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/vufind/Search/Results?filter%5B%5D=format_facet%3A%22Gedruckte+Aufs%C3%A4tze%22&lookfor=%22ClinicalTrials.gov%22&type=JournalTitle&page=11
/vufind/Search/Results?filter%5B%5D=format_facet%3A%22Gedruckte+Aufs%C3%A4tze%22&lookfor=%22ClinicalTrials.gov%22&type=JournalTitle&page=11
Search /vufind/Search2/Results?filter%5B%5D=format_facet%3A%22Gedruckte+Aufs%C3%A4tze%22&lookfor=%22ClinicalTrials.gov%22&type=JournalTitle&page=11
PubPharm (242)
101
Antiviral activity and safety of LB80380 in hepatitis B e antigen-positive chronic hepatitis B patients with lamivudine-resistant diseaseThis study has been registered (registration number NCT00895596) in ClinicalTrials.gov (URL http://clinicaltrials.gov/ct2/show/NCT00895596?term=LB80380&rank=1).This study was supported by LG Life Sciences which also provided the drug LB80380. The data collection and data report were carried out by an independent data management company, Covance Pty Limited, Australia. The analysis and the writing of the manuscript were mainly performed by the first two authors as well as the corresponding author. The drug company employees read and commented on the manuscript, and gave their approval.Potential conflicts of interest: M. F. Y. and C. L. L. have received speakers' honoraria from LG Life Sciences. H. R. K. and C. R. K. are full-time employees of LG Life Sciences. J. K. is a former employee of LG Life Sciences.Correction added after online publication 20 January 2010: Dr. Kwang-
enthalten in:
Hepatology
| 2010
von
Griffiths, W.
|
Mayr, R.
|
McFarlane, I.
| +4
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102
Long-term efficacy of rosiglitazone in nonalcoholic steatohepatitis: Results of the fatty liver improvement by rosiglitazone therapy (FLIRT 2) extension trialMembers of the LIDO Study Group are listed in the acknowledgments.ClinicalTrial.gov identifier number: NCT00492700.Conflict of interest: This was an investigator initiated trial and GlaxoSmithKline Pharmaceuticals had no direct or indirect involvement in the design of the trial, data collection or preparation, or submission of the article. GSK provided rosiglitazone for this trial and partly funded the trial. None of the authors has a personal conflict of interest with the manufacturers of any of the marketed glitazones. V.R. is a consultant to Astellas, Axcan, Gilead, Genentech, Intercept, and Sanofi-Aventis. T.P. is a consultant for and owns 15% of Biopredictive, a company that markets FibroTest and SteatoTest. These conflicts of interest have been disclosed to study participants.
enthalten in:
Hepatology
| 2010
von
Chapman, R.
|
Fevery, J.
|
Kalloo, A.
| +4
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103
Methotrexate polyglutamate concentrations are not associated with disease control in rheumatoid arthritis patients receiving long-term methotrexate therapyClinicalTrials.gov identifier: ACTRN012606000275561.
enthalten in:
Arthritis & rheumatism
| 2010
von
Stamp, L.
|
O'Donnell, J.
|
Chapman, P.
| +4
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104
Tocilizumab in systemic lupus erythematosus: Data on safety, preliminary efficacy, and impact on circulating plasma cells from an open-label phase I dosage-escalation studyClinicalTrials.gov identifier: NCT00046774.
enthalten in:
Arthritis & rheumatism
| 2010
von
Illei, G.
|
Shirota, Y.
|
Yarboro, C.
| +6
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105
Rapid and sustained improvement in bone and cartilage turnover markers with the anti-interleukin-6 receptor inhibitor tocilizumab plus methotrexate in rheumatoid arthritis patients with an inadequate response to methotrexate: Results from a substudy of the multicenter double-blind, placebo-controlled trial of tocilizumab in inadequate responders to methotrexate aloneClinicalTrials.gov identifier: NCT00106548. EudraCT database no. 2004/00374/40.
enthalten in:
Arthritis & rheumatism
| 2010
von
Maciejewska-Rodrigues, H.
|
Al-Shamisi, M.
|
Hemmatazad, H.
| +13
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106
Immunization responses in rheumatoid arthritis patients treated with rituximab: Results from a controlled clinical trialClinicalTrials.gov identifier: NCT00282308.
enthalten in:
Arthritis & rheumatism
| 2010
von
Auger, I.
|
Martin, M.
|
Balandraud, N.
| +1
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107
Effect of long-term belimumab treatment on b cells in systemic lupus erythematosus: Extension of a phase II, double-blind, placebo-controlled, dose-ranging studyClinicalTrials.gov identifier: NCT00071487.
enthalten in:
Arthritis & rheumatism
| 2010
von
Neven, B.
|
Marvillet, I.
|
Terrada, C.
| +10
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108
Nonrenal disease activity following mycophenolate mofetil or intravenous cyclophosphamide as induction treatment for lupus nephritis: Findings in a multicenter, prospective, randomized, open-label, parallel-group clinical trialClinicalTrials.gov identifier: NCT00377637. This is protocol WX17801 from the Aspreva Lupus Management Study Group (see Appendix A for principal investigators and study centers).
enthalten in:
Arthritis & rheumatism
| 2010
von
Brigitte, M.
|
Schilte, C.
|
Plonquet, A.
| +7
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109
Efficacy and safety of rituximab in moderately-to-severely active systemic lupus erythematosus: The randomized, double-blind, phase ii/iii systemic lupus erythematosus evaluation of rituximab trialClinicalTrials.gov identifier: NCT00137969.
enthalten in:
Arthritis & rheumatism
| 2010
von
Reich, N.
|
Maurer, B.
|
Akhmetshina, A.
| +10
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110
ClinicalTrials.gov: A Questionnaire of Industry Experiences and Perceptions
enthalten in:
Drug information journal
| 2010
von
McCarthy, K.
|
Godlew, B.
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