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NCT06652438RecruitingPhase 3

Revumenib in Combination With Azacitidine + Venetoclax in Patients NPM1-mutated or KMT2A-rearranged AML

Randomized Study to Assess Revumenib in Combination With Azacitidine + Venetoclax in Adult Patients With Newly Diagnosed NPM1-mutated or KMT2A-rearranged AML Ineligible for Intensive Chemotherapy

Source: ClinicalTrials.gov · Last updated 2 Sept 2026

Brief summary (registry, in English)

Treatment of patients with newly diagnosed AML who are not eligible for intensive chemotherapy has remained an area of high unmet medical need. The combination therapy with two medicines, azacitidine and venetoclax, is the usual plan of action. This has brought significant progress in the treatment, but it nevertheless is not curative and the disease does relapse over time. Revumenib blocks a specific molecule called menin in the cell nucleus. Some types of AML are reliant on menin working properly. These are leukemia cells with a change in the DNA, i.e. a mutation in the NPM1 or KMT2A gene. Revumenib can prevent the production of these types of leukemia cells by disrupting the production of this menin. The current study investigates whether adding revumenib to the combination therapy improves the prognosis for AML patients with a mutation in the NPM1 or KMT2A gene. This is a randomized, double-blind, placebo-controlled clinical study where subjects will be treated until disease progression, or development of side effects or death. From the moment of inclusion of the last patient, there will be a 4-year observational follow-up study in order to register survival duration and follow-up visits. Approximately 448 previously untreated patients with a mutation in the NPM1 or KMT2A gene and with newly diagnosed AML, who are not eligible for intensive chemotherapy. Patients must be ≥18 years of age.

Status (registry)
Recruiting
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
448 (estimated)
First submitted
2 Oct 2024
Start date
5 May 2025
Primary completion date
13 Dec 2029
Lead sponsor
Stichting Hemato-Oncologie voor Volwassenen Nederland
NCT number
NCT06652438
EU CT number
2024-512733-32-00

What you commit to

  • Study type: Interventional · Phase 3
  • Planned participants: 448
  • From 5 May 2025 to the primary completion date, 13 Dec 2029
  • 197 sites in 18 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Who the study is looking for

  • Central confirmation of NPM1 mutation or KMT2A rearrangement in one of the dedicated central genetic laboratories.
  • Age ≥ 18 years, no upper age limit.
  • Patient is ineligible for intensive induction chemotherapy by meeting at least 1 of the following criteria: * ≥ 75 years of age: ineligible for intensive chemotherapy per physician's discretion (with an ECOG performance status 0-2). * 18-74 years: patient is not eligible for standard chemotherapy because any of the following co-morbidities: * ECOG performance status 2 or 3. * Cardiac history of chronic heart failure requiring treatment; or with an ejection fraction ≤50%; or chronic stable angina. * DLCO ≤ 65% or FEV1 ≤ 65%. * Creatinine clearance ≥ 30 mL/min to \<45 ml/min calculated by the Cockcroft Gault formula. * Moderate hepatic impairment with total bilirubin \> 1.5 to \< 3.0 x upper limit of normal (ULN). * Any other comorbidity that the local physician assesses to be incompatible with intensive chemotherapy must be reviewed and approved by the Sponsor's (co-) Principal Investigator (written approval must be sent to before study enrolment).
  • Patient must have a projected life expectancy of at least 12 weeks (as assessed by the treating physician).
  • Patient must have a white cell blood (WBC) count of \< 25 x 109/L. Hydroxyurea can be used prior to study enrolment to reduce the WBC count to meet this criterion.
  • Adequate renal function as evidenced by serum creatinine ≤ 2.0 × upper limit of norm (ULN) or creatinine clearance \>30 mL/min based on the Cockcroft-Gault glomerular filtration rate (GFR).
  • Adequate hepatic function as evidenced by: * Serum total bilirubin ≤ 3.0 × ULN unless considered due to Gilbert's disease, or leukemic involvement following written approval by the sponsor (Co-)Principal Investigator (copy in ). * Aspartate aminotransferase (AST), alanine aminotransferase (ALT), and alkaline phosphatase (ALP) ≤ 3.0 × ULN, unless considered due to leukemic involvement following written approval by the sponsor (Co-)Principal Investigator (copy in ).
  • Female patient must: * be of nonchildbearing potential: o postmenopausal (defined as at least 1 year without any menses). o documented surgically sterile (e.g. documented hysterectomy, bilateral oophorectomy, bilateral salpingectomy or congenital sterile) or status post hysterectomy (at least 1 month prior to screening). * or, if of childbearing potential (not surgically sterile and not postmenopausal) agree to avoid pregnancy during the study and for 6 months after the final study drug administration. * and have a negative urine or serum pregnancy test at screening. * and, if heterosexually active, agree to consistently apply one highly effective\* method of birth control in combination to a barrier method for the duration of the study and for 6 months after the final study drug administration. \*Highly effective forms of birth control include \- Consistent and correct usage of established hormonal contraceptives that inhibit ovulation for at least 1 month prior to taking study drug. (hormonal contraception is only a highly effective method of birth control, if a combined \[estrogen and progestogen containing\] hormonal contraception or a progestogen-only hormonal contraception - both associated with inhibition of ovulation - is used. \- Established intrauterine device (IUD) or intrauterine system (IUS) \- Bilateral tubal occlusion \- Vasectomy - a vasectomy is highly effective contraception method provided the absence of sperm has been confirmed. If not, an additional highly effective method of contraception should be used. \- Male is sterile due to a bilateral orchiectomy. * Sexual abstinence is considered a highly effective method only if defined as refraining from heterosexual activity during the entire period of risk associated with the study drug. The reliability of sexual abstinence needs to be evaluated in relation to the duration of the clinical study and the preferred and usual lifestyle of the patient. List is not all inclusive. Prior to enrolment, the investigator is responsible for confirming patient will utilize highly effective forms of birth control in combination with a barrier method according to locally accepted standards during the protocol defined period. * agree not to breastfeed starting at screening and throughout the study period. * agree not to donate ova starting at screening and throughout the study period, and for 6 months after the final study drug administration.
  • Men must use a latex condom during any sexual contact with women of childbearing potential (WOCBP), even if they have undergone a successful vasectomy and must agree to avoid to father a child (while on therapy and for 6 months after the final study drug administration). In addition, their female partners of childbearing potential must use a highly effective method of birth control.
  • Male patient must not donate sperm starting at screening and throughout the study period and for 6 months after the final study drug administration.
  • Able to understand and willing to sign an informed consent form (ICF).
  • Institutional Review Board/Independent Ethics Committee-approved written informed consent as per national regulations must be obtained from the patient prior to any study-related procedures (including consent for withdrawal of prohibited medication, if applicable). Exclusion Criteria: Subject has previously been treated for AML; a treatment period with hydroxyurea to control WBC counts is allowed; prior treatment with a hypomethylating agent for MDS-EB is not allowed; prior treatment with erythropoiesis-stimulating agents or luspatercept for MDS is allowed. 2\. Acute promyelocytic leukemia (APL) with t(15;17)(q24.1;q21.2); PML-RARA; or one of the other pathognomonic variant chromosomal translocations / fusion genes. 3. AML with BCR-ABL1; or myeloid blast crisis of CML. 4. Significant active cardiac disease within 3 months prior to the start of study treatment, including: * New York Heart Association (NYHA) class III or IV congestive heart failure
  • Myocardial infarction
  • Unstable angina
  • Severe cardiac arrhythmias
  • Congenital long QT syndrome of family member with this condition QTcF \>450 msec on screening electrogram for males and \>470msec on screening electrogram for females (mean of triplicate recordings; calculated using Fridericia's correction). 5. Severe obstructive or restrictive ventilation disorder. 6. History of stroke or intracranial hemorrhage within 6 months prior to randomization. 7\. Clinical symptoms suggestive of active central nervous system (CNS) leukemia or known CNS leukemia. Evaluation of cerebrospinal fluid (CSF) during screening is only required if there is a clinical suspicion of CNS involvement by leukemia during screening. 8. Active infection, including hepatitis B or hepatitis C or Human Immunodeficiency Virus (HIV) infection, that is uncontrolled prior to first dose of study treatment and may interfere with the study objectives or which could expose the patient to undue risk through the participation in the clinical trial; an infection controlled with an approved antibiotic/ antiviral/ antifungal treatment that is not a strong or moderate CYP3A inducer is allowed. Patients with COVID-19 infection can be enrolled, if the patient has no symptoms and was tested negative twice by PCR test prior to inclusion in the trial. 9. Immediate life-threatening, severe complications of leukemia such as uncontrolled bleeding and/or disseminated intravascular coagulation. 10. Conditions that limit the ingestion or gastrointestinal absorption of orally administered drugs. 11\. Patient with a currently active second malignancy. Patients are not considered to have a currently active malignancy, if they have completed therapy and are considered by their physician to be at \< 30% risk of relapse within one year. However, patients with the following history/concurrent conditions are allowed:
  • Basal or squamous cell carcinoma of the skin;
  • Carcinoma in situ of the cervix;
  • Carcinoma in situ of the breast;
  • Incidental histologic finding of prostate cancer. 12. Receipt of live, attenuated vaccine within 30 days prior to the study inclusion (NOTE: patient, if enrolled, should not receive live vaccine during the study and until 6 months after the therapy). 13\. Severe neurological or psychiatric disorder interfering with ability to give an informed consent. 14\. Contraindication to AZA or VEN (as per Summary of Product Characteristics (SmPC)). 15\. Patient weighing \<40 kg at registration. 16. Participation in other prospective studies with anti-leukemic and/or investigational agents. 17\. Patient taking Dabigatran unless they can be transferred to other medications within ≥5 half-lives prior to dosing. Patients taking other P-gP transporter-sensitive medications (see Appendix H) should be properly monitored during the study if they cannot be transferred to other medications. 18\. Patient taking known strong cytochrome P450 (CYP) 3A4 inducers (see Appendix G), unless they can be transferred to other medications within ≥5 half-lives prior to dosing. 19\. The patient is a pregnant or lactating woman, or plans to become pregnant during the study. 20\. Patient who has once been screened and randomized into this HO177 trial but was considered ineligible cannot re-enter this trial at a later date.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (197)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Vorarlberger Krankenhaus-Betriebsgesellschaft mbH
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FeldkirchAustriaRecruiting
Kepler Universitaetsklinikum GmbH
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LinzAustriaRecruiting
SCRI CCCIT Ges.m.b.H.
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SalzburgAustriaRecruiting
Hanusch Krankenhaus der Wiener Gebietskrankenkasse
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ViennaAustriaRecruiting
AU-Adelaide-RAH
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AdelaideAustraliaNot yet recruiting
AU-Birtinya-SUNSHINECOASTUH General Information
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BirtinyaAustraliaNot yet recruiting
AU-Brisbane-RBWH
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BrisbaneAustraliaRecruiting
AU-Douglas-TOWNSVILLE
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DouglasAustraliaNot yet recruiting
AU-Melbourne-ALFRED
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MelbourneAustraliaRecruiting
AU-Melbourne-MONASH
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MelbourneAustraliaNot yet recruiting
AU-Perth-FSH
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PerthAustraliaWithdrawn
AU-Perth-SCGH
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PerthAustraliaNot yet recruiting
AU-Sydney-RNSH
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SydneyAustraliaNot yet recruiting
AU-Sydney-SVSH
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SydneyAustraliaNot yet recruiting
Institut Jules Bordet
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AnderlechtBelgiumRecruiting
Ziekenhuis Aan De Stroom
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AntwerpBelgiumRecruiting
Az St-Jan Brugge-Oostende A.V.
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BruggeBelgiumRecruiting
Universitair Ziekenhuis Gent
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GentBelgiumRecruiting
UZ Brussel
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JetteBelgiumRecruiting
UZ Leuven
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LeuvenBelgiumRecruiting
Centre Hospitalier Universitaire de Liège
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LiègeBelgiumRecruiting
Cliniques Universitaires Saint-Luc
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Sint-Lambrechts-WoluweBelgiumRecruiting
Centre Hospitalier Universitaire Dinant Godinne Sainte-Elisabeth-UCL-Namur
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YvoirBelgiumRecruiting
CH-Aarau-KSA
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AarauSwitzerlandRecruiting
CH-Basel-USB
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BaselSwitzerlandRecruiting
CH-Bellinzona-IOSI
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BellinzonaSwitzerlandRecruiting
CH-Bern-INSEL
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BernSwitzerlandRecruiting
CH-Geneve (14)-HCUGE
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GenevaSwitzerlandRecruiting
CH-Zürich-USZ
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ZurichSwitzerlandNot yet recruiting
Charite Universitaetsmedizin Berlin KöR
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BerlinGermanyRecruiting
Vivantes Netzwerk fuer Gesundheit GmbH
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BerlinGermanyRecruiting
Universitaetsklinikum Knappschaftskrankenhaus Bochum GmbH
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BochumGermanyRecruiting
Universitaetsklinikum Bonn AöR
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BonnGermanyRecruiting
Gesundheit Nord gGmbH Klinikverbund Bremen
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BremenGermanyRecruiting
Staedtisches Klinikum Braunschweig gGmbH
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BrunswickGermanyRecruiting
Klinikum Darmstadt GmbH
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DarmstadtGermanyRecruiting
KLINIKEN ESSEN SUED Evangelisches Krankenhaus Essen-Werden gGmbH
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EssenGermanyRecruiting
Malteser Norddeutschland gGmbH
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FlensburgGermanyRecruiting
Medical Center- University of Freiburg
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Freiburg im BreisgauGermanyRecruiting
Universitaetsmedizin Greifswald KöR
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GreifswaldGermanyRecruiting
Martin-Luther-Universitaet Halle-Wittenberg
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Halle (Saale)GermanyRecruiting
Asklepios Klinik St George
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HamburgGermanyRecruiting
University Medical Center Hamburg-Eppendorf
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HamburgGermanyRecruiting
Klinikum Region Hannover GmbH
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HanoverGermanyRecruiting
Medizinische Hochschule Hannover
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HanoverGermanyRecruiting
SLK-Kliniken Heilbronn GmbH
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HeilbronnGermanyRecruiting
St. Elisabeth Gruppe GmbH Katholische Kliniken Rhein-Ruhr
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HerneGermanyRecruiting
Universitaet Des Saarlandes
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HomburgGermanyRecruiting
Staedtisches Klinikum Karlsruhe gGmbH
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KarlsruheGermanyRecruiting
Otto Von Guericke Universitaet Magdeburg
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MagdeburgGermanyRecruiting
Universitaetsmedizin der Johannes Gutenberg-Universitaet Mainz KöR
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MainzGermanyRecruiting
Muehlenkreiskliniken AöR
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MindenGermanyRecruiting
Klinikum der Technischen Universitaet Muenchen (TUM Klinikum)
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MunichGermanyRecruiting
Klinikum Oldenburg Aor
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OldenburgGermanyRecruiting
Klinikum Ernst von Bergmann gGmbH
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PotsdamGermanyRecruiting
Universitaetsklinikum Regensburg AöR
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RegensburgGermanyRecruiting
Klinikum Der Landeshauptstadt Stuttgart gKAöR
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StuttgartGermanyRecruiting
Universitaetsklinikum Tuebingen AöR
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TuebingenGermanyRecruiting
Universitaetsklinikum Ulm AoR
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UlmGermanyRecruiting
Helios Universitaetsklinikum Wuppertal
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WuppertalGermanyRecruiting
Aalborg University Hospital
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AalborgDenmarkRecruiting
Region Midtjylland
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Aarhus NDenmarkRecruiting
Rigshospitalet
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Copenhagen OeDenmarkRecruiting
Odense University Hospital
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Odense CDenmarkRecruiting
North Estonia Medical Centre Foundation
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TallinnEstoniaRecruiting
Tartu University Hospital
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Tartu LinnEstoniaRecruiting
Institut Catala d'Oncologia
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BadalonaSpainRecruiting
Hospital Clinic de Barcelona
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BarcelonaSpainRecruiting
Hospital de la Santa Creu i Sant Pau
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BarcelonaSpainRecruiting
Hospital del Mar
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BarcelonaSpainRecruiting
Institut Català d'Oncologia
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GironaSpainRecruiting
Institut Catala D'oncologia
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L'Hospitalet de LlobregatSpainRecruiting
Hospital Universitari Arnau De Vilanova De La Gerencia Territorial De Lleida
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LleidaSpainRecruiting
Hospital General Universitario Gregorio Marañón
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MadridSpainRecruiting
University Hospital Son Espases
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PalmaSpainRecruiting
Hospital Universitari Joan XXIII de Tarragona
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TarragonaSpainRecruiting
Fundacio Assistencial De Mutua De Terrassa Fpc
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TerrassaSpainRecruiting
Hospital Clinico Universitario de Valencia
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ValenciaSpainRecruiting
HUS-Yhtymae
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HelsinkiFinlandRecruiting
Pohjois-Pohjanmaan hyvinvointialue
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OuluFinlandRecruiting
Tampere University Hospital
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TampereFinlandRecruiting
Varsinais-Suomen hyvinvointialue
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TurkuFinlandRecruiting
Centre Hospitalier Universitaire Amiens Picardie
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Amiens Cedex 1FranceRecruiting
Centre Hospitalier Universitaire D'Angers
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AngersFranceRecruiting
CHU Besancon
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Besancon CedexFranceRecruiting
Centre Hospitalier Universitaire De Caen Normandie
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Caen Cedex 9FranceRecruiting
Hopital D Instruction Des Armées Percy
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ClamartFranceRecruiting
University Hospital Of Clermont-Ferrand
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Clermont-FerrandFranceRecruiting
Assistance Publique Hopitaux De Paris
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Creteil CedexFranceRecruiting
Centre Hospitalier Universitaire Grenoble Alpes
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Grenoble Cedex 9FranceRecruiting
Centre Hospitalier De Versailles
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Le Chesnay RocquencourtFranceRecruiting
Centre Hospitalier Universitaire De Lille
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Lille CedexFranceRecruiting
Centre Hospitalier Et Universitaire De Limoges
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Limoges Cedex 1FranceRecruiting
Centre Hospital Region Metz Thionville
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Metz Cedex 03FranceRecruiting
Centre Hospitalier Universitaire De Montpellier
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Montpellier Cedex 5FranceRecruiting
Centre Hospitalier Universitaire de Nantes
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NantesFranceRecruiting
Centre Hospitalier Universitaire de Nice
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NiceFranceRecruiting
Centre Hospitalier Universitaire de Bordeaux
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PessacFranceRecruiting
Hospices Civils de Lyon
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Pierre-BéniteFranceRecruiting
Centre Henri Becquerel
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Rouen CedexFranceRecruiting
Centre Hospitalier Universitaire de Saint Etienne
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Saint-Priest-en-JarezFranceRecruiting
Les Hopitaux Universitaires De Strasbourg
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Strasbourg Cedex 2FranceRecruiting
Belfasttrust
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BelfastUnited KingdomNot yet recruiting
Birmingham-QE
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BirminghamUnited KingdomNot yet recruiting
Blackpool Victoria
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BlackpoolUnited KingdomRecruiting
UK-Bodelwyddan-BCUHB
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BodelwyddanUnited KingdomNot yet recruiting
UK-Bristol-BRISTOLCENTRE
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BristolUnited KingdomRecruiting
University Hospital of Wales
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CardiffUnited KingdomRecruiting
UK-Portsmouth-QUEENALEXANDRA
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CoshamUnited KingdomRecruiting
UK-Coventry-UHCOVENTRYANDWARWICKSHIRE
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CoventryUnited KingdomRecruiting
UK-Derby-ROYALDERBYHOSPITAL
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DerbyUnited KingdomNot yet recruiting
UK-Edinburgh-WGH
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EdinburghUnited KingdomNot yet recruiting
Beatson West of Scotland Cancer Centre
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GlasgowUnited KingdomRecruiting
UK-Harrow-NORTHWICK
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HarrowUnited KingdomNot yet recruiting
UK-Hull-CASTLEHILL
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HullUnited KingdomRecruiting
St. James UH
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LeedsUnited KingdomRecruiting
University Hospitals of Leicester NHS Trust
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LeicesterUnited KingdomRecruiting
King's College Hospital
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LondonUnited KingdomRecruiting
University College Hospital
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LondonUnited KingdomRecruiting
St. Bartholomew's Hospital
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LondonUnited KingdomRecruiting
Christie NHS Foundation Trust
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ManchesterUnited KingdomRecruiting
UK-Manchester-ROYALINFIRMARY
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ManchesterUnited KingdomRecruiting
The Newcastle Upon Tyne Hospitals NHS Foundation Trust
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NewcastleUnited KingdomRecruiting
Nottingham University Hospitals NHS Trust
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NottinghamUnited KingdomRecruiting
Churchill Hospital Oxford
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OxfordUnited KingdomRecruiting
Southampton General Hospital
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SouthamptonUnited KingdomRecruiting
UK-Stoke on Trent-UHNM
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Stoke-on-TrentUnited KingdomNot yet recruiting
The Royal Marsden NHSFT
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SuttonUnited KingdomRecruiting
UK-Swindon-GWH
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SwindonUnited KingdomNot yet recruiting
UK-Cornwall-RCH
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TruroUnited KingdomRecruiting
New cross hospital wolverhampton
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WolverhamptonUnited KingdomRecruiting
Cork University Hospital
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CorkIrelandRecruiting
St Vincent's University Hospital
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Dublin 4IrelandRecruiting
Mater Misericordiae University Hospital
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Dublin 7IrelandRecruiting
St James's Hospital
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Dublin 8IrelandRecruiting
Beaumont Hospital
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Dublin 9IrelandRecruiting
University Hospital Galway
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GalwayIrelandRecruiting
University Hospital Waterford
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WaterfordIrelandRecruiting
Azienda Ospedaliero-Universitaria delle Marche
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AnconaItalyRecruiting
Azienda Ospedaliero-Universitaria Di Bologna IRCCS Istituto Di Ricerca E Di Cura A Carattere Scientifico
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BolognaItalyRecruiting
Azienda Sanitaria Territoriale Di Macerata - Ospedale Civitanova Marche
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Civitanova MarcheItalyRecruiting
ASST Grande Ospedale Metropolitano Niguarda
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MilanItalyRecruiting
Azienda Ospedaliera Ospedali Riuniti Villa Sofia - Cervello
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PalermoItalyRecruiting
Hospital Santa Maria Della Misericordia
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PerugiaItalyRecruiting
Azienda Sanitaria Locale di Pescara
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PescaraItalyRecruiting
Azienda Ospedaliera Policlinico Universitario Tor Vergata
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RomeItalyRecruiting
Azienda Ospedaliero-Universitaria Policlinico Umberto I
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RomeItalyRecruiting
ASL Salerno-PO "Andrea Tortora"
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SalernoItalyRecruiting
Azienda Sanitaria Universitaria Giuliano Isontina
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TriesteItalyRecruiting
Azienda Ospedaliera Universitaria Citta Della Salute E Della Scienza Di Torino
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TurinItalyRecruiting
Vilniaus universiteto ligonine Santaros klinikos VšĮ
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VilniusLithuaniaRecruiting
Meander Medisch Centrum
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AmersfoortNetherlandsRecruiting
Stichting OLVG
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AmsterdamNetherlandsRecruiting
Amsterdam UMC Stichting
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AmsterdamNetherlandsRecruiting
Rijnstate Ziekenhuis Stichting
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ArnhemNetherlandsRecruiting
Amphia Hospital
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BredaNetherlandsRecruiting
Reinier de Graaf Groep
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DelftNetherlandsRecruiting
Albert Schweitzer Ziekenhuis
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DordrechtNetherlandsRecruiting
Máxima Medisch Centrum
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EindhovenNetherlandsRecruiting
Medisch Spectrum Twente
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EnschedeNetherlandsRecruiting
Admiraal De Ruyter Ziekenhuis B.V.
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GoesNetherlandsRecruiting
Universitair Medisch Centrum Groningen
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GroningenNetherlandsRecruiting
Medisch Centrum Leeuwarden B.V.
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LeeuwardenNetherlandsRecruiting
Leids Universitair Medisch Centrum (LUMC)
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LeidenNetherlandsRecruiting
Academisch Ziekenhuis Maastricht
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MaastrichtNetherlandsRecruiting
Sint Antonius Ziekenhuis Stichting
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NieuwegeinNetherlandsRecruiting
Radboud universitair medisch centrum Stichting
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NijmegenNetherlandsRecruiting
Erasmus Universitair Medisch Centrum Rotterdam (Erasmus MC)
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RotterdamNetherlandsRecruiting
Haga Hospital
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's-GravenhageNetherlandsRecruiting
Jeroen Bosch Ziekenhuis Stichting
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'S-HertogenboschNetherlandsRecruiting
Universitair Medisch Centrum Utrecht
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UtrechtNetherlandsRecruiting
Isala Klinieken Stichting
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ZwolleNetherlandsRecruiting
Helse Bergen HF
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BergenNorwayRecruiting
Vestre Viken HF
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DrammenNorwayRecruiting
Akershus University Hospital
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LoerenskogNorwayRecruiting
Oslo University Hospital HF
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OsloNorwayRecruiting
Helse Stavanger HF
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StavangerNorwayRecruiting
Universitetssykehuset Nord-Norge HF
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TromsoeNorwayRecruiting
St. Olavs hospital HF
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TrondheimNorwayRecruiting
Sahlgrenska University Hospital-Vaestra Goetalandsregionen
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GoteborgSwedenRecruiting
Karolinska University Hospital
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HuddingeSwedenRecruiting
Region Skane Skanes Universitetssjukhus
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LundSwedenRecruiting
Uppsala University Hospital
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UppsalaSwedenRecruiting
US-Atlanta GA-EMORY
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AtlantaUnited StatesRecruiting
US-Baltimore MD-UMGCCC
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BaltimoreUnited StatesRecruiting
US-Chapel Hill-UNCNORTHCAROLINA
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Chapel HillUnited StatesRecruiting
US-Cincinnati OH-CINCY
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CincinnatiUnited StatesRecruiting
US-Colombus OH-OSU
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ColumbusUnited StatesRecruiting
US-Dallas TX-SOUTHWESTERN
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DallasUnited StatesNot yet recruiting
US-Kansas City KS-KUMC
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FairwayUnited StatesNot yet recruiting
US-Jacksonville FL-MAYOFL
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JacksonvilleUnited StatesNot yet recruiting
US-Los Angeles CA-UCLA
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Los AngelesUnited StatesNot yet recruiting
US-Pittsburgh PA-PITT
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PittsburghUnited StatesRecruiting
US-Portland OR-OHSU
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PortlandUnited StatesNot yet recruiting
US-Rochester MN-MAYOMN
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RochesterUnited StatesNot yet recruiting
US-San Francisco CA-UCSF
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San FranciscoUnited StatesNot yet recruiting
US-Wheeling WV-WVU
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WheelingUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.