Preclinical Testing of Human Ghrelin and Growth Hormone for Sepsis in the Elderly
Preclinical Testing of Human Ghrelin and Growth Hormone for Sepsis in the Elderly
批准号:
9346602
负责人:
Weng-Lang Yang
金额:
$54.04万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2014
资助国家:
美国
项目状态:
已结题
起止时间:
2014-06-15 至 2019-05-31
关键词:
AftercareAge-YearsAnatomyAnimalsAntisepsisArea Under CurveAttenuatedBacterial TranslocationBloodCardiac OutputCause of DeathCessation of lifeClinicalClinical TrialsCombined Modality TherapyCreatinineDataDoseDrug KineticsElderlyFDA approvedFailureFunctional disorderFundingFutureGoalsHeartHeart RateHepaticHistologicHormonesHumanInbred F344 RatsInflammationInflammatoryInjection of therapeutic agentInjuryInterleukin-1 betaInterleukin-6IntravenousKidneyLethal Dose 50LigationLiverLungMaximum Tolerated DoseModelingMonitorNerveNormal salineOrganOutcomePatientsPerfusionPeripheral ResistancePharmaceutical PreparationsPharmacotherapyPhasePhysiologicalPreclinical TestingPseudomonas aeruginosaPuncture procedureRattusSafetySepsisSeptic ShockSheepSmall Business Innovation Research GrantSmall IntestinesSmoke Inhalation InjurySomatotropinSomatropinStroke VolumeSurvival RateTNF geneTestingTherapeuticTimeTissuesToxic effectUnited Statesagedbasecytokinedrug candidateeffective therapyghrelinhemodynamicshormone therapyhuman old age (65+)improvedjuvenile animalmalenovelolder patientphase 1 studypreclinical evaluationpressurepublic health relevancereceptorrespiratoryresponseseptic
中文摘要
项目描述:该SBIR第二阶段提案旨在进一步开发人生长激素释放肽
(hGhr)和人生长激素(hGH)作为脓毒症老年患者的联合治疗,
败血性休克在美国,每年有超过100万人患败血症,近80%的败血症患者
死亡发生在65岁以上的患者中。目前,没有有效的药物治疗存在
脓毒症的治疗脓毒症临床试验失败的原因之一是,
抗败血症药物候选物仅在幼小动物中进行。例如,Rat Ghr,
改善了年轻而非老年大鼠的脓毒症。我们已经发现,GH的管理上调,
Ghr受体的表达,并恢复脓毒症老年动物Ghr的反应性。在我们
完成SBIR I期项目,hGhr和hGH联合给药(hGhr-hGH)显著改善
脓毒症老年动物中脓毒症相关的肺、肝和肾损伤。我们进一步证明,
联合治疗几乎使脓毒症老年大鼠的存活率加倍。此外,hGH和hGH
已经过临床测试,并用于其他适应症,具有良好的安全性。基于我们
I期结果,我们假设hGhr-hGH可以进一步发展为脓毒症的有效治疗方法
在老年人中。为了推进hGhr-hGH治疗在老年人脓毒症的临床应用,我们计划
以确定联合治疗的最有效剂量和治疗窗口,
伤害和提高生存率。我们还将研究hGhr-hGH对安全性和耐受性的联合作用。
药代动力学(PK)。最后,我们将在绵羊脓毒症模型中进行探索性研究,以评估
hGhr-hGH对血流动力学参数和器官损伤的影响。这些拟议的研究应提供
为今后提交IND申请以在临床试验中进一步开发hGhr-hGH提供重要信息。
我们的最终目标是获得FDA批准使用hGhr-hGH作为安全有效的治疗方法,
老年脓毒症和脓毒性休克患者。
英文摘要
PROJECT DESCRIPTION: This SBIR Phase II proposal is intended to further develop human ghrelin
(hGhr) and human growth hormone (hGH) as a combination therapy for elderly patients with sepsis and
septic shock. In the US, more than one million people develop sepsis every year, and nearly 80% of septic
deaths occur in patients older than 65 years of age. Currently, no effective pharmacotherapy exists for the
treatment of sepsis. One of the reasons for sepsis clinical trial failures is that the preclinical evaluation of
anti-sepsis drug candidates has been conducted exclusively in young animals. Rat Ghr, for example,
ameliorates sepsis in young, but not aged, rats. We have discovered that administration of GH upregulates
the expression of the Ghr receptor and restores Ghr’s responsiveness in aged animals with sepsis. In our
completed SBIR Phase I project, co-administration of hGhr and hGH (hGhr-hGH) significantly ameliorated
sepsis-associated lung, liver, and kidney injury in septic aged animals. We further demonstrated that the
combination therapy nearly doubled the survival rate of septic aged rats. Moreover, both hGhr and hGH
have been clinically tested and used for other indications with an excellent safety profile. Based on our
Phase I results, we hypothesize that hGhr-hGH can be further developed as an effective therapy for sepsis
in the elderly. To advance hGhr-hGH therapy towards its clinical use against sepsis in the elderly, we plan
to determine the combination therapy’s most effective dose and therapeutic window to attenuate tissue
injury and improve survival. We will also study hGhr-hGH’s combination effects on safety and
pharmacokinetics (PK). Finally, we will conduct an exploratory study in an ovine model of sepsis to evaluate
hGhr-hGH’s effects on hemodynamic parameters and organ injury. These proposed studies should provide
crucial information for the future filing of an IND application to further develop hGhr-hGH in clinical trials.
Our ultimate goal is to obtain FDA approval for the use of hGhr-hGH as a safe and effective treatment for
elderly patients with sepsis and septic shock.
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专著(0)
科研奖励(0)
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海外基金