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【求助】AC2993一期、二期臨床研究申報資料
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| 跪求AC2993一期和二期臨床研究的申報資料,現(xiàn)要翻譯臨床研究有關(guān)增大劑量的副反應(yīng)、耐受性、安全性等的相關(guān)資料,可惜沒有電子版,本人英文能力有限,翻譯起來比較困難,最好有中文版的,不勝感激! |
work or phd? |
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Evaluation of the Effect on Glucose Control and Safety of AC2993 in Patients With Type 2 Diabetes Treated With Metformin, Sulfonylurea, or Metformin and Sulfonylurea Combination This study has been completed. First Received: September 3, 2002 Last Updated: November 5, 2007 History of Changes Sponsor: Amylin Pharmaceuticals, Inc. Collaborator: Eli Lilly and Company Information provided by: Amylin Pharmaceuticals, Inc. ClinicalTrials.gov Identifier: NCT00044668 Purpose This multi-center, open-label study is designed to examine the effects on long-term glucose control and safety of AC2993 in patients with type 2 diabetes treated with metformin, sulfonylurea, or metformin and sulfonylurea combination. Condition Intervention Phase Diabetes Mellitus, Type 2 Drug: AC2993 (synthetic exendin-4) Phase III Study Type: Interventional Study Design: Allocation: Non-Randomized Control: Uncontrolled Endpoint Classification: Safety/Efficacy Study Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Treatment Official Title: An Open-Label Study to Examine the Long-Term Effect on Glucose Control (HbA1c) and Safety of AC2993 Given Two Times a Day to Subjects With Type 2 Diabetes Treated With Metformin, a Sulfonylurea, or Metformin and Sulfonylurea Combination Resource links provided by NLM: MedlinePlus related topics: Diabetes Drug Information available for: Exenatide Metformin Metformin hydrochloride U.S. FDA Resources Further study details as provided by Amylin Pharmaceuticals, Inc.: Primary Outcome Measures: •*Examine long-term effect on glucose control of subcutaneously (SC) injected AC2993 administered twice a day (BID) in subjects with type 2 diabetes (T2DM);*Assess long-term safety of SC injected AC2993 administered BID in subjects with T2DM Secondary Outcome Measures: •*Examine long-term effect on various pharmacodynamic measurements of SC injected AC2993 administered BID in subjects with T2DM. Estimated Enrollment: 150 Study Start Date: August 2002 Eligibility Ages Eligible for Study: 20 Years to 75 Years Genders Eligible for Study: Both Accepts Healthy Volunteers: No Criteria Inclusion Criteria: •Subjects with type 2 diabetes •Treated for at least 3 months prior to screening either with metformin, sulfonylurea, or metformin and sulfonylurea combination •BMI 25-45 kg/m^2 •HbA1c between 7.5 % and 12.0 %, inclusive Exclusion Criteria: •Treated with other oral anti-diabetic agents other than metformin and sulfonylureas within 3 months of screening •Patients previously treated with AC2993 •Patients presently treated with insulin Contacts and Locations Please refer to this study by its ClinicalTrials.gov identifier: NCT00044668 Locations Hungary Peterfy Teaching Hospital Budapest, Hungary, H 1076 Diagnostic Units Hungary Kft. Budapest, Hungary, H 1036 Uzsoki Street Municipal Hospital Budapest, Hungary, H 1145 Sponsors and Collaborators Amylin Pharmaceuticals, Inc. Eli Lilly and Company Investigators Study Director: Lisa Porter, MD Amylin Pharmaceuticals, Inc. More Information Additional Information: Link to study results on ClinicalStudyResults.org No publications provided ClinicalTrials.gov Identifier: NCT00044668 History of Changes Other Study ID Numbers: 2993-117 Study First Received: September 3, 2002 Last Updated: November 5, 2007 Health Authority: United States: Food and Drug Administration; Hungary: National Institute of Pharmacy Keywords provided by Amylin Pharmaceuticals, Inc.: exenatide exendin-4 diabetes Amylin Lilly Additional relevant MeSH terms: Diabetes Mellitus Diabetes Mellitus, Type 2 Glucose Metabolism Disorders Metabolic Diseases Endocrine System Diseases Exenatide Metformin Hypoglycemic Agents Physiological Effects of Drugs Pharmacologic Actions |
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http://clinicaltrials.gov/ct2/results?term=AC2993 樓主看下這個帖子吧,英語還是自己翻譯吧,可以鍛煉一下水平,翻譯兩三次你就都熟悉了! 希望對你有幫助! |
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