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The cornerstone of Cell>Point
is metabolic imaging and therapeutic targeting through intracellular
chelator technology. The company is developing universal oncology,
cardiology and stroke molecular imaging agents and intracellular
metallic therapeutic and radiotherapeutic agents. Cell>Point is a
privately held biotechnology company headquartered in Centennial,
Colorado with offices in Houston, Texas and Saratoga, California. The
company's five technology platforms, ethylenedicysteine drug conjugate
technology (“EC Technology”), In-Situ Hydrogel (“In Situ Hydrogel
Technology”), tetraazacyclopentadecane technology (“N4 Technology”),
oligosaccharide conjugate technology (“Dual Agent Technology”) and
mechanism-based targeted pancreatic beta cell technology (“Beta Cell
Technology”) are being developed to create new radiodiagnostic imaging
agents, new intracellular therapeutic agents, and high yield delivery
systems for the administration of local regional radio/chemotherapy.
Each of the company's technology platforms is quite unique. In
radiodiagnostic imaging, the company is developing agents for single
photon emission tomography (“SPECT”) cameras, positron emission
tomography (“PET”) cameras and dual agents for SPECT or PET cameras in
combination with either computed tomography (“CT”) cameras or magnetic
resonance imaging (“MRI”) cameras. In addition, EC Technology, N4
Technology, Dual Agent Technology and Beta Cell Technology are the
foundation for the development of new targeted radiotherapeutic agents.
In-Situ Hydrogel Technology is the foundation for the development of a
new in-situ radio/chemotherapeutic delivery system for the treatment of
inoperable or surgically nonresectable tumors.
EC Technology
Ethylenedicysteine (EC) is a unique (lipophilic)
chelator that forms exceptionally stable functional chelates and
provides significant versatility for the development of
cellular-targeted analogues. Cell>Point has initiated clinical trials of
its first 99mTc-EC analogue, 99mTc-EC-Glucosamine (99mTc-EC-G) for
radiodiagnostic imaging for tumor-specific applications in oncology. The
multicenter clinical trials will compare 99mTc-EC-G /SPECT imaging with
18FDG-PET imaging for assessing and staging patients with (non-small
cell) lung cancer and non-Hodgkin’s lymphoma.
The company is also exploring the application of
99mTc-EC-G in the assessment of myocardial ischemia, myocardial
viability and cardiotoxicity in animal models and has obtained anecdotal
indications of usefulness for myocardial assessment during Phase 1
trials. On the therapy side, EC-G is being labeled with rhenium-187
(“cold metallic”), as an intracellular metallic therapeutic agent for
NHL.
Mechanism based target assessment is crucial in cancer
therapy. EC Technology diagnostic agents can assess pharmacological
response and biochemical process thus providing staging, grading,
treatment follow-up and assistance in the selection of patients who
should be more responsive to the particular treatment being considered.
The versatility of EC Technology has been demonstrated in (i) receptor
targeting (EGF, ER, AR, HER 2, LH, somatostatin, transferrin, etc.),
(ii) transcriptional targeting (glucosamine, deoxyglucose, doxorubicin,
etc.), (iii) tissue hypoxia targeting (metronidazole), (iv) apoptosis
targeting (annexin V), (v) vascular targeting (e.g. angiostatin,
interferon alpha, colchicine, paclitaxel, etc.), (vi) gene expression
targeting (penciclovir, 5-flurocytidine) and (vii) enzymatic targeting
(cox-2, mmp-2 and mmp-9).
In Situ Hydrogel
The second technology platform, In-Situ Hydrogel, is
being developed as a site specific regional chemotherapy and
radiotherapy delivery system. By comparison with other hydrogel
technology, In-Situ Hydrogel is unique in that it is capable of
delivering a high yield dose of a therapeutic radionuclide, such as
rhenium-188 (“188Re”), directly to the tumor site without
collateral leakage into surrounding healthy tissue. In addition, In-Situ
Hydrogel is capable of simultaneously delivering a therapeutic
radionuclide and chemotoxic drug to treat solid tumors and surgically
unresectable tumors. The absence of post injection leakage should help
reduce the side-effects experienced by the patient which are most often
attributable to standard chemotherapy and external beam radiation
treatment. Pre-clinical studies have demonstrated the potential of
In-Situ Hydrogel as an effective high yield delivery system. The
hydrogel formulation traps the radionuclide and/or chemotherapeutic drug
at the tumor site immediately following administration. The radionuclide
remains trapped within the polysaccharide matrix while the
chemotherapeutic drug slowly releases.
N4 Technology
The third technology platform, N4 Technology, is a
covalent lipophilic technology that is being used to develop agents for
the treatment of Alzheimer's, depression and neuroendocrine tumors.
Cell>Point signed a collaboration agreement with Eli Lilly and Company
in November 2007 to study N4 Technology in these and other preclinical
applications.
Dual Agent Technology
The fourth technology platform, Dual Agent Technology,
is facilitating the development of dual use diagnostic agents. For
example, a single agent will combine the radiopharmaceutical for SPECT
imaging with the contrast marker for MRI without interference or
distortion between the radiopharmaceutical and contrast marker. The
company plans to develop dual agents for use with SPECT/CT, SPECT/MRI,
PET/CT and PET/MRI combination cameras. In addition, Dual Agent
Technology will be used to develop special imaging agents for optical
imaging and targeted radio/chemotherapy compounds.
Beta Cell Technology
The fifth technology platform, Beta Cell Technology,
will be used to initially develop a diagnostic imaging agent for SPECT
cameras and a therapeutic agent for the early diagnosis and treatment of
pancreatic cancer. There is a recognized need for tumor-specific
imaging, with an emphasis on the detection of small invasive and
pre-invasive lesions in both the normal and abnormal pancreas. |