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Priya Life Science Compound trial record
Compound · clinical trials

Lomustine clinical trials

Also listed in trial records as CeeNU, Gleostine, 1-Nitrosourea, Belustin, Belustine, Cecenu, Chloroethylcyclohexylnitrosourea, Citostal, Lomeblastin, Lomustinum, Lucostin
Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 11 trials in our France, Switzerland, Canada, USA, Spain, Germany, Netherlands, Belgium, Italy, Israel, Denmark, Austria, Sweden, Australia, Norway, Portugal, Czechia and Mexico registers that name Lomustine as an intervention. Synced 9 Nov 2026
11Current trials
5Recruiting now
10Lead sponsors
18Country registers
At a glance

Lomustine is named as an intervention in 11 current clinical trials in our France, Switzerland, Canada, USA, Spain, Germany, Netherlands, Belgium, Italy, Israel, Denmark, Austria, Sweden, Australia, Norway, Portugal, Czechia and Mexico registers. 5 are recruiting patients now. The most common phase is Phase 3. The sponsor with the most trials is Children's Oncology Group (2). The most-studied condition is Glioblastoma.

Where Lomustine is approved

All regulators →

Of the three regulators tracked here, the first to approve Lomustine was the US, on 4 Aug 1976.

USUnited States (FDA)
4 Aug 1976
Gleostine
NDA017588 on 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.

What health systems spend on Lomustine

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
$23k
13 prescriptions in 2025 · Lomustine
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 Lomustine works

All drug targets →
Diseases it has been tested for in clinical trials, by furthest phase
  • Acute myeloid leukemiaPhase 3
  • Acute myeloid leukemia by FAB classificationPhase 3
  • Anaplastic astrocytomaPhase 3
  • Anaplastic oligoastrocytomaPhase 3
  • Anaplastic oligodendrogliomaPhase 3
  • Astrocytoma (excluding glioblastoma)Phase 3
  • Diffuse intrinsic pontine gliomaPhase 3
  • GlioblastomaPhase 3
  • Grade III gliomaPhase 3
  • Low grade gliomaPhase 3
40 diseases in all

Mechanisms and diseases from ChEMBL via the Open Targets Platform (release 26.09), ChEMBL record CHEMBL514, CC BY-SA 3.0. Targets checked against the IUPHAR/BPS Guide to PHARMACOLOGY (2026.3.1), ligand 7214, 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 Lomustine

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.

Reference identifiers for Lomustine

ATC code
L01AD02
ChEMBL
CHEMBL514
DrugBank
DB01206
PubChem CID
3950
CAS number
13010-47-4
FDA UNII
7BRF0Z81KG
Wikidata
Q415378
Wikipedia
Lomustine

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

  • Recruiting545%
  • Active, closed655%

Trials by phase

  • Phase 3545%
  • Phase 2436%
  • Observational19%
  • Phase 2/319%
01

Clinical trials of Lomustine

11 trials
StudyPhaseStatusLead sponsorRegisters
A Study of Treatment for Medulloblastoma Using Sodium Thiosulfate to Reduce Hearing Loss
NCT05382338 · Childhood Medulloblastoma
Phase 3 Recruiting Children's Oncology Group Canada, Israel
Lomustine With and Without Reirradiation for First Progression of Glioblastoma: a Randomized Phase III Study
NCT05904119 · ClinicalTrials.gov ↗ · First Progression of Glioblastoma
Phase 3 Recruiting European Organisation for Research and Treatment of Cancer - EORTC Germany, France, Spain, Italy, Netherlands, Belgium, Denmark, Switzerland, Austria, Czechia, Norway
Lomustine in Addition to Standard of Care in Patients With MGMT Methylated Glioblastoma
NCT06419946 · ClinicalTrials.gov ↗ · Glioblastoma, IDH-wildtype, MGMT-Methylated Glioblastoma
Phase 3 Recruiting Vastra Gotaland Region Sweden, Denmark, Austria, Norway
A Trial to Evaluate Multiple Regimens in Newly Diagnosed and Recurrent Glioblastoma
NCT03970447 · ClinicalTrials.gov ↗ · Glioblastoma
Phase 2/3 Recruiting Global Coalition for Adaptive Research Germany, France, Switzerland, Canada, Australia
The RECSUR-study: Resection Versus Best Oncological Treatment for Recurrent Glioblastoma (ENCRAM 2302)
NCT06283927 · Glioblastoma, Glioblastoma Multiforme, Glioblastoma, IDH-wildtype
Observational Recruiting Jasper Gerritsen Germany, Netherlands, Belgium, Switzerland
Testing the Addition of the Chemotherapy Drug Lomustine (Gleostine) to the Usual Treatment (Temozolomide and Radiation Therapy) for Newly Diagnosed MGMT Methylated Glioblastoma
NCT05095376 · ClinicalTrials.gov ↗ · Glioblastoma, Gliosarcoma
Phase 3 Active, closed NRG Oncology Canada, Mexico
Sonocloud-9 in Association With Carboplatin Versus Standard-of-Care Chemotherapies (CCNU or TMZ) in Recurrent GBM
NCT05902169 · Glioblastoma, Recurrent Glioblastoma, GBM
Phase 3 Active, closed CarThera USA, Germany, France, Spain, Italy, Netherlands, Belgium, Sweden, Denmark, Switzerland, Austria
Reduced Craniospinal Radiation Therapy and Chemotherapy in Treating Younger Patients With Newly Diagnosed WNT-Driven Medulloblastoma
NCT02724579 · ClinicalTrials.gov ↗ · Medulloblastoma
Phase 2 Active, closed Children's Oncology Group Canada, Australia, Israel
9-ING-41 in Patients With Advanced Cancers
NCT03678883 · Cancer, Pancreatic Cancer, Sarcoma
Phase 2 Active, closed Actuate Therapeutics Inc USA, France, Spain, Netherlands, Belgium, Portugal, Canada
A Study of Berubicin in Adult Subjects With Recurrent Glioblastoma Multiforme
NCT04762069 · Glioblastoma Multiforme, Adult
Phase 2 Active, closed CNS Pharmaceuticals, Inc USA, France, Spain, Italy, Switzerland
A Study With L19TNF in Combination With Lomustine in Patients With Glioblastoma at Progression or Recurrence
NCT06336291 · ClinicalTrials.gov ↗ · Glioblastoma
Phase 2 Active, closed Philogen S.p.A USA, Israel

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 Lomustine

16 conditions
Glioblastoma5Glioblastoma, IDH-wildtype2Glioblastoma Multiforme, Adult1Recurrent Glioblastoma1GBM1Cancer1Pancreatic Cancer1Sarcoma1Renal Cancer1Glioblastoma Multiforme1Glioblastoma Multiforme of Brain1First Progression of Glioblastoma1
All 16 conditions
Condition (as registered)Trials
Glioblastoma5
Glioblastoma, IDH-wildtype2
Glioblastoma Multiforme, Adult1
Recurrent Glioblastoma1
GBM1
Cancer1
Pancreatic Cancer1
Sarcoma1
Renal Cancer1
Glioblastoma Multiforme1
Glioblastoma Multiforme of Brain1
First Progression of Glioblastoma1
MGMT-Methylated Glioblastoma1
Childhood Medulloblastoma1
Gliosarcoma1
Medulloblastoma1
05

Related compounds

06

Questions about Lomustine trials

How many clinical trials are testing Lomustine?

11 current trials in our France, Switzerland, Canada, USA, Spain, Germany, Netherlands, Belgium, Italy, Israel, Denmark, Austria, Sweden, Australia, Norway, Portugal, Czechia and Mexico registers name Lomustine (also registered as 1-Nitrosourea) as a drug or biological intervention, as of the registry sync on 9 November 2026. Completed and withdrawn studies are not counted.

Are Lomustine trials recruiting patients?

Yes. 5 of the 11 trials are recruiting: 2 with sites in France, 3 with sites in Switzerland, 2 with sites in Canada, 1 with sites in Spain, 3 with sites in Germany, 2 with sites in Netherlands, 2 with sites in Belgium, 1 with sites in Italy, 1 with sites in Israel, 2 with sites in Denmark, 2 with sites in Austria, 1 with sites in Sweden, 1 with sites in Australia, 2 with sites in Norway and 1 with sites in Czechia. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.

Who sponsors Lomustine clinical trials?

Children's Oncology Group (2), CNS Pharmaceuticals, Inc (1), Philogen S.p.A (1) and CarThera (1), among 10 lead sponsors in total. 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 Lomustine 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 Lomustine 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 Lomustine (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 9 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.