A Study of Anagrelide Controlled Release (GALE-401) in Patients With High Platelet Counts Due to Bone Marrow Disorders

Completed · Phase 2

Conditions studied: Thrombocytosis, Myeloproliferative Neoplasms

In brief

Anagrelide is a drug that has been shown to slow down how fast platelets are made in the bone marrow, and has been approved by the FDA for treating high platelets counts in patients with bone marrow disorders. Anagrelide Controlled Release ("CR") is a new preparation of anagrelide that is made to dissolve more slowly than currently marketed versions of this drug. Because of this, the anagrelide is taken up into the blood more slowly. Researchers think that this slower release of the drug could help to lower side effects that might be caused by high blood levels when the drug dissolves as quickly as it does with the currently marketed product. The main purposes of this study are to see how well Anagrelide CR can control platelet counts in patients with high platelet levels, to see what kind of side effects it causes, and to measure blood levels of the drug.

Key facts

Study ID: NCT02125318
Run by: Galena Biopharma, Inc.
People needed: 18
Starts: 2014-05-01
Expected to finish: 2016-05-01
Last updated by the study team: 2017-02-27

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

Provide written informed consent prior to any study specific procedure
Male or female patients aged ≥ 18 years
Diagnosis of a myeloproliferative neoplasm (i.e., chronic myelogenous leukemia (CML), polycythemia vera (PV), primary myelofibrosis (PMF), essential thrombocythemia (ET)) as determined by the treating physician, such as based on the 2008 World Health Organization (WHO) classification of myeloid malignancies
Baseline platelet count ≥600 x 10e9/L as determined on two occasions at least 14 days apart prior to the first dose of study drug
Requirement for platelet reduction therapy as assessed by the Investigator
Currently not receiving therapy specifically intended to reduce platelet counts
For patients with ET, prior platelet lowering therapy (e.g., hydroxyurea, anagrelide or interferon) may not be administered within 2 weeks prior to the first dose of study drug.
For patients with MPN diagnoses other than ET, concurrent anti-MPN treatment is permitted provided that the treatment has been administered at stable doses for at least 4 weeks prior to the first dose of study drug. Examples of permitted medications include but are not limited to hydroxyurea for PV, ruxolitinib for MF, and imatinib for CML. All patients must have discontinued anagrelide at least 2 weeks prior to the first dose of study drug.
EXCEPTION: busulfan, melphalan and phosphate P-32 must have been discontinued at least 4 weeks prior to the first dose of study drug.
Adequate hepatic function defined as bilirubin ≤1.5 x ULN, INR ≤1.5 x ULN, albumin >3.5 g/dL, ALT < 3.0 x ULN, AST < 3.0 x ULN
If female, must be of non-childbearing potential, i.e. post- menopausal (defined as > 12 months since last menstrual period) or surgically sterilized (i.e. tubal ligation or hysterectomy at least 6 months prior to screening) or, if of childbearing potential, must not be pregnant or nursing
Males and females of child bearing must agree to use an acceptable form of birth control until 28 days following the last dose of study drug

You may not qualify if…

Other MPN diagnoses not specifically included above: Chronic neutrophilic leukemia, chronic eosinophilic leukemia, mastocytosis, and unclassifiable MPNs
Previously found to be refractory to anagrelide therapy (i.e., failure to achieve a platelet count <600 x 10e9/L for reasons other than anagrelide-related toxicity)
History of coronary artery disease requiring a revascularization procedure within 3 months prior to screening
Left bundle branch block or sustained ventricular tachycardia (>30 seconds) evident on 12-lead ECG at screening
Tachycardia defined as resting heart rate >100 bpm at screening
Unstable angina (characterized by increasingly frequent episodes with modest exertion or at rest, worsening severity, or prolonged duration) within 3 months prior to screening
Transient ischemic attack (TIA) or stroke within 3 months prior to screening
Unstable or clinically significant concurrent medical condition that would, in the opinion of the Investigator, jeopardize the safety of a subject and/or their compliance with the protocol.
Current alcohol or drug abuse, or a significant medical condition that, in the opinion of the Investigator, may impair compliance with the requirements of the protocol
History of allergic hypersensitivity to anagrelide or any component of its formulations
Administration of Type 3 phosphodiesterase (PDE3) inhibitors (e.g., inamrinone, cilostazol, milrinone) within 2 weeks prior to initiating study treatment
Administration of any investigational product within 4 weeks prior to initiating study treatment
History of intolerance of other PDE3 inhibitors

Where it is running

East Valley Hematology and Oncology Medical Group — Burbank, California, United States
California Cancer Associates for Research & Excellence (cCARE) — Encinitas, California, United States
California Cancer Associates for Research & Excellence (cCARE) — Escondido, California, United States
California Cancer Associates For Research and Excellence — Fresno, California, United States
Innovative Medical Research of South Florida, Inc. — Aventura, Florida, United States
Cancer Center of Kansas — Wichita, Kansas, United States
Wake Forest Baptist Health — Winston-Salem, North Carolina, United States
Gettysburg Cancer Center — Hillsdale, Pennsylvania, United States
The University of Texas MD Anderson Cancer Center — Houston, Texas, United States
Cancer Care Centers of South Texas — New Braunfels, Texas, United States
Cancer Care Centers of South Texas — San Antonio, Texas, United States

Full record on ClinicalTrials.gov

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