CCTN - CONTRACEPTIVE CLINICAL TRIALS NETWORK - CORE - FEMALE
CCTN - CONTRACEPTIVE CLINICAL TRIALS NETWORK - CORE - FEMALE
批准号:
8891278
负责人:
LIVIA WAN
金额:
$2.97万
依托单位国家:
美国
项目类别:
财政年份:
2013
资助国家:
美国
项目状态:
已结题
起止时间:
2013-06-26 至 2015-06-25
关键词:
Basic ScienceChemicalsChildChild health careClinical ResearchClinical TrialsClinical Trials NetworkContraceptive AgentsContraceptive methodsContractsDevelopmentDevicesDrug FormulationsEpidemiologic StudiesFemaleFemale Contraceptive AgentsGoalsGrantGynecologicHealth educationHuman DevelopmentInstitutesLeadLeiomyomaMale Contraceptive AgentsMethodsNational Institute of Child Health and Human DevelopmentPharmaceutical PreparationsPhasePopulation ResearchReproductive HealthSafetySiteSocial WelfareTestingUnited States National Institutes of Healthbaseclinical research siteclinical trial phase II/III/IVdrug candidateendometriosispre-clinicalsynthetic peptide
中文摘要
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英文摘要
The National Institutes of Health (NIH), Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), is the lead Federal agency for the conduct of basic, clinical research to develop new contraceptives and to evaluate existing methods of contraception and reproductive health. The Center for Population Research (CPR), within NICHD, was established in 1968 by the Secretary of Health Education and Welfare, with the important goal of developing new
contraceptives through the use of contracts and grants. Within CPR, the Contraception and Reproductive Health Branch (CRHB) has long supported several preclinical contraceptive testing facilities as well as facilities for synthetic chemical and synthetic peptide formulation.
To further expand their contraceptive development capabilities, in 1996 CRHB established the NICHD Contraceptive Clinical Trials Network (CCTN). The current CCTN has conducted Phase I, II, and III clinical trials of both female and male contraceptive methods.
With the recompetition of the CCTN, clinical sites will perform Phase I, II, III, and Phase IV clinical trials of a wide variety of new or existing female contraceptive methods.
The purpose of this contract is to systematically evaluate the safety and efficacy of new female contraceptive drugs and devices as well as gynecologic conditions, such as endometriosis or leiomyoma, in Phase I, II, III, and IV trials
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