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— The Pharmaceutical and Healthcare latest pipeline guide Obesity Pipeline Review, H1 2017, provides comprehensive information on the therapeutics under development for Obesity (Metabolic Disorders), complete with analysis by stage of development, drug target, mechanism of action (MoA), route of administration (RoA) and molecule type. The guide covers the descriptive pharmacological action of the therapeutics, its complete research and development history and latest news and press releases. Browse Obesity Therapeutic Pipeline report has 96 Company Profiles, 154 Tables and 11 Figures, Spread across 495 Pages Report Available at http://www.rnrmarketresearch.com/obesity-pipeline-review-h1-2017-market-report.html . Main companies of Obesity Therapeutic Pipeline - Abeome Corp, Adamas Pharmaceuticals Inc, Advinus Therapeutics Ltd, Aegis Therapeutics LLC, Akron Molecules AG, Alize Pharma SAS, Amabiotics SAS, Amgen Inc, Aoxing Pharmaceutical Company Inc, Arrowhead Pharmaceuticals Inc, AstraZeneca Plc, Asubio Pharma Co Ltd, Athersys Inc, Biophytis SAS, BioRestorative Therapies Inc, Biozeus, Boehringer Ingelheim GmbH, Braasch Biotech LLC, C3J Therapeutics Inc, Camurus AB, Carmot Therapeutics Inc, CohBar Inc, CoMentis Inc, Connexios Life Sciences Pvt Ltd, ConSynance Therapeutics Inc, Corium International Inc, Daiichi Sankyo Company Ltd, DiscoveryBiomed Inc, Eisai Co Ltd, Eli Lilly and Company, Esperion Therapeutics Inc, Eternygen GmbH, Evotec AG, F. Hoffmann-La Roche Ltd, FibroGen Inc, Genmedica Therapeutics SL, Gila Therapeutics Inc, Gilead Sciences Inc, GlaxoSmithKline Plc, Glucox Biotech AB, GTx Inc, HanAll Biopharma Co Ltd, Hanmi Pharmaceuticals Co Ltd, Hyundai Pharmaceutical Co Ltd, Immungenetics AG, Intarcia Therapeutics Inc, Ionis Pharmaceuticals Inc, Ixchel Pharma LLC, Jenrin Discovery Inc, Johnson & Johnson, Laboratorios Silanes SA de CV, Lead Discovery Center GmbH, Leading BioSciences Inc, Lotus Pharmaceutical Co Ltd, M Pharmaceutical Inc, Magnus Life Ltd, MedImmune LLC, Merck & Co Inc, Mitochon Pharmaceuticals Inc, Mitsubishi Tanabe Pharma Corp, NeuroNano Pharma Inc, NGM Biopharmaceuticals Inc, NIBEC, Nordic Bioscience A/S, Novartis AG, Discount Available at http://www.rnrmarketresearch.com/contacts/discount?rname=1019680 (This report is available at upto 25% Discount till June 02nd 2017.) The Obesity (Metabolic Disorders) pipeline guide also reviews of key players involved in therapeutic development for Obesity and features dormant and discontinued projects. The guide covers therapeutics under Development by Companies /Universities /Institutes, the molecules developed by Companies in Phase III, Phase II, Phase I and Preclinical stages are 1, 1, 1 and 4 respectively. Similarly, the Universities portfolio in Preclinical and Discovery stages comprises 3 and 2 molecules, respectively. Scope - The pipeline guide provides a snapshot of the global therapeutic landscape of Obesity (Metabolic Disorders). The pipeline guide reviews pipeline therapeutics for Obesity (Metabolic Disorders) by companies and universities/research institutes based on information derived from company and industry-specific sources. The pipeline guide covers pipeline products based on several stages of development ranging from pre-registration till discovery and undisclosed stages. The pipeline guide features descriptive drug profiles for the pipeline products which comprise, product description, descriptive licensing and collaboration details, R&D brief, MoA & other developmental activities. The pipeline guide reviews key companies involved in Obesity (Metabolic Disorders) therapeutics and enlists all their major and minor projects. The pipeline guide evaluates Obesity (Metabolic Disorders) therapeutics based on mechanism of action (MoA), drug target, route of administration (RoA) and molecule type. The pipeline guide encapsulates all the dormant and discontinued pipeline projects. The pipeline guide reviews latest news related to pipeline therapeutics for Obesity (Metabolic Disorders) Order a copy of this research report at http://www.rnrmarketresearch.com/contacts/purchase?rname=1019680 Table of Contents: Introduction Obesity - Overview Obesity - Therapeutics Development Obesity - Therapeutics Assessment Obesity - Companies Involved in Therapeutics Development Obesity - Drug Profiles Obesity - Dormant Projects Obesity - Discontinued Products Obesity - Product Development Milestones Appendix List of Tables. List of Figures. About Us: RnRMarketResearch.com is your single source for all market research needs. Our database includes 500,000+ market research reports from over 100+ leading global publishers & in-depth market research studies of over 5000 micro markets. With comprehensive information about the publishers and the industries for which they publish market research reports, we help you in your purchase decision by mapping your information needs with our huge collection of reports. Call +1 888 391 5441 with your research requirements or email the details at sales@rnrmarketresearch.com For more information, please visit http://www.rnrmarketresearch.com/obesity-pipeline-review-h1-2017-market-report.html


Thamizhselvi R.K.,Advinus Therapeutics Pvt. Ltd
Indian Journal of Animal Sciences | Year: 2010

A study of 49 contract broiler farmers under 4 leading integrators in and around Puducherry revealed that the contract is one sided favouring the integrator as the contract stipulates standards for the outputs from the farmer but it does not specify any standards for the inputs the integrator supplies such as weight of the day-old chick, quality standards for feed and medicines. The findings also indicated that the weight of the day-old chicks supplied was less than the standard weight of 40 g, an important cause for low body weight gain as well as high mortality. Although the integrators are bearing the risk of production and marketing, the contract broiler farming is exploitative as the integrators are paying on an average 4.61/bird, mostly on the basis of production cost. The integrators may do well by bearing the cost of the miscellaneous inputs being provided by the farmers and by taking feed conversion ratio as the basis for payment rather than production cost on which the farmer has very little control.


Gopinath V.S.,Advinus Therapeutics Pvt. Ltd. | Pinjari J.,Advinus Therapeutics Pvt. Ltd. | Dere R.T.,Advinus Therapeutics Pvt. Ltd. | Verma A.,CSIR - Central Electrochemical Research Institute | And 11 more authors.
European Journal of Medicinal Chemistry | Year: 2013

An analogous library of 2-substituted quinoline compounds was synthesized with the aim to identify a potential drug candidate to treat visceral leishmaniasis. These molecules were tested for their in vitro and in vivo biological activity against Leishmania donovani. Metabolic stability of these compounds was also improved through the introduction of halogen substituents. Compound (26g), found to be the most active; exhibited an IC50 value of 0.2 μM and >180 fold selectivity. The hydrochloride salt of (26g) showed 84.26 ± 4.44 percent inhibition at 50 mg/kg × 5 days (twice daily, oral route) dose in L. donovani/hamster model. The efficacy was well correlated with the PK data observed which indicating that the compound is well distributed. © 2013 Elsevier Masson SAS. All rights reserved.


Sridhara A.M.,Advinus Therapeutics Pvt. Ltd. | Sridhara A.M.,Kuvempu University | Venugopala Reddy K.R.,Kuvempu University | Keshavayya J.,Kuvempu University | And 5 more authors.
European Journal of Medicinal Chemistry | Year: 2010

A series of new 2-substituted [4-(1,3,4-oxadiazol-2-yl)methyl]phthalazin- 1(2H)-one derivatives 7a-h to 9a-h were designed and synthesized from methyl (4-oxo-3,4-dihydrophthalazin-1-yl)acetate (4), which in was turn prepared from phthalic anhydride. The structure of synthesized new compounds were characterized by spectral data and screened for their antimicrobial activities against various bacteria and fungi strains. Several of these compounds showed antimicrobial activity. © 2010 Elsevier Masson SAS. All rights reserved.


Basavaiah K.,University of Mysore | Tharpa K.,University of Mysore | Vinay K.B.,Advinus Therapeutics Pvt. Ltd.
Ecletica Quimica | Year: 2010

Four simple titrimetric procedures are described for the determination of lisinopril (LNP) in bulk and in pharmaceuticals based on the neutralization of basic-amino and acidic carboxylic acid groups present in LNP. Method A is based on the neutralization of basic amino groups using perchloric acid as titrant in anhydrous acetic acid medium. Method B, method C and method D are based on neutralization of carboxylic acid group using NaOH, sodium methoxide and methanolic KOH, as titrants, respectively. Method A is applicable over 2.0-20.0 mg range and the calculations are based in the molar ratio of 1:2 (LNP:HClO4). Method B, method C and method D are applicable over 2.0-20.0 mg, 1.0-10.0 mg and 5.0-15.0 mg range, respectively, and their respective molar ratios are 1:1 (LNP:NaOH), 1:2 (LNP:CH3ONa) and 1:1 (LNP:KOH). Intraday and inter day accuracy and precision of the methods were evaluated and the results showed intra- and inter-day precision less than 2.7% (RSD), and accuracy of < 2.5 % (RE). The developed methods were applied to determine LNP in tablets and the results were validated statistically by comparing the results with those of the reference method by applying the Student's t-test and F-test. The accuracy was further ascertained by recovery studies via standard addition technique. No interferences from common tablet exipients was observed.


Singh U.P.,Indian Institute of Science | Singh U.P.,Advinus Therapeutics Pvt. Ltd.
Journal of Molecular Structure | Year: 2010

Structure of a cyclic water tetramer in channels (pores) formed by self-assembly of N6-methyl-5′-AMP·Na2 molecules is described and a hypothetical model is proposed for growth of water clusters. © 2010 Elsevier B.V. All rights reserved.


Tiwari A.,Advinus Therapeutics Pvt. Ltd.
Drugs of the Future | Year: 2012

Luseogliflozin (TS-071), developed by Taisho Pharmaceutical, is a novel, potent sodium/glucose cotransporter 2 (SGLT2) inhibitor for the potential treatment of type 2 diabetes (T2D) and type 1 diabetes (T1D). Luseogliflozin exhibits high selectivity for SGLT2 over SGLT1 and the glucose transporters GLUT2 and GLUT4, with favorable pharmacokinetic and pharmacodynamic properties. Luseogliflozin exhibited increased urinary glucose excretion, with improved glucose tolerance and a significant reduction in fasting plasma glucose and postprandial plasma glucose, with body weight loss after chronic treatment in different animal models of diabetes and without an increase in plasma insulin. Clinical data in Japanese patients demonstrated that luseogliflozin was orally bioavailable, with a prolonged half-life, suitability for once-daily dosing and effective in significantly reducing glycated hemoglobin and fasting plasma glucose, with body weight loss. Luseogliflozin was well tolerated, without the risk of hypoglycemia and clinically meaningful changes in urinary volume, electrolyte excretion and renal function. The results from phase III clinical trials in T2D and T1D patients will be pivotal; however, the available data suggest that luseogliflozin has potential for success in this niche market segment. Copyright © 2012 Prous Science, S.A.U. or its licensors. All rights reserved.


Hajare A.K.,Advinus Therapeutics Pvt. Ltd | Datrange L.S.,Advinus Therapeutics Pvt. Ltd | Vyas S.,Advinus Therapeutics Pvt. Ltd | Bhuniya D.,Advinus Therapeutics Pvt. Ltd | Reddy D.S.,Advinus Therapeutics Pvt. Ltd
Tetrahedron Letters | Year: 2010

An efficient synthesis of an enantiomer of insect's natural pheromone is reported starting from chiral pool d-(-)-pantolactone. Highly stereoselective tandem conjugate addition/cyclization sequence and hydrogenation of exocyclic double bond are the key steps in the present synthesis. © 2010 Elsevier Ltd. All rights reserved.


Sulaiman S.M.,Dr. M.G.R. Educational and Research Institute | Rajashekhar G.,Dr. M.G.R. Educational and Research Institute | Prakash P.J.,Dr. M.G.R. Educational and Research Institute | Singh D.S.,Advinus Therapeutics Pvt Ltd. | Saleem C.,Advinus Therapeutics Pvt Ltd.
Journal of Pharmacology and Toxicology | Year: 2010

Immunol, a polyherbal formulation was evaluated for its safety and effect on the immune system of rats. The rats were administered a single oral dose of 20 mL kg-1 b.wt. while others were given repeated doses of 1, 5 and 10 mL kg-1 b.wt., orally for 28 days. Immunol treatment did not elicit any abnormalities on the body weight gain, food consumption, neurological assessment, hematology and clinical chemistry parameters, organ weights, gross organ pathology and histopathology and humoral immunity, but it enhanced the cell mediated immunity. It was concluded that Immunol was safe at single oral dose of 20 mL kg-1 b.wt. and repeated dose of 10 mL kg-1 b.wt. in rats for 28 days. © 2010 Academic Journals Inc.


PubMed | Advinus Therapeutics Pvt. Ltd.
Type: | Journal: European journal of medicinal chemistry | Year: 2013

An analogous library of 2-substituted quinoline compounds was synthesized with the aim to identify a potential drug candidate to treat visceral leishmaniasis. These molecules were tested for their in vitro and in vivo biological activity against Leishmania donovani. Metabolic stability of these compounds was also improved through the introduction of halogen substituents. Compound (26g), found to be the most active; exhibited an IC value of 0.2 M and >180 fold selectivity. The hydrochloride salt of (26g) showed 84.26 4.44 percent inhibition at 50 mg/kg 5 days (twice daily, oral route) dose in L. donovani/hamster model. The efficacy was well correlated with the PK data observed which indicating that the compound is well distributed.

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