Ivermectin is named as an intervention in 3 current clinical trials in our Egypt, Ireland, India, Germany, France, Spain, Italy, Netherlands, Belgium, Switzerland, Czechia, Portugal, Canada, Japan, Australia and Israel registers. 2 are recruiting patients now. The most common phase is Phase 3. The sponsor with the most trials is UMC Utrecht (1). The most-studied condition is Community-acquired Pneumonia, Influenza, COVID-19.
| Study | Phase | Status | Lead sponsor | Registers |
|---|---|---|---|---|
|
Randomized, Embedded, Multifactorial Adaptive Platform Trial for Community- Acquired Pneumonia
NCT02735707 · ClinicalTrials.gov ↗ · Community-acquired Pneumonia, Influenza, COVID-19
|
Phase 3 | Recruiting | UMC Utrecht | Ireland, India, Germany, France, Spain, Italy, Netherlands, Belgium, Switzerland, Czechia, Portugal, Canada, Japan, Australia, Israel |
|
The Efficacy of Ivermectin in Larger Doses in COVID-19 Treatment
NCT04351347 · ClinicalTrials.gov ↗ · COVID
|
Phase 2/3 | Recruiting | Tanta University | Egypt |
|
Efficacy of Ivermectin in the Treatment of Plane Warts
NCT07710638 · ClinicalTrials.gov ↗ · Plane Warts
|
Phase 2 | Active, closed | Al-Azhar University | Egypt |
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.
3 single-substance products containing Ivermectin on the HPRA medicines list.
| Lead sponsor | Trials |
|---|---|
| UMC Utrecht | 1 |
| Tanta University | 1 |
| Al-Azhar University | 1 |
A trial with sites in more than one country appears in each of those registers.
3 current trials in our Egypt, Ireland, India, Germany, France, Spain, Italy, Netherlands, Belgium, Switzerland, Czechia, Portugal, Canada, Japan, Australia and Israel registers name Ivermectin as a drug or biological intervention, as of the registry sync on 26 September 2026. Completed and withdrawn studies are not counted.
Yes. 2 of the 3 trials are recruiting: 1 with sites in Egypt, 1 with sites in Ireland, 1 with sites in India, 1 with sites in Germany, 1 with sites in France, 1 with sites in Spain, 1 with sites in Italy, 1 with sites in Netherlands, 1 with sites in Belgium, 1 with sites in Switzerland, 1 with sites in Czechia, 1 with sites in Portugal, 1 with sites in Canada, 1 with sites in Japan, 1 with sites in Australia and 1 with sites in Israel. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.
UMC Utrecht (1), Tanta University (1) and Al-Azhar University (1). The number in brackets is how many trials each organisation leads.
Yes. 1 trial in our Ireland register (ClinicalTrials.gov). Some may be the same study registered in both. See the Irish clinical trials register for sites and contacts.
Yes. The HPRA medicines list includes 3 single-substance products containing Ivermectin, for example Iverscab 3 mg tablets (Substipharm). A licence does not mean a product is currently marketed or reimbursed; see each product's record.
The registers we track list 1 entry for Ivermectin: 1 German notice. 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 Ivermectin 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 Ivermectin 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 Ivermectin (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 26 Sep 2026.