Minutes of the 612Thmeeting Ofthe State
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
FASTKILL FK-20 Antimicrobial
SCC FASTKILL FK-20 Antimicrobial A fast-acting, broad-spectrum biocide for treating raw materials, processing water, and contaminated products Contents Product and Application Overview . 1 Field Test Results . 3 Laboratory Test Results . 7 Physical and Chemical Properties . 9 Decomposition Pathways . 10 Safe Use and Handling . 11 Health and Environment . 15 Regulatory Information . 18 Analytical Test Methods . 19 FASTKILL FK-20 Antimicrobial A fast-acting, broad-spectrum biocide for treating raw materials, processing FASTKILL FK-20 Antimicrobial quickly and economi- cally cleans up these potential sources of contamination water, and contaminated products without requiring you to shut down or delay production. FASTKILL FK-20 Antimicrobial is a fast-acting, broad- spectrum biocide that is ideal for reducing micro- In finished products, FASTKILL FK-20 can be used biological contamination in raw materials or products such effectively in combination with long-term preservatives as aqueous paints and coatings, polymers, slurries, to reduce the bio-burden on the long-term preservative adhesives, latex and resin emulsions, sizing, caulk, process and minimize the likelihood of organism tolerance. This water and specialty industrial products including inks, can lower the chances for field failure, product recall, polishes, waxes, detergents, and cleansers. product rework, and downtime. In some cases overall preservative costs may also be reduced. Many manufacturers who use biocides for in-can preservation of finished products use the same biocide FASTKILL FK-20 also serves as a fast-acting, low cost to treat stored raw materials, wash water, recycle water, preservative for aqueous formulations such as adhesives and contaminated finished product. Although long-term where short-term protection ranging from several days preservatives may eventually get the job done, they to several weeks is desired. -
Oral Antifungal Agent Nailin® Capsules 100Mg Approved in Japan
FOR IMMEDIATE RELEASE January 19, 2018 Sato Pharmaceutical Co., Ltd. Eisai Co., Ltd. ORAL ANTIFUNGAL AGENT NAILIN® CAPSULES 100MG APPROVED IN JAPAN Sato Pharmaceutical Co., Ltd. (Headquarters: Tokyo, President and CEO: Seiichi Sato, “Sato Pharma”) obtained marketing and manufacturing approval for the oral antifungal agent NAILIN® Capsules 100mg containing the active ingredient fosravuconazole L-lysine ethanolate (“fosravuconazole”) for the treatment of onychomycosis in Japan on January 19, 2018. Sato Pharma and Eisai Co., Ltd. (Headquarters: Tokyo, CEO: Haruo Naito, “Eisai”) are jointly providing information on its proper use. Fosravuconazole, the active ingredient of NAILIN® Capsules 100mg, is a new triazole class oral antifungal component discovered by Eisai. Sato Pharma conducted a Phase III clinical study of the agent in patients with onychomycosis in Japan, and after confirming efficacy and safety of the agent in the study, Sato Pharma applied for marketing and manufacturing authorization in January 2017. Onychomycosis affects 1 in every 10 Japanese people, and there are an estimated approximately 11 million sufferers in Japan. With Sato Pharma now having obtained marketing and manufacturing approval for NAILIN® Capsules 100mg, as an oral treatment for onychomycosis, this is the first new treatment for the disease in approximately 20 years. By providing NAILIN® Capsules 100mg as a new option for the treatment of onychomycosis, Sato Pharma and Eisai will strive to fulfil the needs of onychomycosis patients and healthcare professionals. -
Patent Application Publication ( 10 ) Pub . No . : US 2019 / 0192440 A1
US 20190192440A1 (19 ) United States (12 ) Patent Application Publication ( 10) Pub . No. : US 2019 /0192440 A1 LI (43 ) Pub . Date : Jun . 27 , 2019 ( 54 ) ORAL DRUG DOSAGE FORM COMPRISING Publication Classification DRUG IN THE FORM OF NANOPARTICLES (51 ) Int . CI. A61K 9 / 20 (2006 .01 ) ( 71 ) Applicant: Triastek , Inc. , Nanjing ( CN ) A61K 9 /00 ( 2006 . 01) A61K 31/ 192 ( 2006 .01 ) (72 ) Inventor : Xiaoling LI , Dublin , CA (US ) A61K 9 / 24 ( 2006 .01 ) ( 52 ) U . S . CI. ( 21 ) Appl. No. : 16 /289 ,499 CPC . .. .. A61K 9 /2031 (2013 . 01 ) ; A61K 9 /0065 ( 22 ) Filed : Feb . 28 , 2019 (2013 .01 ) ; A61K 9 / 209 ( 2013 .01 ) ; A61K 9 /2027 ( 2013 .01 ) ; A61K 31/ 192 ( 2013. 01 ) ; Related U . S . Application Data A61K 9 /2072 ( 2013 .01 ) (63 ) Continuation of application No. 16 /028 ,305 , filed on Jul. 5 , 2018 , now Pat . No . 10 , 258 ,575 , which is a (57 ) ABSTRACT continuation of application No . 15 / 173 ,596 , filed on The present disclosure provides a stable solid pharmaceuti Jun . 3 , 2016 . cal dosage form for oral administration . The dosage form (60 ) Provisional application No . 62 /313 ,092 , filed on Mar. includes a substrate that forms at least one compartment and 24 , 2016 , provisional application No . 62 / 296 , 087 , a drug content loaded into the compartment. The dosage filed on Feb . 17 , 2016 , provisional application No . form is so designed that the active pharmaceutical ingredient 62 / 170, 645 , filed on Jun . 3 , 2015 . of the drug content is released in a controlled manner. Patent Application Publication Jun . 27 , 2019 Sheet 1 of 20 US 2019 /0192440 A1 FIG . -
For TRADENET VERSION 4.1 Sorted by Chemical Names (Last Updated on 21 Apr 2021)
For TRADENET VERSION 4.1 Sorted by Chemical Names (Last updated on 21 Apr 2021) CHEMICALS CLASSIFIED UNDER HS CODES CONTROLLED BY PCD(HS) OR JOINTLY CONTROLLED WITH OTHER CAs HS CODE PRODUCT CODE DESCRIPTION PRODUCT *CAS Number (AHTN CODE 2017) 29242990 (2R,3S)-N-TERT-BUTOXYCARBONYL-3-AMINO-1-CHLORO-2- PCDCAR115 162536-40-5 HYDROXY-4-PHENYLBUTANE 29242990 [(1S)-3-METHYL-1-[[(2R)-2- PCDCAR118 247068-82-2 METHYLOXIRANYL]CARBONYL]BUTYL]CARBAMIC ACID 1,1- DIMETHYLETHYL ESTER A 28521090 1-(4-CHLOROMERCURIOPHENYLAZO)-2-NAPHTHOL; MERCURY PCDMEO112 3076-91-3 ORANGE 29159090 1,1,3,3-TETRAMETHYLBUTYLPEROXY NEODECANOATE PCDTPN111 51240-95-0 29159090 1,1,3,3-TETRAMETHYLBUTYLPEROXY-2-ETHYLHEXANOATE PCDTPN112 22288-43-3 A 29096000 1,1-DI(TERT-AMYLPEROXY)CYCLOHEXANE PCDDIT116 15667-10-4 A 29096000 1,1-DI(TERT-BUTYLPEROXY)-3,3,5-TRIMETHYLCYCLOHEXANE PCDDIT112 6731-36-8 A 29096000 1,1-DI(TERT-BUTYLPEROXY)CYCLOHEXANE PCDDIT111 3006-86-8 29159090 1,1-DIMETHYL-3-HYDROXYBUTYLPEROXY NEOHEPTANOATE PCDDIM121 110972-57-1 A 29096000 1,1-DIMETHYLPROPYL-1-METHOXYCYCLOHEXYLPEROXIDE PCDDIP119 125768-93-6 29159090 1,1-DIMETHYLPROPYL 3,5,5-TRIMETHYLHEXANEPEROXOATE PCDDIT115 68860-54-8 29291090 1,3-BIS(ISOCYANATOMETHYL)CYCLOHEXANE PCDBIS114 38661-72-2 29291090 1,4-PHENYLENE DIISOCYANATE; P-PHENYL DIISOCYANATE PCDPHD111 104-49-4 29269000 1,6-DICYANOHEXANE; SUBERONITRILE PCDDIC119 629-40-3 A 29189900 2-(2,4,5-TRICHLOROPHENOXY)PROPIONIC ACID PCDTRA113 93-72-1 A 29189900 2-(2,4-DICHLOROPHENOXY)PROPANOIC ACID PCDDIA115 120-36-5 29339990 2-(P-CHLOROPHENYL)-3-CYANO-4-BROMO-5- -
Federal Register/Vol. 84, No. 230/Friday, November 29, 2019
Federal Register / Vol. 84, No. 230 / Friday, November 29, 2019 / Proposed Rules 65739 are operated by a government LIBRARY OF CONGRESS 49966 (Sept. 24, 2019). The Office overseeing a population below 50,000. solicited public comments on a broad Of the impacts we estimate accruing U.S. Copyright Office range of subjects concerning the to grantees or eligible entities, all are administration of the new blanket voluntary and related mostly to an 37 CFR Part 210 compulsory license for digital uses of increase in the number of applications [Docket No. 2019–5] musical works that was created by the prepared and submitted annually for MMA, including regulations regarding competitive grant competitions. Music Modernization Act Implementing notices of license, notices of nonblanket Therefore, we do not believe that the Regulations for the Blanket License for activity, usage reports and adjustments, proposed priorities would significantly Digital Uses and Mechanical Licensing information to be included in the impact small entities beyond the Collective: Extension of Comment mechanical licensing collective’s potential for increasing the likelihood of Period database, database usability, their applying for, and receiving, interoperability, and usage restrictions, competitive grants from the Department. AGENCY: U.S. Copyright Office, Library and the handling of confidential of Congress. information. Paperwork Reduction Act ACTION: Notification of inquiry; To ensure that members of the public The proposed priorities do not extension of comment period. have sufficient time to respond, and to contain any information collection ensure that the Office has the benefit of SUMMARY: The U.S. Copyright Office is requirements. a complete record, the Office is extending the deadline for the extending the deadline for the Intergovernmental Review: This submission of written reply comments program is subject to Executive Order submission of written reply comments in response to its September 24, 2019 to no later than 5:00 p.m. -
Rpt POL-TOXIC AIR POLLUTANTS 98 BY
SWCAA TOXIC AIR POLLUTANTS '98 by CAS ASIL TAP SQER CAS No HAP POLLUTANT NAME HAP CAT 24hr ug/m3 Ann ug/m3 Class lbs/yr lbs/hr none17 BN 1750 0.20 ALUMINUM compounds none0.00023 AY None None ARSENIC compounds (E649418) ARSENIC COMPOUNDS none0.12 AY 20 None BENZENE, TOLUENE, ETHYLBENZENE, XYLENES BENZENE none0.12 AY 20 None BTEX BENZENE none0.000083 AY None None CHROMIUM (VI) compounds CHROMIUM COMPOUN none0.000083 AY None None CHROMIUM compounds (E649962) CHROMIUM COMPOUN none0.0016 AY 0.5 None COKE OVEN COMPOUNDS (E649830) - CAA 112B COKE OVEN EMISSIONS none3.3 BN 175 0.02 COPPER compounds none0.67 BN 175 0.02 COTTON DUST (raw) none17 BY 1,750 0.20 CYANIDE compounds CYANIDE COMPOUNDS none33 BN 5,250 0.60 FIBROUS GLASS DUST none33 BY 5,250 0.60 FINE MINERAL FIBERS FINE MINERAL FIBERS none8.3 BN 175 0.20 FLUORIDES, as F, containing fluoride, NOS none0.00000003 AY None None FURANS, NITRO- DIOXINS/FURANS none5900 BY 43,748 5.0 HEXANE, other isomers none3.3 BN 175 0.02 IRON SALTS, soluble as Fe none00 AN None None ISOPROPYL OILS none0.5 AY None None LEAD compounds (E650002) LEAD COMPOUNDS none0.4 BY 175 0.02 MANGANESE compounds (E650010) MANGANESE COMPOU none0.33 BY 175 0.02 MERCURY compounds (E650028) MERCURY COMPOUND none33 BY 5,250 0.60 MINERAL FIBERS ((fine), incl glass, glass wool, rock wool, slag w FINE MINERAL FIBERS none0.0021 AY 0.5 None NICKEL 59 (NY059280) NICKEL COMPOUNDS none0.0021 AY 0.5 None NICKEL compounds (E650036) NICKEL COMPOUNDS none0.00000003 AY None None NITROFURANS (nitrofurans furazolidone) DIOXINS/FURANS none0.0013 -
R&D Model & Portfolio
R&D MODEL & PORTFOLIO ADAPTED TREATMENTS FOR THE BENEFIT OF NEGLECTED PATIENTS The R&D strategies developed by DNDi since its inception aim to Phase II trials as a potential single- address the immediate needs of patients by improving existing dose oral treatment and is the first therapeutic options in the short term, whilst undertaking longer molecule to arise from DNDi’s lead term research to identify and develop entirely new compounds optimization programme. which will be valuable adapted tools, particularly for elimination targets set by the World Health Organization. Although not Leishmaniasis is a complex family necessarily breakthrough medicines, six new treatments have of diseases, and the identification been delivered to date as a result of the short-term strategy, of new compounds has proved which have brought significant benefits to patients. challenging. Compound libraries from a variety of sources have been screened and, despite the inevitable The year 2015 has been a turning are orally available compounds for loss of compounds to attrition, NCEs point for DNDi, as long-term systemic use. The most clinically from the nitroimidazole, oxaborole, investments have now filled the advanced of these are for sleeping and aminopyrazole chemical drug development pipeline with sickness: fexinidazole, which was families are undergoing lead thirteen new chemical entities identified from compound mining optimization to combat Leishmania (NCEs) included by the end of the and is a ten day oral treatment, infections, with the nitroimidazole year, the vast majority of which and SCYX-7158, which is entering VL-0690 selected to go forward to 14 › DNDi Annual Report 2015 R&D MODEL & PORTFOLIO pre-clinical development in 2015. -
Stembook 2018.Pdf
The use of stems in the selection of International Nonproprietary Names (INN) for pharmaceutical substances FORMER DOCUMENT NUMBER: WHO/PHARM S/NOM 15 WHO/EMP/RHT/TSN/2018.1 © World Health Organization 2018 Some rights reserved. This work is available under the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 IGO licence (CC BY-NC-SA 3.0 IGO; https://creativecommons.org/licenses/by-nc-sa/3.0/igo). Under the terms of this licence, you may copy, redistribute and adapt the work for non-commercial purposes, provided the work is appropriately cited, as indicated below. In any use of this work, there should be no suggestion that WHO endorses any specific organization, products or services. The use of the WHO logo is not permitted. If you adapt the work, then you must license your work under the same or equivalent Creative Commons licence. If you create a translation of this work, you should add the following disclaimer along with the suggested citation: “This translation was not created by the World Health Organization (WHO). WHO is not responsible for the content or accuracy of this translation. The original English edition shall be the binding and authentic edition”. Any mediation relating to disputes arising under the licence shall be conducted in accordance with the mediation rules of the World Intellectual Property Organization. Suggested citation. The use of stems in the selection of International Nonproprietary Names (INN) for pharmaceutical substances. Geneva: World Health Organization; 2018 (WHO/EMP/RHT/TSN/2018.1). Licence: CC BY-NC-SA 3.0 IGO. Cataloguing-in-Publication (CIP) data. -
A Abacavir Abacavirum Abakaviiri Abagovomab Abagovomabum
A abacavir abacavirum abakaviiri abagovomab abagovomabum abagovomabi abamectin abamectinum abamektiini abametapir abametapirum abametapiiri abanoquil abanoquilum abanokiili abaperidone abaperidonum abaperidoni abarelix abarelixum abareliksi abatacept abataceptum abatasepti abciximab abciximabum absiksimabi abecarnil abecarnilum abekarniili abediterol abediterolum abediteroli abetimus abetimusum abetimuusi abexinostat abexinostatum abeksinostaatti abicipar pegol abiciparum pegolum abisipaaripegoli abiraterone abirateronum abirateroni abitesartan abitesartanum abitesartaani ablukast ablukastum ablukasti abrilumab abrilumabum abrilumabi abrineurin abrineurinum abrineuriini abunidazol abunidazolum abunidatsoli acadesine acadesinum akadesiini acamprosate acamprosatum akamprosaatti acarbose acarbosum akarboosi acebrochol acebrocholum asebrokoli aceburic acid acidum aceburicum asebuurihappo acebutolol acebutololum asebutololi acecainide acecainidum asekainidi acecarbromal acecarbromalum asekarbromaali aceclidine aceclidinum aseklidiini aceclofenac aceclofenacum aseklofenaakki acedapsone acedapsonum asedapsoni acediasulfone sodium acediasulfonum natricum asediasulfoninatrium acefluranol acefluranolum asefluranoli acefurtiamine acefurtiaminum asefurtiamiini acefylline clofibrol acefyllinum clofibrolum asefylliiniklofibroli acefylline piperazine acefyllinum piperazinum asefylliinipiperatsiini aceglatone aceglatonum aseglatoni aceglutamide aceglutamidum aseglutamidi acemannan acemannanum asemannaani acemetacin acemetacinum asemetasiini aceneuramic -
Fosravuconazole L-Lysine Ethanolate | Medchemexpress
Inhibitors Product Data Sheet Fosravuconazole L-lysine ethanolate • Agonists Cat. No.: HY-16779B CAS No.: 914361-45-8 Molecular Formula: C₃₁H₄₀F₂N₇O₈PS • Molecular Weight: 739.73 Screening Libraries Target: Fungal; Parasite Pathway: Anti-infection Storage: Powder -20°C 3 years 4°C 2 years In solvent -80°C 6 months -20°C 1 month SOLVENT & SOLUBILITY In Vitro DMSO : 50 mg/mL (67.59 mM; Need ultrasonic) H2O : < 0.1 mg/mL (ultrasonic) (insoluble) Mass Solvent 1 mg 5 mg 10 mg Concentration Preparing 1 mM 1.3518 mL 6.7592 mL 13.5184 mL Stock Solutions 5 mM 0.2704 mL 1.3518 mL 2.7037 mL 10 mM 0.1352 mL 0.6759 mL 1.3518 mL Please refer to the solubility information to select the appropriate solvent. In Vivo 1. Add each solvent one by one: 10% DMSO >> 40% PEG300 >> 5% Tween-80 >> 45% saline Solubility: ≥ 2.5 mg/mL (3.38 mM); Clear solution 2. Add each solvent one by one: 10% DMSO >> 90% (20% SBE-β-CD in saline) Solubility: ≥ 2.5 mg/mL (3.38 mM); Clear solution BIOLOGICAL ACTIVITY Description Fosravuconazole L-lysine ethanolate (BMS-379224 L-lysine ethanolate), a prodrug of Ravuconazole, is an orally active broad spectrum antifungal agent. Fosravuconazole L-lysine ethanolate can be used for candidiasis, onychomycosis and parasitemia research[1][2][3]. In Vitro Fosravuconazole has potent in vitro antifungal activity against a wide range of fungal species, including Candida, Aspergillus , and Trichophyton species[1]. MCE has not independently confirmed the accuracy of these methods. -
Surveillance of Antifungal Use in Japan Oral Medicine + Injection Change in Antifungal Use for All of Japan by Rout of Administration 1
Surveillance of antifungal use in Japan Oral medicine + Injection Change in antifungal use for all of Japan by rout of administration 1 0.9 / day 0.8 0.7 0.6 0.5 0.4 Dose / inhabitants / 1,000 Dose 0.3 Daily 0.2 0.1 Defined 0 2013 2014 2015 2016 2017 2018 2019 Injection注射薬 内服薬Oral medicine(テルビナフィン・ホスラブコナゾールを除く (except for terbinafine and fosravuconazole) ) ホスラブコナゾールFosravuconazole テルビナフィンTerbinafine Oral medicine Change in antifungal use (oral medicine) for all of Japan 1 0.9 / day 0.8 0.7 0.6 0.5 0.4 Dose / inhabitants / 1,000 Dose 0.3 Daily 0.2 0.1 Defined 0 2013 2014 2015 2016 2017 2018 2019 フルシトシンFlucytosine ボリコナゾールVoriconazole イトラコナゾールItraconazole フルコナゾールFluconazole ホスラブコナゾールFosravuconazole テルビナフィンTerbinafine Injection Change in antifungal use (injection) for all of Japan 0.035 / day 0.03 0.025 0.02 0.015 Dose / inhabitants / 1,000 Dose 0.01 Daily 0.005 Defined 0 2013 2014 2015 2016 2017 2018 2019 Amphotericinアムホテリシン BB ミコナゾールMiconazole フルコナゾールFluconazole イトラコナゾールItraconazole Voriconazoleボリコナゾール Caspofunginカスポファンギン ミカファンギンMicafungin 〇The data are calculated from claims registered in the NDB. The data do not always reflect the precise antibiotic use because the data of patients who receive publicly funded health care are not always included. The numerical values are different from those of the surveillance of antibiotic sales (http://amrcrc.ncgm.go.jp/surveillance/020/20190902163931.html) due to the different data source. 〇The figures indicate drug utilization standardized by defined daily dose (DDD) per population and drug, called DID (DDDs/1,000 inhabitants/day) (Reference:https://www.whocc.no/atc_ddd_index/ ). -
Mining Sudanese Medicinal Plants for Natural Compounds Against Malaria and Neglected Tropical Diseases
Mining Sudanese Medicinal Plants for Natural Compounds against Malaria and Neglected Tropical Diseases INAUGURALDISSERTATION zur Erlangung der Würde eines Doktors der Philosophie vorgelegt der Philosophisch-Naturwissenschaftlichen Fakultät der Universität Basel von Abdelhalim Babiker Mohamed Mahmoud aus dem Sudan Basel, 2020 Originaldokument gespeichert auf dem Dokumentenserver der Universität Basel edoc.unibas.ch Genehmigt von der Philosophisch-Naturwissenschaftlichen Fakultät auf Antrag von Prof. Dr. Pascal Mӓser Prof. Dr. Thomas J. Schmidt Basel, den 23.06.2020 Prof. Dr. Martin Spiess Dekan To my father Who taught me that perseverance and hard work always pays off. May your inspiring soul rest in peace. Table of Contents Acknowledgment ...................................................................................................................................................... I Abbreviations .......................................................................................................................................................... III Summary .................................................................................................................................................................... V 1. INTRODUCTION: Neglected Tropical Diseases, Drug Discovery, and the Sudan .................... 1 1.1 Neglected Tropical Diseases ............................................................................................................................ 3 1.1.1 NTDs and Sudan .........................................................................................................................................