Ireland
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Priya Life Science Compound trial record
Compound · clinical trials

Roginolisib clinical trials

Also listed in trial records as IOA-244
Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 6 trials in our Italy, UK, Spain, France, Belgium and Australia registers that name Roginolisib as an intervention. Synced 10 Nov 2026
6Current trials
3Recruiting now
3Lead sponsors
6Country registers
At a glance

Roginolisib is named as an intervention in 6 current clinical trials in our Italy, UK, Spain, France, Belgium and Australia registers. 3 are recruiting patients now. The most common phase is Phase 1/2. The sponsor with the most trials is iOnctura (4). The most-studied condition is Solid Tumor, Adult.

Where Roginolisib is approved

All regulators →
USUnited States (FDA)
No FDA approval of a single-substance product in Drugs@FDA
First original NDA/BLA approval
EUEuropean Union (EMA)
No centralised EU authorisation (it may be authorised nationally)
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.

How Roginolisib works

All drug targets →
Diseases it has been tested for in clinical trials, by furthest phase
  • Uveal melanomaPhase 2
  • B-cell chronic lymphocytic leukemiaPhase 1/2
  • Mature T-cell and NK-cell non-Hodgkin lymphomaPhase 1/2
  • MyelofibrosisPhase 1/2
  • Non-small cell lung carcinomaPhase 1/2
  • Cutaneous melanomaPhase 1
  • MesotheliomaPhase 1
  • Primary myelofibrosisPhase 1

Mechanisms and diseases from ChEMBL via the Open Targets Platform (release 26.09), ChEMBL record CHEMBL3683575, CC BY-SA 3.0. Targets checked against the IUPHAR/BPS Guide to PHARMACOLOGY (2026.3.1), ligand 12487, 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 Roginolisib

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

  • Recruiting350%
  • Active, closed350%

Trials by phase

  • Phase 1/2350%
  • Phase 1233%
  • Phase 2117%
01

Clinical trials of Roginolisib

6 trials
StudyPhaseStatusLead sponsorRegisters
A Study of Roginolisib in Combination With Ruxolitinib in Patients With Myelofibrosis (MF) Who Are Unresponsive to JAK Inhibitors
NCT06887803 · Myelofibrosis (MF)
Phase 1/2 Recruiting iOnctura UK, Spain, Italy
A Platform Trial Evaluating New Drugs or Combination in R/R Peripheral T-cell Lymphomas
NCT07018752 · ClinicalTrials.gov ↗ · Peripheral T Cells Lymphoma (PTCL), Follicular Helper T-Cell Lymphoma
Phase 1/2 Recruiting The Lymphoma Academic Research Organisation France
Tebentafusp and Roginolisib in Uveal Melanoma to Prolong T-cell Homeostasis
NCT07203391 · Uveal Melanoma, Metastatic
Phase 1 Recruiting St Vincent's Hospital, Sydney Australia
A Randomised Phase II Study of Roginolisib in Patients With Advanced/Metastatic Uveal Melanoma
NCT06717126 · Uveal Melanoma, Ocular Melanoma
Phase 2 Active, closed iOnctura UK, Spain, Italy
A Study of Roginolisib (IOA-244) in Combination With Dostarlimab With or Without Docetaxel in Metastatic Non Small-cell Lung Cancer (NSCLC) Patients
NCT06879717 · ClinicalTrials.gov ↗ · Non-Squamous Non-Small Cell Lung Cancer (NSCLC), Advanced Non Squamous NSCLC
Phase 1/2 Active, closed iOnctura Spain, Italy, Belgium
A Study to Assess a PI3Kδ Inhibitor (IOA-244) in Patients With Metastatic Cancers
NCT04328844 · Solid Tumor, Adult, Non-Hodgkin Lymphoma, Adult, NSCLC
Phase 1 Active, closed iOnctura UK, Italy

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

Conditions studied with Roginolisib

12 conditions
Solid Tumor, Adult1Non-Hodgkin Lymphoma, Adult1NSCLC1Myelofibrosis1Uveal Melanoma1Ocular Melanoma1Myelofibrosis (MF)1Peripheral T Cells Lymphoma (PTCL)1Follicular Helper T-Cell Lymphoma1Non-Squamous Non-Small Cell Lung Cancer (NSCLC)1Advanced Non Squamous NSCLC1Uveal Melanoma, Metastatic1
03

Sponsors

lead sponsor per trial
Lead sponsorTrials
iOnctura4
The Lymphoma Academic Research Organisation1
St Vincent's Hospital, Sydney1
04

By country register

RegisterTrialsRecruiting
Clinical trials in Italy41
Clinical trials in UK31
Clinical trials in Spain31
Clinical trials in France11
Clinical trials in Belgium10
Clinical trials in Australia11

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

05

Related compounds

06

Questions about Roginolisib trials

How many clinical trials are testing Roginolisib?

6 current trials in our Italy, UK, Spain, France, Belgium and Australia registers name Roginolisib (also registered as IOA-244) as a drug or biological intervention, as of the registry sync on 10 November 2026. Completed and withdrawn studies are not counted.

Are Roginolisib trials recruiting patients?

Yes. 3 of the 6 trials are recruiting: 1 with sites in Italy, 1 with sites in UK, 1 with sites in Spain, 1 with sites in France and 1 with sites in Australia. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.

Who sponsors Roginolisib clinical trials?

iOnctura (4), The Lymphoma Academic Research Organisation (1) and St Vincent's Hospital, Sydney (1). 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 Roginolisib 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 Roginolisib 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 Roginolisib (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.