Published: June 06, 2010
Calistoga Pharmaceuticals' CAL-101, an Oral Delta Isoform-Selective PI3K Inhibitor, Demonstrates Clinical Benefit in Patients with Relapsed or Refractory Indolent Non Hodgkin's Lymphoma, Mantle Cell Lymphoma and Chronic Lymphocytic Leukemia
SEATTLE - (BUSINESS WIRE) - Calistoga Pharmaceuticals, Inc., the leader in the development of
isoform-selective phosphatidylinositol 3 kinase (PI3K) inhibitors for
the treatment of cancer and inflammatory diseases, today presented
updated clinical data on CAL-101, the Company's oral, delta selective
PI3K inhibitor, demonstrating anti-tumor activity in patients with
hematologic malignancies treated during a Phase 1 clinical trial. Data
were presented at the American Society of Clinical Oncology (ASCO)
Annual Meeting in Chicago, IL.
The results presented were from an interim assessment of 106 patients
enrolled in the ongoing Phase 1 study of CAL-101 in patients with
relapsed or refractory chronic lymphocytic leukemia, indolent and
aggressive non-Hodgkin's lymphoma, acute myeloid leukemia and multiple
myeloma. Over half of the patients enrolled in the trial were refractory
to their last therapy prior to entering the study, and the median number
of prior treatment regimens was five. Patients received continuous,
twice daily, oral dosing of CAL-101 on a 28-day cycle for up to 12
cycles.
Single agent CAL-101 treatment in patients with relapsed or refractory
indolent non-Hodgkin's lymphoma (NHL), mantle cell lymphoma (MCL), and
chronic lymphocytic leukemia (CLL) resulted in overall response rates of
57 percent, 67 percent, and 30 percent, respectively. Furthermore, 94
percent of patients with CLL had greater than 50 percent decrease in
their lymph node disease, demonstrating a high degree of biologic
activity.
The majority of responding patients remain on CAL-101 treatment. The
median duration of response is not yet achieved at this interim
assessment, although 12 patients have experienced a duration of response
of more than 6 months. Three of these patients have completed more than
12 cycles (336 days) of treatment and are continuing to receive
treatment with CAL-101 as part of an extension protocol.
Overall, CAL-101 was generally well tolerated. A low incidence of
hematological toxicity was observed. Some patients had elevation of
liver transaminases, which was monitorable and reversible following
discontinuation of dosing. Most patients who experienced an elevation in
transaminases resumed CAL-101 at a reduced dose.
"The single agent activity demonstrated by CAL-101 in heavily pretreated
patients with NHL and CLL is impressive," said Richard R. Furman, M.D.,
Weill Cornell Medical College. "This oral, small molecule targeted
therapy approach may provide a new paradigm of treatment for patients
with lymphoid malignancies."
"As we have treated more patients with CAL-101, we are pleased to see a
consistent response in indolent NHL, mantle cell lymphoma, and CLL
patients," said Albert Yu, M.D., Chief Medical Officer of Calistoga
Pharmaceuticals. "With over a 100 patients now evaluated, we are
developing a good understanding of the clinical activity and
tolerability of CAL-101."
CAL-101 is a first-in-class inhibitor of the PI3K delta isoform. It is
an orally administered small molecule, and exhibits a greater than
200-fold selectivity in cell-based assays for the delta isoform as
compared to other class 1 PI3K isoforms. CAL-101 is designed to induce
cancer cell death (apoptosis) and to inhibit the signaling pathways
associated with cancer cell dependence on the tumor microenvironment.
"CAL-101 continues to show promise as a novel, first in class, treatment
for patients with hematologic malignancies," said Carol Gallagher,
Pharm.D., Chief Executive Officer of Calistoga Pharmaceuticals. "We look
forward to initiating a registration program for CAL-101 later this
year."
In addition to CAL-101, Calistoga Pharmaceuticals has a pipeline of
isoform-selective PI3K inhibitors including CAL-263, a delta
isoform-selective PI3K inhibitor for treatment of patients with
inflammatory diseases such as asthma, chronic obstructive pulmonary
disease and rheumatoid arthritis.
About Calistoga Pharmaceuticals
Calistoga Pharmaceuticals is dedicated to developing targeted therapy to
improve the health of patients with cancer and inflammatory diseases.
Calistoga Pharmaceuticals has a portfolio of proprietary compounds
selectively targeting isoforms of the PI3K pathway. The Company's most
advanced compound, CAL-101, a selective PI3K delta inhibitor, is under
clinical evaluation in patients with B cell malignancies. Calistoga is a
private company headquartered in Seattle, Washington. For more
information, visit the Company's website at: www.calistogapharma.com.

Rathbun Communications, Inc.
Julie Rathbun, 206-769-9219
Julie@rathbuncomm.com
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