Immunomedics Reports Multiple Objective Responses in Solid Cancers With
-- Partial Responses in Colorectal, Triple-Negative Breast, and
Small-Cell-Lung Cancers --
-- Clinical Trial Expanding to Phase II Focusing on Select Tumor Types --
BOSTON, Oct. 22, 2013 (GLOBE NEWSWIRE) -- Immunomedics, Inc. (Nasdaq:IMMU), a
biopharmaceutical company primarily focused on the development of monoclonal
antibody-based products for the targeted treatment of cancer, autoimmune and
other serious diseases, today announced that its newest antibody-drug
conjugate (ADC), IMMU-132, has produced durable partial responses in three
different cancer types in early phase of clinical evaluation.
Results from the multicenter, dose-escalation Phase I trial were presented by
Dr. Alexander N. Starodub of the Indiana University Health Goshen Center for
Cancer Care, Goshen, IN, at the AACR-NCI-EORTC International Conference on
Molecular Targets and Cancer Therapeutics in Boston, Massachusetts.
In addition to the 3 partial responses observed by computed tomography (CT)
using RECIST criteria, 15 patients also reported stable disease as their best
response for an overall disease control rate of 86% in 21 patients with at
least 1 CT assessment reported at the Conference. In terms of CT-confirmed
tumor shrinkage, about half of the patients showed this result.
"We, as well as our clinical investigators, are very encouraged by these early
promising results with IMMU-132 in this refractory, advanced cancer patient
population with difficult-to-treat tumors that failed multiple prior
therapies," commented Cynthia L. Sullivan, President and Chief Executive
Officer of Immunomedics. "This is the first time these results have been
presented at a scientific meeting after peer-review of the submitted abstract.
The study has now transitioned to Phase II for additional safety and efficacy
data in patients with certain tumor types using doses that were found active
and tolerable in Phase I," Ms. Sullivan added.
At the time of reporting, a total of 25 patients with 12 different types of
epithelial cancers have been enrolled into the Phase I trial. These patients
had failed a median of 3 (range 1-6) prior standard therapies for their tumor
types and were enrolled with disease progression. IMMU-132 was administered
weekly for 2 consecutive weeks, followed by one week off, in 3-week cycles.
Treatments may continue for up to 8 cycles until unacceptable toxicity or
progression of disease. Currently, 10 patients are continuing treatments.
The major side-effects of IMMU-132 are neutropenia and controllable diarrhea,
consistent with the toxicity experienced with irinotecan, the parent drug of
SN-38, despite this agent releasing about 20-fold more SN-38 than when
irinotecan is given.
This study was supported in part by Award Number R43CA171388 from the National
Cancer Institute. The content is solely the responsibility of the Company and
does not necessarily represent the official views of the National Cancer
Institute or the National Institutes of Health.
IMMU-132 is composed of hRS7, a humanized antibody that binds to the
trophoblast cell-surface antigen (TROP-2), also know as the epithelial
glycoprotein-1 antigen (EGP-1). TROP-2 is expressed by many human tumors, such
as cancers of the breast, cervix, colon and rectum, kidney, liver, lung,
ovary, pancreas, and prostate, but with only limited expression in normal
human tissues. hRS7 internalizes into cancer cells following binding to
TROP-2, making it a suitable candidate for the delivery of cytotoxic drugs.
SN-38 is the active metabolite of irinotecan, which is a standard therapy for
patients with metastatic colorectal cancer, but has major gastrointestinal and
hematologic toxicity. By attaching SN-38 to tumor-targeting antibodies,
delivery of SN-38 to the tumor may be increased several-fold while mitigating
systemic toxicity. Preclinical studies have shown that the antibody-drug
linkage was susceptible to cleavage in serum, with 50% of SN-38 released in
~1.0 day, leading to a locally enhanced concentration within the tumor site.
In various animal models of human cancers, IMMU-132 significantly improved
survival and tumor regression.
Immunomedics is a New Jersey-based biopharmaceutical company primarily focused
on the development of monoclonal antibody-based products for the targeted
treatment of cancer, autoimmune and other serious diseases.We have developed
a number of advanced proprietary technologies that allow us to create
humanized antibodies that can be used either alone in unlabeled or "naked"
form, or conjugated with radioactive isotopes, chemotherapeutics, cytokines or
toxins, in each case to create highly targeted agents.Using these
technologies, we have built a pipeline of therapeutic product candidates that
utilize several different mechanisms of action.Our lead product candidate,
epratuzumab, is currently in two Phase III clinical trials in lupus. In
oncology, we are planning to launch a Phase III pivotal trial for clivatuzumab
labeled with a radioisotope in advanced pancreatic cancer patients. Other
solid tumor therapeutics in Phase II clinical development include 2
antibody-drug conjugates, labetuzumab-SN-38 (IMMU-130) and hRS7-SN-38
(IMMU-132).We also have a majority ownership in IBC Pharmaceuticals, Inc.,
which is developing a novel DOCK-AND-LOCK™ (DNL™) method with us for making
fusion proteins and multifunctional antibodies. DNL™ is being used
particularly to make bispecific antibodies targeting cancers and infectious
diseases as a T-cell redirecting immunotherapy, as well as bispecific
antibodies for next-generation cancer and autoimmune disease therapies. We
believe that our portfolio of intellectual property, which includes
approximately 231 active patents in the United States and more than 400
foreign patents, protects our product candidates and technologies.Our
strength in intellectual property has resulted in the top-10 ranking in the
2012 IEEE Spectrum Patent Power Scorecards in the Biotechnology and
Pharmaceuticals category.For additional information on us, please visit our
website at www.immunomedics.com. The information on our website does not,
however, form a part of this press release.
This release, in addition to historical information, may contain
forward-looking statements made pursuant to the Private Securities Litigation
Reform Act of 1995. Such statements, including statements regarding clinical
trials, out-licensing arrangements (including the timing and amount of
contingent payments), forecasts of future operating results, potential
collaborations, and capital raising activities, involve significant risks and
uncertainties and actual results could differ materially from those expressed
or implied herein. Factors that could cause such differences include, but are
not limited to, risks associated with any cash payment that the Company might
receive in connection with a sublicense involving a third party and UCB, which
is not within the Company's control, new product development (including
clinical trials outcome and regulatory requirements/actions), our dependence
on UCB for the further development of epratuzumab for non-cancer indications,
competitive risks to marketed products and availability of required financing
and other sources of funds on acceptable terms, if at all, as well as the
risks discussed in the Company's filings with the Securities and Exchange
Commission.The Company is not under any obligation, and the Company expressly
disclaims any obligation, to update or alter any forward-looking statements,
whether as a result of new information, future events or otherwise.
CONTACT: For More Information:
Dr. Chau Cheng
Senior Director, Investor Relations & Grant Management
(973) 605-8200, extension 123
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