• Also provided are methods of treatment as Janus Kinase inhibitors and pharmaceutical compositions containing the compounds of the invention and combinations thereof with other therapeutic agents. (justia.com)
  • This invention also is directed to compositions comprising said compounds, methods for making such compounds, and methods for treating and preventing conditions mediated by JAKs, and in particular TYK2/JAK1. (justia.com)
  • pharmaceutical compositions comprising a pharmaceutically acceptable carrier and a compound of formula I, or a pharmaceutically acceptable salt thereof. (justia.com)
  • EP 0474 098 relates to the formulation of solid compositions comprising a hardly soluble drug substance co-precipitated with 3 carrfer comprising a water-soluble excipient (PVP) and a blodegradable excipient (polyactic acid). (allindianpatents.com)
  • US 4 639 370 rotates to the formulation of powdery compositions comprising a poorly water-soluble drug in combination with a water Insoluble carrier (cross-linked PVP). (allindianpatents.com)
  • US 6 027 747 relates to the formulation of solid compositions comprising a hardly soluble drug substance together with a carrier (PVP). (allindianpatents.com)
  • Watanabe T et al relates to the formulation of solid compositions comprising indomethacin and silica. (allindianpatents.com)
  • Related methods and compositions that can be used for diagnosis, prognosis, and treatment of those medical conditions are disclosed," the abstract adds. (genomeweb.com)
  • These modified oligomeric compounds are used as single compounds or in compositions, including pharmaceutical compositions, to modulate or mimic the targeted nucleic acid comprising or encoding miR-122a. (genomeweb.com)
  • The invention relates to "compounds, compositions, and methods for the study, diagnosis, and treatment of traits, diseases and conditions that respond to the modulation of 11 beta-hydroxysteroid dehydrogenase-1 gene expression and/or activity," the patent application's abstract states. (genomeweb.com)
  • The invention "is also directed to compounds, compositions, and methods relating to traits, diseases and conditions that respond to the modulation of expression and/or activity of genes involved in 11 beta-hydroxysteroid dehydrogenase-1 gene expression pathways or other cellular processes that mediate the maintenance or development of such traits, diseases, and conditions. (genomeweb.com)
  • The present invention relates to pharmaceutical compositions suitable for the treatment of chronic diseases associated with the presence of abnormal or an abnormal distribution of microflora in the gastrointestinal tract of a mammalian host, which compositions comprise viable non-pathogenic or attenuated pathogenic Clostridia. (patsnap.com)
  • The present invention also provides pharmaceutical compositions suitable for the treatment of the same chronic diseases comprising viable non-pathogenic or attenuated pathogenic Escherichia coli, at least one strain of viable non-pathogenic or attenuated pathoenic Bacteroides and at least one strain of viable non-pathogenic or attenuated pathogenic microorganism. (patsnap.com)
  • [0001] The present invention relates to the use of erythritol as a stable soluble filler in spray-dried pharmaceutical compositions and, in particular, to novel compositions comprising eythritol as excipient and the NK 3 receptor antagonist talnetant. (patentsencyclopedia.com)
  • Many are related to the production of cannabis products and involve cannabis plant breeding methods, cannabis processing methods and apparatuses such as for extraction, analytical methods for quality control, and cannabis compositions . (internetandtechnologylaw.com)
  • A patent in the name of Colgate-Palmolive Company relating to pearlised cleansing compositions was opposed by The Procter & Gamble Company and Sasol Germany GmbH. (blogspot.com)
  • The present Invention relates to the field of pharmaceutical formulation science, In particular wfth respect to methods of improving solubility and bioavailability of lipophilic compounds. (allindianpatents.com)
  • Poor bioavailability of lipophilic compounds is a well-known problem, In particular in connection with per oral administration, wherein the compound Is to be dissolved In the gastric fluid and or intestinal fluid before being absorbed from the gastro-intestinal tract into the blood circulation. (allindianpatents.com)
  • Both compounds are a preferred object of the present invention. (allindianpatents.com)
  • The present invention also relates to specific compounds that have been identified, using such screening methods, as useful in the treatment and/or the prevention of HCC/cirrhosis. (sumobrain.com)
  • Molecules, including those of pharmaceutical compounds, have three-dimensional structures. (patentology.com.au)
  • In his role at Thomas Jefferson University Innovation Pillar, which handles the patent portfolio for the university, including all submission and procurement of patents and licensure of inventions by the faculty, Hackett helped to prepare communications with the US Patent and Trademark Office (USPTO) in furtherance of securing patents on inventions for TJU. (temple.edu)
  • Though cannabis is still illegal under federal law, the U.S. Patent and Trademark Office (USPTO) is not precluded from granting patents on inventions related to cannabis. (internetandtechnologylaw.com)
  • The present invention relates to a propellant-free aerosol formulation of a pharmaceutically acceptable salt of tiotropium dissolved in water. (allindianpatents.com)
  • The patent application, according to its abstract, claims "methods … for the treatment of cardiovascular or metabolic diseases characterized by elevated serum total cholesterol, elevated serum LDL-cholesterol, or elevated serum triglycerides, through the administration of an oligomeric compound which modulates the levels or activity of miR-122a. (genomeweb.com)
  • Categories 1 and 3 were relevant to the question of the steps in the development of a tiotriopium dry powder formulation for a capsule, and the moisture-sensitivity thereof in respect of the Capsule Patent. (eagar.com.au)
  • The collegial panel opined that the language attests that claim 1 is not a mere feature of the drug administration method but a feature that would indirectly affect the product's preparation, suggesting that the product is a combination of two dosage forms, namely the injection formulation and the oral formulation, and their respective excipients thereof. (managingip.com)
  • His Honour held that the expression " at least one water-soluble therapeutic agent " in the context of claims 1 and 26 referred to either a drug, a prodrug or a salt thereof, depending on which is actually added to the formulation. (maddocks.com.au)
  • To achieve an optimum distribution of active substances in the lung it makes sense to use a liquid formulation without propellant gases administered using suitable inhalers. (allindianpatents.com)
  • Those inhalers which are capable of nebulising a small amount of a liquid formulation in the dosage needed for therapeutic purposes within a few seconds into an aerosol suitable for therapeutic inhalation are particularly suitable. (allindianpatents.com)
  • An inhalable unit dose liquid formulation containing SAE-CD and corticosteroid is provided. (patsnap.com)
  • Pharmaceutical preparation consisting of tiotropium bromide as active substance, in a concentration based on tiotropium of between 0.02g per 100ml of formulation and 0.05g per 100ml of formulation, the tiotropium bromide being present in the pharmaceutical preparation is totally dissolved form. (allindianpatents.com)
  • Among the Examples disclosed there is a formulation containing tiotropium bromide with a pH of 3.2 or 3.4. (allindianpatents.com)
  • 2008203057 (Capsule Patent) and 757008 (Powder Patent) broadly relate to preparations containing inhalable forms of tiotropium, as either capsules or an inhalable powder. (eagar.com.au)
  • The specification of each patent particularly refers to use of tiotropium for the treatment of asthma and Chronic Obstructive Pulmonary Disease, where inhalable administration of tiotropium is desirable. (eagar.com.au)
  • Tiotropium is a highly effective active pharmaceutical substance and as such, requires significant dilution with excipients during formulation. (eagar.com.au)
  • Diluting tiotropium raises the potential for instability of the substance in the final product formulation, which in turn may give rise to heterogenous dosage and administration of the active substance. (eagar.com.au)
  • The invention as claimed in each of the patents addresses the stability issue in inhaled forms of tiotropium. (eagar.com.au)
  • Teva presented similar arguments and evidence in support of discovery for category 4 and 5 documents (laboratory notes and reports, and protocols or standard operating procedures) relating to development of formulations of tiotropium with different grades or different particle sizes of lactose, during the period from October 1998 to October 2001 regarding the Powder document. (eagar.com.au)
  • We coined the name DehydraTECH to recognize the fact that our patented formulation and processing methodology is rooted in effecting a molecular association between any given lipophilic bioactive substance of interest (e.g., cannabidiol (CBD), tetrahydrocannabinol, antiviral drugs, etc.) and certain long chain triglyceride rich oils (e.g., high oleic sunflower oil) together with certain emulsifying substrate powders that is enabled by way of our dehydration processing technique. (extractionmagazine.com)
  • Our research is indeed a testament to how high-quality scientific findings from the hemp/cannabis CPG [consumer packaged goods] industry can be applicable to the broader pharmaceutical industry, as we are now investigating for certain oral antiviral drug therapies," Bunka says. (extractionmagazine.com)
  • For aqueous formulations of solutions which are to be converted into inhalable aerosols using the inhaler described above, the specification favours a minimum concentration of sodium edetate of 50 mg/100 ml, in order to reduce the incidence of spray anomalies. (allindianpatents.com)
  • The formulation is administered as an aqueous solution or concentrated composition. (patsnap.com)
  • The present invention provides pharmaceutically active aminopyrimidinyl ligands and analogues. (justia.com)
  • Accordingly, the present invention provides novel JAK inhibitors which are both potent JAK inhibitors, and in particular TYK2/JAK1 inhibitors, but also display high clearance in human hepatocytes, thus affording significantly improved systemic clearance, and thereby reducing the risk of adverse side effects upon topical administration while retaining efficacy in the skin. (justia.com)
  • The specific formulation technique of the present invention relates to stabilised supersaturated solid solutions of lipophilic drugs, such as steroidal molecules and hormones In general. (allindianpatents.com)
  • relates to the formulation of solid dispersions comprising a hardly soluble drug substance together with a carrier (PVP), wherein the the drug substance is present in amorphous form or in crystalline form (Khougaz K et al. (allindianpatents.com)
  • SAE-CD present in the formulation significantly enhances the chemical stability of corticosteroid, such as budesonide. (patsnap.com)
  • The present invention provides good patient convenience in terms of administration due to exhibition of an excellent pharmacological activity effect upon administration and a significant increase of half-life in blood over existing interferon formulations. (justia.com)
  • The present invention provides a tumour vasculature permeabilising molecule for use in permeabilising vasculature of a tumour for treating, detecting or diagnosing said tumour wherein said tumour vasculature permeabilising molecule is formulated for systemic administration to said patient. (justia.com)
  • In the present patent embodiment, the combination of injection and oral dosage forms does indeed produce a good immunological effect, and the substantial contribution of the invention is the combination of the injection and oral dosage forms. (managingip.com)
  • The present invention provides a method for stabilizing an anti-dementia drug in a pharmaceutical composition containing the anti-dementia drug and a high molecular weight basic substance by adding a high molecular weight acidic substance to said pharmaceutical composition. (drugs.com)
  • Further, the present invention provides a pharmaceutical composition containing an anti-dementia drug and a high molecular basic substance in which a high molecular weight acidic substance is contained for stabilizing the anti-dementia drug. (drugs.com)
  • Furthermore, the present invention provides a method for manufacturing a pharmaceutical composition which comprises steps wherein a solution or suspension containing a high molecular weight acidic substance is added to a mixture of an anti-dementia drug and a high molecular weight basic substance for the sake of stabilizing the anti-dementia drug. (drugs.com)
  • The present invention provides a simple and robust human liver cell-based system in which persistent hepatitis C infection, persistent hepatitis B infection or ethanol exposure induces a clinical Prognostic Liver Signature (PLS) high-risk gene signature. (sumobrain.com)
  • However, concerns related to vaccine equity become the biggest obstacle to addressing this global pandemic and future pandemics. (medrxiv.org)
  • Zoetis Services LLC owns an invention patent, No. ZL200780048424.3, which relates to a vaccine for treating canine diseases. (managingip.com)
  • On November 10 2021, a petitioner launched an invalidity attack against the patent at issue, arguing that adjusting the vaccine dosage form, excipients, and other composition in so far as it adapts to different routes of administration is a conventional technical means in this field, which is common knowledge among technical personnel and is devoid of novelty. (managingip.com)
  • But with the arrival of COVID-19, his focus shifted to inventions that were directed to the novel coronavirus, including potential vaccine formulations among others. (temple.edu)
  • He also did work concerning a licensing deal for a previously patented vaccine formulation that may prove to be a useful platform against COVID-19. (temple.edu)
  • The formulation is prepared by mixing SAE-CD, in solid or liquid (dissolved) form, with an inhalable suspension-based unit dose formulation. (patsnap.com)
  • WO 03/04360 relates to the formulation of solid dispersions comprising a poorly water-soluble drug in combination with a carrier (PVP). (allindianpatents.com)
  • 7. Although one might have thought that the actual invention should have been characterised as a disclosure that pemetrexed could be administered safely if it was combined in a medicament with vitamin B12, the claimed invention in the Patent is, as mentioned in para 4 above, the manufacture of such a medicament. (bailii.org)
  • Inappropriate kinase activity triggers a variety of biological cellular responses relating to cell growth, cell differentiation, cell function, survival, apoptosis, and cell mobility implicated in the aforementioned and related diseases. (justia.com)
  • In this review, a search for literature and patent technological prospecting has been performed on the use of EO to treat and prevent diseases as well as to prepare pharmaceutical formulations. (mdpi.com)
  • The LASER ART developed by the UNMC scientists is a formulation of injectable drugs, he said. (unemed.com)
  • However, injectable administration requires the involvement of a medical practitioner, which may not be easily accessible for the masses and usually increases a medicine's cost. (extractionmagazine.com)
  • The formulation according to the invention is particularly suitable for nebulising the active substance using an atomiser in order to administer the active substance by inhalation. (allindianpatents.com)
  • An apparatus of this kind for the propellant-free administration of a metered amount of a liquid pharmaceutical composition for inhalation is described in detail for example in International Patent Application WO 91/14468 "Atomizing Device and Methods" and also in WO 97/12687, cf. (allindianpatents.com)
  • The formulation is employed in an improved nebulization system for administering corticosteroid by inhalation. (patsnap.com)
  • A method of administering the formulation by inhalation is provided. (patsnap.com)
  • water as the only solvent, acid for adjusting the pH to between 2.7 and 3.1, preferably 2.8 and 3.05, benzalkonium chloride in a concentration of between 8mg/100ml and 12mg/100ml, sodium edentate in an amount of between 8mg/ 100ml of formulation and 12mg/100ml of formulation. (allindianpatents.com)
  • WO 98/27959 discloses formulations of solutions for the inhaler described above which contain as additive the disodium salt of editic acid (or disodium ethylenediamine tetraacetate dihydrate or sodium edetate). (allindianpatents.com)
  • standardised the Summary for failure in 10 history of dysfunctions, and the fecal problem of a exercise heart, we apply the linkage Contact of a circular and vivo pharmaceutical XO Sodium to beat purified currently over a five Source Uterus. (siriuspixels.com)
  • In April 2018, Juno Pharmaceuticals Pty Ltd obtained registration on the Australian Register of Therapeutic Goods ( ARTG ) of formulations of parecoxib (as sodium) (the Juno Products ). (maddocks.com.au)
  • Specifically, the invention relates to double stranded nucleic acid molecules … capable of mediating RNA interference against 11 beta-hydroxysteroid dehydrogenase-1 gene expression, including cocktails of such small nucleic acid molecules and lipid nanoparticle (LNP) formulations of such small nucleic acid molecules. (genomeweb.com)
  • More specifically, the composition is an orally administered pharmaceutical formulation in the form of a spontaneous emulsion comprising cyclosporine, ethanol ethyl oleate and polyoxyethylene glycerol trioleate. (patsnap.com)
  • In November 2019, the two offices issued the Opinions on Strengthening the Protection of Intellectual Property Rights, specifically requiring the "strict regulation of evidence standards" and the "formulation of judicial interpretations on rules for evidence in civil lawsuits involving intellectual property. (wipo.int)
  • Registers of approved drugs are maintained by goverment authorities, and specifically the Food and Drug Administration (FDA) in the US, and the Therapeutic Goods Administration (TGA) in Australia. (patentology.com.au)
  • it takes specifically now inherited by fat of the abnormal vitamins, upon which congestive urine relates commonly achieved. (seabaygame.com)
  • The LASER ART research breakthrough is significant, as the invention could be broadly applied. (unemed.com)
  • JAK inhibitors known in the art often have properties which render them generally better suited for oral administration and less well suited for topical administration. (justia.com)
  • and (three) a therapeutic enhancer is offered, which upon admixing with a liquefied gas propellant in an aerosol container releases a breakable foam that is appropriate for topical administration. (kollamdistrictsportscouncil.org)
  • OBJECTIVE: The purpose of this article is based on the review of patents of new products of principal topical administration for the treatment of acne in recent years 2016-2020, to evaluate and analyze novel synthetic molecules and semi-synthetics with potential therapeutic and preventive in the acne treatment. (bvsalud.org)
  • It is essential that the active substance formulations used are sufficiently stable when stored and at the same time are such that they can be administered directly, if possible without any further handling, in accordance with their medical purpose. (allindianpatents.com)
  • In this formulation the active substance is dissolved in water. (allindianpatents.com)
  • Teva adduced evidence that a formulator would seek to minimise moisture in the formulation, including in the capsule, and that the formulator would contact capsule suppliers to obtain information about low-moisture capsules which were suitable for use, and test the capsules that were recommended. (eagar.com.au)
  • Background Single unit dosage forms suitable for oral administration of the active pharmaceutical ingredients are usually formulated in the form of solid formulations. (uni-lj.si)
  • The invention relates to an alcohol-free cosmetic or pharmaceutical foam composition comprising water, a hydrophobic solvent, a floor-lively agent, a gelling agent, an active element selected from the group of urea, hydroxy acid and a therapeutic enhancer and a propellant. (kollamdistrictsportscouncil.org)
  • This led to inventions which otherwise might have been expected to be expressed as being new therapeutic treatments being cast as manufacturing claims. (bailii.org)
  • Pharmacia LLC is the patentee of Australian Patent Number 2002256031 (the Patent ), which relates to the formulation and administration of selective cyclooxygenase-2 ( COX-2 ) inhibitors. (maddocks.com.au)
  • Lyophilized ODT formulations may use proprietary technologies but can produce a tablet that has a faster disintegration rate, for example the Zydis ODT typically dissolves in the mouth in less than 5 seconds without water and Lyophilized Freeze drying tablets - ODT typically dissolves in the mouth in few seconds depending on the molecules and strength. (wikipedia.org)
  • Preservation of authenticity of any invention within its original sources is more often than not, tied along with the concept of Intellectual Property Rights. (legalserviceindia.com)
  • Any mediation relating to disputes arising under the licence shall be conducted in accordance with the mediation rules of the World Intellectual Property Organization (http://www.wipo.int/amc/en/mediation/rules). (who.int)
  • Catalent Pharma Solutions (formerly Scherer DDS) in the U.K., Cima Labs and Fuisz Technologies (whose founder Richard Fuisz went on to pioneer orally soluble films, a separate but related dosage form) in the U.S. and Takeda Pharmaceutical Company in Japan led the development of ODTs. (wikipedia.org)
  • The use of erythritol as soluble filler in the preparation of a stable pharmaceutical composition is disclosed. (patentsencyclopedia.com)
  • It's no wonder, then, that Lexaria Bioscience, a leader in oral drug delivery and fat-soluble drugs, is pushing the envelope of both those fields, in addition to others like nicotine and pharmaceuticals, and even the field that has practically become one with everyday life - COVID 19 - with its patented DehydraTECH technology. (extractionmagazine.com)
  • The formulation can also be administered by conventional nasal delivery apparatus. (patsnap.com)
  • Ms. Brougher is a patent attorney who focuses on all aspects of services related to patents in the areas of biotechnology, pharmaceuticals and medical devices, including patentability opinions, due diligence, patent drafting, domestic and foreign patent prosecution, development and management of patent portfolios, and general client counseling during all phases of a product's lifecycle, from concept to commercialization. (straffordpub.com)
  • The court agreed with Juno that " about 90% " in claim 1 extends to 90.49% as its upper limit, especially given the evidence of the typical use of precise measurements in pharmaceutical sciences, and the examples in the patent descending to measurements to two decimal places. (maddocks.com.au)
  • This method was adapted to pharmaceutical use with the invention of microparticles containing a drug, which would be released upon effervescence of the tablet and swallowed by the patient. (wikipedia.org)
  • The first ODT form of a drug to get approval from the U.S. Food and Drug Administration (FDA) was a Zydis ODT formation of Claritin (loratadine) in December 1996. (wikipedia.org)
  • the development of America's gargantuan pharmaceutical markets must be understood alongside the growth of the illicit drug market. (dissentmagazine.org)
  • The new drug formulation is not an anti-HIV medicine, Dr. Gorantla said, but rather one that opens storage areas inside cells where drugs can be maintained for a long period of time. (unemed.com)
  • This feature, if interpreted literally, appears to be a description of the drug administration process, which would be categorised as a simple feature of drug use, thus does not have any impact on the drug structure or composition, nor does it limit the scope of the claims. (managingip.com)
  • As a result, the CNIPA, in assessing novelty and inventiveness of the patent, focused on ascertaining whether the corresponding combination product was disclosed in the prior art, rather than solely on whether the drug administration method was disclosed. (managingip.com)
  • In China, dosage regimen is generally viewed as a feature of drug administration, which, in principle, does not have a limiting effect on the product. (managingip.com)
  • The Food and Drug Administration Amendments Act of 2007 gave the FDA the authority to require a REMS from drug manufacturers to ensure that the benefits of a drug or biological product outweigh its risks. (straffordpub.com)
  • Thus a subsequent patent, directed for example to an improved formulation ( ie a better way of delivering the same drug to a patient), would not be eligible for extension if the underlying drug had previously been registered in its own right. (patentology.com.au)
  • In the case of pharmaceutical products, different enantiomers may have different bioactivity, that is one or other of them may be more or less effective as a drug. (patentology.com.au)
  • The Lundbeck case in Australia relates to the antidepressant drug citalopram , which comprises two enantiomers of which one, escitalopram was ultimately isolated and found to be the more effective. (patentology.com.au)
  • Another drug, fusidic acid, has been used in Europe for over 40 years and is available in oral or IV formulations in many countries. (medscape.com)
  • This formulation technique aims at solving the problem of providing controlled release formulations. (allindianpatents.com)
  • The Biological Diversity Act aims to control access to biological resources and related traditional knowledge. (legalserviceindia.com)
  • With necessity being the mother of invention, an old Plato attribution, both scientists and clinicians have either gone to the attic or tried to help improve old drugs to see if we can get a bit more mileage with agents that we already have. (medscape.com)
  • A pharmaceutical composition contains cyclosporine as the active ingredient. (patsnap.com)
  • 3. A spray-dried pharmaceutical composition comprising (i) a pharmaceutical active, (ii) povidone, (iii) substantially crystalline erythritol and (iv) a surfactant. (patentsencyclopedia.com)
  • The Board of Appeal disagreed with the Opposition Division and found that, although "sole active ingredient" was not mentioned expressis verbis in the application as filed, monotherapy was the preferred method of administration disclosed in the application. (blogspot.com)
  • A method for preparing an orally administered pharmaceutical composition involves first dissolving cyclosporine in ethanol. (patsnap.com)
  • Taking into account various parameters - including the literal interpretation of claim 1, the material contribution of the invention, and the consensus of the parties over the scope of protection of the patent at issue - the CNIPA affirmed that claim 1, in its essence, protects a combination product. (managingip.com)
  • So, the skilled person would be aware of the concept of the invention, but the question was whether the scope of protection of EP '508 went beyond the literal wording of the claims. (vennershipley.com)
  • Public health authorities, pharmaceutical companies, healthcare organizations, and other stakeholders must work together to guarantee a willing and timely response to PMR outbreaks. (diseaselandscape.com)
  • This synergistic combination of product offerings and superior data analytics is poised to benefit all stakeholders and consumers within the pharmaceutical industry. (smallcaprelations.com)
  • This litigation, relating to the painkiller pregabalin marketed by Warner-Lambert for the treatment of pain under the name Lyrica®, has been keenly followed as the first detailed analysis of infringement of 'second medical use' patents by generically available medicines. (patentdocs.org)
  • Article 66 paragraph 1 provides for the burden of proof in new product manufacturing process invention patent infringement cases (see Section 4.3.2.5.4 of this chapter for further detail). (wipo.int)
  • Article 71 stipulates that people's courts may order an infringer to provide account books and materials related to patent infringement (see Section 4.4.3.4 of this chapter for further detail). (wipo.int)
  • The impact of this decision was significant as it challenged the UK's long established approach to the assessment of infringement, and saw re-formulation of the approach adopted by the UK Courts to determine the scope of claims and infringement by equivalents. (vennershipley.com)
  • No generic formulation of the following product is available. (drugs.com)
  • In such cases, the racemic mixture may be a useful pharmaceutical product, since it includes the effective enantiomer. (patentology.com.au)
  • It is therefore not uncommon for an initial patent to cover a particular pharmaceutical product, in terms of its general chemical formula, and a subsequent patent to cover a specific enantiomer, once the more bioactive molecule has been identified and successfully isolated. (patentology.com.au)
  • There, he was gaining firsthand experience in understanding the compliance and regulatory risks of a major healthcare organization, including work in privacy matters related to HIPAA and HITECH (the regulations that address information privacy, data security and breach response processes for healthcare compliance officers). (temple.edu)
  • Given the growth of investments in and shift of regulatory views regarding cannabis-related products, many companies in industries like medicine, lifestyle and foods/beverages are looking to carve out niches and be leaders in the relatively new space . (internetandtechnologylaw.com)
  • The average was skewed upwards by patents related to the pharmaceutical industry, chemistry, and electronics. (ustechnews.net)
  • A new frontloading strategy may mean that it has a new life as monotherapy and is currently being explored by the pharmaceutical industry. (medscape.com)
  • Actavis, along with other generics companies, developed products in which a different pemetrexed salt was used, assuming that such formulations would not fall within the scope of the claims of Lilly's patent. (vennershipley.com)
  • In Pharmacia LLC v Juno Pharmaceuticals Pty Ltd [2022] FCA 92 the Federal Court held at first instance that three out of six representative batches of Juno's generic parecoxib products fell within the claims of Pharmacia's patent. (maddocks.com.au)
  • With respect to promoting research and development (Element 2), concern was expressed about an open-source model for research and development of pharmaceutical products. (who.int)
  • Other inventions are consumer oriented, such as smokable products like vapes , beverage pods , food additives ( cannabis juice popsicles , anyone? (internetandtechnologylaw.com)
  • Director and CEO Xiaodong (Sean) Chen has over 20 years of experience creating, developing and producing toys and games related products. (serioustraders.com)
  • In the pharmaceutical field, there are inventions that address newly discovered dosage regimens for known drugs, such as new dosage or administration intervals, rather than new indications. (managingip.com)
  • Further provided are methods for reducing hepatic steatosis or liver tissue triglyceride accumulation through the administration of an oligomeric compound which modulates the levels or activity of miR-122a. (genomeweb.com)
  • The invention relates to the use of cytolytic bi-component protein complexes deriving from the fungal genus Pleurotus for controlling CPB and WCR. (uni-lj.si)
  • The use of IoT-enabled technologies can aid in the early detection of signs and the formulation of treatment strategies depending on the level of the infection. (datachief.club)
  • This formulation was required by the then-prevailing law contained in article 52(4) of the European Patent Convention 1973 ( EPC 1973 ), which prohibited from patentability any method of treatment of humans or animals. (bailii.org)
  • Watson & Band's IP-related services cover agency and consulting services concerning trademarks, patents, copyrights and other new types of IP rights, enforcement and litigation services, and commercial IP-related legal services. (watsonband.com)
  • With respect to issues concerning evidence in civil lawsuits, detailed provisions exist in the Civil Procedure Law, Interpretation of the Civil Procedure Law, Provisions on Evidence in Civil Procedures, and related judicial interpretations. (wipo.int)
  • Based on the characteristics of patent cases, the Patent Law and related judicial interpretations also contain some special provisions related to evidence. (wipo.int)
  • In order to do so, we will need to provide a little background, firstly on the provisions for extending the term of pharmaceutical patents, and secondly on the specific chemical issues in these cases. (patentology.com.au)
  • The EPO explicitly recognises the patentability of use claims that are limited to a dosage regimen, whereas the CNIPA is of the opinion that the distinguishing features of an administration process cannot be used to establish novelty in a use claim. (managingip.com)
  • It was noted that the parties agreed on the literal wording of the claims (which only covered pemetrexed disodium), whilst the person skilled in the art would recognise that the idea of the invention behind those words is not so limited. (vennershipley.com)
  • In this article, Ben Miller and Jenny Wong examine the recent Federal Court decision in Pharmacia v Juno Pharmaceuticals, and particularly the challenges to the pharma and biopharma industries presented by the practice of the Australian Patent Office of allowing imprecise terms in patent claims. (maddocks.com.au)
  • In other words, Lexaria's invention has game-changing potential to make ingestion a worthy contender for the ultimate mode of CBD consumption. (extractionmagazine.com)
  • Pfizer Australia Pty Ltd, a related entity, is the exclusive licensee in Australia of the Patent. (maddocks.com.au)
  • In a 2018 randomized, double-blind, placebo-controlled, human clinical study , DehydraTECH delivered 317% more CBD to the blood than the control formulation at the 30-minute mark. (extractionmagazine.com)
  • These generally apply to patent-related civil cases. (wipo.int)
  • E.W. MARTIN: "ReJnington 's Pharmaceutical Sciences", 1990, MACK PUBLISHING CO. (sumobrain.com)
  • Meanwhile, at pharmaceutical giant Johnson & Johnson, rising 2L Thomas McCann was working as an end-to-end strategic lead focusing on 3D Printing in Healthcare. (temple.edu)