Duloxetine is named as an intervention in 2 current clinical trials in our China register. 2 are recruiting patients now. The most common phase is Phase 2. The sponsor with the most trials is Yan Yang, MD, Ph.D (1). The most-studied condition is Chemotherapy-induced Peripheral Neuropathy.
| Study | Phase | Status | Lead sponsor | Registers |
|---|---|---|---|---|
|
Efficacy and Safety of Duloxetine in Chinese Solid Tumor Patients With Taxanes-induced Painful Peripheral Neuropathy
NCT04970121 · ClinicalTrials.gov ↗ · Chemotherapy-induced Peripheral Neuropathy, Pain, Solid Tumor
|
Phase 2 | Recruiting | Yan Yang, MD, Ph.D | China |
|
Sequenced Treatment Alternatives to Relieve Adolescent Depression (STAR-AD)
NCT05814640 · ClinicalTrials.gov ↗ · Depression, Sequestra
|
Phase 1/2 | Recruiting | First Affiliated Hospital of Chongqing Medical 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.
The same active substance in our other registers, matched by its exact name. Each entry links to the register record it comes from.
20 single-substance products containing Duloxetine on the HPRA medicines list.
+ 1 more German shortage notices.
| Lead sponsor | Trials |
|---|---|
| Yan Yang, MD, Ph.D | 1 |
| First Affiliated Hospital of Chongqing Medical University | 1 |
| Register | Trials | Recruiting |
|---|---|---|
| Clinical trials in China | 2 | 2 |
A trial with sites in more than one country appears in each of those registers.
2 current trials in our China register name Duloxetine as a drug or biological intervention, as of the registry sync on 25 September 2026. Completed and withdrawn studies are not counted.
Yes. 2 of the 2 trials are recruiting: 2 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.
Yan Yang, MD, Ph.D (1) and First Affiliated Hospital of Chongqing Medical University (1). The number in brackets is how many trials each organisation leads.
Yes. The HPRA medicines list includes 20 single-substance products containing Duloxetine, for example Duloxetine Accord 30 mg hard gastro-resistant capsules (Accord Healthcare Ireland Ltd.). A licence does not mean a product is currently marketed or reimbursed; see each product's record.
The registers we track list 7 entries for Duloxetine: 7 German notices. Shortages are product- and country-specific; check with a pharmacist.
Every trial, status, phase and sponsor on this page is copied from public ClinicalTrials.gov records by a daily sync. Nothing here describes how Duloxetine works or whether it is effective, and it is not medical advice.
Everything on this page is copied from public ClinicalTrials.gov registry records — it is not written from memory, and nothing here describes how Duloxetine works or whether it is effective. Each trial links to its own record so you can check it yourself.
This page is built automatically: a daily sync job reads the registry records behind our country trial registers, collects every trial that lists Duloxetine (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 25 Sep 2026.