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Radiotherapy of Multiple Brain Metastases Using AGuIX® (NANORAD2)

Primary Purpose

Brain Metastases, Adult, Radiotherapy

Status
Recruiting
Phase
Phase 2
Locations
France
Study Type
Interventional
Intervention
AGuIX®
Whole Brain Radiation Therapy
Sponsored by
University Hospital, Grenoble
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Brain Metastases, Adult focused on measuring gadolinium nanoparticles, AGuIX

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients with brain metastases, from a histologically confirmed solid tumor, eligible for WBRT
  • At least 18 years old
  • Signed informed consent after informing the patient
  • ECOG (Eastern Cooperative Oncology Group) performance status 0-2
  • Extracranial disease:

    • Complete or partial response or stability under systemic treatment
    • No extracranial disease
    • Or first line of treatment
  • Life expectancy greater than 6 weeks
  • Effective contraceptive method for all patient of childbearing potential
  • Affiliated to a social security regimen

Exclusion Criteria:

  • Leptomeningeal metastasis
  • Evidence of metastasis with recent large hemorrhage
  • Progressive and threatening extracranial disease under systemic treatment
  • Previous cranial irradiation (except stereotactic irradiation)
  • Known contra-indication, sensitivity or allergy to gadolinium
  • Known contra-indication for Magnetic Resonance Imaging
  • Renal insufficiency (glomerular filtration rate ≤ 50 mL/min/1.73m²)
  • Pregnancy or breastfeeding
  • Subject under administrative or judicial control

Sites / Locations

  • Institut Régional du CancerRecruiting
  • Institut Claudius Regaud Institut Universitaire du Cancer Toulouse Oncopole RadiothérapieRecruiting
  • Centre Leon Berard LyonRecruiting
  • Centre Hospitalier Annecy GenevoisRecruiting
  • Centre Hospitalier Universitaire Grenoble-AlpesRecruiting
  • CRLCC - Institut BergoniéRecruiting
  • Crlcc Francois BaclesseRecruiting
  • Centre Georges François LeclercRecruiting
  • Hospices Civils de Lyon-Hôpital Lyon SudRecruiting
  • Hôpital Européen Georges PompidouRecruiting
  • La Pitié Salpêtrière - Charles FoixRecruiting
  • Institut Curie Saint CloudRecruiting
  • Crlcc Paul StraussRecruiting
  • Institut de Cancérologie de Lorraine ALEXIS VAUTRINRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

AGuIX® + Whole Brain Radiation Therapy

Whole Brain Radiation Therapy

Arm Description

Intervention: Drug: AGuIX® + WBRT Other Names: Gadolinium-chelated polysiloxane based nanoparticles 3 intravenous injections at 100mg/kg D0: AGuIX® injection followed by MRI (within 7 days before commencement of WBRT) Fr1: AGuIX® injection before the first radiation session Fr6: AGuIX® injection before the sixth radiation session 30 Gy in 10 fractions of 3 Gy over 2-3 weeks

Intervention: Radiation: Whole Brain Radiation Therapy ( WBRT) 30 Gy in 10 fractions of 3 Gy over 2-3 weeks

Outcomes

Primary Outcome Measures

Best objective intracranial response rate - intent-to-treat
Evaluation of brain metastases response, according to RECIST v1.1 criteria (or modified RECIST) by MRI, with MRI centralized reading
Best objective intracranial response rate - intent-to-treat
Evaluation of brain metastases response, according to RECIST v1.1 criteria (or modified RECIST) by MRI, with MRI centralized reading

Secondary Outcome Measures

Evaluation of the quality of life
Quality of life test score EORTC QLQ C30
Evaluation of the quality of life
Quality of life test score EORTC QLQ BN20
Neurocognitive evaluation
Neurocognitive test (MoCA)
Best objective intracranial response rate - per-protocol
Evaluation of brain metastases response on per-protocol population, according to RECIST v1.1 criteria (or modified RECIST), by MRI with centralized reading
Evaluation of the intracranial response rate
Evaluation of brain metastases response, according to RANO, to RECIST v1.1 criteria, and as the evolution of the sum of longest diameters (for all metastases with a sum of diameters > 1cm), by MRI, at 6 weeks and 3, 6, 9 and 12 months
Evaluation of individual metastasis response
Evaluation of individual brain metastasis response, for all metastases with the sum of diameters > 1cm, by MRI rate
Intracranial progression-free survival
Evaluation of the time between the start of the treatment and the occurence of intracranial progression or neuriologic death
Intracranial progression-free survival, brain survival
Death related to brain metastases progression
Overall survival
Death
Change in steroid dependence
Reporting of daily steroid dose
Incidence of adverse events
Reporting of adverse events by type, frequency and severity for both treatments (WBRT and AGuIX® + WBRT)
MRI study of the distribution of the product in brain metastases
MRI evaluation of contrast enhancement at D0 after AGuIX® injection

Full Information

First Posted
December 11, 2018
Last Updated
August 16, 2023
Sponsor
University Hospital, Grenoble
Collaborators
NH TherAguix SAS
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1. Study Identification

Unique Protocol Identification Number
NCT03818386
Brief Title
Radiotherapy of Multiple Brain Metastases Using AGuIX®
Acronym
NANORAD2
Official Title
Radiotherapy of Multiple Brain Metastases Using AGuIX® Gadolinium-chelated Polysiloxane Based Nanoparticles: a Prospective Randomized Phase II Clinical Trial.
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Recruiting
Study Start Date
March 26, 2019 (Actual)
Primary Completion Date
June 26, 2024 (Anticipated)
Study Completion Date
March 26, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Grenoble
Collaborators
NH TherAguix SAS

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This is a Prospective Randomized Open Blinded Endpoint phase II clinical trial. The study will be adaptive: an interim analysis is planned after enrolment of 20 patients in each arm of treatment (WBRT and AGuIX® + WBRT), to select and continue the study with group(s) that present the best response rate to the experimental treatment (AGuIX® + WBRT). The main endpoint will be evaluated by a blinded endpoint committee.
Detailed Description
The occurrence of brain metastases is a common event in the history of cancer and negatively affects the life expectancy of patients. Their incidence varies between 15 and 50% according to the histologic types. Surgery, stereotactic radiosurgery, radiotherapy and chemotherapy are the main treatments currently proposed. For patients with multiple brain metastases, whole brain radiation therapy (WBRT) remains the standard of care. However, the median overall survival is less than 6 months and new approaches need to be developed to improve treatment of these patients. In this context, the weak control of the disease comes from three main factors: the multiplicity of the brain lesions, the radioresistance of certain histologies and the poor distribution of cytotoxic agents in brain metastases. The use of radiosensitizing agents is here of great interest. The radiosensitizing agent chosen in this study is AGuIX®. It is a Gadolinium-chelated polysiloxane based nanoparticle developed by NH TherAguix company for its theranostic properties (radiosensitization and diagnosis by multimodal imaging). Preclinical studies have demonstrated the radiosensitizing effect of AGuIX® in vivo in 8 tumor models xenografted in rodents, and particularly in brain tumors.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Brain Metastases, Adult, Radiotherapy
Keywords
gadolinium nanoparticles, AGuIX

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Model Description
Prospective Randomized Open Blinded Endpoint phase II clinical trial.
Masking
Outcomes Assessor
Masking Description
The main endpoint will be evaluated by a blinded endpoint committee.
Allocation
Randomized
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
AGuIX® + Whole Brain Radiation Therapy
Arm Type
Experimental
Arm Description
Intervention: Drug: AGuIX® + WBRT Other Names: Gadolinium-chelated polysiloxane based nanoparticles 3 intravenous injections at 100mg/kg D0: AGuIX® injection followed by MRI (within 7 days before commencement of WBRT) Fr1: AGuIX® injection before the first radiation session Fr6: AGuIX® injection before the sixth radiation session 30 Gy in 10 fractions of 3 Gy over 2-3 weeks
Arm Title
Whole Brain Radiation Therapy
Arm Type
Active Comparator
Arm Description
Intervention: Radiation: Whole Brain Radiation Therapy ( WBRT) 30 Gy in 10 fractions of 3 Gy over 2-3 weeks
Intervention Type
Drug
Intervention Name(s)
AGuIX®
Other Intervention Name(s)
Gadolinium-chelated polysiloxane based nanoparticles
Intervention Description
3 intravenous injection at 100mg/kg D0: AGuIX® injection followed by MRI (within 7 days before commencement of WBRT) Fr1: AGuIX® injection before the first radiation session Fr6: AGuIX® injection before the sixth radiation session
Intervention Type
Radiation
Intervention Name(s)
Whole Brain Radiation Therapy
Other Intervention Name(s)
WBRT
Intervention Description
30 Gy in 10 fractions of 3 Gy over 2-3 weeks
Primary Outcome Measure Information:
Title
Best objective intracranial response rate - intent-to-treat
Description
Evaluation of brain metastases response, according to RECIST v1.1 criteria (or modified RECIST) by MRI, with MRI centralized reading
Time Frame
at 6 weeks
Title
Best objective intracranial response rate - intent-to-treat
Description
Evaluation of brain metastases response, according to RECIST v1.1 criteria (or modified RECIST) by MRI, with MRI centralized reading
Time Frame
at 3 months
Secondary Outcome Measure Information:
Title
Evaluation of the quality of life
Description
Quality of life test score EORTC QLQ C30
Time Frame
at D0, 6 weeks, 3, 6, 9, 12 months
Title
Evaluation of the quality of life
Description
Quality of life test score EORTC QLQ BN20
Time Frame
at day 0, 6 weeks, 3, 6, 9, 12 months
Title
Neurocognitive evaluation
Description
Neurocognitive test (MoCA)
Time Frame
at Day 0, 6 weeks, 3, 6, 9, 12 months
Title
Best objective intracranial response rate - per-protocol
Description
Evaluation of brain metastases response on per-protocol population, according to RECIST v1.1 criteria (or modified RECIST), by MRI with centralized reading
Time Frame
at 6 weeks and 3 months
Title
Evaluation of the intracranial response rate
Description
Evaluation of brain metastases response, according to RANO, to RECIST v1.1 criteria, and as the evolution of the sum of longest diameters (for all metastases with a sum of diameters > 1cm), by MRI, at 6 weeks and 3, 6, 9 and 12 months
Time Frame
for 12 months
Title
Evaluation of individual metastasis response
Description
Evaluation of individual brain metastasis response, for all metastases with the sum of diameters > 1cm, by MRI rate
Time Frame
at 6 weeks and 3, 6, 9 and 12 months
Title
Intracranial progression-free survival
Description
Evaluation of the time between the start of the treatment and the occurence of intracranial progression or neuriologic death
Time Frame
at 12 months
Title
Intracranial progression-free survival, brain survival
Description
Death related to brain metastases progression
Time Frame
at 12 months
Title
Overall survival
Description
Death
Time Frame
at 12 months
Title
Change in steroid dependence
Description
Reporting of daily steroid dose
Time Frame
at 6 weeks and 3, 6, 9 and 12 months
Title
Incidence of adverse events
Description
Reporting of adverse events by type, frequency and severity for both treatments (WBRT and AGuIX® + WBRT)
Time Frame
at 6 weeks and 3, 6, 9 and 12 months
Title
MRI study of the distribution of the product in brain metastases
Description
MRI evaluation of contrast enhancement at D0 after AGuIX® injection
Time Frame
Day 0

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with brain metastases, from a histologically confirmed solid tumor, eligible for WBRT At least 18 years old Signed informed consent after informing the patient ECOG (Eastern Cooperative Oncology Group) performance status 0-2 Extracranial disease: Complete or partial response or stability under systemic treatment No extracranial disease Or first line of treatment Life expectancy greater than 6 weeks Effective contraceptive method for all patient of childbearing potential Affiliated to a social security regimen Exclusion Criteria: Leptomeningeal metastasis Evidence of metastasis with recent large hemorrhage Progressive and threatening extracranial disease under systemic treatment Previous cranial irradiation (except stereotactic irradiation) Known contra-indication, sensitivity or allergy to gadolinium Known contra-indication for Magnetic Resonance Imaging Renal insufficiency (glomerular filtration rate ≤ 50 mL/min/1.73m²) Pregnancy or breastfeeding Subject under administrative or judicial control
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Camille VERRY, MD
Phone
+33 (0)4 76 76 54 35
Email
cverry@chu-grenoble.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Tinaïg LE COSTAOUEC
Phone
+33 (0)4 76 76 68 13
Email
TLecostaouec@chu-grenoble.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Camille VERRY, MD
Organizational Affiliation
University Hospital, Grenoble
Official's Role
Principal Investigator
Facility Information:
Facility Name
Institut Régional du Cancer
City
Montpellier
State/Province
Occitanie
ZIP/Postal Code
34298
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Olivier RIOU, Dr
Phone
+33 (0)4 67 61 24 43
Email
Olivier.Riou@icm.unicancer.fr
First Name & Middle Initial & Last Name & Degree
Justine ROCHER, Study Co
Phone
+33 4 67 61 23 71
Email
justine.rochet@icm.unicancer.fr
First Name & Middle Initial & Last Name & Degree
OLIVIER RIOU, Dr
Facility Name
Institut Claudius Regaud Institut Universitaire du Cancer Toulouse Oncopole Radiothérapie
City
Toulouse
State/Province
Occitanie
ZIP/Postal Code
31059
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ciprian CHIRA
Phone
+33 (0)5 31 15 60 50
Email
chira.ciprian@iuct-oncopole.fr
First Name & Middle Initial & Last Name & Degree
Stella MANTA, Study Co
Phone
05 31 15 58 01
Email
manta.stella@iuct-oncopole.fs
First Name & Middle Initial & Last Name & Degree
CIPRIAN CHIRA
Facility Name
Centre Leon Berard Lyon
City
Lyon
State/Province
Rhones Alpes
ZIP/Postal Code
69373
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ronan TANGUY
Phone
+33(0)4 78 78 28 28
Email
Ronan.TANGUY@lyon.unicancer.fr
First Name & Middle Initial & Last Name & Degree
Cécile BACHELIER, Study Co
Phone
+33(0)4 78 78 28 85
Email
Cecile.BACHELIER@lyon.unicancer.fr
First Name & Middle Initial & Last Name & Degree
RONAN TANGUY
Facility Name
Centre Hospitalier Annecy Genevois
City
Annecy
State/Province
Rhones-Alpes
ZIP/Postal Code
74374
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Alexandre TESSIER, MD
Phone
04 50 63 63 63
Ext
585380
Email
atessier@ch-annecygenevois.fr
First Name & Middle Initial & Last Name & Degree
Fanny BOCHE, Study Co
Phone
+33 4 56 49 74 69
Email
fboche@ch-annecygenevois.fr
First Name & Middle Initial & Last Name & Degree
ALEXANDRE TESSIER, MD
First Name & Middle Initial & Last Name & Degree
JOHAN KRISTIANSEN, MD
Facility Name
Centre Hospitalier Universitaire Grenoble-Alpes
City
Grenoble
State/Province
Rhones-Alpes
ZIP/Postal Code
38700
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Camille VERRY, MD, PHD
Phone
+33476765435
Email
cverry@chu-grenoble.fr
First Name & Middle Initial & Last Name & Degree
Mélanie GATALETA, Study Co
Phone
+33476768339
Email
MGataleta1@chu-grenoble.fr
First Name & Middle Initial & Last Name & Degree
Camille VERRY, MD, PHD
First Name & Middle Initial & Last Name & Degree
Julie VILLA
First Name & Middle Initial & Last Name & Degree
Andréa DESAGNEAUX
Facility Name
CRLCC - Institut Bergonié
City
Bordeaux
ZIP/Postal Code
33000
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Nicolas MILHADE, MD PHD
Email
n.milhade@bordeaux.unicancer.fr
First Name & Middle Initial & Last Name & Degree
Laurence VIRMOUX, Study Co
Phone
05 56 33 33 33
Ext
3531
Email
l.virmoux@bordeaux.unicancer.fr
First Name & Middle Initial & Last Name & Degree
NICOLAS MILHADE, MD PHD
Facility Name
Crlcc Francois Baclesse
City
Caen
ZIP/Postal Code
14000
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Paul LESUEUR, PHD
Email
p.lesueur@baclesse.unicancer.fr
First Name & Middle Initial & Last Name & Degree
Bérénice LEGRAND, Study Co
Phone
02 31 45 50 50
Email
b.legrand@baclesse.unicancer.fr
First Name & Middle Initial & Last Name & Degree
PAUL LESUEUR, MD
Facility Name
Centre Georges François Leclerc
City
Dijon
ZIP/Postal Code
21079
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Gilles TRUC, PUPH
Phone
03 80 73 75 18
Email
gtruc@cgfl.fr
First Name & Middle Initial & Last Name & Degree
Philippe BATAILLARD, Study Co
Email
PBataillard@cgfl.fr
First Name & Middle Initial & Last Name & Degree
GILLES TRUC, PUPH
Facility Name
Hospices Civils de Lyon-Hôpital Lyon Sud
City
Lyon
ZIP/Postal Code
69495
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Anne D'HOMBRES
Email
anne.dhombres@chu-lyon.fr
First Name & Middle Initial & Last Name & Degree
Célia PREVOST, Study Co
Phone
04 78 86 42 99
Email
celia.prevost@chu-lyon.fr
First Name & Middle Initial & Last Name & Degree
ANNE D'HOMBRES
Facility Name
Hôpital Européen Georges Pompidou
City
Paris
ZIP/Postal Code
75015
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Philippe GIRAUD, MD, PHD
Phone
01 56 09 54 65
Email
philippe.giraud@aphp.fr
First Name & Middle Initial & Last Name & Degree
Virginie RIEB, Study Co
Phone
01 56 09 50 09
Email
virginie.rieb@aphp.fr
First Name & Middle Initial & Last Name & Degree
PHILIPPE GIRAUD, MD, PHD
Facility Name
La Pitié Salpêtrière - Charles Foix
City
Paris
ZIP/Postal Code
75651
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Julian JACOB, MD, PHD
Phone
+33 (0) 1 42 17 81 71
Email
julian.jacob@aphp.fr
First Name & Middle Initial & Last Name & Degree
Audie BAVOUIDIBIO, Study Co
Phone
+33 (0) 1 42 16 00 25
Email
audie.bavouidibio2@aphp.fr
First Name & Middle Initial & Last Name & Degree
JULIAN JACOB, MD, PHD
Facility Name
Institut Curie Saint Cloud
City
Saint-Cloud
ZIP/Postal Code
92210
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Maxime LOO
Email
maxime.loo@curie.fr
First Name & Middle Initial & Last Name & Degree
Agnès BABARIT, Study Co
Phone
+33(0) 1 47 11 18 55
Email
agnes.babarit@curie.fr
First Name & Middle Initial & Last Name & Degree
MAXIME LOO
Facility Name
Crlcc Paul Strauss
City
Strasbourg
ZIP/Postal Code
67085
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
George NOEL, MD PHD
Email
gnoel@strasbourg.unicancer.fr
First Name & Middle Initial & Last Name & Degree
Laurence KLEIDER, Study Co
Phone
03 68 76 73 60
Email
l.kleider@icans.eu
First Name & Middle Initial & Last Name & Degree
GEORGE NOEL, MD PHD
Facility Name
Institut de Cancérologie de Lorraine ALEXIS VAUTRIN
City
Vandœuvre-lès-Nancy
ZIP/Postal Code
54519
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Anaïs STEFANI, MD
Phone
03 83 59 84 27
Email
a.stefani@nancy.unicancer.fr
First Name & Middle Initial & Last Name & Degree
Fabienne BONNICHON, Study Co
Phone
03 83 59 84 27
Ext
87 23
Email
f.polet@nancy.unicancer.fr
First Name & Middle Initial & Last Name & Degree
ANAIS STEFANI, MD

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
22040385
Citation
Le Duc G, Miladi I, Alric C, Mowat P, Brauer-Krisch E, Bouchet A, Khalil E, Billotey C, Janier M, Lux F, Epicier T, Perriat P, Roux S, Tillement O. Toward an image-guided microbeam radiation therapy using gadolinium-based nanoparticles. ACS Nano. 2011 Dec 27;5(12):9566-74. doi: 10.1021/nn202797h. Epub 2011 Nov 9.
Results Reference
background
PubMed Identifier
30226413
Citation
Lux F, Tran VL, Thomas E, Dufort S, Rossetti F, Martini M, Truillet C, Doussineau T, Bort G, Denat F, Boschetti F, Angelovski G, Detappe A, Cremillieux Y, Mignet N, Doan BT, Larrat B, Meriaux S, Barbier E, Roux S, Fries P, Muller A, Abadjian MC, Anderson C, Canet-Soulas E, Bouziotis P, Barberi-Heyob M, Frochot C, Verry C, Balosso J, Evans M, Sidi-Boumedine J, Janier M, Butterworth K, McMahon S, Prise K, Aloy MT, Ardail D, Rodriguez-Lafrasse C, Porcel E, Lacombe S, Berbeco R, Allouch A, Perfettini JL, Chargari C, Deutsch E, Le Duc G, Tillement O. AGuIX(R) from bench to bedside-Transfer of an ultrasmall theranostic gadolinium-based nanoparticle to clinical medicine. Br J Radiol. 2019 Jan;92(1093):20180365. doi: 10.1259/bjr.20180365. Epub 2018 Sep 18.
Results Reference
background
PubMed Identifier
27529506
Citation
Verry C, Dufort S, Barbier EL, Montigon O, Peoc'h M, Chartier P, Lux F, Balosso J, Tillement O, Sancey L, Le Duc G. MRI-guided clinical 6-MV radiosensitization of glioma using a unique gadolinium-based nanoparticles injection. Nanomedicine (Lond). 2016 Sep;11(18):2405-17. doi: 10.2217/nnm-2016-0203. Epub 2016 Aug 16.
Results Reference
background

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Radiotherapy of Multiple Brain Metastases Using AGuIX®

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