A Phase 1/2, First in Human, Dose Escalation Study of MGD006, a CD123 x CD3 DART® Bi-Specific Antibody Based Molecule, in Patients With Relapsed or Refractory AML or Intermediate-2/High Risk Myelodysplastic Syndrome (MDS)

Who is this study for? Patients with relapsed or refractory AML or intermediate-2/high risk myelodysplastic syndrome
What treatments are being studied? Flotetuzumab
Status: Terminated
Location: See all (43) locations...
Intervention Type: Biological, Drug
Study Type: Interventional
Study Phase: Phase 1/Phase 2
SUMMARY

Open-label, multi-dose, single-arm, multi-center, Phase 1/2 study conducted in three segments: the Single Patient Dose Escalation Segment (complete), followed by the Multi-Patient Dose Escalation Segment (complete) and the Maximum Tolerated Dose and Schedule (MTDS) Expansion Cohort Segment (closed). Having characterized safety and determined the maximum tolerated dose and schedule, the primary objective of this study now is to assess the anti-neoplastic activity of flotetuzumab in patients with PIF/ER AML, as determined by the proportion of patients who achieve CR or CRh. Starting with Cycle 2, patients who are benefiting from flotetuzumab may receive up to a maximum of 8 cycles of treatment. Patients will receive daily increasing doses of flotetuzumab for the first week of Cycle 1 (Lead-In Dosing) followed by 3 weeks of continuous intravenous infusion at a the assigned dose. Subsequent cycles are each 4 weeks of continuous infusion at the assigned dose. Dosing may continue for up to 8 cycles. Follow up visits may continue for 6 months after treatment is discontinued.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Confirmed diagnosis of primary or secondary AML \[any subtype except acute promyelocytic leukemia (APL)\] according to World Health Organization (WHO) classification

• Patients with AML must meet one of the following criteria, a or b:

‣ Primary Induction Failure (PIF) AML, defined as disease refractory to either, i or ii:

• i. An intensive induction attempt, per institution. Induction attempts include high-dose and/or standard-dose cytarabine ± an anthracyclines/anthracenedione ± an anti-metabolite, with or without growth factor or targeted therapy containing regimens. Examples include but are not limited to: 1 cycle of high dose cytarabine (HiDAC) containing regimen, 1 cycle of liposomal cytarabine and daunorubicin, 2 cycles of standard dose cytarabine containing regimen

∙ ii. For adults who are age 75 years or older, or who have comorbidities that preclude use of intensive induction chemotherapy; PIF is defined as AML refractory to one of the following less intensive regimens: i ≥ 2 but ≤ 4 cycles of Bcl-2 inhibitors in combination with azacitidine, decitabine, or low dose cytarabine, or ii ≥ 2 but ≤ 4 cycles of gemtuzumab ozogamicin monotherapy

⁃ Early relapse (ER) AML, defined as AML in first relapse with initial CR1 duration \< 6 months

• Limit of 3 prior lines of therapy (excluding focal radiation therapy for palliative purposes): up to 2 induction (induction, re-induction) or 1 induction plus/minus 1 consolidation attempt, followed by a maximum of 1 salvage/re-induction attempt.

• Eastern Cooperative Oncology Group (ECOG) performance status ≤2

• Life expectancy of at least 4 weeks

• Peripheral blast count \</= 20,000/mm3 at the time of first dose

• Acceptable laboratory parameters and adequate organ reserve

Locations
United States
California
City of Hope National Medical Center
Duarte
UCSD Moores Cancer Center
La Jolla
UCSF - Helen Diller Family Comprehensive Cancer Center
San Francisco
University of California, San Francisco
San Francisco
Washington, D.c.
Georgetown University - Lombardi Cancer Center
Washington
Florida
Moffitt Cancer Center
Tampa
Georgia
Emory University
Atlanta
Illinois
Loyola University Chicago - Cardinal Bernadin Cancer Center
Maywood
Maryland
University of Maryland
Baltimore
Michigan
University of Michigan
Ann Arbor
Missouri
Washington University School of Medicine
Saint Louis
North Carolina
University of North Carolina Lineberger Comprehensive Cancer Center
Chapel Hill
Duke University Medical Center
Durham
New York
Stony Brook Medicine
Stony Brook
Ohio
Cleveland Clinic
Cleveland
Oregon
Providence Portland Medical Center
Portland
Tennessee
Vanderbilt-Ingram Cancer Center
Nashville
Texas
The University of Texas MD Anderson Cancer Center
Houston
Washington
Fred Hutchinson Cancer Research Center
Seattle
Wisconsin
Medical College of Wisconsin
Milwaukee
Other Locations
France
Institut Paoli-Calmettes
Marseille
Centre Hospitalier Universitaire de Nantes
Nantes
Institut Universitaire du Cancer de Toulouse-Oncopole
Toulouse
CHRU de Tours - Hôpital Bretonneau
Tours
Germany
Charité - Universitätsmedizin Berlin
Berlin
Universitätsklinikum Carl Gustav Carus an der Technischen Universität Dresden
Dresden
Universitätsklinik Hamburg-Eppendorf
Hamburg
Universitätsklinikum Leipzig
Leipzig
Universitätsmedizin der Johannes Gutenberg-Universität Mainz
Mainz
III. Med. Klinik-Klinikum rechts der Isar-Technische Universität München
Munich
Medizinische Klinik und II, Universitätsklinikum Würzburg
Würzbur
Israel
Rambam Health Care Campus
Haifa
Shaare Zedek Medical Center
Jerusalem
Italy
Policlinico Sant'Orsola Malpighi
Bologna
Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori (IRST)
Meldola
University Vita-Salute San Raffaele
Milano
Unità Operativa di Ematologia Ospedale Santa Maria delle Croci
Ravenna
Netherlands
University Medical Center Groningen
Groningen
Erasmus University Medical Center
Rotterdam
Spain
Universitat Autonomaa de Barcelona (UAB) - Hospital de la Santa Creu i de Sant Pau
Barcelona
Hospital Universitario 12 de Octubre
Madrid
United Kingdom
King's Health Partners
London
The Christie NHS Foundation Trust
Manchester
Time Frame
Start Date: 2014-06-09
Completion Date: 2022-07-05
Participants
Target number of participants: 244
Treatments
Experimental: Cohort 0-a
Experimental: Cohort 0-b
Experimental: Cohort 0-c
Experimental: Cohort 0-d
Experimental: Cohort 1
Experimental: Cohort 2
Experimental: Cohort 2a
Experimental: Cohort 3
Experimental: Cohort 6
Experimental: Cohort 7
Experimental: Cohort 8
Experimental: MTD Expansion
Experimental: MTD expansion with Ruxolitinib
Related Therapeutic Areas
Sponsors
Leads: MacroGenics

This content was sourced from clinicaltrials.gov

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