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A critical step to effectively fighting cancer is detecting it at a very early stage. Currently the clinical diagnosis of cancer mainly relies on imaging techniques such as X-ray, mammography, ultrasound, endoscopy, computed tomography (CT), magnetic resonance imaging (MRI) and histopathology [e.g., examination of a tissue biopsy under a microscope]). However, these techniques often cannot distinguish differences between healthy and diseased cells/tissues at the early stage of cancer, when the malignancy of tissues are not sufficiently visible, but the alternation of far more subtle protein and molecular markers due to the cancer have already presented. Although notable successful techniques have been developed in the molecular analysis such as enzyme-linked immunosorbent assay (ELISA), polymerase chain reaction (PCR), and fluorescence in situ hybridization (FISH), these techniques are labor intensive, involving complex operational procedures, and requiring high stability of reagents. Therefore, the market is calling to develop new techniques and tools to enhance the biomarker detection at the very early stages of cancer.

Dilworth IP has now added a Resources page to our website which will offer electronic versions of the Firm’s publications for download. Our intention is to provide you with relevant information on cutting-edge technologies, evolving patent trends and the best strategies for protecting your IP. Please CLICK HERE to visit our resources page, and be sure to check back for future publications.

Frederick A. Spaeth, Partner at Dilworth IP, will be hosting a FREE webinar on Wednesday, October 19th at 1:00 PM (EDT). This installment in the Dilworth IP Webinar Series is entitled Advanced Strategies for Drafting CDAs – Beyond the Boilerplate, and will focus on properly structuring Confidentiality Agreements (CDAs), or Nondisclosure Agreements (NDAs). NDAs seem to be used by everyone: businesses, politicians, religious organizations, celebrities, governmental bodies, etc., the single common denominator being an obligation not to share certain information with others. Beyond that…

A split of opinions on the scope of authorization for accessing a computer that is needed to avoid violation of the Computer Fraud and Abuse Act (“CFAA” or “Act”), 18 U.S.C. § 1030 was examined in Phillips Medical v. GIS (U.S. Dist. Of Puerto Rico) Aug. 2016, in which Magistrate Judge Bruce McGiverin adopted an inclusive view of the entities whose authorization is needed under 18 U.S.C. § 1030(a)(2).

Dilworth IP welcomes Nicholas Vincent, a Technology Specialist who will be joining the Firm’s growing Biotech and Pharmaceutical Practice. Nick is currently working toward his doctorate in Microbiology at Yale University where he received the Gruber Science Fellowship, awarded to the highest ranked PhD candidate in his/her field. He also currently serves as the Chairman of the Yale Graduate Student Assembly, and has previously served as the co-Editor-in-Chief of the Yale Journal of Biology and Medicine. Nick has a specialized background in microbiology, molecular and cellular biology, biochemistry, protein biology, RNA biology, microbial pathogenesis, and immunology. His expertise in these cutting-edge technologies further strengthens the Firm’s Biotech and Pharmaceutical Practice area and strengthens Dilworth IP’s commitment to providing our clients with the highest level of technical proficiency. We are excited to welcome Nick to our team.

Dr. Anthony D. Sabatelli, Partner and Chair of the Life Sciences group at Dilworth IP, will be presenting a FREE webinar on Wednesday, September 7th at 1:00 PM (EDT). This installment in the Dilworth IP Webinar Series is entitled What is Patent Eligible: The Ever-evolving Section 101 Standard, and will focus on the inconsistencies in how patent subject matter eligibility is interpreted by the USPTO and the courts. Despite the Supreme Court’s articulation of a two-part test for determining such eligibility (i.e. the Mayo/Alice test), it is often not easy to predict how this test will actually be applied by the U.S. Patent Office or the courts. Dr. Sabatelli’s presentation will offer clarity to those dealing with this uncertainty.

Nanoparticles, due to their unique structure, often possess an enhanced permeability and retention (EPR) effect. These particles can preferentially accumulate in tumors, resulting in higher drug concentrations at targeted sites and consequently higher therapeutic efficacy with lower toxicity for surrounding normal tissue. Also nanoparticle carriers can be designed to encapsulate and deliver cancer drugs having poor water solubility. These favorable characteristics render nanoparticles as promising potential delivery systems for cancer therapies.

Interestingly, the court unearthed an 1864 Supreme Court decision, Godfrey v. Eames, 68 U.S. 317 (1864), for the origin of same-day continuations and the idea of copendency. The court opined that the intent of the drafters of the 1952 Patent Act was to codify the longstanding practice of following Godfrey’s rule

This year Congress gave business owners a new tool to combat theft of their trade secrets: the Defend Trade Secrets Act of 2016, Public Law No: 114-153 (18 U.S.C. 1836(b)) (“DTSA”). Even prior to DTSA, theft of trade secrets was a federal offense under 18 U.S.C.1832 (“Theft of Trade Secrets”)(“ToTS”), exposing offenders to penalties up to $5 million. However, only the U.S. Attorney General was authorized to take action against wrongdoers under this statute, so victims of trade secret theft hoping for compensation or enforcement when the AG would not act had to rely on state law. DTSA now gives victims of trade secret misappropriation a right of private action, with a remedy not available under state l

For clinical therapeutics, there is a great need to develop new approaches to fight chronic and incurable diseases and further improve the efficiency of medical treatments. The current research focus and opportunities for nanomedicine in therapeutics include the development of rapid and accurate analytical techniques, safe and targeted drug delivery systems, improved controlled drug release systems, and the discovery of alternative and innovative therapeutic methods. In this article, I will specifically discuss the use of nanoparticles for drug delivery.