Ireland
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Priya Life Science Compound trial record
Compound · clinical trials

Efavirenz clinical trials

Also listed in trial records as Sustiva, Teva-Efavirenz, Mylan-Efavirenz, Jamp-Efavirenz, Auro-Efavirenz
Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 4 trials in our China and Canada registers that name Efavirenz as an intervention. Synced 10 Nov 2026
4Current trials
3Recruiting now
4Lead sponsors
2Country registers
At a glance

Efavirenz is named as an intervention in 4 current clinical trials in our China and Canada registers. 3 are recruiting patients now. The most common phase is Phase 3. The sponsor with the most trials is Xuanwu Hospital, Beijing (1). The most-studied condition is Creutzfeldt-Jakob Disease. The EU clinical trials register (CTIS) separately lists 1 authorised or ongoing trial.

Where Efavirenz is approved

All regulators →

Of the three regulators tracked here, the first to approve Efavirenz was the US, on 17 Sep 1998. It is approved in 3 of the 3 regulators tracked here.

USUnited States (FDA)
17 Sep 1998
Sustiva
NDA020972 on Drugs@FDA
First original NDA/BLA approval
EUEuropean Union (EMA)
28 May 1999
Stocrin
EMA product page
First centralised authorisation
CACanada (Health Canada)
19 Mar 1999
Sustiva
Notice of Compliance 1766
First new-drug NOC

From the regulators' own registers: FDA Drugs@FDA, the EMA medicines list and Health Canada's Notice of Compliance database. Dates are the first listed approval of a product containing only this substance; combination products and nationally authorised EU medicines are not counted.

What health systems spend on Efavirenz

All medicines →
ENNHS England
Not dispensed in the community in England in the last 12 months under this name
Net ingredient cost, community prescriptions
USUS Medicaid
$170k
1,502 prescriptions in 2025 · Efavirenz
-39% on 2024
Amount Medicaid reimbursed, before rebates

From NHSBSA Prescription Cost Analysis (Open Government Licence v3.0) and CMS State Drug Utilization Data. Both are gross amounts: neither system publishes its discounts or rebates per drug. Products combining several substances are not counted here.

How Efavirenz works

All drug targets →
  • Human immunodeficiency virus type 1 reverse transcriptase inhibitor Inhibitor
    ChEMBL only
Diseases it has been tested for in clinical trials, by furthest phase
  • AIDSPhase 3
  • Creutzfeldt Jacob diseasePhase 3
  • Kaposi's sarcomaPhase 3
  • SepsisPhase 3
  • Hepatitis B virus infectionPhase 3
  • Hepatitis C virus infectionPhase 3
  • Inherited lipid metabolism disorderPhase 3
  • PneumoniaPhase 3
  • TuberculosisPhase 3
  • Viral loadPhase 3
27 diseases in all

Mechanisms and diseases from ChEMBL via the Open Targets Platform (release 26.09), ChEMBL record CHEMBL223228, CC BY-SA 3.0. Targets checked against the IUPHAR/BPS Guide to PHARMACOLOGY (2026.3.1), ligand 11287, CC BY-SA 4.0. Trial phases are not approvals: approved uses are shown from the regulators' own records where we hold them.

Patient leaflets for Efavirenz

The package leaflet is the official guide for patients that comes with every medicine. These links go to the regulators that publish it.

  • IE
    Ireland: 10 products on the HPRA list
    Each product record links to the HPRA, which publishes the leaflet and SmPC.
  • EU
    European Union: Efavirenz Teva (generic)
    EMA product information: package leaflet and summary of product characteristics in every EU language.
  • 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.

Reference identifiers for Efavirenz

ATC code
J05AG03
ChEMBL
CHEMBL223228
DrugBank
DB00625
PubChem CID
64139
CAS number
154598-52-4
FDA UNII
JE6H2O27P8
Wikidata
Q422645
Wikipedia
Efavirenz

Codes that identify this medicine in other databases, from Wikidata (CC0), matched by its ChEMBL ID. The ATC code is the WHO classification of what the medicine is used for.

Trials by status

  • Recruiting375%
  • Not yet open125%

Trials by phase

  • Phase 3125%
  • Phase 1125%
  • Phase 2125%
  • Not applicable125%
01

Clinical trials of Efavirenz

4 trials
StudyPhaseStatusLead sponsorRegisters
Efavirenz for the Treatment of Creutzfeldt-Jakob Disease
NCT07482085 · ClinicalTrials.gov ↗ · Creutzfeldt-Jakob Disease
Phase 3 Recruiting Xuanwu Hospital, Beijing China
Reverse Triple Negative Immune Resistant Breast Cancer
NCT05076682 · ClinicalTrials.gov ↗ · Triple-negative Breast Cancer
Phase 2 Recruiting Fudan University China
The T Cell Activator of Cell Killing ("TACK") IT ON" STUDY
NCT06823596 · ClinicalTrials.gov ↗ · Hiv
Not applicable Recruiting University of Toronto Canada
A Single-center, Randomized, Open-label, Parallel-design Clinical Study to Evaluate the Pharmacokinetic Effects of Itraconazole, Fluconazole or Efavirenz on a Single Dose of Clifutinib in Healthy Participants
NCT07341672 · ClinicalTrials.gov ↗ · Healthy Adult Subject
Phase 1 Not yet open Sunshine Lake Pharma Co., Ltd 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.

02

Efavirenz in the EU trials register (CTIS)

1 trial

Authorised or ongoing trials in the EU Clinical Trials Information System that list a product containing Efavirenz. 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 3, Randomized, Open-label Study to Evaluate the Efficacy and Safety of Switching to a Regimen of Broadly Neutralizing Antibodies Teropavimab and Zinlirvimab in Combination with Capsid Inhibitor Lenacapavir Twice Yearly in Virologically Suppressed Adults with HIV-1 Infection on Stable Oral Treatment Regimens
2025-524336-19-00 · Virus Diseases
Phase 3 Ongoing Gilead Sciences Inc Poland, Italy, France + 3 more
03

Efavirenz across our data

Ireland · EU · US

The same active substance in our other registers, matched by its exact name. Each entry links to the register record it comes from.

Licensed in Ireland (HPRA)

10 single-substance products containing Efavirenz on the HPRA medicines list.

All 10 Irish products →

Supply shortages

No entry for Efavirenz in the EMA, FDA or German BfArM shortage lists we track.

04

Conditions studied with Efavirenz

4 conditions
Creutzfeldt-Jakob Disease1Healthy Adult Subject1Triple-negative Breast Cancer1Hiv1
05

Sponsors

lead sponsor per trial
Lead sponsorTrials
Xuanwu Hospital, Beijing1
Sunshine Lake Pharma Co., Ltd1
Fudan University1
University of Toronto1
06

By country register

RegisterTrialsRecruiting
Clinical trials in China32
Clinical trials in Canada11
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.

07

Related compounds

08

Questions about Efavirenz trials

How many clinical trials are testing Efavirenz?

4 current trials in our China and Canada registers name Efavirenz as a drug or biological intervention, as of the registry sync on 10 November 2026. Completed and withdrawn studies are not counted.

Are Efavirenz trials recruiting patients?

Yes. 3 of the 4 trials are recruiting: 2 with sites in China and 1 with sites in Canada. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.

Who sponsors Efavirenz clinical trials?

Xuanwu Hospital, Beijing (1), Sunshine Lake Pharma Co., Ltd (1), Fudan University (1) and University of Toronto (1). The number in brackets is how many trials each organisation leads.

Is Efavirenz licensed in Ireland?

Yes. The HPRA medicines list includes 10 single-substance products containing Efavirenz, for example Efavirenz Teva 600 mg film-coated tablets (Teva B.V.). A licence does not mean a product is currently marketed or reimbursed; see each product's record.

Is there a Efavirenz shortage?

Not in the lists we track: Efavirenz has no entry in the EMA, FDA or German BfArM shortage registers as of their latest sync.

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 Efavirenz 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 Efavirenz 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 Efavirenz (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.