Jan 27 2010
Neoprobe Corporation (OTCBB: NEOP), a diversified developer of
innovative oncology surgical and diagnostic products, announced today
that it has completed a license amendment with The Dow Chemical Company
(NYSE: DOW) for a variety of antibodies used in its proprietary surgical
oncology system called radioimmunoguided surgery or RIGS®.
The license amendment covers antibodies that target a variety of cancers
including colon, rectal, breast, bladder, ovarian and endometrial. The
antibodies were developed in the research laboratories of the National
Institutes of Health (NIH) and Dow. In addition, Neoprobe and Dow have
agreed that Neoprobe will assume direct responsibility for the licensing
agreements. Dow will be compensated for its contributions when Neoprobe
successfully introduces commercial products.
“The completion of the agreements for the portfolio of antibodies with
both NIH and Dow clarifies the development rights for the RIGS
technology”
“The completion of the agreements for the portfolio of antibodies with
both NIH and Dow clarifies the development rights for the RIGS
technology,” said David Bupp, Neoprobe’s President and CEO. “We
commenced updated cell line development activities for the antibodies
last year and we are pleased with the results to date. Our clinical and
pharmaceutical development teams have been working on the clinical and
regulatory strategies for the program including the recently filed Phase
3 trial design which has been submitted to FDA under the special
protocol assessment provisions,” concluded Mr. Bupp.
The most clinically evaluated RIGS antibody is called RIGScan™
CR, which when combined with a hand-held gamma radiation detection
probe, provides surgeons with real-time information used to locate tumor
components not detectable by conventional methods, and assists in the
more thorough removal of the potentially cancerous tissue. The RIGScan
CR targeting agents are monoclonal antibodies labeled with a radioactive
isotope that emits low energy gamma rays. Before surgery, a cancer
patient is injected with the monoclonal antibody targeting agent, which
circulates throughout the patient’s body and binds specifically to
cancer cell components (cancer antigens). Concentrations of the
targeting agent are then located during surgery by the gamma detection
device, which emits an audible tone to direct the surgeon to
tumor-involved tissue. Information on the clinical history and current
development status of RIGScan CR can be obtained from Neoprobe’s recent
press releases and filings with the U.S. Securities and Exchange
Commission.
Source: Neoprobe Corporation