Acute Myeloid Leukemia Clinical Trial

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

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). 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.

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Full 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.

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Eligibility Criteria

Inclusion Criteria:

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.

Exclusion Criteria:

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).
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.

Study is for people with:

Acute Myeloid Leukemia

Phase:

Phase 2

Estimated Enrollment:

317

Study ID:

NCT02088541

Recruitment Status:

Completed

Sponsor:

Karyopharm Therapeutics Inc

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There are 41 Locations for this study

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Jonsson Comprehensive Cancer Center / University of California, Los Angeles
Los Angeles California, 90024, United States
Sutter Oncology & Hematology
Sacramento California, 95816, United States
Stanford Cancer Institute / Stanford University
Stanford California, 94304, United States
Colorado Blood Cancer Institute/Sarah Cannon Research Institute
Denver Colorado, 80218, United States
Yale Cancer Center / Yale University
New Haven Connecticut, 06510, United States
H. Lee Moffitt Cancer Center and Research Institute
Tampa Florida, 33612, United States
Winship Cancer Institute / Emory University
Atlanta Georgia, 30322, United States
Northwestern University
Chicago Illinois, 60611, United States
University of Chicago Medicine
Chicago Illinois, 60637, United States
University of Kansas Hospital
Kansas City Kansas, 66160, United States
Sidney Kimmel Comprehensive Cancer Center / John Hopkins University
Baltimore Maryland, 21287, United States
University of Massachusetts Medical School
Worcester Massachusetts, 01655, United States
University of Michigan Comprehensive Cancer Center
Ann Arbor Michigan, 48109, United States
Hackensack University Medical Center
Hackensack New Jersey, 07601, United States
Roswell Park Cancer Institute
Buffalo New York, 14263, United States
Westchester Medical Center / New York Medical College
Hawthorne New York, 10532, United States
Memorial Sloan Kettering Cancer Center
New York New York, 10065, United States
New York Presbyterian Hospital / Weill Cornell Medical College
New York New York, 10065, United States
Duke Cancer Care
Durham North Carolina, 27705, United States
Gabrail Cancer Center
Canton Ohio, 44718, United States
Ohio State University Comprehensive Cancer Center
Columbus Ohio, 43210, United States
Milton S. Hershey Medical Center / Penn State
Hershey Pennsylvania, 17033, United States
Tennessee Oncology/Sarah Cannon Research Institute
Nashville Tennessee, 37203, United States
Vanderbilt-Ingram Cancer Center / Vanderbilt University
Nashville Tennessee, 37215, United States
MD Anderson Cancer Center / University of Texas
Houston Texas, 77030, United States
Texas Transplant Institute/Sarah Cannon Research Institute
San Antonio Texas, 78229, United States
Tom Baker Cancer Centre
Calgary Alberta, T2N 4, Canada
University of Alberta
Edmonton Alberta, T6G 2, Canada
Sir Mortimer B. Davis Jewish General Hospital / McGill University
Montreal Quebec, H2W1S, Canada
Aarhus University Hospital
Aarhus , , Denmark
Department of Haematology, National University Hospital, Rigshospitalet
Copenhagen , , Denmark
Herlev Hospital
Herlev , , Denmark
Odense University Hospital, Department of Hematology
Odense , , Denmark
CHU Bordeaux- Hôpital Haut Lévêque
Bordeaux , , France
Centre Hospitalier Lyon
Lyon , , France
Hopital Saint Louis
Paris , , France
Hôpital Avicenne
Paris , , France
Institut Universitaire du Cancer Toulouse
Toulouse , , France
Stellvertretende Klinikleiterin Charité, Campus Benjamin Franklin
Berlin , 12203, Germany
Ev. Diakonie-Krankenhaus Gemeinnutzige GMBH Medizinische Klinik 2
Bremen , , Germany
UNIVERSITÄTSKLINIKUM TU DRESDEN Medizinische Klinik und Poliklinik I,
Dresden , , Germany
University Hospital Frankfurt
Frankfurt , , Germany
Medizinische Hochschule Hannover (Hannover Medical School) Dept. of Hematology, Hemostasis, Oncology, and Stem Cell Transplantation
Hanover , , Germany
Abteilung Hämatologie, internistische Onkologie und Hämostaseologie
Leipzig , , Germany
UNIVERSITY HOSPITAL OF MÜNSTER Medizinische Klinik und Poliklinik A, Universitätsklinikum Münster
Münster , , Germany
Universitätsklinikum Ulm
ULM , , Germany
Sororka MC
Beer Sheva , 85025, Israel
Rambam Health Care Campus
Haifa , 31096, Israel
Wolfson Medical Center
Holon , , Israel
Hadassah Medical Center
Jerusalem , 91120, Israel
Rabin Medical Center
Petach Tikva , 49414, Israel
Tel Aviv Sourasky Medical Centre
Tel Aviv , , Israel
Chaim Sheba Medical Center
Tel Hashomer , 52621, Israel
AOU Ospedali Riuniti di Ancona
Ancona , , Italy
A.O Spedali Civili di Brescia
Brescia , , Italy
AORN Cardarelli / UOSC di Ematologia con TMO
Naples , , Italy
AMC, Academisch Medisch Centrum Afdeling Klinische Hematologie
Amsterdam , , Netherlands
VU University Medical Center
Amsterdam , , Netherlands
Universitair Medisch Centrum Groningen Department of Haematology
Groningen , , Netherlands
Radboud University Medical Center Department of Haematology (476)
Nijmegen , , Netherlands
Erasmus MC, location Daniel den Hoed
Rotterdam , , Netherlands
University Medical Center Utrecht
Utrecht , , Netherlands
Isala Kliniecken Zwolle
Zwolle , , Netherlands
Wojewódzki Szpital Specjalistyczny im. M. Kopernika, Klinika Hematologii
Lodz , , Poland
Samodzielny Publiczny Zakład Opieki Zdrowotnej Ministerstwa Spraw Wewnętrznych
Olsztyn , , Poland
Instytut Hematologii i Transfuzjologii
Warszawa , , Poland
Samodzielny Publiczny Szpital Kliniczny Nr 1 we Wrocławiu
Wroclaw , , Poland
ICO Badalona
Badalona , 08916, Spain
Hospital del Mar
Barcelona , , Spain
Hospital Universitario de Salamanca Servicio de Hematologia
Salamanca , , Spain
Hospital Universitario y Politécnico La Fe
Valencia , , Spain
Northwick Park Hospital
Harrow England, HA1 3, United Kingdom
Royal Liverpool University Hospital, Dept of Cellular and Molecular Physiology, Molecular and Clinical Cancer Medicine
Liverpool Lancashire, L7 8X, United Kingdom
Royal Marsden NHS Trust
Sutton Surrey, SM2 5, United Kingdom
University Hospital Wales
Cardiff Wales, CF14 , United Kingdom
Hull and East Yorkshire Hospitals NHS Trust Queens Centre for Oncology and Haematology
Hull Yorkshire, HU3 2, United Kingdom
Ninewells Hospital and Medical School NHS Tayside
Dundee , DD1 9, United Kingdom
Plymouth Hospitals NHS Trust/Derriford Hospital
Plymouth , , United Kingdom

How clear is this clinincal trial information?

Study is for people with:

Acute Myeloid Leukemia

Phase:

Phase 2

Estimated Enrollment:

317

Study ID:

NCT02088541

Recruitment Status:

Completed

Sponsor:


Karyopharm Therapeutics Inc

How clear is this clinincal trial information?

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