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Chronic Lymphocytic Leukemia (CLL)VeRVeNCT03342144

Study of the Use of Venetoclax in Participants With Chronic Lymphocytic Leukemia (CLL) Under Real-Life Setting

An observational study of Chronic Lymphocytic Leukemia (CLL), run by AbbVie at 74 sites in 3 countries.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record

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Trial summary

An observational study to assess the effectiveness, health economic-relevant costs and participant reported outcomes in participants with Chronic lymphocytic leukemia (CLL) receiving venetoclax as a monotherapy or in combination with rituximab, obinutuzumab, ibrutinib, or acalabrutinib as prescribed at the discretion… Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Chronic Lymphocytic Leukemia (CLL)
How many people
500 participants
Where
74 sitesin 3 countries
Study dates
4 Dec 2017to Dec 2030
Phase
Observational

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Participants with chronic lymphocytic leukemia (CLL) administering venetoclax per the local label.

Who may be able to join

  • Participant with chronic lymphocytic leukemia (CLL) who start venetoclax therapy can be included in the study if treated as specified in the local label for any specific line of treatment.

Who cannot join

  • None

Trial locations and contacts

74 sites in 3 countries. Contact the study team or a site near you to ask about taking part.

Stefan Lorenz contact

stefan.lorenz@abbvie.com

74 sites in 3 countries

Germany61 sites, 4 recruiting
  • MVZ am Klinikum Aschaffenburg Onkologie /ID# 201548

    Aschaffenburg, Bavaria, 63739

    Completed
  • Studienzentrum Aschaffenburg /ID# 204125

    Aschaffenburg, Bavaria, 63739

    Completed
  • Gemeinschaftspraxis Dr. Heinrich und Prof. Bangerter /ID# 200950

    Augsburg, Bavaria, 86150

    Completed
  • Praxis Dr. Kreher /ID# 202604

    Bad Liebenwerda, Brandenburg, 04924

    Completed
  • Caritas-Krankenhaus gGmbH /ID# 243212

    Bad Mergentheim, 97980

    Completed
  • Drs. Tanzer, Chirca, Stoeberl /ID# 202613

    Bad Reichenhall, Bavaria, 83435

    Completed
  • MVZ Klinikum Mittelbaden GmbH /ID# 206207

    Baden-Baden, 76532

    Completed
  • Praxis für Hämatologie und Onkologie /ID# 241763

    Berlin, 10117

    Completed
  • Onkologische Schwerpunktpraxis /ID# 200953

    Berlin, 10707

    Completed
  • Praxis am Volkspark /ID# 243195

    Berlin, 10715

    Completed
  • Onkologie am Segelfliegerdamm /ID# 202603

    Berlin, 12487

    Completed
  • Ambulantes Tumorzentrum Bremerhaven /ID# 224353

    Bremerhaven, Free Hanseatic City of Bremen, 27576

    Completed
  • Pioh Dres. Draube & Partner /ID# 239507

    Cologne, 50674

    Completed
  • Donauisar Klinikum Deggendorf /ID# 289012

    Deggendorf, Bavaria, 94469

    Recruiting
  • Onkozentrum Dresden /ID# 202599

    Dresden, Saxony, 01127

    Completed
  • BAG Freiberg-Richter, Jacobasch, Illmer, Wolf /ID# 201532

    Dresden, Saxony, 01307

    Completed
  • Praxis Dres. Prange-Krex/Mohm /ID# 210049

    Dresden, 01307

    Completed
  • St. Georg Klinikum Eisenach gemeinnützige GmbH (GKE) /ID# 250200

    Eisenach, 99817

    Completed
  • Internistische Schwerpunktpraxen, Erlangen /ID# 200949

    Erlangen, Bavaria, 91052

    Completed
  • Praxis Dres. Kiehl/Stein /ID# 210052

    Frankfurt (Oder), Brandenburg, 15236

    Completed
  • Centrum fuer Haematologie und Onkologie Bethanien /ID# 206701

    Frankfurt am Main, Hesse, 60389

    Completed
  • MVZ Dres. Cordes & Partner /ID# 202598

    Frankfurt am Main, Hesse, 60596

    Completed
  • Klinikum Frankfurt Hoechst /ID# 210048

    Frankfurt am Main, Hesse, 65929

    Completed
  • Varisano Klinikum Frankfurt Hoechst /ID# 288028

    Frankfurt am Main, Hesse, 65929

    Recruiting
  • Praxis fuer interdisziplinaere Onkolologie und Haematologie /ID# 206999

    Freiburg im Breisgau, 79110

    Completed
  • Onkologische Kooperation Harz /ID# 201550

    Goslar, Lower Saxony, 38642

    Completed
  • MVZ Onkologie GmbH /ID# 212376

    Hagen, 58095

    Completed
  • Evidia MVZ III Oncology Halle /ID# 218354

    Halle, Saxony-Anhalt, 06110

    Completed
  • OncoResearch Lerchenfeld GmbH /ID# 205237

    Hamburg, 22081

    Completed
  • Onkologische Gemeinschaftspraxis /ID# 205239

    Hamburg, 22767

    Completed
  • Evangelisches Krankenhaus Hamm /ID# 206703

    Hamm, 59063

    Completed
  • Onkologische Schwerpunktpraxis Hanau /ID# 287948

    Hanau, Hesse, 63450

    Recruiting
  • OAZ Hannover /ID# 201538

    Hanover, Lower Saxony, 30171

    Completed
  • Studienzentrum am Raschplatz /ID# 250180

    Hanover, 30161

    Completed
  • Studienbüro Kamal und Dorn GBR /ID# 234105

    Hanover, 30625

    Completed
  • Onkologie Hof /ID# 201531

    Hof, Bavaria, 95028

    Completed
  • Klinikum Idar-Oberstein GmbH /ID# 210046

    Idar-Oberstein, 55743

    Completed
  • Hämatologie und Onkologie /ID# 205247

    Kaiserslautern, Rhineland-Palatinate, 67655

    Completed
  • Praxis Dres. Tebbe/Mayer /ID# 206730

    Kassel, Hesse, 34125

    Completed
  • Praxis Dr. Stauch /ID# 202611

    Kronach, Bavaria, 96317

    Completed
  • VK&K Studien GbR /ID# 202614

    Landshut, Bavaria, 84036

    Completed
  • Praxis Fuchs/Koehler /ID# 243215

    Langenhessen, 63225

    Completed
  • Luebecker Oncology Practice /ID# 200952

    Lübeck, Schleswig-Holstein, 23562

    Completed
  • Gemeinschaftspraxis fuer Haematologie und Onkologie /ID# 281328

    Magdeburg, 39104

    Recruiting
  • Haemato-Onkologie /ID# 205236

    Munich, Bavaria, 81241

    Completed
  • Stauferklinikum Schwaebisch Gmuend /ID# 201518

    Mutlangen, Baden-Wurttemberg, 73557

    Completed
  • Friedrich-Ebert-Krankenhaus GmbH /ID# 206206

    Neumünster, Schleswig-Holstein, 24534

    Completed
  • Praxis Dr. Klaproth/Cura /ID# 216413

    Neunkirchen, Saarland, 66538

    Completed
  • Praxis Dres. Plewe/Losem /ID# 202606

    Neuss, North Rhine-Westphalia, 41462

    Completed
  • Onkolologische Praxis Oldenburg /ID# 202607

    Oldenburg, Lower Saxony, 26121

    Completed
  • MVZ der Paracelsus-Klinik /ID# 201541

    Osnabrück, Lower Saxony, 49076

    Completed
  • Bruederkrankenhaus St. Josef Paderborn /ID# 202600

    Paderborn, 33098

    Completed
  • Onkologische Praxis GbR /ID# 206705

    Porta Westfalica, 32457

    Completed
  • MVZ f. Blut- u.Krebserkrankungen /ID# 206704

    Potsdam, Brandenburg, 14467

    Completed
  • Praxis Dres. Krober/Stosiek /ID# 206729

    Regensburg, State of Berlin, 93053

    Completed
  • Praxis Dres. Decker/Lakner/Leithäuser /ID# 206208

    Rostock, 18057

    Completed
  • Diakonieklinikum Schwaebisch Hall /ID# 206205

    Schwäbisch Hall, 74523

    Completed
  • MVZ am Schlossgarten GmbH /ID# 210043

    Schwetzingen, 68723

    Completed
  • Onkologische Praxis /ID# 201545

    Stuttgart, Baden-Wurttemberg, 70174

    Completed
  • Schwarzwald-Baar-Klinikum /ID# 208176

    Villingen-Schwenningen, Baden-Wurttemberg, 78052

    Completed
  • Med. Studiengesellschaft Nord West GmbH /ID# 201535

    Westerstede, Lower Saxony, 26655

    Completed

Other trials in Germany

Switzerland9 sites, 1 recruiting
  • Kantonsspital Aarau AG /ID# 210034

    Aarau, Canton of Aargau, 5001

    Completed
  • EOC Ospedale Regionale di Bellinzona e Valli /ID# 208782

    Bellinzona, Canton Ticino, 6500

    Completed
  • Inselspital, Universitaetsspital Bern /ID# 210031

    Bern, 3010

    Completed
  • Luzerner Kantonsspital /ID# 210029

    Lucerne, Canton of Lucerne, 6000

    Completed
  • Kantonsspital Münsterlingen /ID# 210035

    Münsterlingen, Thurgau, 8596

    Completed
  • Réseau Hospitalier Neuchâtelois /ID# 227865

    Neuchâtel, Canton of Neuchâtel, 2000

    Recruiting
  • Kantonsspital St. Gallen /ID# 223037

    Sankt Gallen, Canton of St. Gallen, 9007

    Completed
  • Spital Thun /ID# 233714

    Thun, Canton of Bern, 3600

    Completed
  • KSW Kantonsspital Winterthur /ID# 211068

    Winterthur, Canton of Zurich, 8400

    Completed

Other trials in Switzerland

Austria4 sites
  • Medizinische Universitaet Graz /ID# 221155

    Graz, Styria, 8010

    Completed
  • Landeskrankenhaus Salzburg-Universitaetsklinikum der PMU (LKH) /ID# 221153

    Salzburg, 5020

    Active, not recruiting
  • Universitaetsklinikum St. Poelten /ID# 221152

    Sankt Pölten, Lower Austria, 3100

    Completed
  • Hanusch Krankenhaus /ID# 221151

    Vienna, 1140

    Completed

Other trials in Austria

About this study

Official title: Observational Study of the Use of Venetoclax in Patients With Chronic Lymphocytic Leukemia (CLL) Under Real-Life Setting in Austria, Germany and Switzerland

An observational study to assess the effectiveness, health economic-relevant costs and participant reported outcomes in participants with Chronic lymphocytic leukemia (CLL) receiving venetoclax as a monotherapy or in combination with rituximab, obinutuzumab, ibrutinib, or acalabrutinib as prescribed at the discretion of the physician and in accordance with local clinical practice and label.

Keywords
Chronic Lymphocytic Leukemia (CLL), Cancer, Leukemia, venetoclax, rituximab, obinutuzumab, ABT-199, venclexta, venclyxto
Medical subject headings
Leukemia, Lymphocytic, Chronic, B-Cell, Neoplasms, Leukemia

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT03342144
Study groupRoleWhat they receive
Participants Receiving VenetoclaxParticipants with Chronic Lymphocytic Leukemia (CLL) receiving venetoclax.
Participants Receiving Venetoclax + RituximabParticipants with CLL receiving venetoclax in combination with rituximab.
Participants Receiving Venetoclax + ObinutuzumabParticipants with CLL receiving venetoclax in combination with obinutuzumab.
Participants Receiving Venetoclax + IbrutinibParticipants with CLL receiving venetoclax in combination with ibrutinib.
Participants Receiving Venetoclax + AcalabrutinibParticipants with CLL receiving venetoclax in combination with acalabrutinib.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Percentage of Participants Achieving Best Overall Response Rate (ORR)

    ORR is defined as the percentage of participants achieving partial response (PR) and complete response with incomplete regeneration of bone marrow (CRi) and complete response (CR) according to physician's assessment to therapy with venetoclax.

    Measured: Up to 12 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted14 Nov 2017
  2. Study start4 Dec 2017
  3. Primary completionDec 2030 (estimated)
  4. Study completionDec 2030 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
500 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03342144
Sponsor's protocol ID
P17-132
Acronym
VeRVe
Status last verified
Oct 2026
First submitted
10 Nov 2017
Last updated
21 Oct 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Publications

  • Schwaner I, Kuhn T, Losem C, Wolff T, Otremba B, Zaiss M, Hulsenbeck J, Famulla K, Nosslinger T, Rossi D. Low incidence of tumor lysis syndrome in elderly patients with chronic lymphocytic leukemia treated with venetoclax under real-world conditions: results from the prospective observational VeRVe study. Ann Hematol. 2024 Jun;103(6):2013-2020. doi: 10.1007/s00277-024-05638-7. Epub 2024 Feb 29.

    PubMed 38421404

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