CapOx(Capecitabine clinical trials
CapOx(Capecitabine is named as an intervention in 2 current clinical trials in our China register. 1 is recruiting patients now. All registered phases are Phase 3. The sponsor with the most trials is Fudan University (1). The most-studied condition is Locally Advanced Colon Cancer.
Patient leaflets for CapOx(Capecitabine
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 CapOx(Capecitabine
2 trials| Study | Phase | Status | Lead sponsor | Registers |
|---|---|---|---|---|
|
A Phase III Study of SHR-A1811 in Combination With Chemotherapy and Adebrelimab in Previously Untreated Patients With Gastric or Gastroesophageal Junction Adenocarcinoma
NCT07118527 · ClinicalTrials.gov ↗ · Patients With Unresectable Locally Advanced or Metastatic Untreated Gastric or Gastroesophageal Junction Adenocarcinoma
|
Phase 3 | Recruiting | Suzhou Suncadia Biopharmaceuticals Co., Ltd | China |
|
Chemotherapy Combined With or Without Short-Course Radiotherapy Versus Chemotherapy Alone as Neoadjuvant Therapy for High-Risk Locally Advanced Colon Cancer With pMMR/MSS
NCT07877597 · ClinicalTrials.gov ↗ · Locally Advanced Colon Cancer, pMMR
|
Phase 3 | Not yet open | Fudan University | 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 CapOx(Capecitabine
3 conditionsSponsors
lead sponsor per trial| Lead sponsor | Trials |
|---|---|
| Fudan University | 1 |
| Suzhou Suncadia Biopharmaceuticals Co., Ltd | 1 |
By country register
| Register | Trials | Recruiting |
|---|---|---|
| Clinical trials in China | 2 | 1 |
A trial with sites in more than one country appears in each of those registers.
Related compounds
Questions about CapOx(Capecitabine trials
How many clinical trials are testing CapOx(Capecitabine?
2 current trials in our China register name CapOx(Capecitabine as a drug or biological intervention, as of the registry sync on 17 October 2026. Completed and withdrawn studies are not counted.
Are CapOx(Capecitabine trials recruiting patients?
Yes. 1 of the 2 trials is recruiting: 1 with sites in China. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.
Who sponsors CapOx(Capecitabine clinical trials?
Fudan University (1) and Suzhou Suncadia Biopharmaceuticals Co., Ltd (1). 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 CapOx(Capecitabine 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 CapOx(Capecitabine 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 CapOx(Capecitabine (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 17 Oct 2026. How every register is built: methodology · fixes we have made: corrections log.