Approximately 21 subjects with amyotrophic lateral sclerosis (ALS) will be randomized (6 to 1) to receive by mouth seven morning doses of CC100 or placebo for 7 days. Subjects are required to stay in the Clinic for approximately 9 hours following the first and last dose. Subjects will also have a mid-week clinic visit and will be contacted by phone within 3 to 5 days after the last dose.
Funding Source - FDA OOPD

开始日期2017-04-07

申办/合作机构

Chemigen, Inc.

NCT02050334 / Completed临床1期

Protocol CC100A CC100: Safety and Tolerability of Single Doses

The purpose of this study is to see if CC100, given by mouth, is safe and is tolerated in increasing doses. How long the drug remains in the body will also be calculated.

开始日期2013-11-01

申办/合作机构

Chemigen, Inc.

NCT02744703 / CompletedN/AIIT

Professor, Ege University Faculty of Dentistry

Matrix metalloproteinases (MMPs); activated by the application of adhesive systems on dentin cause degradation of the collagen proteins and loss of bond strength in adhesive restorations. Caffeic acid phenethyl ester (CAPE) showed inhibitory activities on dentinal MMPs. It is hypothesised that dentin pretreatment with CAPE, as an MMP inhibitor, would be beneficial for the bonding of resin material and tooth substrate over the course of time. This study evaluated the effect of 5 % CAPE pretreatment on the microtensile bond strength of a nanohybrid resin restoration applied with total-etch or self-etch adhesive systems on 10 patients (12-18 yrs). Two standard cavities (3 x 3 x 4 mm) prepared on the occlusal surfaces of one of the two premolar teeth in each patient were randomly assigned into four treatment groups (n=10); 5% CAPE pretreatment and total-etch adhesive (TC), Total-etch adhesive (control) (T), 5% CAPE pretreatment and self-etch adhesive (SC), Self-etch adhesive (control) (S) followed by restoration and 3 months of intra-oral functioning. After teeth extraction, the specimens were stored in distilled water+thymol solution at 4°C to inhibit microbial growth and used in one week period. Dentin-composite sticks were obtained from each restoration for µTBS tests and scanning electron microscopy (SEM) evaluation. Failure mode analysis was performed microscopically. Data were analysed statistically using Repeated Measure ANOVA (p < 0.05). Dentin pretreatment with CAPE solution (5%) for 60 seconds significantly increased the composite resin restorations' bond strengths to dentin applied with either total-etch or self-etch adhesive system. Thus it can be used as an MMP inhibitor prior to the the resin restorations. However further long term clinical studies are needed to support the use of CAPE pretreatment along with self-etch and total-etch adhesive systems.

开始日期2013-04-01

申办/合作机构

Ege Universitesi

100 项与 Caffeic acid phenethyl ester 相关的临床结果

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100 项与 Caffeic acid phenethyl ester 相关的转化医学

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100 项与 Caffeic acid phenethyl ester 相关的专利（医药）

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项与 Caffeic acid phenethyl ester 相关的文献（医药）

2024-12-31·Renal Failure

Caffeic acid phenethyl ester restores mitochondrial homeostasis against peritoneal fibrosis induced by peritoneal dialysis through the AMPK/SIRT1 pathway

Article

作者: Zeng, Ying ; Zhang, Wenwen ; Lu, Ying ; Gao, Luyan ; Hu, Ji ; Song, Kai

Increasing evidence suggests that peritoneal fibrosis induced by peritoneal dialysis (PD) is linked to oxidative stress. However, there are currently no effective interventions for peritoneal fibrosis. In the present study, we explored whether adding caffeic acid phenethyl ester (CAPE) to peritoneal dialysis fluid (PDF) improved peritoneal fibrosis caused by PD and explored the molecular mechanism. We established a peritoneal fibrosis model in Sprague-Dawley rats through intraperitoneal injection of PDF and lipopolysaccharide (LPS). Rats in the PD group showed increased peritoneal thickness, submesothelial collagen deposition, and the expression of TGFβ1 and α-SMA. Adding CAPE to PDF significantly inhibited PD-induced submesothelial thickening, reduced TGFβ1 and α-SMA expression, alleviated peritoneal fibrosis, and improved the peritoneal ultrafiltration function. In vitro, peritoneal mesothelial cells (PMCs) treated with PDF showed inhibition of the AMPK/SIRT1 pathway, mitochondrial membrane potential depolarization, overproduction of mitochondrial reactive oxygen species (ROS), decreased ATP synthesis, and induction of mesothelial-mesenchymal transition (MMT). CAPE activated the AMPK/SIRT1 pathway, thereby inhibiting mitochondrial membrane potential depolarization, reducing mitochondrial ROS generation, and maintaining ATP synthesis. However, the beneficial effects of CAPE were counteracted by an AMPK inhibitor and siSIRT1. Our results suggest that CAPE maintains mitochondrial homeostasis by upregulating the AMPK/SIRT1 pathway, which alleviates oxidative stress and MMT, thereby mitigating the damage to the peritoneal structure and function caused by PD. These findings suggest that adding CAPE to PDF may prevent and treat peritoneal fibrosis.

2024-12-01·Clinical and Experimental Pharmacology and Physiology

Caffeic acid phenethyl ester ameliorates colistin‐induced nephrotoxicity in rats via modulation of FOXO1/Nrf2/Sirt1 axis

Article

作者: Abdel‐Naim, Ashraf B. ; Noor, Ahmad O. ; Bagalagel, Alaa A. ; Neamtalllah, Thikryat ; Nasrullah, Mohammed Z. ; Bakhsh, Hussain T. ; Alshibani, Mohannad

AbstractBackgroundColistin (Cst) is one of the antimicrobial peptides and is reserved for use against multi‐drug‐resistant Gram‐negative bacteria. However, the clinical value of Cst is limited by its nephrotoxic adverse effects. Caffeic acid phenethyl ester (CAPE) is a honeybee propolis flavonoid recognised for its diverse pharmacological potential. It has demonstrated d antioxidant and anti‐inflammatory properties, as well as protective effects against chemically induced toxicity in variuos biological systems. This study aimed to investigate the impact of CAPE on nephrotoxicity induced in rats by Cst.MethodsAnimals were randomly divided into five groups. Group 1 served as control, group 2 received CAPE (10 mg/kg) orally, group 3 received Cst IP, group 4 received Cst + CAPE (5 mg/kg) and group 5 received Cst + CAPE (10 mg/kg). All treatments were given daily for 10 consecutive days.ResultsCAPE notably attenuated Cst‐inducednephrotoxicity as shown by reducing urea serum levels, creatinine, cystatin C, urinary protein contents and urinary N‐acetyl‐β‐D‐glucosaminidase (NAG). This was confirmed by histological investigations that indicated amelioration of histopathological changes in the kidney architecture as well as the deposition of collagen in renal tissues. CAPE exhibited antioxidant effects supported by the prevention of rise in Cst‐induced lipid peroxidation and depletion of superoxide dismutase and catalase enzymatic activities. In addition, CAPE inhibited the expression of the inflammatory markers including tumour necrosis factor‐α, nuclear factor kappa B and interleukin‐6. These actions were associated with modulation of messenger ribonucleic acid (mRNA) expression of Bax and Bcl‐2 in favour of anti‐apoptosis. CAPE inhibited Cst‐induced rise in forkhead box O1 (FOXO1) expression and downregulation of nuclear factor erythroid 2–related factor 2 (Nrf2) and Sirtuin 1 (Sirt1) immune‐expression.ConclusionCAPE protects against nephrotoxicity induced by Cst in ratsprimarily through its antioxidant, antiinflammatory and antiapoptotic activities. These pritective effects are mediated via modulation of FOXO1/Nrf2/Sirt1 axis.

2024-12-01·Molecular Biology Reports

Interaction of olive oil-based propolis and caffeic acid phenethyl ester with methylprednisolone used in the treatment of human acute myeloid leukemia

Article

作者: Ozcimen, A Ata ; Silici, Sibel ; Dogan, Hamide

BACKGROUNDMethylprednisolone (MP) is a pharmaceutical agent employed in the management of Leukemia, which is a systemic malignancy that arises from abnormalities in the hematological system. Numerous investigations in the field of cancer research have directed their attention towards propolis, a natural substance with significant potential as a treatment-supportive agent. Its utilization aims to mitigate the potential adverse effects associated with chemotherapy medications. The objective of this study was to examine the impact of olive oil-based propolis (OEP) and caffeic acid phenethyl ester (CAPE) on the treatment of acute myeloid leukemia, as well as to determine if they exhibit a synergistic effect when combined with the therapeutic support product methylprednisolone.METHODS AND RESULTSThe proliferation of HL-60 cells was quantified using the WST-8 kit. The PI Staining technique was employed to do cell cycle analysis of DNA in cells subjected to OEP, CAPE, and MP, with subsequent measurement by flow cytometry. The apoptotic status of cells was determined by analyzing them using flow cytometry after staining with the Annexin V-APC kit. The quantification of apoptotic gene expression levels was conducted in HL-60 cells. In HL-60 cells, the IC₅₀ dosages of CAPE and MP were determined to be 1 × 10^- 6 M and 5 × 10^- 4 M, respectively. The HL-60 cells were subjected to apoptosis and halted in the G₀/G₁ and G₂/M phases of the cell cycle after being treated with MP, CAPE, and OEP.CONCLUSIONSPropolis and its constituents have the potential to serve as effective adjunctive therapies in chemotherapy.

项与 Caffeic acid phenethyl ester 相关的新闻（医药）

2023-02-27

·PRNewswire

Cymbiotika Announces Launch of New Supplement, ParaX ™

This all-natural formula supports overall whole-body wellness SAN DIEGO, Feb. 27, 2023 /PRNewswire/ -- Cymbiotika, the leading supplement brand known for creating clean, science-backed supplements, announced its newest product, ParaX™. ParaX is a comprehensive approach to balancing the gut microbiome, enhancing detox pathways, fortifying the immune system, and providing whole-body wellness. ParaX utilizes vitamins, minerals, standardized herbal extracts, fatty acids, and phenols encapsulated within powerful ozonated, oxygen-infused oils. What makes ParaX unique is that it was designed inside a gel capsule with suspended ParaX-Spheres. The formula also contains a powerful blend of ozonated oils made of monolaurin, coconut, thyme, clove, olive, and oregano. This combination provides a wide range of antimicrobial and antiseptic agents. The formula also contains CAPE (Caffeic Acid Phenethyl Ester), a highly bioactive compound found in bee propolis and utilized for its extraordinary antioxidant and immune properties, and Andrographolide, which is shown to support the immune system, promote a healthy inflammatory response and support the body during bacterial and viral infections. "We designed this formula to offer a proactive approach to combating the overgrowth of bacteria, microbes, and other foreign invaders in our microbiome that can cause many diverse health issues. ParaX is a daily supplement intentionally formulated for overall wellness and immune support rather than act as a harsh, one-time cleanse," said Dr. Pejman Taghavi, a Cymbiotika's Board of Advisors member. Cymbiotika's ParaX is a powerful supplement that provides an extra line of defense against bacteria, microbes, and foreign invaders that the body is exposed to. ParaX retails for $92 and is available for purchase through the Cymbiotika website. Customers over the age of 18 should take three capsules daily, with water or juice, as directed by a qualified healthcare practitioner. The formula was designed for individuals to take three weeks on and one week off. ParaX can be taken any time of the day, but it is crucial to be consistent with the time it is taken. For increased effectiveness, take alongside Cymbiotika's Liposomal Vitamin C. About Cymbiotika Cymbiotika is an innovative wellness brand based in San Diego. With the motto, "Your mind and body deserve the best," Cymbiotika is driven by the higher purpose of inspiring everyday people to achieve their optimal health. Founded in 2018, Cymbiotika uses the most advanced bioavailable absorption technology and sources only the highest quality plant-based nutrients to resolve specific nutritional deficiencies and support healthy aging, detoxification, and longevity. Cymbiotika never uses synthetics, GMOs, fillers, chemicals, preservatives, or additives in its products. For more information, visit . SOURCE Cymbiotika

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100 项与 Caffeic acid phenethyl ester 相关的药物交易

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适应症	最高研发状态	国家/地区	公司	日期
肌萎缩侧索硬化	临床1期	美国	Chemigen, Inc.	2013-10-27
口腔鳞状细胞癌	临床前	中国台湾	Mackay Medical College	2017-09-01
结直肠癌	临床前	美国	The National Institute of Environmental Health Sciences	2007-05-01
结直肠癌	临床前	韩国	Andong National University	2007-05-01
结直肠癌	临床前	美国	University of Tennessee	2007-05-01

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研究	分期	人群特征	评价人数	分组	结果	评价	发布日期


NCT02050334 (CC100A, CTgov)	临床1期	-	18	CC100 (CC100 (3 Single Doses))	築選構鑰蓋網憲醖範壓(衊艱選鏇簾齋鏇獵鏇鑰) = 願鑰繭範夢糧獵鹽壓憲構淵築鬱衊廠鹽淵顧網 (願夢鬱襯繭餘鹽醖憲鑰, 壓網積鬱鑰衊積壓餘窪 ~ 衊窪醖夢獵鑰繭窪構夢) 更多	-	2015-04-29
				Placebo+CC100 (CC100 (2 Single Doses) & Placebo(1 Dose))	築選構鑰蓋網憲醖範壓(衊艱選鏇簾齋鏇獵鏇鑰) = 鑰顧鏇構醖鹹膚衊願淵構淵築鬱衊廠鹽淵顧網 (願夢鬱襯繭餘鹽醖憲鑰, 獵遞願壓鏇鏇廠蓋鑰鬱 ~ 窪窪遞憲獵積積築蓋膚) 更多