Study of ACY-1215 Alone and in Combination With Bortezomib and Dexamethasone in Multiple Myeloma



Status:Completed
Conditions:Blood Cancer, Hematology
Therapuetic Areas:Hematology, Oncology
Healthy:No
Age Range:18 - Any
Updated:4/7/2017
Start Date:July 2011
End Date:December 3, 2016

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A Phase 1/2, Open-Label, Multicenter Study of ACY-1215 Administered Orally as Monotherapy and in Combination With Bortezomib and Dexamethasone for the Treatment of Relapsed or Relapsed/Refractory Multiple Myeloma

Phase 1(a & b): To evaluate the side effects and determine the best dose of oral ACY-1215 as
monotherapy, and also in combination with bortezomib and dexamethasone in patients with
relapsed or relapsed/refractory multiple myeloma.

Phase 2a: To determine the objective response rate of oral ACY-1215 in combination with
bortezomib and dexamethasone in patients with relapsed or relapsed/refractory multiple
myeloma.


Inclusion Criteria:

- Patient has relapsed or relapsed/refractory MM with measurable disease parameters
according to the International Myeloma Working Group (IMWG) Criteria

- Refractory is defined as experiencing less than minimal response (MR) to or
progressive disease (PD) within 60 days after completion of the most recent
anti-MM regimen

- Relapsed is defined as experiencing PD that requires therapy but which is not
refractory following the achievement of stable disease (SD) or better to the
most recent anti-MM regimen.

- Patient received at least 2 prior regimens for MM.

- Patient received prior treatment for MM with a proteasome inhibitor and an
immunomodulatory drug, unless not a candidate for a proteasome inhibitor or an
immunomodulatory drug.

- Patient either is not a candidate for autologous stem cell transplant (ASCT), has
declined the option of ASCT, or has relapsed after prior ASCT.

- Patient is ≥18 years of age.

- Patient has a Karnofsky Performance Status score of ≥70

- Patient has adequate bone marrow reserve, as evidenced by:

- Absolute neutrophil count (ANC) of ≥1.0x109/L.

- Platelet count of ≥ 75x109/L in patients in whom <50% of bone marrow nucleated
cells are plasma cells and ≥50x109/L in patients in whom more than 50% of bone
marrow nucleated cells are plasma cells.

- Patient has adequate renal function (calculated creatinine clearance of ≥30 mL/min
according to the Cockroft-Gault)

- Patient has adequate hepatic function (serum bilirubin values <2.0 mg/dL and ALT
and/or AST values <3 × the upper limit of normal ULN).

- Patient has a corrected serum calcium ≤ULN.

Exclusion Criteria

- Patient has received any of the following therapies:

- Radiotherapy or systemic therapy within 2 weeks of baseline

- Prior peripheral autologous stem cell transplant within 12 wks of Baseline.

- Prior allogeneic stem cell transplant.

- Prior treatment with an HDAC inhibitor.

- Patient has an active systemic infection requiring treatment.

- Patient has a history of other malignancies unless has undergone definitive treatment
more than 5 yrs prior to study and without evidence of recurrent malignant disease
(excluding basal cell carcinoma of the skin; superficial carcinoma of the bladder;
carcinoma of the prostate with a current prostate-specific antigen <0.1 ng/mL; or
cervical intraepithelial neoplasia).

- Patient has known or suspected HIV, positive for hepatitis B or is known or suspected
to have active hepatitis C infection.

- Patient has a history of significant cardiovascular, neurological, endocrine,
gastrointestinal, respiratory, or inflammatory illness including recent myocardial
infarction (within 6 months)or stroke; hypertension requiring >2 medications for
adequate control; diabetes mellitus with >2 episodes of ketoacidosis in the preceding
12 months; or chronic obstructive pulmonary disease (COPD) requiring >2
hospitalizations in the preceding 12 months.

- Patient has a QTcF value of >480 msec; family or personal history of long QTc
syndrome or ventricular arrhythmias including ventricular bigeminy; previous history
of drug-induced QTc prolongation

- Patient has > Grade 2 painful neuropathy or peripheral neuropathy

- Patient has a history of allergic reaction attributable to bortezomib or other
compounds containing boron or mannitol (Phase 1b and 2a only)
We found this trial at
6
sites
185 Cambridge Street
Boston, Massachusetts 02114
617-724-5200
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1365 Clifton Rd NE
Atlanta, Georgia 30322
(404) 778-1900
Winship Cancer Institute at Emory University Winship Cancer Institute of Emory University is Georgia
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Houston, Texas 77030
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Milwaukee, WI
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New York, New York 10029
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3451 Walnut St
Philadelphia, Pennsylvania 19104
1 (215) 898-5000
Univ of Pennsylvania Penn has a long and proud tradition of intellectual rigor and pursuit...
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Philadelphia, PA
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