Berg Pharma presents at ASCO, poised to lead field in cancer metabolism with Phase II trials of BPM 31510
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Berg Pharma presents at ASCO, poised to lead field in cancer metabolism with Phase II trials of BPM 31510

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2 pages
English
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Berg Pharma presents at ASCO, poised to lead field in cancer metabolism with Phase II trials of BPM 31510 PR Newswire CAMBRIDGE, Massachusetts, June 12, 2012 CAMBRIDGE, Massachusetts, June 12, 2012 /PRNewswire/ -- Berg Pharma, a Boston-based pharmaceutical company presented at the 2012 American Society of Clinical Oncology meeting in Chicago on BPM 31510, the lead molecule in the Berg's cancer portfolio that targets the metabolism of cancer cells by reversing the Warburg phenotype. BPM 31510, an endogenous small molecule resident in mitochondria restores oxidative phosphorylation and confers re-capitulation of the BCL-2 protein family potential to induce cell death, a process that cancer evades. Mechanistic studies show that BPM 31510 does not adversely affect normal tissue but rather optimizes the bioenergetic balance in the tumor microenvironment to "normalize" a cancer cell into behaving much like a healthy cell. Vikas P. Sukhatme, MD PhD, Victor J. Aresty Professor of Medicine at Harvard Medical School and Chief Academic Officer at Beth Israel Deaconess Medical Center commented, "Targeting metabolic pathways that differ between cancer cells and normal cells holds considerable promise for cancer therapy and this study falls squarely in this category. It will be instructive to see if the degree of reversal of the Warburg effect by BPM 31510 correlates with clinical outcomes.

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Nombre de lectures 33
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Berg Pharma presents at ASCO, poised to lead
field in cancer metabolism with Phase II trials
of BPM 31510
PR Newswire
CAMBRIDGE, Massachusetts, June 12, 2012
CAMBRIDGE, Massachusetts
,
June 12, 2012
/PRNewswire/ -- Berg Pharma, a
Boston
-based pharmaceutical company presented at the 2012 American
Society of Clinical Oncology meeting in
Chicago
on BPM 31510, the lead
molecule in the Berg's cancer portfolio that targets the metabolism of cancer
cells by reversing the Warburg phenotype. BPM 31510, an endogenous small
molecule resident in mitochondria restores oxidative phosphorylation and
confers re-capitulation of the BCL-2 protein family potential to induce cell
death, a process that cancer evades. Mechanistic studies show that BPM 31510
does not adversely affect normal tissue but rather optimizes the bioenergetic
balance in the tumor microenvironment to "normalize" a cancer cell into
behaving much like a healthy cell.
Vikas P. Sukhatme, MD PhD,
Victor J. Aresty Professor of Medicine
at Harvard
Medical School and
Chief Academic Officer at
Beth Israel Deaconess Medical
Center commented, "Targeting metabolic pathways that differ between cancer
cells and normal cells holds considerable promise for cancer therapy and this
study falls squarely in this category. It will be instructive to see if the degree of
reversal of the Warburg effect by BPM 31510 correlates with clinical
outcomes."
Results presented at ASCO in the Phase I trial on advanced, refractory, solid
tumors revealed that BPM 31510 was well-tolerated with no serious side
effects. The Phase I is on-going as the MTD has not been reached to date
however, there has already been very encouraging signs of efficacy with 1
patient showing a near complete response in addition to a few significant
partial responses and stable disease profile in various patient cohorts. Linda
Vahdat, MD,
Professor of Medicine, Head, Solid Tumor Service, and Director of
the Breast Cancer Research Program
at Weill Cornell Medical School said, "It is
terrific to see the implementation of targeting metabolism in treating cancer
finally underway. I am cautiously optimistic, based on the preliminary safety
and efficacy results of BPM 31510 in the phase I in solid tumors, that we will be
able to quickly move this agent into phase II trials in selected cancers."
Berg plans to move into Phase II trials in late 2012 with specific focus on
cancers that demonstrate an aggressive/highly metabolic phenotype such as
pancreatic, triple-negative breast, and colorectal cancers. Pre-clinical models
presented at the 2012 AACR meeting showed that BPM 31510 has a synergistic
effect with various chemotherapy regimens in aggressive cancers. Niven R.
Narain,
Co-Founder, President & CTO
of Berg Pharma said, "We are excited
about moving this agent into Phase II trials with an astute combination strategy
based on pre-clinical scientific guidance. BPM 31510 is showing promising
activity in early trials as a monotherapy and we are eager to assess activity in
combination with standard of care."
The company also has other clinical programs with a topical form of BPM 31510
for skin cancer and BPM 31543 for supportive care in cancer that prevents hair
loss during chemotherapy. Berg's robust pipeline is fueled by the
Interrogative
Biology
®
platform which has developed therapeutics targets in cancer,
endocrinology, and CNS diseases with a focus on mitochondrial metabolism.
About Berg Pharma
Berg Pharma is a
Boston
based pharmaceutical company and parent company
to Berg Biosystems and Berg Diagnostics. Our research focus seeks to
understand how alterations in metabolism relate to disease onset. We have
uncovered key insight into metabolic control factors and namely into underlying
elements in the Warburg Hypothesis. The company has a deep pipeline of
early-stage technologies in CNS diseases and metabolic diseases that
complement its late-stage clinical trial activity in cancer and prevention of
chemotoxicity. Armed with use of the discovery platform that translates
biological output into viable therapeutics and a robust biomarker library,
Berg
Pharma is poised to realize its pursuit of a healthier tomorrow.
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