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Cardurion Pharmaceuticals clinical trials

Source: ClinicalTrials.gov, U.S. National Library of Medicine and the EU Clinical Trials Information System (CTIS) — current trials in our USA and EU (CTIS) registers with Cardurion Pharmaceuticals as lead sponsor. Synced 26 Sep 2026
3Current trials
2Recruiting now
1Drug in these trials
2Trial registers
Maintained by Sreepriya Prasannan
MSc Digital Transformation of Life Sciences (Innopharma Education / Griffith College); MSc & BSc Botany HSE Spark Ignite 2026 — Top 14 finalist
Compiled from ClinicalTrials.gov and CTIS registry records · Last verified · Editorial standards
At a glance

Cardurion Pharmaceuticals is the lead sponsor of 3 current clinical trials in our USA and EU (CTIS) registers. 2 are recruiting patients now. All registered phases are Phase 2. The drugs named most often in its trials are CRD-4730. The most-studied condition is Catecholaminergic Polymorphic Ventricular Tachycardia.

ClinicalTrials.gov trials by status

  • Recruiting2100%

Trials by phase

  • Phase 22100%
01

Clinical trials sponsored by Cardurion Pharmaceuticals

2 on ClinicalTrials.gov
StudyPhaseStatusStartRegisters
A Phase 2 Study of CRD-4730 in CPVT
NCT06658899 · Catecholaminergic Polymorphic Ventricular Tachycardia
Drug: CRD-4730
Phase 2 Recruiting 2025-12 USA
A Trial of CRD-4730 in HFrEF
NCT07750873 · ClinicalTrials.gov ↗ · Heart Failure With Reduced Ejection Fraction (HFrEF)
Drug: CRD-4730
Phase 2 Recruiting 2026-07 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. Titles and statuses are copied from the registry as published.

02

Cardurion Pharmaceuticals in the EU trials register (CTIS)

1 trial

Authorised or ongoing trials in the EU Clinical Trials Information System with Cardurion Pharmaceuticals as sponsor. Some are the same study as a ClinicalTrials.gov record above; the two registries share no common ID. Trials with a site in Ireland are listed first.

StudyPhaseStatusCountries
A Phase 2, randomized, double-blind, placebo-controlled trial to evaluate the efficacy, safety, and tolerability of CRD-4730 in patients with heart failure with reduced ejection fraction (HFREF) (CALIBRATE-HF)
2025-525033-31-00 · Cardiovascular Diseases
Drug: CRD-4730
Phase 2 Authorised Latvia, Slovakia, Lithuania + 7 more
03

Drugs in Cardurion Pharmaceuticals trials

1 compound

Drugs and biologicals named as interventions in these trials, with the number of this sponsor's trials that name each one. Placebos and generic comparators are excluded.

04

Conditions in Cardurion Pharmaceuticals trials

2 conditions
Catecholaminergic Polymorphic Ventricular Tachycardia1Heart Failure With Reduced Ejection Fraction (HFrEF)1
05

By trial register

RegisterTrialsRecruiting
Clinical trials in USA22
EU register (CTIS)1—

A trial with sites in more than one country appears in each of those registers.

06

Other sponsors in Catecholaminergic Polymorphic Ventricular Tachycardia

SponsorTrials
Solid Biosciences1

Sponsors with the most current trials registered for this condition.

07

Questions about Cardurion Pharmaceuticals trials

How many clinical trials does Cardurion Pharmaceuticals sponsor?

Cardurion Pharmaceuticals is the lead sponsor of 2 current trials on ClinicalTrials.gov in our USA register, and 1 authorised or ongoing trial in the EU register (CTIS), as of the registry sync on 26 September 2026. Completed and withdrawn studies are not counted.

Are Cardurion Pharmaceuticals trials recruiting?

Yes. 2 of its 2 ClinicalTrials.gov trials are recruiting. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.

Which drugs is Cardurion Pharmaceuticals testing?

Its current trials name 1 drug or biological as interventions. The most frequent are CRD-4730 (3). The number in brackets is how many of its trials name each drug.

Where does this information come from?

Every trial, status, phase and condition on this page is copied from public ClinicalTrials.gov and EU CTIS records by a daily sync, grouped by the sponsor name each registry records. It says nothing about the organisation beyond its registered trials, and it is not medical advice.

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How this page is built

Everything on this page is copied from public registry records — it is not written from memory, and nothing here describes the organisation beyond its registered trials. 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 trial registers and groups every current trial by its lead sponsor name, ignoring legal-form suffixes such as Inc. or Ltd. A small, hand-checked list joins the same organisation's different registry names (for example its EU legal entity). There is no AI drafting and no per-sponsor editorial pass. 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 the registries data on this page was last retrieved on 26 Sep 2026.

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.