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Amgen Announces Top-Line Results Of Phase 3 Talimogene Laherparepvec Trial In Melanoma
Publish date: Mar 19, 2013
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PR Newswire THOUSAND OAKS, Calif., March 19, 2013
THOUSAND OAKS, Calif., March 19, 2013 /PRNewswire/ -- Amgen
(NASDAQ:AMGN) today announced top-line results from the Phase 3 trial in melanoma, which evaluated the efficacy and safety
of talimogene laherparepvec for the treatment of unresected stage IIIB, IIIC or IV melanoma compared to treatment
with subcutaneous granulocyte-macrophage colony-stimulating factor (GM-CSF). The study met its primary endpoint of durable response rate (DRR), defined as the rate of complete or partial response
lasting continuously for at least six months. A statistically significant difference was observed in DRR: 16 percent in the
talimogene laherparepvec arm versus two percent in the GM-CSF arm. The analysis of overall survival (OS), a key secondary
endpoint of the study, is event driven. A pre-planned interim analysis conducted with the analysis of DRR has shown
an OS trend in favor of talimogene laherparepvec as compared to GM-CSF. The OS data is expected to mature in late 2013 in
line with previous guidance. "These are the first Phase 3 results of this novel approach to cancer therapy," said Sean E. Harper,
M.D., executive vice president of Research and Development at Amgen. "A high unmet need exists in melanoma and we believe
the innovative mechanism of action of talimogene laherparepvec may offer a promising approach for these patients." The most frequent adverse events observed in this trial were fatigue, chills and pyrexia. The most common serious adverse
events include disease progression, cellulitis and pyrexia. Among the various types of skin cancer, melanoma is the most aggressive and also the most serious. Although melanoma accounts
for less than five percent of skin cancer cases, or 132,000 cases globally each year, melanoma accounts for 75 percent of
all skin cancer deaths.[i] Talimogene laherparepvec is an investigational oncolytic immunotherapy designed to work in two important and complementary
ways - to cause local lytic destruction of tumors while also stimulating a systemic anti-tumor immune response. Additional safety and efficacy data will be submitted to the American Society of Clinical Oncology (ASCO) for the 2013
Annual Meeting.
Trial Design (NCT00769704) Patients were randomized 2:1 to receive either talimogene laherparepvec intralesionally every two weeks or GM-CSF subcutaneously
for the first 14 days of each 28 day cycle. Treatment could last for up to 18 months. Where appropriate, stable or responding
patients could receive additional treatment on an extension protocol.
About Talimogene Laherparepvec
About Amgen
Forward-Looking Statements No forward-looking statement can be guaranteed and actual results may differ materially from those we project. Discovery
or identification of new product candidates or development of new indications for existing products cannot be guaranteed and
movement from concept to product is uncertain; consequently, there can be no guarantee that any particular product candidate
or development of a new indication for an existing product will be successful and become a commercial product. Further,
preclinical results do not guarantee safe and effective performance of product candidates in humans. The complexity
of the human body cannot be perfectly, or sometimes, even adequately modeled by computer or cell culture systems or animal
models. The length of time that it takes for us to complete clinical trials and obtain regulatory approval for product
marketing has in the past varied and we expect similar variability in the future. We develop product candidates internally
and through licensing collaborations, partnerships and joint ventures. Product candidates that are derived from
relationships may be subject to disputes between the parties or may prove to be not as effective or as safe as we may have
believed at the time of entering into such relationship. Also, we or others could identify safety, side effects or manufacturing
problems with our products after they are on the market. Our business may be impacted by government investigations,
litigation and products liability claims. If we fail to meet the compliance obligations in the corporate integrity agreement
between us and the U.S. government, we could become subject to significant sanctions. We depend on third parties for
a significant portion of our manufacturing capacity for the supply of certain of our current and future products and limits
on supply may constrain sales of certain of our current products and product candidate development. In addition, sales of our products are affected by the reimbursement policies imposed by third-party payors, including
governments, private insurance plans and managed care providers and may be affected by regulatory, clinical and guideline
developments and domestic and international trends toward managed care and healthcare cost containment as well as U.S. legislation
affecting pharmaceutical pricing and reimbursement. Government and others' regulations and reimbursement policies may
affect the development, usage and pricing of our products. In addition, we compete with other companies with respect
to some of our marketed products as well as for the discovery and development of new products. We believe that some
of our newer products, product candidates or new indications for existing products, may face competition when and as they
are approved and marketed. Our products may compete against products that have lower prices, established reimbursement, superior
performance, are easier to administer, or that are otherwise competitive with our products. In addition, while we routinely
obtain patents for our products and technology, the protection offered by our patents and patent applications may be challenged,
invalidated or circumvented by our competitors and there can be no guarantee of our ability to obtain or maintain patent protection
for our products or product candidates. We cannot guarantee that we will be able to produce commercially successful
products or maintain the commercial success of our existing products. Our stock price may be affected by actual or perceived
market opportunity, competitive position, and success or failure of our products or product candidates. Further, the
discovery of significant problems with a product similar to one of our products that implicate an entire class of products
could have a material adverse effect on sales of the affected products and on our business and results of operations. The scientific information discussed in this news release related to our product candidates is preliminary and investigative.
Such product candidates are not approved by the U.S. Food and Drug Administration (FDA), and no conclusions can or should
be drawn regarding the safety or effectiveness of the product candidates. Only the FDA can determine whether the product
candidates are safe and effective for the use(s) being investigated. Healthcare professionals should refer to and
rely upon the FDA-approved labeling for the products, and not the information discussed in this news release. CONTACT: Amgen, Thousand Oaks
(Logo: http://photos.prnewswire.com/prnh/20081015/AMGENLOGO) [i] Skin Cancers. World Health Organization, http://www.who.int/uv/faq/skincancer/en/index1.html.
Accessed March 8, 2013. SOURCE Amgen
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