Evaluation of ACT1 to Treat Diabetic Keratopathy
Evaluation of ACT1 to Treat Diabetic Keratopathy
批准号:
10261233
负责人:
Donald Lo
金额:
$25.84万
依托单位国家:
美国
项目类别:
财政年份:
--
资助国家:
美国
项目状态:
未结题
起止时间:
至
关键词:
ADME StudyBindingBlindnessBurn injuryC-terminalCellsCollaborationsConnexin 43CorneaCorneal InjuryDefectDevelopmentDiabetes MellitusDiseaseDrug KineticsEpithelialEpitheliumEthanolEvaluationExtravasationFibrosisFormulationGranulation TissueHumanImmuneIndividualInjuryInvestigational DrugsKeratopathyLeadMediator of activation proteinMorbidity - disease ratePeptidesPharmaceutical PreparationsPlayPre-Clinical ModelRoleSafetySignal TransductionTherapeuticThinnessToxicologyTreatment ProtocolsVisual impairmentbaseconventional therapycorneal burndesigndiabeticdiabetic ratepithelial woundphase 1 studyresearch clinical testingsafety studywound closurewound healing
中文摘要
点击翻译按钮获取中文摘要
英文摘要
FirstStrings lead peptide, ACT1, is based on the C-terminal sequence of connexin43 (Cx43) and is designed to enter the cell and competitively inhibit the binding of endogenous Cx43. Cx43 plays critical roles in multiple aspects of wound healing, including spread of injury signals, extravasation of immune cells, granulation tissue formation, and fibrosis.
Studies in preclinical models of efficacy show significant enhancement in corneal re-epithelialization and wound closure following ethanol-induced corneal burn injuries in diabetic rats, as compared with controls. This project will involve further development and safety studies of ACT1, a potential therapeutic compound for diabetic keratopathy.
The BrIDGs team is collaborating on the completion of the following studies on ACT1:
-Formulation development and manufacture of drug product to support Phase I studies
-Pharmacokinetic/absorption, distribution, metabolism, and excretion (PK/ADME) studies
-Investigational New Drug (IND)-directed toxicology
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