WSD0922-FU clinical trials
WSD0922-FU is named as an intervention in 3 current clinical trials in our China, USA and France registers. 3 are recruiting patients now. The most common phase is Phase 1/2. The lead sponsor is Wayshine Biopharm, Inc. The most-studied condition is Non Small Cell Lung Cancer.
Patient leaflets for WSD0922-FU
The package leaflet is the official guide for patients that comes with every medicine. These links go to the regulators that publish it.
- UKUnited Kingdom: Search MHRA ProductsPatient information leaflets and SmPCs for UK-licensed products.
- USUnited States: Search DailyMedFDA-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
Trials by phase
Clinical trials of WSD0922-FU
3 trials| Study | Phase | Status | Lead sponsor | Registers |
|---|---|---|---|---|
|
A Study to Assess the Efficacy of WSD0922-FU in Patients With C797S+ Advanced Non-small Cell Lung Cancer
NCT06868485 · Non Small Cell Lung Cancer
|
Phase 2 | Recruiting | Wayshine Biopharm, Inc | USA, China, France |
|
A Study to Assess the Efficacy and Safety of WSD0922-FU in Patients With EGFRm+ Advanced Non-small Cell Lung Cancer
NCT06631989 · ClinicalTrials.gov ↗ · EGFR Mutation Positive Advanced Non-Small Cell Lung Cancer
|
Phase 1/2 | Recruiting | Wayshine Biopharm, Inc | China |
|
A Study to Evaluate Safety and Efficacy of WSD0922-FU Combo With Osimertinib for NSCLC
NCT07206498 · ClinicalTrials.gov ↗ · Non Small Cell Lung Cancer (NSCLC)
|
Phase 1/2 | Recruiting | Wayshine Biopharm, Inc | China |
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 WSD0922-FU
3 conditionsSponsors
lead sponsor per trial| Lead sponsor | Trials |
|---|---|
| Wayshine Biopharm, Inc | 3 |
By country register
| Register | Trials | Recruiting |
|---|---|---|
| Clinical trials in China | 3 | 3 |
| Clinical trials in USA | 1 | 1 |
| Clinical trials in France | 1 | 1 |
A trial with sites in more than one country appears in each of those registers.
Related compounds
Questions about WSD0922-FU trials
How many clinical trials are testing WSD0922-FU?
3 current trials in our China, USA and France registers name WSD0922-FU (also registered as WSD0922) as a drug or biological intervention, as of the registry sync on 9 November 2026. Completed and withdrawn studies are not counted.
Are WSD0922-FU trials recruiting patients?
Yes. 3 of the 3 trials are recruiting: 3 with sites in China, 1 with sites in USA and 1 with sites in France. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.
Who sponsors WSD0922-FU clinical trials?
The lead sponsor is Wayshine Biopharm, Inc. 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 WSD0922-FU 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 WSD0922-FU 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 WSD0922-FU (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.