NCT02242942

Brief Summary

This open-label, multicenter, randomized Phase III study is designed to compare the efficacy and safety of a combined regimen of obinutuzumab and venetoclax versus obinutuzumab + chlorambucil in participants with chronic lymphocytic leukemia (CLL) and coexisting medical conditions. The time on study treatment was approximately one year and the follow-up period will be up to 9 years

Trial Health

98
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
445

participants targeted

Target at P50-P75 for phase_3

Timeline
Completed

Started Dec 2014

Longer than P75 for phase_3

Geographic Reach
19 countries

99 active sites

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

September 16, 2014

Completed
1 day until next milestone

First Posted

Study publicly available on registry

September 17, 2014

Completed
4 months until next milestone

Study Start

First participant enrolled

December 31, 2014

Completed
3.6 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 17, 2018

Completed
1.1 years until next milestone

Results Posted

Study results publicly available

October 1, 2019

Completed
5.9 years until next milestone

Study Completion

Last participant's last visit for all outcomes

August 27, 2025

Completed
Last Updated

November 6, 2025

Status Verified

November 1, 2025

Enrollment Period

3.6 years

First QC Date

September 16, 2014

Results QC Date

August 15, 2019

Last Update Submit

November 3, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • Progression Free Survival (PFS) Based on Investigator Assessment According to IWCLL Criteria

    PFS was determined according to IWCLL 2008 criteria and defined as the time from randomization to the first occurrence of PD or death from any cause. Disease progression was characterized by at least one of the following: 1) \>/= 50% increase in the absolute number of circulating lymphocytes to at least 5\*10\^9/L, 2) Appearance of new palpable lymph nodes (\> 15 mm in longest diameter) or any new extra-nodal lesion; 3) \>/= 50% increase in the longest diameter of any previous site of lymphadenopathy; 4) \>/= 50% increase in the enlargement of the liver and/or spleen; 5) Transformation to a more aggressive histology.

    Baseline until disease progression or death up to approximately 3.75 years

Secondary Outcomes (22)

  • Progression Free Survival (PFS) Based on Institutional Review Committee (IRC)-Assessments According to International Workshop on Chronic Lymphocytic Leukemia (IWCLL) Criteria

    Baseline until disease progression or death up to approximately 3.75 years

  • Percentage of Participants With an Overall Response (OR) at Completion of Treatment, as Determined by the Investigator According to IWCLL Criteria

    At the completion of treatment assessment 3 months after treatment completion (at approximately 15 months)

  • Percentage of Participants With a Complete Response Rate (CRR) at the Completion of Treatment Assessment as Determined by the Investigator According to IWCLL Criteria

    At the completion of treatment assessment 3 months after treatment completion (at approximately 15 months)

  • Percentage of Participants With Minimal Residual Disease (MRD) Negativity in Peripheral Blood as Measured by Allele-Specific Oligonucleotide Polymerase Chain Reaction (ASO-PCR) at Completion of Treatment

    At the completion of treatment assessment 3 months after treatment completion (at approximately 15 months)

  • Percentage of Participants With MRD Negativity in Bone Marrow as Measured by ASO-PCR at Completion of Treatment

    At the completion of treatment assessment 3 months after treatment completion (at approximately 15 months)

  • +17 more secondary outcomes

Study Arms (3)

Safety Run-in Obinutuzumab + Venetoclax

EXPERIMENTAL

Subjects received obinutuzumab for 6 cycles and venetoclax for 12 cycles. Cycles comprised of 28 days.

Drug: VenetoclaxDrug: Obinutuzumab

Obinutuzumab + Chlorambucil

EXPERIMENTAL

Participants will receive obinutuzumab for 6 cycles and chlorambucil for 12 cycles. Cycles will comprise 28 days.

Drug: ChlorambucilDrug: Obinutuzumab

Obinutuzumab + Venetoclax

EXPERIMENTAL

Participants will receive obinutuzumab for 6 cycles and venetoclax for 12 cycles. Cycles will comprise 28 days.

Drug: VenetoclaxDrug: Obinutuzumab

Interventions

Chlorambucil 0.5 milligrams per kilogram (mg/kg) orally at Day 1 and Day 15 at of each 28 day cycle for 12 cycles.

Obinutuzumab + Chlorambucil

Venetoclax, oral tablet: 20 mg daily during Cycle 1, Day 22-28; 50 mg daily during Cycle 2, Day 1-7; 100 mg daily during Cycle 2, Day 8-14; 200 mg daily during Cycle 2, Day 15-21; 400 mg daily during Cycle 2, Day 22-28 and on Day 1-28 for all subsequent cycles until the end of Cycle 12.

Also known as: ABT-0199, GDC-0199
Obinutuzumab + VenetoclaxSafety Run-in Obinutuzumab + Venetoclax

Obinutuzumab, IV infusion: 100 mg or 1000 mg, depending on splitting rules, at Cycle 1, Day 1 (if 100 mg was received on Day 1, 900 mg will be administered on Cycle 1, Day 2); 1000 mg at Cycle 1, Day 8 and Day 15; 1000 mg at Day 1 for all subsequent cycles until the end of Cycle 6

Also known as: GA-101; Gazyva
Obinutuzumab + ChlorambucilObinutuzumab + VenetoclaxSafety Run-in Obinutuzumab + Venetoclax

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Documented previously untreated CLL according to the International Workshop on Chronic Lymphocytic Leukemia (IWCLL) criteria
  • CLL requiring treatment according to IWCLL criteria
  • Total Cumulative Illness Rating Scale (CIRS score) greater than (\>) 6
  • Adequate marrow function independent of growth factor or transfusion support within 2 weeks of screening as per protocol, unless cytopenia is due to marrow involvement of CLL
  • Adequate liver function
  • Life expectancy \> 6 months
  • Agreement to use highly effective contraceptive methods per protocol

You may not qualify if:

  • Transformation of CLL to aggressive Non-Hodgkin's lymphoma (Richter's transformation or pro-lymphocytic leukemia)
  • Known central nervous system involvement
  • Participants with a history of confirmed progressive multifocal leukoencephalopathy (PML)
  • An individual organ/ system impairment score of 4 as assessed by the CIRS definition limiting the ability to receive the treatment regimen of this trial with the exception of eyes, ears, nose, throat organ system
  • Participants with uncontrolled autoimmune hemolytic anemia or immune thrombocytopenia
  • Inadequate renal function
  • History of prior malignancy, except for conditions as listed in the protocol if participants have recovered from the acute side effects incurred as a result of previous therapy
  • Use of investigational agents or concurrent anti-cancer treatment within the last 4 weeks of registration
  • Participants with active bacterial, viral, or fungal infection requiring systemic treatment within the last two months prior to registration
  • History of severe allergic or anaphylactic reactions to humanized or murine monoclonal antibodies or known sensitivity or allergy to murine products
  • Hypersensitivity to chlorambucil, obinutuzumab, or venetoclax or to any of the excipients
  • Pregnant women and nursing mothers
  • Positive test results for chronic hepatitis B virus (HBV) infection (defined as positive hepatitis B surface antigen \[HBsAg\] serology) or positive test result for hepatitis C (hepatitis C virus \[HCV\] antibody serology testing)
  • Participants with known infection with human immunodeficiency virus (HIV) or human T-cell leukemia virus-1 (HTLV-1)
  • Requires the use of warfarin, marcumar, or phenprocoumon
  • +1 more criteria

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (122)

Banner MD Anderson Cancer Center

Gilbert, Arizona, 85234, United States

Location

City of Hope

Duarte, California, 91010, United States

Location

UC San Diego Health System

La Jolla, California, 92093, United States

Location

Moffitt Cancer Center

Tampa, Florida, 33612-9497, United States

Location

Winship Cancer Institute

Atlanta, Georgia, 30322, United States

Location

Ingalls Memorial Hospital

Harvey, Illinois, 60426, United States

Location

Henry Ford Hospital

Detroit, Michigan, 48202-2689, United States

Location

Joe Arrington Cancer Center

Lubbock, Texas, 79410, United States

Location

Hospital Italiano

Buenos Aires, C1181ACH, Argentina

Location

Liverpool Hospital

Liverpool BC, New South Wales, 1871, Australia

Location

Tweed Hospital

Tweed Heads, New South Wales, 2485, Australia

Location

The Townsville Hospital

Douglas, Queensland, 4814, Australia

Location

Princess Alexandra Hospital Woolloongabba

Woolloongabba, Queensland, 4102, Australia

Location

Royal Adelaide Hospital

Adelaide, South Australia, 5000, Australia

Location

Ashford Cancer Centre Research

Ashford, South Australia, 5035, Australia

Location

Box Hill Hospital

Box Hill, Victoria, 3128, Australia

Location

The Northern Hospital

Epping, Victoria, 3076, Australia

Location

Monash Medical Centre

Melbourne, Victoria, 3168, Australia

Location

Tiroler Landeskrankenanstalten Ges.M.B.H.

Innsbruck, 6020, Austria

Location

Medizinische Universität Wien

Vienna, 1090, Austria

Location

Hanusch-Krankenhaus

Vienna, 1140, Austria

Location

Hospital das Clinicas - UFRGS

Porto Alegre, Rio Grande do Sul, 90035-903, Brazil

Location

Instituto de Ensino e Pesquisa Sao Lucas - IEP

São Paulo, São Paulo, 01236-030, Brazil

Location

Hospital Sírio-Libanês

São Paulo, São Paulo, 01308-050, Brazil

Location

Hospital das Clinicas - FMUSP

São Paulo, São Paulo, 05403-000, Brazil

Location

UMHAT Dr Georgi Stranski

Pleven, 5800, Bulgaria

Location

UMHAT " Sveti Georgi" Plovdiv - Clinic of Oncology and Hematology

Plovdiv, 4002, Bulgaria

Location

University Hospital Sv.Georgi Clnic of Hematology

Plovdiv, 4002, Bulgaria

Location

University Multiprofile Hospital For Active Treatment "Sveti Ivan Rilski" EAD

Sofia, 1431, Bulgaria

Location

MHAT Hristo Botev

Vratsa, 3000, Bulgaria

Location

Arthur J.E. Child Comprehensive Cancer Center

Calgary, Alberta, T2N 4N2, Canada

Location

Queen Elizabeth II Health Sciences Centre

Halifax, Nova Scotia, B3H 2Y9, Canada

Location

Jewish General Hospital

Montreal, Quebec, H3T 1E2, Canada

Location

University Hospital Center Zagreb

Zagreb, 10000, Croatia

Location

University Hospital Merkur Clinic for Internal Medicine/ Hematology

Zagreb, 10000, Croatia

Location

Herlev Hospital

Herlev, 2730, Denmark

Location

Rigshospitalet

København Ø, 2100, Denmark

Location

Sjaellands Universitetshospital, Roskilde

Roskilde, 4000, Denmark

Location

Sygehus Lillebælt, Vejle

Vejle, 7100, Denmark

Location

North Estonia medical Centre

Tallinn, 13419, Estonia

Location

Tartu Uni Hospital

Tartu, 51014, Estonia

Location

Institut d'Hématologie de Basse Normandie

Caen, 14000, France

Location

Hopital Henri Mondor

Créteil, 94000, France

Location

CHU de Grenoble

Grenoble, 38043, France

Location

Centre Jean Bernard

Le Mans, 72000, France

Location

Centre Leon Berard

Lyon, 69373, France

Location

Hôpital Saint Eloi

Montpellier, 34295, France

Location

Hopital Hotel Dieu Et Hme

Nantes, 44093, France

Location

Hopital Saint Louis

Paris, 75475, France

Location

Hopital Pontchaillou

Rennes, 35033, France

Location

Centre Henri Becquerel

Rouen, 76038, France

Location

CH de Toulon Hôpital Sainte Musse

Toulon, 83056, France

Location

Institut Gustave Roussy - Hematologie

Villejuif, 94805, France

Location

Uniklinik RWTH Aachen

Aachen, 52074, Germany

Location

Charite - Campus Virchow-Klinikum

Berlin, 13353, Germany

Location

Charite - Universitätsmedizin Berlin

Berlin, 13353, Germany

Location

Universitätsklinikum Köln

Cologne, 50937, Germany

Location

BAG Freiberg-Richter, Jacobasch, Illmer, Wolf

Dresden, 01307, Germany

Location

Uniklinikum "Carl Gustav Carus";Med. Klinik 1

Dresden, 01307, Germany

Location

Universitätsklinikum Essen

Essen, 45122, Germany

Location

Klinik Esslingen

Esslingen am Neckar, 73730, Germany

Location

Klinikum Frankfurt/Oder

Frankfurt (Oder), 15236, Germany

Location

Uniklinikum Freiburg

Freiburg im Breisgau, 79106, Germany

Location

Universitaetsklinikum Heidelberg

Heidelberg, 69120, Germany

Location

Stiftung Kathol. Krankenhaus Marienhospital Herne Klinik Mitte

Herne, 44625, Germany

Location

Praxisklinik für Hämatologie und Onkologie Koblenz

Koblenz, 56068, Germany

Location

Kliniken Maria Hilf GmbH Innere Medizin I

Mönchengladbach, 41063, Germany

Location

Klinikum Schwäbisch Gmünd

Mutlangen, 73557, Germany

Location

München Klinik Schwabing

München, 80804, Germany

Location

Klinikum rechts der Isar der Technischen Universität München

München, 81675, Germany

Location

Klinikum der Universität München, Campus Großhadern

München, 83177, Germany

Location

Brüderkrankenhaus St. Josef Paderborn

Paderborn, 33098, Germany

Location

Krankenhaus Barmherzige Bruder Regensburg

Regensburg, 93049, Germany

Location

Marienhospital

Stuttgart, 70199, Germany

Location

Robert-Bosch-Krankenhaus

Stuttgart, 70376, Germany

Location

Universitatsklinikum Tubingen

Tübingen, 72076, Germany

Location

Universtitätsklinikum Ulm

Ulm, 89081, Germany

Location

Arcispedale S. Anna

Ferrara, Emilia-Romagna, 44100, Italy

Location

Uni Cattolica

Rome, Lazio, 00168, Italy

Location

AOU Città della Salute e della Scienza di Torino - Presidio Le Molinette

Torino, Lazio, 10126, Italy

Location

Ospedale San Raffaele

Milan, Lombardy, 20132, Italy

Location

Az. Osp. S. Maria

Terni, Umbria, 05100, Italy

Location

Ospedale dell' Angelo

Venezia Mestre, Veneto, 30174, Italy

Location

Hospital General de Culiacan

Culiacán, Sinaloa, 80230, Mexico

Location

Canterbury Health Laboratories

Christchurch, 8011, New Zealand

Location

Dunedin Hospital

Dunedin, New Zealand

Location

Midcentral District Health Board

Palmerston North, 4442, New Zealand

Location

Wellington Hospital

Wellington, 6012, New Zealand

Location

Samodzielny Public Zaklad

Chorzów, 41-500, Poland

Location

Wojewódzki Szpital Specjalistyczny im. Miko?aja Kopernika

Lodz, 9351, Poland

Location

Wojewodzki Szpital Specjalistyczny im. J. Korczaka

Słupsk, 76-200, Poland

Location

Samodzielny Publiczny Szpital Kliniczny Nr 1 we Wroc?awiu

Wroclaw, 5036, Poland

Location

Fundeni Clinical Inst.

Bucharest, 022328, Romania

Location

Institutul Regional de Oncologie Iasi

Iași, 700483, Romania

Location

Spitalul Clinic Judetean de Urgenta Targu-Mures

Târgu Mureş, 540136, Romania

Location

SBEI of HPE ?Bashkir State Medical University? of MoH RF

Ufa, Bashkortostan Republic, 450000, Russia

Location

Regional Clinical Hospital N.A. Semashko

Nizhny Novgorod, Niznij Novgorod, 603126, Russia

Location

Republican Clinical Oncologic Dispensary of Republic Of Tatarstan

Kazan', Tatarstan Republic, 420029, Russia

Location

Penza Regional Oncology Dispensary

Penza, 440071, Russia

Location

Clinical MSCh No1

Perm, 614077, Russia

Location

Complejo Hospitalario de Navarra

Pamplona, Navarre, 31008, Spain

Location

Hospital Universitario de Canarias

San Cristóbal de La Laguna, Tenerife, 38320, Spain

Location

Hospital del Mar

Barcelona, 08003, Spain

Location

Hospital Universitari Vall d'Hebron

Barcelona, 08035, Spain

Location

Hospital Clínic i Provincial

Barcelona, 08036, Spain

Location

Hospital Universitario de la Princesa

Madrid, 28006, Spain

Location

Hospital Universitario Ramón y Cajal

Madrid, 28034, Spain

Location

Hospital Univ. 12 de Octubre

Madrid, 28041, Spain

Location

Hospital Universitario La Paz

Madrid, 28046, Spain

Location

Hospital Clinico Universitario de Salamanca

Salamanca, 37007, Spain

Location

Hospital Universitario Virgen del Rocio

Seville, 41013, Spain

Location

Complejo Hospitalario de Toledo- H. Virgen de la Salud

Toledo, 45004, Spain

Location

Hospital Clinico Universitario de Valencia

Valencia, 46010, Spain

Location

Hospital Arnau de Vilanova (Valencia) Servicio de Hematologia

Valencia, 46015, Spain

Location

Inselspital Bern

Bern, 3010, Switzerland

Location

Luzerner Kantonsspital, Hämatologie

Lucerne, 6000, Switzerland

Location

Universitätsspital Zürich Medizin Hämatologie

Zurich, 8091, Switzerland

Location

Birmingham Heartlands Hospital

Birmingham, B9 5SS, United Kingdom

Location

Boston Pilgrim Hospital

Boston,Lincolnshire, PE21 9QS, United Kingdom

Location

Western General Hospital

Edinburgh, EH4 2XU, United Kingdom

Location

Lincoln County Hospital

Lincoln, LN2 5QY, United Kingdom

Location

University Hospital Southampton NHS Foundation Trust

Southhampton, SO16 6YD, United Kingdom

Location

Related Publications (9)

  • Munir T, Martinez-Calle N, Xu S, Yang K, Ge X, Ali AK, Mohseninejad L, Dobi B, Rakonczai P, Ma H, Williams R, Aldairy W, Lamanna N. Indirect Comparisons of the Efficacy and Safety of Zanubrutinib versus Venetoclax plus Obinutuzumab in Treatment-Naive Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma. Oncol Ther. 2025 Dec;13(4):1055-1070. doi: 10.1007/s40487-025-00380-0. Epub 2025 Sep 13.

  • Al-Sawaf O, Robrecht S, Zhang C, Olivieri S, Chang YM, Fink AM, Tausch E, Schneider C, Ritgen M, Kreuzer KA, Sivchev L, Niemann CU, Schwarer A, Loscertales J, Weinkove R, Strumberg D, Kilfoyle A, Manzoor BS, Jawaid D, Emechebe N, Devine J, Boyer M, Runkel ED, Eichhorst B, Stilgenbauer S, Jiang Y, Hallek M, Fischer K. Venetoclax-obinutuzumab for previously untreated chronic lymphocytic leukemia: 6-year results of the randomized phase 3 CLL14 study. Blood. 2024 Oct 31;144(18):1924-1935. doi: 10.1182/blood.2024024631.

  • Langerbeins P, Giza A, Robrecht S, Cramer P, von Tresckow J, Al-Sawaf O, Fink AM, Furstenau M, Kutsch N, Simon F, Goede V, Hoechstetter M, Niemann CU, da Cunha-Bang C, Kater A, Dubois J, Gregor M, Staber PB, Tausch E, Schneider C, Stilgenbauer S, Eichhorst B, Fischer K, Hallek M. Reassessing the chronic lymphocytic leukemia International Prognostic Index in the era of targeted therapies. Blood. 2024 Jun 20;143(25):2588-2598. doi: 10.1182/blood.2023022564.

  • Al-Sawaf O, Zhang C, Jin HY, Robrecht S, Choi Y, Balasubramanian S, Kotak A, Chang YM, Fink AM, Tausch E, Schneider C, Ritgen M, Kreuzer KA, Chyla B, Paulson JN, Pallasch CP, Frenzel LP, Peifer M, Eichhorst B, Stilgenbauer S, Jiang Y, Hallek M, Fischer K. Transcriptomic profiles and 5-year results from the randomized CLL14 study of venetoclax plus obinutuzumab versus chlorambucil plus obinutuzumab in chronic lymphocytic leukemia. Nat Commun. 2023 Apr 18;14(1):2147. doi: 10.1038/s41467-023-37648-w.

  • Badawi M, Chen X, Marroum P, Suleiman AA, Mensing S, Koenigsdorfer A, Schiele JT, Palenski T, Samineni D, Hoffman D, Menon R, Salem AH. Bioavailability Evaluation of Venetoclax Lower-Strength Tablets and Oral Powder Formulations to Establish Interchangeability with the 100 mg Tablet. Clin Drug Investig. 2022 Aug;42(8):657-668. doi: 10.1007/s40261-022-01172-4. Epub 2022 Jul 13.

  • Samineni D, Gibiansky L, Wang B, Vadhavkar S, Rajwanshi R, Tandon M, Sinha A, Al-Sawaf O, Fischer K, Hallek M, Salem AH, Li C, Miles D. Pharmacokinetics and Exposure-Response Analysis of Venetoclax + Obinutuzumab in Chronic Lymphocytic Leukemia: Phase 1b Study and Phase 3 CLL14 Trial. Adv Ther. 2022 Aug;39(8):3635-3653. doi: 10.1007/s12325-022-02170-w. Epub 2022 Jun 16.

  • Al-Sawaf O, Zhang C, Lu T, Liao MZ, Panchal A, Robrecht S, Ching T, Tandon M, Fink AM, Tausch E, Schneider C, Ritgen M, Bottcher S, Kreuzer KA, Chyla B, Miles D, Wendtner CM, Eichhorst B, Stilgenbauer S, Jiang Y, Hallek M, Fischer K. Minimal Residual Disease Dynamics after Venetoclax-Obinutuzumab Treatment: Extended Off-Treatment Follow-up From the Randomized CLL14 Study. J Clin Oncol. 2021 Dec 20;39(36):4049-4060. doi: 10.1200/JCO.21.01181. Epub 2021 Oct 28.

  • Al-Sawaf O, Zhang C, Tandon M, Sinha A, Fink AM, Robrecht S, Samoylova O, Liberati AM, Pinilla-Ibarz J, Opat S, Sivcheva L, Le Du K, Fogliatto LM, Niemann CU, Weinkove R, Robinson S, Kipps TJ, Tausch E, Schary W, Ritgen M, Wendtner CM, Kreuzer KA, Eichhorst B, Stilgenbauer S, Hallek M, Fischer K. Venetoclax plus obinutuzumab versus chlorambucil plus obinutuzumab for previously untreated chronic lymphocytic leukaemia (CLL14): follow-up results from a multicentre, open-label, randomised, phase 3 trial. Lancet Oncol. 2020 Sep;21(9):1188-1200. doi: 10.1016/S1470-2045(20)30443-5.

  • Fischer K, Al-Sawaf O, Bahlo J, Fink AM, Tandon M, Dixon M, Robrecht S, Warburton S, Humphrey K, Samoylova O, Liberati AM, Pinilla-Ibarz J, Opat S, Sivcheva L, Le Du K, Fogliatto LM, Niemann CU, Weinkove R, Robinson S, Kipps TJ, Boettcher S, Tausch E, Humerickhouse R, Eichhorst B, Wendtner CM, Langerak AW, Kreuzer KA, Ritgen M, Goede V, Stilgenbauer S, Mobasher M, Hallek M. Venetoclax and Obinutuzumab in Patients with CLL and Coexisting Conditions. N Engl J Med. 2019 Jun 6;380(23):2225-2236. doi: 10.1056/NEJMoa1815281. Epub 2019 Jun 4.

MeSH Terms

Conditions

Leukemia, Lymphocytic, Chronic, B-Cell

Interventions

Chlorambucilvenetoclaxobinutuzumab

Condition Hierarchy (Ancestors)

Leukemia, B-CellLeukemia, LymphoidLeukemiaNeoplasms by Histologic TypeNeoplasmsHematologic DiseasesHemic and Lymphatic DiseasesLymphoproliferative DisordersLymphatic DiseasesImmunoproliferative DisordersImmune System DiseasesChronic DiseaseDisease AttributesPathologic ProcessesPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Nitrogen Mustard CompoundsMustard CompoundsHydrocarbons, HalogenatedHydrocarbonsOrganic Chemicals

Results Point of Contact

Title
Medical Communications
Organization
Hoffmann-La Roche

Study Officials

  • Clinical Trials

    Hoffmann-La Roche

    STUDY DIRECTOR

Publication Agreements

PI is Sponsor Employee
No
Restriction Type
OTHER
Restrictive Agreement
Yes

Study Design

Study Type
interventional
Phase
phase 3
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
INDUSTRY
Responsible Party
SPONSOR

Study Record Dates

First Submitted

September 16, 2014

First Posted

September 17, 2014

Study Start

December 31, 2014

Primary Completion

August 17, 2018

Study Completion

August 27, 2025

Last Updated

November 6, 2025

Results First Posted

October 1, 2019

Record last verified: 2025-11

Locations