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Priya Life Science Compound trial record
Compound · clinical trials

Rimonabant clinical trials

Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 2 trials in our Spain register that name Rimonabant as an intervention. Synced 4 Nov 2026
2Current trials
0Recruiting now
1Lead sponsor
1Country register
At a glance

Rimonabant is named as an intervention in 2 current clinical trials in our Spain register. None are recruiting at the moment. The most common phase is Phase 1/2. The lead sponsor is Sinfatin S.L. The most-studied condition is Cervical Spinal Cord Injury. The EU clinical trials register (CTIS) separately lists 1 authorised or ongoing trial.

Where Rimonabant is approved

All regulators →

Of the three regulators tracked here, the first to approve Rimonabant was the EU, on 19 Jun 2006.

USUnited States (FDA)
No FDA approval of a single-substance product in Drugs@FDA
First original NDA/BLA approval
EUEuropean Union (EMA)
19 Jun 2006
Zimulti
EMA product page
First centralised authorisation
CACanada (Health Canada)
No new-drug Notice of Compliance since 1994
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.

NICE appraisals of Rimonabant

All NICE appraisals →

NICE, which decides whether the NHS in England should fund new medicines, has published 1 technology appraisal of Rimonabant. 1 is current, and 1 of it recommends it for at least some patients.

AppraisalNICE recommendationPublishedStatus
Rimonabant for the treatment of overweight and obese adults
NICE TA144
Optimised23 Jun 2008Current

NICE decisions apply to the NHS in England. In Ireland the HSE decides on reimbursement, advised by the National Centre for Pharmacoeconomics. Titles, categories and dates link to the guidance on nice.org.uk. © NICE 2026 technology appraisal guidance. Available from www.nice.org.uk/guidance. All rights reserved. Subject to Notice of rights. NICE guidance is prepared for the National Health Service in England. All NICE guidance is subject to regular review and may be updated or withdrawn. NICE accepts no responsibility for the use of its content in this product/publication.

Patient leaflets for Rimonabant

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

  • Not yet open150%
  • Active, closed150%

Trials by phase

  • Phase 1/2150%
  • Phase 2150%
01

Clinical trials of Rimonabant

2 trials
StudyPhaseStatusLead sponsorRegisters
Rimonabant for Improving Walking Ability in Patients With Chronic Stroke
NCT07913763 · ClinicalTrials.gov ↗ · Chronic Stroke
Phase 2 Not yet open Sinfatin S.L Spain
Effect of Rimonabant on Hand Function in Patients With Spinal Cord Injury
NCT07843108 · ClinicalTrials.gov ↗ · Cervical Spinal Cord Injury
Phase 1/2 Active, closed Sinfatin S.L Spain

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

Rimonabant in the EU trials register (CTIS)

1 trial

Authorised or ongoing trials in the EU Clinical Trials Information System that list a product containing Rimonabant. 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
Effects of a CB1 Receptor Antagonist/Inverse Agonist (Rimonabant) on the Improvement of Cognitive Impairment in Patients with Post-COVID-19 Syndrome (RIMOCOVID-1)
2023-507870-42-00 · Virus Diseases
Phase 2 Ongoing Sinfatin S.L Spain
03

Conditions studied with Rimonabant

2 conditions
Cervical Spinal Cord Injury1Chronic Stroke1
04

Sponsors

lead sponsor per trial
Lead sponsorTrials
Sinfatin S.L2
05

By country register

RegisterTrialsRecruiting
Clinical trials in Spain20
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

Questions about Rimonabant trials

How many clinical trials are testing Rimonabant?

2 current trials in our Spain register name Rimonabant as a drug or biological intervention, as of the registry sync on 4 November 2026. Completed and withdrawn studies are not counted.

Are Rimonabant trials recruiting patients?

Not at the moment. None of the 2 trials in our registers is recruiting; they are active but closed to enrolment, not yet open, or enrolling by invitation. Only the study team can confirm whether a patient is eligible.

Who sponsors Rimonabant clinical trials?

The lead sponsor is Sinfatin S.L. 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 Rimonabant 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 Rimonabant 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 Rimonabant (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 4 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.