Posts Tagged: "breast cancer"

The Unpredictable Prospects of Patenting Cancer Innovation

Art Unit 1618 and 1621 are both identified as relating to “organic compounds – part of the class 532-570 series.” However, the patenting probability for cancer related applications is markedly different between these two art units. 70.5% of the cancer patent applications assigned to Art Unit 1621 were patented, while only 42.3% assigned to Art Unit 1618 were patented. Indeed, nearly one-quarter of all cancer applications are assigned to art units with low allowance rates, while 16% were assigned to art units with much higher allowance rates… The cancer-application allowance rates range from 20.5% to 100.0% in various art units (with the general allowance rate of these art units ranging from 25.7% to 97.8%). Thus, the probability of securing patent protection on a cancer-related innovation exhibits marked variability and appears to be highly dependent on art-unit assignment.

Patent-Ineligibility of Medical Diagnostics, Life Sciences Discoveries Arrests U.S. Progress

In a research project funded by the Austrian Science Fund (FWF), evidence emerged that a higher expression of the GIRK1 protein in malignant tissue samples was linked to higher relapse and mortality rates in breast cancer patients who have gone through surgery. The novel use of the GIRK1 protein as a biomarker could have a great impact on breast cancer diagnostics and treatments and further research could yield more discovery on the interdependence of GIRK1 with other important biological pathways critical to cancer management… Unfortunately, discovery of GIRK1 as a biomarker for breast cancer diagnostics would run into 35 U.S.C. § 101, the basic threshold statute for determining patentability of subject matter, under the Supreme Court’s March 2012 ruling in Mayo Collaborative Services v. Prometheus Laboratories, Inc. In that case, the Court held that processes involving correlations between blood test results and patient health is not patent-eligible subject matter because the process incorporates laws of nature. This would seemingly render any processes involving the application of GIRK1 as a biomarker for breast cancer prognoses unpatentable as well as the expression of GIRK1 occurs naturally.

Blue Ribbon Panel of Advisors Announced for Biden Cancer Moonshot Initiative

Earlier this week the National Cancer Institute (NCI), which is part of the National Institutes of Health, announced a Blue Ribbon Panel of scientific experts, cancer leaders, and patient advocates that will work to inform the scientific direction and goals for Vice President Joe Biden’s National Cancer Moonshot Initiative. “Thanks to advances in science, we are now in a historically unique position to make profound improvements in the way we treat, detect, and prevent cancer,” said NIH Director Francis S. Collins, M.D., Ph.D. He is correct, and here is why.

Bolder initiatives needed to take next steps in fight against cancer

February 4 is World Cancer Day… There has been steady progress made in the history of treating cancers of many types since the administration of former U.S President Richard Nixon, according to Dr. Boris Pasche, the Director of the Wake Forest Baptist Medical Center’s Comprehensive Cancer Center. “In my opinion, government should embark on bold new initiatives in cancer treatment,” Pasche said. He did note that, while what President Obama says as a statesman doesn’t change the humbling reality that many cancers have so far stumped medical scientists. Nevertheless, increased investments into cancer research have dramatically impacted survival rates. Over the past decade, most cancers show a better outcome than they did ten years ago. “Bolder initiatives with disruptive approaches to cancer are in order if we want to make leaps forward more quickly,” Pasche said.

Federal funding for a cancer moonshot is not a terrible idea

To hear Ars Technica say it is ”a terrible idea” to devote increased funding in order to eradicate cancer is astonishing on many levels. As part of the reason why he believes increased funding for cancer research is a terrible idea he explains that great strides have been made with respect to treatments and cures, which is true. Of course, it is also true that people are dying and they are dying horrible deaths. With the victories and advances that have been made over the last generation it is no longer fanciful to dream of a day when cancer can become eradicated. So why is it a terrible idea to devote more resources on a so-called cancer moonshot to attempt to once and for all put an end to this scourge? For anyone to call President Obama’s cancer moonshot a terrible idea is nothing short of cruel, and is frankly incredibly stupid.

General Electric beats recent earnings estimates, focuses on healthcare and energy R&D

Medical and healthcare technologies were again prevalent when taking a survey of GE patent applications recently published by the USPTO. Techniques for determining a better course of treatment when dealing with cancer are described within U.S. Patent Application No. 20150198599, filed under the title TLE3 as a Marker for Chemotherapy. The patent application would protect a method of identifying a breast cancer that will not respond favorably to a chemotherapy treatment that includes either taxane or a taxane derivative; the method involves performing immunohistochemical staining for TLE3 polypeptide on a cancer sample. This technology enables a more effective process of selecting chemotherapies to administer to a patient, especially when the therapy in question is paclitaxel, which carries adverse side effects.

Despite diminishing resources HBCUs contribute to medical innovations

Research and development of cancer treatments seemed to be a particularly strong focus area for Morehouse School of Medicine. A pharmaceutical composition designed to modulate receptors within a cancer patient which play an important role in the progression of cancers is disclosed and protected by U.S. Patent No. 8796422, which is titled Chemokine-Immunoglobulin Fusion Polypeptides, Compositions, Method of Making and Use Thereof.

Merck seeks patents on cancer treatments, medications for Alzheimer’s

Merck & Co. (NYSE: MRK), which is headquartered in Whitehouse Station, NJ, and also does business under the name Merck Sharp & Dohme MSD, is one of the world’s largest and most renowned pharmaceutical development companies. The company just made a major acquisition in the middle of December, investing $8.4 billion in the purchase of Cubist Pharmaceuticals, a deal which…

A Passionate Fight Against Breast Cancer

She thought about a new approach to get these patents off the shelf: launching an international competition for teams to develop business plans for a start-up company around some of the most promising inventions… Eleven new companies have already been formed, five have completed their licensing negotiations with NIH, most of the new companies have secured venture funding, several have letters of intent from large drug companies and one team landed an additional $700K after winning a separate business plan competition.

Pharma & Biotech Update: News for October 2013

Mouse Model of Parkinson’s Disease Shows Improved Brain Function — DARPA Awards $25 Million To Develop Messenger RNA Therapeutics™ — Actavis Files ANDA for Generic Suboxone® Sublingual Film — AzaSite® Patents Upheld in Patent Infringement Lawsuit Against Sandoz — Surgeons Successfully Remove “Inoperable” Metastatic Breast Cancer — Actavis Files ANDA on Acanya® Gel, Gets Sued by Dow, Valeant — NYSE Inquires About Unusual Market Activity for Ampio Pharmaceuticals — Cannabis Biotech Hires Patent Attorney to Protect Medical Marijuana Innovation — Merck’s Hepatitis C Drug Gets Breakthrough Therapy Designation — Therapeutic Vaccine for Hepatitis C Enters Phase I — Urine Test for Cancer Monitoring — Popular Prenatal Vitamin Patent Upheld in District Court — Clinical Trials on Brain Technology to Assist ALS Patients — Teva Gets Favorable Ruling on COPAXONE in the Netherlands — BVGH Recruits Dr. Linda Venczel as New Program Director — Actavis’s settles with FTC over $8.5 Billion acquisition of Warner Chilcott

Patent Pending: Corporations, the Constitution, and the Human Gene

The Honorable Alex Kozinski immediately posed the question—by way of an analogy to scientists who stare at the stars—of why should someone be able to get a gene patent just because there was a significant amount of effort put in to discover that gene. Throughout the event, Judge Kozinski took on the role of the generalist judge, who would need to be convinced that the invention in the lab is anything other than a product of nature. Professor David Winickoff of UC Berkeley followed that question up by discussing James Watson’s amicus brief and the idea that genes are both symbolic in our culture and shared by all humans, thus making them a unique item in our world.

Gene Patents: Getting Beyond Witch Trials

The USPTO Roundtable on genetic testing exposed claims that have driven the debate so far to a rare scrutiny.  Perhaps the bonfires being prepared for the accused are premature. One critic condemned universities issuing exclusive licenses as culprits responsible for preventing physician-run laboratories “that are begging to do the test” from offering competing testing services. The underlying notion appears that exclusive licensees who spend millions on test development and clinical validation actually provide shoddy lab work in practice, and that physician-run laboratories could do a better job. If so, no supporting evidence was given.

Patent Granted on Long-Acting Drug for Multiple Sclerosis

The conjugates covered by this patent could enable less frequent and better tolerated dosing of one of the most widely used treatments worldwide for relapsing-remitting multiple sclerosis, interferon-beta-1b. The invention described in the European Patent relates to methods for the preparation of conjugates of poly(ethylene glycol), and derivatives thereof, with interferon-beta-1b. Compared to the corresponding unconjugated bioactive components, the conjugates of the invention have increased stability (i.e., longer shelf life and longer half-lives in vivo). In addition, compared to conjugates of the same bioactive component prepared with polymer chains that are attached randomly to solvent-accessible sites along the polypeptide chains, the conjugates of the invention have increased receptor-binding activity and increased potency.

US Oncologists Report Crucial Cancer Drug Shortages

The mantra of the anti-patent community is nearly in unison on the issue of patented drugs. Of course, everyone wants drugs to be developed, but no one wants to pay the exorbitant prices charged for blockbuster, patented drugs. You can add me to that list of individuals who doesn’t like the prices, but at least there is a benefit. Without appropriate financial incentives in place drugs would not be patented, but then again they wouldn’t be developed either. But what is the justification for scarcity and exorbitant prices of old drugs that are off patent?

FDA: No to Breast Cancer Drug, Could Cost Genetech $1 Billion

Contrary to the FDA, the European Medicines Agency confirmed that the benefits of Avastin® in combination with paclitaxel outweigh the risks, further determining that the combination of Avastin® and paclitaxel remains a valuable treatment option for patients suffering from metastatic breast cancer. If the FDA is successful in removing the breast cancer indication from Avastin® Genentech (a member of the Roche Group and the maker of Avastin®) could lose $1 billion of its $6 billion in annual sales of Avastin® due to the lost sales associated with use to treat breast cancer.