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Trial of Cladribine, Cytarabine, Mitoxantrone, Filgrastim (CLAG-M) in Relapsed Acute Lymphoblastic Leukemia

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified January 2012 by New York Medical College.
Recruitment status was:  Recruiting
Information provided by (Responsible Party):
Karen Seiter, New York Medical College Identifier:
First received: January 11, 2012
Last updated: January 19, 2012
Last verified: January 2012
CLAG-M is an active, well tolerated regimen in acute myelogenous leukemia. Each of the agents is active in Acute Lymphoblastic Leukemia (ALL) as well. The current trial will determine the efficacy of the regimen in patients with relapsed ALL.

Condition Intervention Phase
Acute Lymphoblastic Leukemia
Lymphoblastic Lymphoma
Burkitts Leukemia/Lymphoma
Chronic Myelogenous Leukemia
Drug: CLAG-M
Phase 2

Study Type: Interventional
Study Design: Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: Phase II Trial of CLAG-M in Relapsed ALL

Resource links provided by NLM:

Further study details as provided by New York Medical College:

Primary Outcome Measures:
  • Complete remission percentage [ Time Frame: 1 month ]

Secondary Outcome Measures:
  • Survival [ Time Frame: 2 years ]

Estimated Enrollment: 50
Study Start Date: January 2012
Estimated Study Completion Date: January 2014
Estimated Primary Completion Date: January 2014 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: CLAG-M Drug: CLAG-M
IV times 5 days
Other Names:
  • Leustatin
  • Ara-C
  • Novantrone
Drug: CLAG-M
Other Names:
  • Cladribine (Leustatin)
  • Cytarabine (Ara-c)
  • Mitoxantrone (Novantrone)

Detailed Description:
Patients will receive standard dose CLAG-M (cladribine, cytarabine, mitoxantrone, filgrastim). Standard support care will be given. Efficacy will be assessed through bone marrow examinations and blood tests.

Ages Eligible for Study:   Child, Adult, Senior
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Relapsed or refractory acute lymphoblastic leukemia,
  • Burkitts leukemia/lymphoma,
  • Lymphoid blastic CML,
  • Lymphoblastic lymphoma.
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its identifier: NCT01513603

Contact: Karen Seiter, MD 914 493 7514
Contact: Nasir Ahmed, MD 914 493 7514

United States, New York
Westchester Medical Center/New York Medical College Recruiting
Valhalla, New York, United States, 10595
Contact: Karen Seiter, MD    914-493-7514   
Principal Investigator: Karen Seiter, MD         
Sub-Investigator: Delong Liu, MD, PhD         
Sub-Investigator: Claudio Sandoval, MD         
Sponsors and Collaborators
New York Medical College
Principal Investigator: Karen Seiter, MD New York Medical College
  More Information

Responsible Party: Karen Seiter, Professor of Medicine, New York Medical College Identifier: NCT01513603     History of Changes
Other Study ID Numbers: L-10,442
Study First Received: January 11, 2012
Last Updated: January 19, 2012

Additional relevant MeSH terms:
Precursor Cell Lymphoblastic Leukemia-Lymphoma
Leukemia, Lymphoid
Leukemia, Myeloid
Leukemia, Myelogenous, Chronic, BCR-ABL Positive
Burkitt Lymphoma
Neoplasms by Histologic Type
Lymphoproliferative Disorders
Lymphatic Diseases
Immunoproliferative Disorders
Immune System Diseases
Myeloproliferative Disorders
Bone Marrow Diseases
Hematologic Diseases
Epstein-Barr Virus Infections
Herpesviridae Infections
DNA Virus Infections
Virus Diseases
Tumor Virus Infections
Lymphoma, B-Cell
Lymphoma, Non-Hodgkin
Antimetabolites, Antineoplastic
Molecular Mechanisms of Pharmacological Action
Antineoplastic Agents processed this record on April 28, 2017