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Sponsor · clinical trials

Cerenome clinical trials

Source: ClinicalTrials.gov, U.S. National Library of Medicine — current trials in our USA register with Cerenome as lead sponsor. Synced 26 Sep 2026
5Current trials
4Recruiting now
1Drug in these trials
1Trial register
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

Cerenome is the lead sponsor of 5 current clinical trials in our USA register. 4 are recruiting patients now. The most common phase is Phase 1. The drugs named most often in its trials are 186RNL. The most-studied condition is Glioma.

ClinicalTrials.gov trials by status

  • Recruiting480%
  • Active, closed120%

Trials by phase

  • Phase 1360%
  • Phase 1/2240%
01

Clinical trials sponsored by Cerenome

5 on ClinicalTrials.gov
StudyPhaseStatusStartRegisters
Maximum Tolerated Dose, Safety, and Efficacy of Rhenium Nanoliposomes in Recurrent Glioma (ReSPECT)
NCT01906385 · Glioma
Phase 1/2 Recruiting 2015-06 USA
Determine Maximum Tolerated Dose, Safety, and Tolerability of Rhenium (186Re) in Pediatric Recurrent, Refractory or Progressive Ependymoma and High-Grade Glioma
NCT07061626 · Ependymoma, High Grade Gliomas
Phase 1 Recruiting 2026-08 USA
Multiple Dose Intraventricular Administration of Rhenium-186 NanoLiposome for Leptomeningeal Metastases
NCT07098806 · ClinicalTrials.gov ↗ · Leptomeningeal Metastasis
Drug: 186RNL
Phase 1/2 Recruiting 2025-07 USA
Safety & Efficacy/Tolerability of Rhenium-186 NanoLiposomes (186RNL) for Patients Who Received a Prior 186RNL Treatment
NCT05460507 · ClinicalTrials.gov ↗ · Glioma
Phase 1 Recruiting 2024-12 USA
Intraventricular Administration of Rhenium-186 NanoLiposome for Leptomeningeal Metastases
NCT05034497 · Leptomeningeal Metastasis
Drug: 186RNL
Phase 1 Active, closed 2021-12 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

Drugs in Cerenome 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.

03

Conditions in Cerenome trials

4 conditions
Glioma2Leptomeningeal Metastasis2Ependymoma1High Grade Gliomas1
04

By trial register

RegisterTrialsRecruiting
Clinical trials in USA54

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

05

Other sponsors in Glioma

SponsorTrials
Tata Memorial Centre5
Huashan Hospital4
The First Affiliated Hospital of Zhengzhou University4
Nuvation Bio2
The Third Affiliated hospital of Zhejiang Chinese Medical University2
HighField Biopharmaceuticals Corporation1
Beijing Neurosurgical Institute1

Sponsors with the most current trials registered for this condition.

06

Questions about Cerenome trials

How many clinical trials does Cerenome sponsor?

Cerenome is the lead sponsor of 5 current trials on ClinicalTrials.gov in our USA register, as of the registry sync on 26 September 2026. Completed and withdrawn studies are not counted.

Are Cerenome trials recruiting?

Yes. 4 of its 5 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 Cerenome testing?

Its current trials name 1 drug or biological as interventions. The most frequent are 186RNL (2). 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.