14-ICML Accepted Abstracts
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												  Understanding Understanding Non-Hodgkin Non-Hodgkin Lymphoma Lymphoma This Patient Guide Is Supported Through Unrestricted Educational Grants FromUnderstanding Understanding Non-Hodgkin Non-Hodgkin Lymphoma Lymphoma This patient guide is supported through unrestricted educational grants from: A Guide for Patients, 8th Edition Survivors, and Loved Ones Contact the Lymphoma Research Foundation Helpline: (800) 500-9976 [email protected] Website: lymphoma.org Fall 2020 Lymphoma Research Foundation (LRF) Helpline and Clinical Trials FOCUS ON LYMPHOMA Information Service MOBILE APP CONTACT THE LRF HELPLINE The Lymphoma Research Foundation’s Trained staff are available to answer questions mobile app, Focus on Lymphoma, is a and provide support to patients, caregivers and great tool and resource for lymphoma healthcare professionals in any language. patients to manage their disease. Our support services include: Focus on Lymphoma is the fi rst mobile • Information on lymphoma, treatment options, app that provides patients and side effect management and current research fi ndings caregivers comprehensive content • Financial assistance for eligible patients and based on their lymphoma subtype and tools to help manage their diagnosis, referrals for additional fi nancial, legal and including a medication manager, doctor sessions tool and side effects tracker. insurance help • Clinical trial searches based on patient’s The Focus on Lymphoma mobile app was recently named Best App by PR News and diagnosis and treatment history is available for free download for iOS and Android devices in the Apple App Store • Support through LRF’s Lymphoma Support and Google Play. Network, a national one-to one volunteer patient peer program For further information on LRF’s award winning mobile app or any of our Monday through Friday programs and services, call the LRF Helpline toll free (800) 500-9976, 9:30 am − 7:30 pm Eastern Standard Time (EST) Toll-Free (800) 500-9976 email [email protected] or visit us at lymphoma.org.
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												  Journal of Cancer Biology and TherapeuticsISSN: 2379-5972 Research Article Journal of Cancer Biology and Therapeutics Administration of Beta-Emitting Anti-CD37 Radioimmunoconjugate Lutetium (177Lu) Lilotomab Satetraxetan as Weekly Multiple Injections Increases Maximum Tolerated Activity in Nude Mice with Non- Hodgkin Lymphoma Xenografts Heyerdahl H*, Repetto-Llamazares AHV and Dahle J Department of Research and Development, Nordic Nanovector ASA, Norway *Correspondence: Helen Heyerdahl, Department of Research and Development, Nordic Nanovector ASA, Kjelsåsveien 168 B, 0884 Oslo, Norway, Tel: +(47) 22 18 33 01; Fax: +(47) 22 58 00 07; E-mail: [email protected] Received: Apr 20, 2018; Accepted: Aug 23, 2018; Published: Aug 28, 2018 Abstract Lutetium (177Lu) lilotomab satetraxetan (177Lu-lilotomab) is a novel anti-CD37 radioimmunoconjugate (RIC) currently in Phase 2b clinical trial for treatment of non-Hodgkin lymphoma (NHL). The aim of the current study was to investigate tolerability and anti-tumor efficacy of multiple dosing of 177Lu-lilotomab in vivo. Nude mice with subcutaneous (s.c.) NHL (Ramos) xenografts were given 2, 3 or 4 weekly injections of 300 MBq/kg 177Lu-lilotomab or NaCl. Treatment tolerability was assessed by body weight, hematology and histopathological evaluation. A separate experiment in mice without xenografts was performed to collect long term toxicity data. Mice in this study were dosed more conservatively with the intention that all mice should survive until end of experiment and were administered 2 or 4 weekly injections of 200 MBq/kg 177Lu-lilotomab or NaCl. Total accumulated activity of 900 MBq/kg 177Lu-lilotomab given as three weekly injections was tolerated by nude mice with s.c. Ramos xenografts, which is 50 % higher than the maximum tolerated activity (MTA) of a single injection of 530-600 MBq/kg.
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												  Kinetics Model Analysis and Technical Optimization Study on the Elite Men S Triple Jump BTAIJ, 10(2) 2014 FULL PAPERid147288218 pdfMachine by Broadgun Software - a great PDF writer! - a great PDF creator! - http://www.pdfmachine.com http://www.broadgun.com BBiiooTTISSNe e: 097cc4 - h7h435 nnooVlolluomoe 1g0g Issuyye 2 An Indian Journal FULL PAPER BTAIJ, 10(2), 2014 [068-076] Kinetics model analysis and technical optimization study on the ’ elite men s triple jump Su Jin1*, Fang Liu2 1College of Physical Education, Northeast Normal University, Changchun130024, Jilin, (CHINA) 2The Ated School Beijing Education Institute Shijingshan Branch, Beijing 100043, (CHINA) ABSTRACT KEYWORDS For the existing action defect problem of Chinese Triple jump athletes, this Kinematic model; paper studies the motion parameters and technical actions of triple jump Mathematical statistics; athletes through the analysis of kinematics, combines the whole process Jumping angle; of triple jump, uses the mathematical statistical methods, by comparing Triple jump. Chinese elite athletes with foreign elite athletes, and concludes that Chinese ’ speed and take-off angle is too small, they have deficiency in the athletes integrity and continuity of the action. Therefore, in the future training we should pay attention to strengthening the training of speed, increasing the ground pedaling angle when taking off, adjusting the power ratio of triple jump, focusing on strength training of upper body; it studies the taking-off angle of the third jump to find the best jumping angle. Through the study of the triple jump technique, this paper raises rationalization proposals for the improvement of technological level, which is aiming at improvement the technological level of China triple jump. 2014 Trade Science Inc. - INDIA INTRODUCTION cal skills of triple jump deeply, find a more efficient way, and come up with better improvement sugges- In 1986, the triple jump officially emergences as tions for the Chinese athletes.
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												  Classification Decisions Taken by the Harmonized System Committee from the 47Th to 60Th Sessions (2011CLASSIFICATION DECISIONS TAKEN BY THE HARMONIZED SYSTEM COMMITTEE FROM THE 47TH TO 60TH SESSIONS (2011 - 2018) WORLD CUSTOMS ORGANIZATION Rue du Marché 30 B-1210 Brussels Belgium November 2011 Copyright © 2011 World Customs Organization. All rights reserved. Requests and inquiries concerning translation, reproduction and adaptation rights should be addressed to [email protected]. D/2011/0448/25 The following list contains the classification decisions (other than those subject to a reservation) taken by the Harmonized System Committee ( 47th Session – March 2011) on specific products, together with their related Harmonized System code numbers and, in certain cases, the classification rationale. Advice Parties seeking to import or export merchandise covered by a decision are advised to verify the implementation of the decision by the importing or exporting country, as the case may be. HS codes Classification No Product description Classification considered rationale 1. Preparation, in the form of a powder, consisting of 92 % sugar, 6 % 2106.90 GRIs 1 and 6 black currant powder, anticaking agent, citric acid and black currant flavouring, put up for retail sale in 32-gram sachets, intended to be consumed as a beverage after mixing with hot water. 2. Vanutide cridificar (INN List 100). 3002.20 3. Certain INN products. Chapters 28, 29 (See “INN List 101” at the end of this publication.) and 30 4. Certain INN products. Chapters 13, 29 (See “INN List 102” at the end of this publication.) and 30 5. Certain INN products. Chapters 28, 29, (See “INN List 103” at the end of this publication.) 30, 35 and 39 6. Re-classification of INN products.
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												  2017 Immuno-Oncology Medicines in Development2017 Immuno-Oncology Medicines in Development Adoptive Cell Therapies Drug Name Organization Indication Development Phase ACTR087 + rituximab Unum Therapeutics B-cell lymphoma Phase I (antibody-coupled T-cell receptor Cambridge, MA www.unumrx.com immunotherapy + rituximab) AFP TCR Adaptimmune liver Phase I (T-cell receptor cell therapy) Philadelphia, PA www.adaptimmune.com anti-BCMA CAR-T cell therapy Juno Therapeutics multiple myeloma Phase I Seattle, WA www.junotherapeutics.com Memorial Sloan Kettering New York, NY anti-CD19 "armored" CAR-T Juno Therapeutics recurrent/relapsed chronic Phase I cell therapy Seattle, WA lymphocytic leukemia (CLL) www.junotherapeutics.com Memorial Sloan Kettering New York, NY anti-CD19 CAR-T cell therapy Intrexon B-cell malignancies Phase I Germantown, MD www.dna.com ZIOPHARM Oncology www.ziopharm.com Boston, MA anti-CD19 CAR-T cell therapy Kite Pharma hematological malignancies Phase I (second generation) Santa Monica, CA www.kitepharma.com National Cancer Institute Bethesda, MD Medicines in Development: Immuno-Oncology 1 Adoptive Cell Therapies Drug Name Organization Indication Development Phase anti-CEA CAR-T therapy Sorrento Therapeutics liver metastases Phase I San Diego, CA www.sorrentotherapeutics.com TNK Therapeutics San Diego, CA anti-PSMA CAR-T cell therapy TNK Therapeutics cancer Phase I San Diego, CA www.sorrentotherapeutics.com Sorrento Therapeutics San Diego, CA ATA520 Atara Biotherapeutics multiple myeloma, Phase I (WT1-specific T lymphocyte South San Francisco, CA plasma cell leukemia www.atarabio.com
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												  Asian Championships Statistics – Men's TJAsian Championships Statistics – Men’s TJ Can two-time Asian Games champion Li Yanxi win the Asian Championships? All time performance list at the Asian Championships Performance Performer Distance Wind Name Nat Pos Venue Year 1 1 17.22 Chen Yanping CHN 1 Kuala Lumpur 1991 2 2 17.05 Zhou Zhenxian CHN 1 Tokyo 1981 3 17.02 Zhou Zhenxian 1 Tokyo 1979 4 3 17.00 1.8 Kim Duk-Hyun KOR 2 Amman 2007 5 16.95 Chen Yanping 1 New Delhi 1989 5 4 16.95 Zou Sixin CHN 2 Kuala Lumpur 1991 7 5 16.89 Aleksey Fatyanov AZE 1 Manila 1993 8 6 16.88 1.1 Kazuyoshi Ishikawa 2 Incheon 2005 9 7 16.82 Oleg Sakirkin KAZ 2 Manila 1993 10 8 16.79 Duan Qifeng CHN 1 Fukuoka 1998 11 9 16.78 Sergey Arzamasov KAZ 3 Manila 1993 11 9 16.78 Zheng Lizhi CHN 1 Djakarta 1995 11 16.78 -0.6 Kim Duk-Hyun 3 Incheon 2005 14 16.72 0.7 Kazuyoshi Ishikawa 1 Manila 2003 15 11 16.70 0.6 Roman Valiyev KAZ 1 Guangzhou 2009 16 12 16.68 Du Benzhong CHN 2 New Delhi 1989 16 16.68 Aleksey Fatyanov 2 Djakarta 1995 16 12 16.68 -0.4 Gu Junjie CHN 2 Manila 2003 19 14 16.67 0.7 Wu Ji CHN 3 Manila 2003 19 16.67 0.8 Roman Valiyev 1qB Incheon 2005 19 14 16.67 1.4 Zhu Shujing CHN 2 Guangzhou 2009 22 16 16.65 Nai Hui-Fang TPE 3 New Delhi 1989 23 17 16.61 Masami Nakanishi JPN 2 Tokyo 1981 23 17 16.61 -0.5 Salem Mouled Al-Ahmadi KSA 1 Colombo 2002 25 19 16.53 Vasif Asadov AZE 3 Djakarta 1995 25 19 16.53 0.4 Nattapol Nomkunha THA 1 Djakarta 2000 27 21 16.50 Takanori Sugibayashi JPN 2 Fukuoka 1998 28 22 16.49 0.1 Mohamad Hamdi Awadh QAT 4 Manila 2003 28 22 16.49 1.6 Yevgeniy Ektov KAZ 3 Guangzhou 2009 All time
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												  The Two Tontti Tudiul Lui Hi Ha UnitTHETWO TONTTI USTUDIUL 20170267753A1 LUI HI HA UNIT ( 19) United States (12 ) Patent Application Publication (10 ) Pub. No. : US 2017 /0267753 A1 Ehrenpreis (43 ) Pub . Date : Sep . 21 , 2017 ( 54 ) COMBINATION THERAPY FOR (52 ) U .S . CI. CO - ADMINISTRATION OF MONOCLONAL CPC .. .. CO7K 16 / 241 ( 2013 .01 ) ; A61K 39 / 3955 ANTIBODIES ( 2013 .01 ) ; A61K 31 /4706 ( 2013 .01 ) ; A61K 31 / 165 ( 2013 .01 ) ; CO7K 2317 /21 (2013 . 01 ) ; (71 ) Applicant: Eli D Ehrenpreis , Skokie , IL (US ) CO7K 2317/ 24 ( 2013. 01 ) ; A61K 2039/ 505 ( 2013 .01 ) (72 ) Inventor : Eli D Ehrenpreis, Skokie , IL (US ) (57 ) ABSTRACT Disclosed are methods for enhancing the efficacy of mono (21 ) Appl. No. : 15 /605 ,212 clonal antibody therapy , which entails co - administering a therapeutic monoclonal antibody , or a functional fragment (22 ) Filed : May 25 , 2017 thereof, and an effective amount of colchicine or hydroxy chloroquine , or a combination thereof, to a patient in need Related U . S . Application Data thereof . Also disclosed are methods of prolonging or increasing the time a monoclonal antibody remains in the (63 ) Continuation - in - part of application No . 14 / 947 , 193 , circulation of a patient, which entails co - administering a filed on Nov. 20 , 2015 . therapeutic monoclonal antibody , or a functional fragment ( 60 ) Provisional application No . 62/ 082, 682 , filed on Nov . of the monoclonal antibody , and an effective amount of 21 , 2014 . colchicine or hydroxychloroquine , or a combination thereof, to a patient in need thereof, wherein the time themonoclonal antibody remains in the circulation ( e . g . , blood serum ) of the Publication Classification patient is increased relative to the same regimen of admin (51 ) Int .
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												  Combination of 177Lu‐Lilotomab with Rituximab Significantly Improves TheReceived: 18 April 2018 | Accepted: 5 July 2018 DOI: 10.1111/ejh.13139 ORIGINAL ARTICLE Combination of 177Lu- lilotomab with rituximab significantly improves the therapeutic outcome in preclinical models of non- Hodgkin’s lymphoma Ada H. V. Repetto-Llamazares1 | Marion M. Malenge1,2,3 | Adam O’Shea1 | Bergthóra Eiríksdóttir4 | Trond Stokke2 | Roy H. Larsen5 | Jostein Dahle1 1Nordic Nanovector ASA, Oslo, Norway Abstract 2Department of Radiation Biology, Institute for Cancer Research, Oslo University Objectives: To investigate the therapeutic potential of the next- generation anti- CD37 ra- Hospital, Oslo, Norway dioimmunoconjugate 177Lu- lilotomab satetraxetan (177Lu- lilotomab) in combination with 3Institute of Clinical Medicine, Faculty of the anti- CD20 antibody rituximab for treatment of mice with non- Hodgkin’s lymphoma Medicine, University of Oslo, Oslo, Norway 4ArcticLAS Ltd. CRO, Reykjavík, Iceland (NHL) xenografts. 5Sciencons AS, Oslo, Norway Methods: Nude mice with subcutaneous (s.c.) Burkitt’s lymphoma Daudi xenografts and SCID mice intravenously (i.v.) injected with Mantle cell lymphoma Rec- 1 cells were Correspondence 177 Ada H. V. Repetto-Llamazares, Nordic treated with either Lu- lilotomab or rituximab alone or with the combination of both Nanovector ASA, Kjelsåsveien 168B, 0884 treatments. Tumour volume, body weight, blood counts and clinical status were moni- Oslo, Norway. Email: [email protected] tored. CD20 expression was measured using flow cytometry with fluorescence- labelled rituximab. Funding information 177 Norges Forskningsråd, Grant/Award Results: The combination of Lu- lilotomab and rituximab was synergistic for treat- Number: Industrial PhD program, project ment of nude mice with s.c. Daudi xenografts while it was additive for treatment of number 260203; Nordic Nanovector ASA SCID mice with i.v.
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												  “Villages” in Shenzhen Dissertation Bauhaus-Universität Weimar“Villages” in Shenzhen Persistence and Transformation of an Old Social System in an Emerging Mega City Dissertation Zur Erlangung des akademischen Grades Doktor-Ingenieur an der Fakultät Architektur der Bauhaus-Universität Weimar vorgelegt von M.Arch. Ma Hang Geboren am 25. April 1974 in Ji lin Weimar, 2006 Mentor: Prof.Dr. phil.habil. Dieter Hassenpflug “Villages” in Shenzhen Contents Acknowledgments .................................................................................VI Introduction ............................................................................................1 1 Study Background ..............................................................................11 1.1 Concepts of Villages in China ........................................................11 1.1.1 Traditional Villages in China ................................................... 11 1.1.2 Urbanization in China............................................................ 19 1.1.3 Current “Villages” in China .................................................... 25 1.2 Concepts of Villages in Shenzhen .................................................30 1.2.1 History of Villages in Shenzhen .............................................. 30 1.2.2 From a Fish Village to Chinese Mega City ................................. 32 1.2.3 “Villages” as an Urban Corporate Community ........................... 39 2 Persistence & Transformation of Social Structures.............................53 2.1 Composition of Population & Social Stratification .........................53
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												  The Use of Stems in the Selection of International Nonproprietary Names (INN) for Pharmaceutical Substances" WHO/EMP/RHT/TSN/2013.1INN Working Document 18.435 31/05/2018 Addendum1 to "The use of stems in the selection of International Nonproprietary names (INN) for pharmaceutical substances" WHO/EMP/RHT/TSN/2013.1 Programme on International Nonproprietary Names (INN) Technologies Standards and Norms (TSN) Regulation of Medicines and other health technologies (RHT) World Health Organization, Geneva © World Health Organization 2018 - All rights reserved. The contents of this document may not be reviewed, abstracted, quoted, referenced, reproduced, transmitted, distributed, translated or adapted, in part or in whole, in any form or by any means, without explicit prior authorization of the WHO INN Programme. This document contains the collective views of the INN Expert Group and does not necessarily represent the decisions or the stated policy of the World Health Organization. Addendum1 to "The use of stems in the selection of International Nonproprietary Names (INN) for pharmaceutical substances" - WHO/EMP/RHT/TSN/2013.1 1 This addendum is a cumulative list of all new stems selected by the INN Expert Group since the publication of "The use of stems in the selection of International Nonproprietary Names (INN) for pharmaceutical substances" 2013. ------------------------------------------------------------------------------------------------------------ -apt- aptamers, classical and mirror ones (a) avacincaptad pegol (113), egaptivon pegol (111), emapticap pegol (108), lexaptepid pegol (108), olaptesed pegol (109), pegaptanib (88) (b) -vaptan stem: balovaptan (116), conivaptan
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												  Vedlegg INSPIRE:Lungekreft 1 Virkestoff, Type Behandling, TilordningVedlegg INSPIRE:lungekreft 1 Virkestoff, type behandling, tilordning A B CD E G 1 Virkestoff_tilordning_mapping Virkestoff_fra sykehusene ATC-kode ATC nivå 2 ATC nivå 3 Type behandling_gruppert 2 Afatinib afatinib L01XE13 Antineoplastiske midler Andre antineoplastiske midler Proteinkinasehemmere 3 Aflibercept/Placebo Aflibercept/Placebo Ingen Utprøving 4 Alektinib alektinib L01XE36 Antineoplastiske midler Andre antineoplastiske midler Proteinkinasehemmere 5 Alemtuzumab ALEMTUZUMAB L04AA34 Immunsuppressiver Immunsuppressiver Immunterapi 6 Alemtuzumab Alemtuzumab L04AA34 Immunsuppressiver Immunsuppressiver Immunterapi 7 Alemtuzumab Alemtuzumab act-1 L04AA34 Immunsuppressiver Immunsuppressiver Immunterapi 8 Alemtuzumab Alemtuzumab HOVON 68 L04AA34 Immunsuppressiver Immunsuppressiver Immunterapi 9 Alemtuzumab zzz Alemtuzumab ACT-1-studien L04AA34 Immunsuppressiver Immunsuppressiver Immunterapi 10 Amphinex PCI A202 12 Amphinex PCI A202 12 Ingen Utprøving 11 Amphinex PCIA 203 18 Amphinex PCIA 203 18 Ingen Utprøving 12 Amsakrin AMSAKRIN L01XX01 Antineoplastiske midler Andre antineoplastiske midler Kjemoterapi 13 Amsakrin Amsakrin L01XX01 Antineoplastiske midler Andre antineoplastiske midler Kjemoterapi 14 Amsakrin Amsakrin HOVON 102 AML/SAKK L01XX01 Antineoplastiske midler Andre antineoplastiske midler Kjemoterapi 15 Antitymocytt immunglobulin Anti-human thym. imm. (Kanin) L04AA04 Immunsuppressiver Immunsuppressiver Immunterapi 16 Antitymocytt immunglobulin Anti-humant T-lymfocyt imm.globulin (ATG) (Kanin) L04AA04 Immunsuppressiver Immunsuppressiver
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												  Understanding Non-Hodgkin LymphomaUnderstanding Non-Hodgkin Lymphoma A Guide for Patients, Survivors, and Loved Ones July 2018 Lymphoma Research Foundation (LRF) Helpline and Clinical Trials Information Service CONTACT THE LRF HELPLINE Trained staff are available to answer questions and provide support to patients, caregivers and healthcare professionals in any language. Our support services include: • Information on lymphoma, treatment options, side effect management and current research fi ndings • Financial assistance for eligible patients and referrals for additional fi nancial, legal and insurance help • Clinical trial searches based on patient’s diagnosis and treatment history • Support through LRF’s Lymphoma Support Network, a national one-to one volunteer patient peer program Monday through Friday, Toll-Free (800) 500-9976 or email [email protected] Understanding Non-Hodgkin Lymphoma A Guide For Patients, Survivors, and Loved Ones July 2018 This guide is an educational resource compiled by the Lymphoma Research Foundation to provide general information on adult non- Hodgkin lymphoma. Publication of this information is not intended to replace individualized medical care or the advice of a patient’s doctor. Patients are strongly encouraged to talk to their doctors for complete information on how their disease should be diagnosed, treated, and followed. Before starting treatment, patients should discuss the potential benefits and side effects of cancer therapies with their physician. Contact the Lymphoma Research Foundation Helpline: (800) 500-9976 [email protected] Website: lymphoma.org This patient guide is supported through unrestricted educational grants from: © 2018 Lymphoma Research Foundation. Information contained herein is the property of the Lymphoma Research Foundation (LRF). Any portion may be reprinted or reproduced provided that LRF is acknowledged to be the source and the Foundation’s website (lymphoma.org) is included in the citation.