Ireland
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Priya Life Science Compound trial record
Compound · clinical trials

ENV-294 clinical trials

Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 3 trials in our USA register that name ENV-294 as an intervention. Synced 10 Nov 2026
3Current trials
3Recruiting now
1Lead sponsor
1Country register
At a glance

ENV-294 is named as an intervention in 3 current clinical trials in our USA register. 3 are recruiting patients now. All registered phases are Phase 2. The lead sponsor is Enveda Therapeutics. The most-studied condition is Atopic Dermatitis (AD). The EU clinical trials register (CTIS) separately lists 1 authorised or ongoing trial.

Patient leaflets for ENV-294

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

  • Recruiting3100%

Trials by phase

  • Phase 23100%
01

Clinical trials of ENV-294

3 trials
StudyPhaseStatusLead sponsorRegisters
Study of ENV-294 in Adults With Moderate-to-Severe Atopic Dermatitis
NCT07298395 · Atopic Dermatitis (AD)
Phase 2 Recruiting Enveda Therapeutics USA
ENV-294 for Moderate-to-Severe Asthma: A 12-Week Study in Adults
NCT07301255 · Asthma
Phase 2 Recruiting Enveda Therapeutics USA
A Phase 2b Dose-Ranging Study to Evaluate the Efficacy and Safety of ENV-294 in Adults With Moderate-to-Severe Atopic Dermatitis
NCT07643766 · Atopic Dermatitis
Phase 2 Recruiting Enveda Therapeutics USA

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.

02

ENV-294 in the EU trials register (CTIS)

1 trial

Authorised or ongoing trials in the EU Clinical Trials Information System that list a product containing ENV-294. Many trials are registered in both CTIS and ClinicalTrials.gov, so these are shown separately rather than added to the count above. Trials with a site in Ireland are listed first.

StudyPhaseStatusSponsorCountries
A Phase 2b, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Dose-Ranging Study to Evaluate the Efficacy and Safety of ENV-294 in Adult Participants with Moderate-to-Severe Atopic Dermatitis
2026-526184-38-00 · Skin and Connective Tissue Diseases
Phase 2 Authorised Enveda Therapeutics Inc Germany, Czechia, Bulgaria + 2 more
03

Conditions studied with ENV-294

3 conditions
04

Sponsors

lead sponsor per trial
Lead sponsorTrials
Enveda Therapeutics3
05

By country register

RegisterTrialsRecruiting
Clinical trials in USA33
EU register (CTIS)1—

A trial with sites in more than one country appears in each of those registers. CTIS does not publish a recruiting flag; its trials may also appear in the registers above.

06

Related compounds

07

Questions about ENV-294 trials

How many clinical trials are testing ENV-294?

3 current trials in our USA register name ENV-294 as a drug or biological intervention, as of the registry sync on 10 November 2026. Completed and withdrawn studies are not counted.

Are ENV-294 trials recruiting patients?

Yes. 3 of the 3 trials are recruiting: 3 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 ENV-294 clinical trials?

The lead sponsor is Enveda Therapeutics. 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 ENV-294 works or whether it is effective, and it is not medical advice.

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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 ENV-294 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 ENV-294 (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 10 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.