Advancing New Drug Regimens for MDR/XDR TB
Advancing New Drug Regimens for MDR/XDR TB
批准号:
8274822
负责人:
ERIC L NUERMBERGER
金额:
$42.7万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-06-15 至 2014-05-31
关键词:
AcademiaAnimal ModelAntimycobacterial AgentsBacteriaBacterial ProteinsBiological ModelsCarbapenemsCell Culture SystemCell Culture TechniquesCell WallCharacteristicsChronicClavulanateClinicalClinical TrialsCultured CellsDataDevelopmentDoseDrug CombinationsDrug KineticsDrug Resistant TuberculosisDrug resistanceDrug resistance in tuberculosisDrug usageDrug-sensitiveEmergency SituationEnsureEthambutolEthylenediaminesExtreme drug resistant tuberculosisFutureGoalsHumanImipenemIn VitroInfectionInstitutionLaboratoriesLactamaseLiquid substanceMarketingMeasuresMeropenemModelingMusMycobacterium tuberculosisNew AgentsOralOxazolidinonesPharmaceutical PreparationsPharmacologic SubstancePlasmaPreventionProdrugsProgram DevelopmentProtein BiosynthesisProtein Synthesis InhibitorsRegimenRelapseResistanceStagingSterilizationTechniquesTestingTissuesTuberculosisVertebral columnWhole BloodWorld Healthcombatdrug candidatedrug developmentextracellularglobal healthimprovedinhibitor/antagonistinnovationkillingsmathematical modelmembermouse modelnovelpharmacodynamic modelpreventresearch studyresistant strainsuccesstuberculosis drugstuberculosis treatment
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The global emergence of highly drug resistant tuberculosis (MDR and XDR TB) poses a serious and growing threat to world health. New classes of TB drugs are urgently needed to combat these infections, but new regimens comprised of 2 or more members of such new classes of TB drugs are thought to have the greatest chances of long-term success. The current paradigm is to study new drugs individually, but this does not inform the development of new regimens. Moreover, the perceived lack of a viable market has deterred many companies from developing new drugs for TB. This project is a unique partnership between big pharma, biotech and academia that will examine a novel 3-drug combination of new agents in which 2 drugs attack different components of the bacterial cell wall and the third blocks bacterial protein synthesis. Two of the drugs are currently in separate clinical development programs for a TB indication. The third is in clinical development for indications other than TB and would not likely be developed for TB without independent support. This proposed drug combination will be studied intensively to with regard its ability to rapidly kill TB bacteria and prevent emergence of resistance. These characteristics as well as the optimal combinations and dosing regimens will be determined using innovative liquid culture and cell culture systems and a well established mouse model in an effort integrated with sophisticated mathematical modeling techniques. Additional new agents in clinical development may be incorporated as the project evolves. The goal is to identify potent drug combinations that are likely to be safe and effective and that could be subsequently tested in human clinical trials.
New drug regimens comprised of 2 or more new drug classes are urgently needed to combat the serious and growing global health emergency posed by highly drug resistant tuberculosis (MDR and XDR TB). This project proposes a unique partnership between a major pharmaceutical company, a small biotech company and 2 academic institutions to examine a novel combination of 3 new agents expected to have a synergistic killing effect against TB bacteria. The goal is to identify potent drug combinations that are likely to be safe and effective and that could be subsequently tested in human clinical trials.
期刊论文(6)
专著(0)
科研奖励(0)
会议论文
Reply to Seddon, Schaaf, and Hesseling.
回复 Seddon、Schaaf 和 Hesseling。
DOI:
10.1093/cid/cis820
发表时间:
2013
期刊:
Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
影响因子:
--
作者:
[Dooley,KellyE, Mitnick,Carole, Degroote,MaryAnn, Obuku,Ekwaro, Hamilton,CarolD, Makhene,Mamodikoe, Shah,Sarita, Brust,JamesCM, Durakovic,Nadza, Nuermberger,Eric, EfficacySubgroup,RESIST-TB]
通讯作者:
EfficacySubgroup,RESIST-TB
High-dose fluoroquinolones in short-course regimens for treatment of MDR-TB: the way forward?
高剂量氟喹诺酮类药物短程治疗耐多药结核病:前进之路?
DOI:
10.5588/ijtld.13.0301
发表时间:
2013
期刊:
The international journal of tuberculosis and lung disease : the official journal of the International Union against Tuberculosis and Lung Disease
影响因子:
--
作者:
[Yew,Wing-Wai, Nuermberger,Eric]
通讯作者:
Nuermberger,Eric
Pharmacology and Pharmacometrics Core
-
批准号:10593158
-
项目类别:
-
资助金额:$12.73万
-
财政年份:2022
-
负责人:ERIC L NUERMBERGER
-
依托单位:
Harnessing potent next-generation diarylquinolines for long-acting injectable formulations to prevent and treat tuberculosis
-
批准号:10437843
-
项目类别:
-
资助金额:$63.12万
-
财政年份:2021
-
负责人:ERIC L NUERMBERGER
-
依托单位:
Harnessing potent next-generation diarylquinolines for long-acting injectable formulations to prevent and treat tuberculosis
-
批准号:10631987
-
项目类别:
-
资助金额:$61.77万
-
财政年份:2021
-
负责人:ERIC L NUERMBERGER
-
依托单位:
JHU- Optimal regimen development on a Ribosome inhibitor backbone.
-
批准号:10388415
-
项目类别:
-
资助金额:$85.09万
-
财政年份:2019
-
负责人:ERIC L NUERMBERGER
-
依托单位:
JHU- Optimal regimen development on a Ribosome inhibitor backbone.
-
批准号:10595587
-
项目类别:
-
资助金额:$54.64万
-
财政年份:2019
-
负责人:ERIC L NUERMBERGER
-
依托单位:
Development of novel penems for drug-resistant tuberculosis
-
批准号:10320850
-
项目类别:
-
资助金额:$74.58万
-
财政年份:2018
-
负责人:ERIC L NUERMBERGER
-
依托单位:
Development of novel penems for drug-resistant tuberculosis
-
批准号:10077824
-
项目类别:
-
资助金额:$75.9万
-
财政年份:2018
-
负责人:ERIC L NUERMBERGER
-
依托单位:
Closing the Gaps on Buruli Ulcer Diagnosis, Treatment, and Prevention
-
批准号:9030108
-
项目类别:
-
资助金额:$94.57万
-
财政年份:2015
-
负责人:ERIC L NUERMBERGER
-
依托单位:
Advancing New Drug Regimens for MDR/XDR TB
-
批准号:7988845
-
项目类别:
-
资助金额:$38.98万
-
财政年份:2010
-
负责人:ERIC L NUERMBERGER
-
依托单位:
Advancing New Drug Regimens for MDR/XDR TB
-
批准号:8089314
-
项目类别:
-
资助金额:$42.17万
-
财政年份:2010
-
负责人:ERIC L NUERMBERGER
-
依托单位:
Defining Moxifloxacin as a First-line TB Drug
-
批准号:7241463
-
项目类别:
-
资助金额:$12.93万
-
财政年份:2004
-
负责人:ERIC L NUERMBERGER
-
依托单位:
Defining Moxifloxacin as a First-line TB Drug
-
批准号:6899907
-
项目类别:
-
资助金额:$11.77万
-
财政年份:2004
-
负责人:ERIC L NUERMBERGER
-
依托单位:
Defining Moxifloxacin as a First-line TB Drug
-
批准号:7428881
-
项目类别:
-
资助金额:$12.93万
-
财政年份:2004
-
负责人:ERIC L NUERMBERGER
-
依托单位:
Defining Moxifloxacin as a First-line TB Drug
-
批准号:7060036
-
项目类别:
-
资助金额:$12.93万
-
财政年份:2004
-
负责人:ERIC L NUERMBERGER
-
依托单位:
Defining Moxifloxacin as a First-line TB Drug
-
批准号:6757621
-
项目类别:
-
资助金额:$11.69万
-
财政年份:2004
-
负责人:ERIC L NUERMBERGER
-
依托单位:
JHU- Optimal regimen development on a Ribosome inhibitor backbone.
-
批准号:9904485
-
项目类别:
-
资助金额:$50.51万
-
财政年份:--
-
负责人:ERIC L NUERMBERGER
-
依托单位:
海外基金