Atopic Dermatitis1Allergic Asthma1

By country register

Register	Trials	Recruiting
Clinical trials in China	2	2
Clinical trials in Taiwan	2	2
Clinical trials in USA	1	1

A trial with sites in more than one country appears in each of those registers.

Related compounds

Questions about FB825 trials

How many clinical trials are testing FB825?

2 current trials in our China, Taiwan and USA registers name FB825 as a drug or biological intervention, as of the registry sync on 9 November 2026. Completed and withdrawn studies are not counted.

Are FB825 trials recruiting patients?

Yes. 2 of the 2 trials are recruiting: 2 with sites in China, 2 with sites in Taiwan and 1 with sites in USA. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.

Who sponsors FB825 clinical trials?

The lead sponsor is Oneness Biotech Co., Ltd. The number in brackets is how many trials each organisation leads.

Where does this information come from?

Every trial, status, phase and sponsor on this page is copied from public ClinicalTrials.gov records by a daily sync. Nothing here describes how FB825 works or whether it is effective, and it is not medical advice.

How this page is built

Everything on this page is copied from public ClinicalTrials.gov registry records — it is not written from memory, and nothing here describes how FB825 works or whether it is effective. Each trial links to its own record so you can check it yourself.

ClinicalTrials.gov (U.S. National Library of Medicine) ↗ Trial IDs, titles, intervention names and synonyms, phase, overall status, lead sponsor and conditions for every trial on this page

This page is built automatically: a daily sync job reads the registry records behind our country trial registers, collects every trial that lists FB825 (or a registered synonym) as a drug or biological intervention, and tabulates the registry fields directly. Placebos and generic comparators are excluded. There is no AI drafting and no per-compound editorial pass, and the page has not been clinically reviewed. The “last verified” date above is the timestamp of that sync, not a review date. Our general editorial approach is described in our editorial standards and corrections policy. The ClinicalTrials.gov data on this page was last retrieved on 9 Nov 2026. How every register is built: methodology · fixes we have made: corrections log.

Please verify before you rely on this. This page is general information for life-science and pharmaceutical professionals. It is not medical advice, and it has not been reviewed by a clinician — our editorial team holds life-science qualifications, not clinical ones. It is not exhaustive and may not reflect the most recent label change. Always check the official prescribing information (US Prescribing Information or EU SmPC) and speak to your doctor or pharmacist before acting on anything here. Drugs in the same class are not automatically interchangeable, and approvals, brand names and indications differ between the US, the EU/Ireland (EMA/HPRA) and other regions. Spotted an error? Tell us — we correct promptly and log it.