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Acute Myeloid Leukemia (AML)Phase 2SOPRANCT02088541

Selinexor (KPT-330) in Older Patients With Relapsed AML

A Phase 2 study testing Selinexor, Hydroxyurea and Ara-C in people with Acute Myeloid Leukemia (AML), run by Karyopharm Therapeutics Inc at 78 sites in 11 countries.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

Trial summary

This is a randomized, multicenter, open-label, phase 2 study of the SINE compound, selinexor given orally versus specified investigator choices (one of three potential salvage therapies). Read more about this study

Who is it for?
Ages 60 years and older
Conditions the study is for
Acute Myeloid Leukemia (AML)
What is being tested?
Selinexor, Hydroxyurea and Ara-C
Could I receive a placebo?
No, everyone receives an active treatment
How many people
317 participants
Where
78 sitesin 11 countries
Study dates
Mar 2014to 8 Jan 2018
Phase
Phase 2
Are there results?
Yes, posted in the registrySummary in the doctors' view

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

Who may be able to join

  • Age ≥ 60 years with relapsed or refractory AML of any type except for acute promyelocytic leukemia (APL; AML M3), after at least 1 prior AML therapy , who have never undergone, and who are not currently eligible for, stem cell transplantation, and are currently deemed unfit for intensive chemotherapy.
  • Eastern Cooperative Oncology Group (ECOG) ≤ 2.
  • Must have available archival or recently acquired bone marrow biopsy/aspiration or tumor tissue for central review to be eligible.
  • Relapsed or refractory AML, defined as either: recurrence of disease after a complete remission (CR), or failure to achieve CR with initial therapy.
  • Must have received at least 1 prior line of AML therapy given at standard doses and must have progressed after their most recent therapy. Prior therapy must have included: a hypomethylating agent with at least 2 cycles.
  • At least 2 weeks must have elapsed since the last anti-leukemia treatment (with the exception of hydroxyurea) before first dose in this study.

Who cannot join

  • Treatment with any investigational agent within 3 weeks prior to first dose in this study.
  • Presence of central nervous system (CNS) leukemia.
  • In blast transformation of chronic myeloid leukemia (CML). Prior myelodysplastic syndrome (MDS) is acceptable; prior treatment for MDS does not count as an AML therapy.
  • Major surgery within 2 weeks of first dose of study drug. Participants must have recovered from the effects of any surgery performed greater than 2 weeks previously.
  • Concurrent active malignancy under treatment.
  • Known active hepatitis B virus (HBV) or C virus (HCV) infection; or known to be positive for HCV ribonucleic acid (RNA) or HBsAg (HBV surface antigen).
Show all 9Show fewer
  • Known HIV infection.
  • Unable to swallow tablets, or participants with malabsorption syndrome, or any other disease significantly affecting gastrointestinal function.
  • Participants whose AML is classified as favorable according to the European LeukemiaNet (ELN) disease risk assessment.

Trial locations and contacts

78 sites in 11 countries.

78 sites in 11 countries

United States26 sites
  • University of Michigan Comprehensive Cancer Center

    Ann Arbor, Michigan, 48109-0944

  • Winship Cancer Institute / Emory University

    Atlanta, Georgia, 30322

  • Sidney Kimmel Comprehensive Cancer Center / John Hopkins University

    Baltimore, Maryland, 21287

  • Roswell Park Cancer Institute

    Buffalo, New York, 14263

  • Gabrail Cancer Center

    Canton, Ohio, 44718

  • Northwestern University

    Chicago, Illinois, 60611

  • University of Chicago Medicine

    Chicago, Illinois, 60637

  • Ohio State University Comprehensive Cancer Center

    Columbus, Ohio, 43210

  • Colorado Blood Cancer Institute/Sarah Cannon Research Institute

    Denver, Colorado, 80218

  • Duke Cancer Care

    Durham, North Carolina, 27705

  • Hackensack University Medical Center

    Hackensack, New Jersey, 07601

  • Westchester Medical Center / New York Medical College

    Hawthorne, New York, 10532

  • Milton S. Hershey Medical Center / Penn State

    Hershey, Pennsylvania, 17033

  • MD Anderson Cancer Center / University of Texas

    Houston, Texas, 77030

  • University of Kansas Hospital

    Kansas City, Kansas, 66160

  • Jonsson Comprehensive Cancer Center / University of California, Los Angeles

    Los Angeles, California, 90024

  • Tennessee Oncology/Sarah Cannon Research Institute

    Nashville, Tennessee, 37203

  • Vanderbilt-Ingram Cancer Center / Vanderbilt University

    Nashville, Tennessee, 37215

  • Yale Cancer Center / Yale University

    New Haven, Connecticut, 06510

  • Memorial Sloan Kettering Cancer Center

    New York, New York, 10065

  • New York Presbyterian Hospital / Weill Cornell Medical College

    New York, New York, 10065

  • Sutter Oncology & Hematology

    Sacramento, California, 95816

  • Texas Transplant Institute/Sarah Cannon Research Institute

    San Antonio, Texas, 78229

  • Stanford Cancer Institute / Stanford University

    Stanford, California, 94304

  • H. Lee Moffitt Cancer Center and Research Institute

    Tampa, Florida, 33612

  • University of Massachusetts Medical School

    Worcester, Massachusetts, 01655

Other trials in United States

Germany8 sites
  • Stellvertretende Klinikleiterin Charité, Campus Benjamin Franklin

    Berlin, 12203

  • Ev. Diakonie-Krankenhaus Gemeinnutzige GMBH Medizinische Klinik 2

    Bremen

  • UNIVERSITÄTSKLINIKUM TU DRESDEN Medizinische Klinik und Poliklinik I,

    Dresden

  • University Hospital Frankfurt

    Frankfurt

  • Medizinische Hochschule Hannover (Hannover Medical School) Dept. of Hematology, Hemostasis, Oncology, and Stem Cell Transplantation

    Hanover

  • Abteilung Hämatologie, internistische Onkologie und Hämostaseologie

    Leipzig

  • UNIVERSITY HOSPITAL OF MÜNSTER Medizinische Klinik und Poliklinik A, Universitätsklinikum Münster

    Münster

  • Universitätsklinikum Ulm

    Ulm

Other trials in Germany

Israel7 sites
  • Sororka MC

    Beersheba, 85025

  • Rambam Health Care Campus

    Haifa, 3109601

  • Wolfson Medical Center

    Holon

  • Hadassah Medical Center

    Jerusalem, 91120

  • Rabin Medical Center

    Petah Tikva, 4941492

  • Tel Aviv Sourasky Medical Centre

    Tel Aviv

  • Chaim Sheba Medical Center

    Tel HaShomer, 52621

Other trials in Israel

Netherlands7 sites
  • AMC, Academisch Medisch Centrum Afdeling Klinische Hematologie

    Amsterdam

  • VU University Medical Center

    Amsterdam

  • Universitair Medisch Centrum Groningen Department of Haematology

    Groningen

  • Radboud University Medical Center Department of Haematology (476)

    Nijmegen

  • Erasmus MC, location Daniel den Hoed

    Rotterdam

  • University Medical Center Utrecht

    Utrecht

  • Isala Kliniecken Zwolle

    Zwolle

Other trials in Netherlands

United Kingdom7 sites
  • University Hospital Wales

    Cardiff, Wales, CF14 4XW

  • Ninewells Hospital and Medical School NHS Tayside

    Dundee, DD1 9SY

  • Northwick Park Hospital

    Harrow, England, HA1 3UJ

  • Hull and East Yorkshire Hospitals NHS Trust Queens Centre for Oncology and Haematology

    Hull, Yorkshire, HU3 2JZ

  • Royal Liverpool University Hospital, Dept of Cellular and Molecular Physiology, Molecular and Clinical Cancer Medicine

    Liverpool, Lancashire, L7 8XP

  • Plymouth Hospitals NHS Trust/Derriford Hospital

    Plymouth

  • Royal Marsden NHS Trust

    Sutton, Surrey, SM2 5PT

Other trials in United Kingdom

France5 sites
  • CHU Bordeaux- Hôpital Haut Lévêque

    Bordeaux

  • Centre Hospitalier Lyon

    Lyon

  • Hopital Saint Louis

    Paris

  • Hôpital Avicenne

    Paris

  • Institut Universitaire du Cancer Toulouse

    Toulouse

Other trials in France

Denmark4 sites
  • Aarhus University Hospital

    Aarhus

  • Department of Haematology, National University Hospital, Rigshospitalet

    Copenhagen

  • Herlev Hospital

    Herlev

  • Odense University Hospital, Department of Hematology

    Odense

Other trials in Denmark

Poland4 sites
  • Wojewódzki Szpital Specjalistyczny im. M. Kopernika, Klinika Hematologii

    Lodz

  • Samodzielny Publiczny Zakład Opieki Zdrowotnej Ministerstwa Spraw Wewnętrznych

    Olsztyn

  • Instytut Hematologii i Transfuzjologii

    Warsaw

  • Samodzielny Publiczny Szpital Kliniczny Nr 1 we Wrocławiu

    Wroclaw

Other trials in Poland

Spain4 sites
  • ICO Badalona

    Badalona, 08916

  • Hospital del Mar

    Barcelona

  • Hospital Universitario de Salamanca Servicio de Hematologia

    Salamanca

  • Hospital Universitario y Politécnico La Fe

    Valencia

Other trials in Spain

Canada3 sites
  • Tom Baker Cancer Centre

    Calgary, Alberta, T2N 4N2

  • University of Alberta

    Edmonton, Alberta, T6G 2G3

  • Sir Mortimer B. Davis Jewish General Hospital / McGill University

    Montreal, Quebec, H2W1S6

Other trials in Canada

Italy3 sites
  • AOU Ospedali Riuniti di Ancona

    Ancona

  • A.O Spedali Civili di Brescia

    Brescia

  • AORN Cardarelli / UOSC di Ematologia con TMO

    Naples

Other trials in Italy

About this study

Official title: A Randomized, Open Label, Phase 2 Study of the Selective Inhibitor of Nuclear Export (SINE) Selinexor (KPT-330) Versus Specified Physician's Choice in Patients ≥ 60 Years Old With Relapsed or Refractory Acute Myeloid Leukemia (AML) Who Are Ineligible for Intensive Chemotherapy and/or Transplantation

This is a randomized, multicenter, open-label, phase 2 study of the SINE compound, selinexor given orally versus specified investigator choices (one of three potential salvage therapies). Participants age ≥ 60 years with relapsed or refractory AML of any type except for AML M3, after one prior therapy only, who have never undergone and who are not currently eligible for stem cell transplantation and are currently deemed unfit for intensive chemotherapy.

Read the detailed description

This is a randomized, multicenter, open-label phase 2 study of the SINE compound, selinexor given orally versus restricted investigator choice (i.e., one of three potential salvage therapies).

Participants who have never been transplant eligible, are currently deemed unfit for intensive chemotherapy, ≥ 60 years old, who have AML (except Acute Promyelocytic Leukemia: APL, AML M3) after one prior treatment of either hypomethylating agent or a regimen including Ara-C, and are meeting the inclusion and exclusion criteria will be randomized to receive either oral selinexor or physician's choice (one of three potential treatments: best supportive care (BSC) alone, or BSC + hypomethylating agent, or BSC + low dose Ara-C until disease progression, death or intolerance has occurred.

Being tested
Selinexor, Hydroxyurea, Ara-C
Keywords
Relapsed/Refractory Acute Myeloid Leukemia, Acute Myeloid Leukemia, AML, Karyopharm, Selinexor, KPT-330
Medical subject headings
Leukemia, Myeloid, Acute

What participants receive

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

  • SelinexorDrug

    Also called KPT-330

    Selinexor oral tablet.

  • HydroxyureaDrug

    Also called Hydroxycarbamide

  • Ara-CDrug

    Also called Cytarabine, Cytosine arabinoside, Cytosar-U, Depocyt

    Ara-C Subcutaneous Injection.

Study groups in NCT02088541
Study groupRoleWhat they receive
Selinexor approximately 55 mg/m^2 (60 to 120 mg based on BSA)ExperimentalParticipants under protocol versions (PV) less than (<) 5.0 (those who had one prior line of acute myeloid leukemia (AML) therapy), receive oral selinexor tablets at a dose of approximately 55 mg/m^2 (milligrams per square meter) (60 to 120 mg based on body surface area [BSA]) twice weekly, on Day 1 and 3 of each week of 4-week cycle (28 days per cycle).
Receives: Drug: Selinexor
Selinexor 60 mg (PV <5) (Equivalent to 35 mg/m^2)ExperimentalParticipants under PV < 5.0 (those who had one prior line of AML therapy), receive oral selinexor tablets at a fixed dose of 60 mg (equivalent to 35 mg/m^2), based on BSA, twice weekly, on Day 1 and 3 of each week of 4-week cycle (28 days per cycle).
Receives: Drug: Selinexor
Selinexor 60 mg (PV >=5) (Equivalent to 35 mg/m^2)ExperimentalParticipants under PV >= 5 (PV 5: those who had at least one prior line of AML therapy, PV 5.1: who had at least two prior line of AML therapy), receive oral selinexor tablets at a dose of 60 mg (equivalent to 35 mg/m^2) twice weekly, on Day 1 and 3 of each week of 4-week cycle (28 days per cycle).
Receives: Drug: Selinexor
Physician's Choice 1 (PV <5)Active comparatorParticipants under PV < 5.0 (those who had one prior line of AML therapy) received Best Supportive Care (BSC) which included blood product transfusions, antimicrobials, growth factors as needed, and hydroxyurea.
Receives: Drug: Hydroxyurea
Physician's Choice 2 (PV >=5)Active comparatorParticipants under PV >= 5 (PV 5: those who had at least one prior line of AML therapy, PV 5.1: who had at least two prior line of AML therapy), received BSC along with subcutaneous injection of arabinoside cytosine (Ara-C), 20 mg, twice daily, for 10 days, repeated at 28 to 42 day intervals.
Receives: Drug: Ara-C

What is being measured

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

  1. Overall Survival

    Overall survival was defined as the time (in days) from the date of randomization to the date of death due to any cause. Participants last known to be alive were censored at date of last contact.

    Measured: Baseline until disease progression or discontinuation from the study, or death, whichever occurred first (up to a maximum of approximately 104 weeks)

Secondary outcomes (11)
  1. Percentage of Participants With Overall Survival of at Least 3 Months (OS3.0)

    Overall survival was defined as the time (in days) from the date of randomization to the date of death due to any cause. Participants last known to be alive were censored at date of last contact. Analysis was performed using Kaplan-Meier method.

    Measured: From randomization (Day 1) up to 3 months

  2. Percentage of Participants With Complete Remission Rate (CRR) for Those Who Achieved Complete Remission (CR)

    CRR was analyzed using International Working Group (IWG) 2003 criteria, as the difference in the proportions of participants with IWG results of CR. CR per IWG 2003 criteria was defined as morphologic presence of < 5 percentage (%) myeloblasts in bone marrow, the absence of circulating blasts, hematologic recovery (as evidenced by a peripheral blood absolute neutrophil count (ANC) > 1000 cells/microliter (microL) and platelet count > 100,000/microL, with no need for red blood cell (RBC) transfusions), and the absence of extramedullary disease.

    Measured: Baseline until disease progression or discontinuation from the study, or death, whichever occurred first (up to a maximum of approximately 104 weeks)

  3. Median Disease-Free Survival (DFS) for Participants Who Achieved Complete Remission (CR)

    DFS for CRR based on IWG criteria, was calculated from the first date of response of CR to the date of progression or recurrence, or date of death if progression or recurrence did not occur. Participants who discontinued prior to disease progression or recurrence or did not progress as of the time of the analysis were censored at the time of last radiologic assessment. CR per IWG 2003 criteria was defined as morphologic presence of < 5 % myeloblasts in bone marrow, the absence of circulating blasts, hematologic recovery (as evidenced by a peripheral blood ANC > 1000 cells/microL and platelet count > 100,000/microL, with no need for RBC transfusions), and the absence of extramedullary disease.

    Measured: Baseline until disease progression or discontinuation from the study, or death, whichever occurred first (up to a maximum of approximately 104 weeks)

  4. Percentage of Participants With Modified Complete Remission Rate (mCRR) for Those Who Achieved Complete Remission (CR) or Complete Remission With Incomplete Hematologic Recovery (Cri)

    mCRR was defined as the point estimate of the percentage of participants who had CR, CRi, or CRp. Responses defined as per IWG 2003 response criteria: Morphologic CR:< 5% myeloblasts in bone marrow, the absence of circulating blasts, hematologic recovery (as evidenced by a peripheral blood ANC > 1000 cells/microL and platelet count > 100,000/microL, with no need for RBC transfusions), and the absence of extramedullary disease. Morphologic CRp: All criteria for CR except for residual neutropenia (<1x10^9/L) or thrombocytopenia (<100 x10^9/L), Cri (< 5% bone marrow blasts with residual neutropenia [ANC < 1000 cells/microL] or thrombocytopenia [platelets < 100,000/microL]), normal maturation of all cellular components in the bone marrow, no extramedullary disease and transfusion independent.

    Measured: Baseline until disease progression or discontinuation from the study, or death, whichever occurred first (up to a maximum of approximately 104 weeks)

  5. Median Disease-Free Survival (DFS) for Participants Who Achieved Complete Remission or CR With Incomplete Hematologic Recovery (CRi) or Complete Remission With Incomplete Platelet Recovery (CRp)

    DFS based on IWG criteria was defined as the duration from start of the complete response achieved until disease progression or death from any cause. Responses defined by IWG 2003 Response Criteria: Morphologic CR: < 5% myeloblasts in bone marrow, the absence of circulating blasts, hematologic recovery (as evidenced by a peripheral blood ANC > 1000 cells/microL and platelet count > 100,000/microL, with no need for RBC transfusions), and the absence of extramedullary disease. Morphologic CRp: All criteria for CR except for residual neutropenia (<1x10^9/L) or thrombocytopenia (<100 x10^9/L), Cri (< 5% bone marrow blasts with residual neutropenia [ANC < 1000 cells/microL] or thrombocytopenia [platelets < 100,000/microL]), normal maturation of all cellular components in the bone marrow, no extramedullary disease and transfusion independent.

    Measured: Baseline until disease progression or discontinuation from the study, or death, whichever occurred first (up to a maximum of approximately 104 weeks)

  6. Percentage of Participants With Overall Response Rate (ORR)

    Overall response rate was defined as the point estimate of the percentage of participants who achieved CR (disappearance of all target and non-target lesions), partial response (PR) (>=30 % decrease in sum of longest diameters of target lesions taking as reference baseline sum longest diameters associated to non-progressive disease response for non-target lesions). CRi; < 5% BM blasts with residual neutropenia [ANC < 1000 cells/microL] or thrombocytopenia [platelets < 100,000/microL]. CRp; All criteria for CR except for residual neutropenia (<1x10^9/L) or thrombocytopenia (<100 x10^9/L) and morphologic leukemia-free state (MLFS); morphologic BM blast clearance to <5% in a marrow sample in which <=200 cells enumerated or cellularity is ≥10%, in absence of blasts with Auer rods, no hematologic recovery required.

    Measured: Baseline until disease progression or discontinuation from the study, or death, whichever occurred first (up to a maximum of approximately 104 weeks)

  7. Duration of Response (DOR)

    DOR was calculated from date of response of CR, CRi, CRp, MLFS, or PR to date of progression or recurrence based on IWG criteria. CR: <5% myeloblasts in bone marrow,absence of circulating blasts, hematologic recovery (peripheral blood ANC >1000 cells/microL, platelet count > 100,000/microL, no need for RBC transfusions), absence of extramedullary disease. PR: No circulating blasts, neutrophil count > =1.0 x10^9/L, platelet count >= 100 x10^9/L, >= 50 % reduction in bone marrow blast to 6% to 25%, or blasts less than or equal to (<=) 5% if Auer rods are present. CRp: All criteria for CR except for residual neutropenia (<1x10^9/L) or thrombocytopenia (<100 x10^9/L), CRi; < 5% bone marrow blasts with residual neutropenia [ANC < 1000 cells/microL] or thrombocytopenia [platelets < 100,000/microL]. MLFS: morphologic bone marrow blast clearance to < 5% in marrow sample, <= 200 cells enumerated/cellularity is ≥ 10%, in absence of blasts with Auer rods, no hematologic recovery required.

    Measured: Baseline until disease progression or discontinuation from the study, or death, whichever occurred first (up to a maximum of approximately 104 weeks)

  8. Percentage of Participants With Disease Control Rate (DCR)

    DCR:Point estimate of % of participants with CR,CRi,CRp,MLFS,PR, or SD for <=4 weeks.CR:<5% myeloblasts in bone marrow (BM),absence of circulating blasts,hematologic recovery(peripheral blood ANC >1000 cells/microL and platelet count >100,000/microL, no need of RBC transfusions),absence of extramedullary disease. PR:No circulating blasts,Neutrophil count >=1.0 x10^9/L, Platelet count >= 100*10^9/L, >=50% reduction in BM blast to 6% to 25%, or blasts <=5% if Auer rods are present.CRp:All criteria for CR except for residual neutropenia (<1*10^9/L) or thrombocytopenia(<100 x10^9/L),CRi;< 5% BM blasts with residual neutropenia [ANC < 1000 cells/microL] or thrombocytopenia [platelets < 100,000/microL]. MLFS:morphologic BM blast clearance to <5% in a marrow sample in which <=200 cells enumerated or cellularity is ≥10%,in absence of blasts with Auer rods,no hematologic recovery required,SD:failure to achieve a response but not meeting criteria for disease progression over period of >4 weeks.

    Measured: Up to 4 weeks from the date of randomization to the date of progression or recurrence based on IWG criteria

  9. Duration of Disease Control Rate

    Duration of DCR calculated for all participants with DCR. CR: < 5% myeloblasts in BM, absence of circulating blasts, hematologic recovery (peripheral blood ANC >1000 cells/microL and platelet count > 100,000/microL, no need for RBC transfusions), absence of extra medullary disease. PR: No circulating blasts, Neutrophil count >=1.0 x 10^9/L, Platelet count >= 100 x 10^9/L, >= 50 % reduction in BM blast to 6% to 25%, or blasts <= 5% if Auer rods are present. CRp: All criteria for CR except for residual neutropenia (<1 x 10^9/L) or thrombocytopenia (<100 x 10^9/L), CRi; < 5% BM blasts with residual neutropenia [ANC < 1000 cells/microL] or thrombocytopenia [platelets < 100,000/microL]. MLFS; morphologic BM blast clearance to < 5% in a marrow sample in which <=200 cells enumerated/cellularity is >= 10%, in absence of blasts with Auer rods, no hematologic recovery required and SD; failure to achieve a response but not meeting criteria for disease progression over period of > 4 weeks.

    Measured: Up to 4 weeks from the date of randomization to the date of progression or recurrence based on IWG criteria

  10. Change From Baseline in Quality of Life (QoL) and Patient-Reported Outcomes (Functional Assessment of Cancer Therapy -Leukemia [FACT-Leu]

    QoL was assessed by the FACT-Leu. FACT-Leu combines the General version of the Functional Assessment of Cancer Therapy (FACT-G) with a leukemia-specific sub-scale (17 items). The sub-scales for the FACT-G are Physical Well-Being (7 items), Social/Family Well-Being (7 items), Emotional Well-Being (6 items), and Functional Well-Being (7 items). The trial outcomes index (TOI; total of 31 items) was the primary measurement of interest, comprising the Physical and Functional sub-scales plus the leukemia - specific sub-scale. Each item was rated on a 5-point Likert scale. Range from 0 = (Not at all) to 4 = (Very much); therefore, the TOI had a score ranging from 0 to 124. Higher scores indicated improvement in well being. The QoL assessment was performed at baseline (prior to first dose of study treatment), Day 1 of each cycle on or after the second, and at the final visit.

    Measured: Baseline, Day 1 of each treatment cycle (a maximum of 20 cycles: 28 days per cycle) up to 30 days after last dose of study drug (final visit)

  11. Change From Baseline in European Quality of Life-5 Dimension (EQ-5D) Health Questionnaire Visual Analogue Scale (VAS)

    EQ-5D descriptive system comprises of 5 dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each dimension has 5 levels: 1=no problems, 2=slight problems, 3=moderate problems, 4=severe problems, and 5=extreme problems. EQ-5D-5L is a standardized instrument that measures health-related quality of life for men with prostate cancer. EQ-5D consists of EQ-5D descriptive system and EQ VAS. EQ-5D-5-VAS records participant's self-rated health on a vertical VAS that allows them to indicate their health state that can range from 0 (worst imaginable) to 100 (best imaginable), higher scores indicating a better health state.

    Measured: Baseline, Day 1 of each treatment cycle (a maximum of 20 cycles: 28 days per cycle) up to 30 days after last dose of study drug (final visit)

Timeline

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

  1. First posted17 Mar 2014 (estimated)
  2. Study startMar 2014
  3. Primary completion8 Jan 2018
  4. Study completion8 Jan 2018

Resources

More details

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

Study design
Study type
Interventional
Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
317 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02088541
Sponsor's protocol ID
KCP-330-008
Acronym
SOPRA
Status last verified
Jan 2023
First submitted
9 Mar 2014
Last updated
26 Jan 2023
Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
Individual data sharing
Yes

Publications

  • Sweet K, Bhatnagar B, Dohner H, Donnellan W, Frankfurt O, Heuser M, Kota V, Liu H, Raffoux E, Roboz GJ, Rollig C, Showel MM, Strickland SA Jr, Vives S, Tang S, Unger TJ, Joshi A, Shen Y, Alvarez MJ, Califano A, Crochiere M, Landesman Y, Kauffman M, Shah J, Shacham S, Savona MR, Montesinos P. A 2:1 randomized, open-label, phase II study of selinexor vs. physician's choice in older patients with relapsed or refractory acute myeloid leukemia. Leuk Lymphoma. 2021 Dec;62(13):3192-3203. doi: 10.1080/10428194.2021.1950706. Epub 2021 Jul 29.

    PubMed 34323164

Questions about this trial

What is this clinical trial studying?

A Phase 2 study testing Selinexor, Hydroxyurea and Ara-C in people with Acute Myeloid Leukemia (AML), run by Karyopharm Therapeutics Inc at 78 sites in 11 countries.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 9 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 26 Jan 2023. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 78 sites in United States, Germany, Israel, Netherlands, United Kingdom and 6 more countries. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

Yes. Results are posted in the registry (first posted 8 Oct 2020). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Overall Survival (time frame: Baseline until disease progression or discontinuation from the study, or death, whichever occurred first (up to a maximum of approximately 104 weeks)). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT02088541, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 26 Jan 2023.

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