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Expert opinion on investigational drugs最新文献

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Safety, tolerability, and pharmacokinetics of the novel RdRp inhibitor SHEN26 against SARS-CoV-2: a randomized, placebo-controlled, double-blind phase I study in healthy subjects 新型 RdRp 抑制剂 SHEN26 对抗 SARS-CoV-2 的安全性、耐受性和药代动力学:一项针对健康受试者的随机、安慰剂对照、双盲 I 期研究
IF 6.1 2区 医学 Q1 PHARMACOLOGY & PHARMACY Pub Date : 2024-04-25 DOI: 10.1080/13543784.2024.2347302
Cheng Sun, Hao Liu, Ziwei Ouyang, Jie Ding, Qin Zhang, Hongjie Ma, Dandan Xu, Qian Zhang, Renpeng Zhou, Mingming Yang, Wei Hu
SHEN26, an oral broad-spectrum antiviral drug, possesses potent preclinical activity against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and has a favorable safety profile.We repor...
SHEN26是一种口服广谱抗病毒药物,对严重急性呼吸系统综合征冠状病毒2(SARS-CoV-2)具有很强的临床前活性,并具有良好的安全性。
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引用次数: 0
Experimental and new investigational drugs for the treatment of uterine fibroids 治疗子宫肌瘤的试验性药物和新研究药物
IF 6.1 2区 医学 Q1 PHARMACOLOGY & PHARMACY Pub Date : 2024-04-15 DOI: 10.1080/13543784.2024.2343786
Giulio Evangelisti, Simone Ferrero, Umberto Perrone, Claudio Gustavino, Eugenio Volpi, Alberto Izzotti, Fabio Barra
Uterine fibroids, the most prevalent benign tumors among reproductive-age women, pose treatment challenges that range from surgical interventions to medical therapies for symptom control. Progestin...
子宫肌瘤是育龄妇女中最常见的良性肿瘤,它给治疗带来了挑战,包括从手术干预到控制症状的药物疗法。孕激素...
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引用次数: 0
Investigational agents for autosomal dominant polycystic kidney disease: preclinical and early phase study insights 常染色体显性多囊肾病的研究药物:临床前和早期阶段研究的启示
IF 6.1 2区 医学 Q1 PHARMACOLOGY & PHARMACY Pub Date : 2024-04-15 DOI: 10.1080/13543784.2024.2342327
Irene Capelli, Sarah Lerario, Francesca Ciurli, Gian Marco Berti, Valeria Aiello, Michele Provenzano, Gaetano Manna
Autosomal Dominant Polycystic Kidney Disease (ADPKD) is the most common inherited kidney condition caused by a single gene mutation. It leads patients to kidney failure in more than 50% of cases by...
常染色体显性多囊肾(ADPKD)是由单基因突变引起的最常见的遗传性肾病。50%以上的患者会因基因突变而导致肾衰竭。
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引用次数: 0
Sodium/Bile acid co-transporter inhibitors currently in preclinical or early clinical development for the treatment of primary biliary cholangitis 目前正处于临床前或早期临床开发阶段的钠/胆酸协同转运体抑制剂,用于治疗原发性胆汁性胆管炎
IF 6.1 2区 医学 Q1 PHARMACOLOGY & PHARMACY Pub Date : 2024-04-13 DOI: 10.1080/13543784.2024.2343789
Abhishek Gairola, Aaron Wetten, Jessica Dyson
Pruritus is common and often undertreated in patients with primary biliary cholangitis (PBC). Existing treatments largely have an aging and low-quality evidence base, and studies included only smal...
瘙痒是原发性胆汁性胆管炎(PBC)患者常见的症状,但往往治疗不足。现有的治疗方法大多证据基础老化且质量不高,而且研究仅包括少量的...
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引用次数: 0
Investigational regenerative medicine for non-traumatic osteonecrosis of the femoral head: a survey of registered clinical trials. 治疗非创伤性股骨头坏死的再生医学研究:注册临床试验调查。
IF 6.1 2区 医学 Q1 PHARMACOLOGY & PHARMACY Pub Date : 2024-04-01 Epub Date: 2024-03-05 DOI: 10.1080/13543784.2024.2326622
Yutaka Kuroda, Toshiyuki Kawai, Yaichiro Okuzu, Yugo Morita, Shuichi Matsuda

Introduction: Osteonecrosis of the femoral head (ONFH) is a refractory disease requiring joint replacement in young patients. Regenerative therapies have been developed.

Areas covered: This study surveyed clinical trials on regenerative medicine for ONFH. We extracted clinical trials on non-traumatic ONFH from the websites of five publicly available major registries (EuropeanUnion Clinical Trials Register ([EU-CTR],ClinicalTrials.gov, Chinese ClinicalTrial Registry [ChiCTR], University Hospital Medical InformationNetwork - Clinical Trial Registry [UMIN-CTR] and Australian New Zealand Clinical Trials Registry [ANZCTR]).The trials were classified into six categories based on purpose: surgical treatment, non-drug conservative treatment, conservative drug treatment, therapeutic strategy, diagnosis and pathogenesis, and regenerative therapy.) We extracted 169 clinical trials on ONFH. Of these, 37 were on regenerative medicine, including 29 on cell therapy. Surgical treatment was the most common treatment, followed by regenerative therapy.There were 9 clinical trials registered in the EU-CTR, with 5 on regenerative medicine; 79 trials registered on ClinicalTrials.gov, with 24 on regenerativemedicine; 54 trials registered in the ChiCTR, with 6 on regenerative medicine.

Expert opinion: The focus of the joint-preserving surgery has shifted to regenerative therapy based on using cell therapy in early-stage ONFH. The global standardisation of regenerative therapy is still ongoing.

简介:股骨头骨坏死(ONFH)是一种难治性疾病,年轻患者需要进行关节置换。目前已开发出再生疗法:本研究调查了再生医学治疗股骨头坏死的临床试验。我们从五个公开的主要登记处(欧盟临床试验登记处(EU-CTR)、ClinicalTrials.gov、中国临床试验登记处[ChiCTR]、大学医院医学信息网-临床试验登记处[UMIN-CTR]和澳大利亚-新西兰临床试验登记处[ANZCTR])的网站上提取了有关非创伤性 ONFH 的临床试验。根据目的将试验分为六类:手术治疗、非药物保守治疗、药物保守治疗、治疗策略、诊断和发病机制以及再生治疗。)我们提取了 169 项有关 ONFH 的临床试验。其中 37 项涉及再生医学,包括 29 项细胞疗法。手术治疗是最常见的治疗方法,其次是再生疗法。在欧盟临床试验中心(EU-CTR)登记的临床试验有9项,其中5项涉及再生医学;在ClinicalTrials.gov登记的临床试验有79项,其中24项涉及再生医学;在ChiCTR登记的临床试验有54项,其中6项涉及再生医学:专家观点:关节保留手术的重点已转向再生疗法,即在早期ONFH中使用细胞疗法。再生疗法的全球标准化工作仍在进行中。
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引用次数: 0
Investigational drugs for the treatment of dysmenorrhea. 治疗痛经的研究药物。
IF 6.1 2区 医学 Q1 PHARMACOLOGY & PHARMACY Pub Date : 2024-04-01 Epub Date: 2024-03-19 DOI: 10.1080/13543784.2024.2326627
Amelia K Mardon, Lucy Whitaker, Toobah Farooqi, Jane Girling, Claire Henry, Carolyn Ee, Jordan Tewhaiti-Smith, Mike Armour

Introduction: Dysmenorrhea is the most common cause of gynecological pain among women that has considerable impact on quality of life and psychosocial wellbeing. Non-steroidal anti-inflammatory drugs (NSAIDs) and hormonal therapies are most commonly used to treat dysmenorrhea. However, given these drugs are often associated with bothersome side effects and are less effective when there is an underlying cause contributing to dysmenorrhea (e.g. endometriosis), a patient-centered approach to managing dysmenorrhea is important. Various new drugs are currently being investigated for the treatment of primary and secondary dysmenorrhea.

Areas covered: This review provides an updated overview on new therapeutic targets and investigational drugs for the treatment of primary and secondary dysmenorrhea. The authors describe the clinical development and implications of these drugs.

Expert opinion: Among the investigative drugs discussed in this review, anti-inflammatories show the most promising results for the treatment of dysmenorrhea. However, given some trials have considerable methodological limitations, many drugs cannot be currently recommended. Research focused on understanding the mechanisms involved in menstruation and its associated symptoms will be important to identify new therapeutic targets for dysmenorrhea. Further robust clinical trials are required to better understand the efficacy and safety of investigational drugs for treating primary and secondary dysmenorrhea.

简介痛经是女性最常见的妇科疼痛原因,对生活质量和社会心理健康有很大影响。非甾体抗炎药(NSAIDs)和激素疗法是治疗痛经最常用的方法。然而,鉴于这些药物通常会产生令人烦恼的副作用,而且当痛经的根本原因(如子宫内膜异位症)存在时,这些药物的疗效就会大打折扣,因此,以患者为中心的痛经治疗方法非常重要。目前正在研究用于治疗原发性和继发性痛经的各种新药:本综述概述了治疗原发性和继发性痛经的新治疗靶点和在研药物的最新情况。作者介绍了这些药物的临床开发和影响:专家观点:在本综述讨论的研究药物中,抗炎药在治疗痛经方面显示出最有希望的结果。然而,由于试验在方法上存在相当大的局限性,这些药物目前还不能付诸实施。研究重点在于了解月经及其相关症状的发病机制,这对于确定治疗痛经的新靶点非常重要。要更好地了解治疗原发性和继发性痛经的研究药物的疗效和安全性,还需要进一步开展强有力的临床试验。
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引用次数: 0
Novel preclinical developments of the primary sclerosing cholangitis treatment landscape. 原发性硬化性胆管炎治疗的临床前新进展。
IF 6.1 2区 医学 Q1 PHARMACOLOGY & PHARMACY Pub Date : 2024-04-01 Epub Date: 2024-03-18 DOI: 10.1080/13543784.2024.2330738
Aalam Sohal, Kris V Kowdley

Introduction: Primary sclerosing cholangitis (PSC) is a chronic cholestatic liver disease associated with inflammation, fibrosis, and destruction of intra- and extrahepatic bile ducts. Despite substantial recent advances in our understanding of PSC, the only proven treatment of PSC is liver transplantation. There is an urgent unmet need to find medical therapies for this disorder.

Areas covered: Multiple drugs are currently under evaluation as therapeutic options for this disease. This article summarizes the literature on the various novel therapeutic options that have been investigated and are currently under development for the treatment of PSC.

Expert opinion: In the next decade, more than one drug will likely be approved for the treatment of the disease, and we will be looking at combination therapies for the optimal management of the disease.

导言--:原发性硬化性胆管炎(PSC)是一种慢性胆汁淤积性肝病,与肝内外胆管的炎症、纤维化和破坏有关。尽管近年来我们对 PSC 的认识有了长足的进步,但治疗 PSC 的唯一行之有效的方法是肝移植。我们迫切需要找到治疗这种疾病的药物:目前正在对多种药物进行评估,作为治疗该疾病的选择。这篇文章总结了有关各种新型治疗方案的文献,这些方案已经过研究,目前正在开发中,用于治疗PSC:在未来十年中,可能会有一种以上的药物被批准用于治疗该疾病,我们将寻求联合疗法来优化该疾病的治疗。
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引用次数: 0
Investigational new drugs for the treatment of chronic renal failure: an overview of the literature. 治疗慢性肾功能衰竭的试验性新药:文献综述。
IF 6.1 2区 医学 Q1 PHARMACOLOGY & PHARMACY Pub Date : 2024-04-01 Epub Date: 2024-03-28 DOI: 10.1080/13543784.2024.2326624
Chiara Terzo, Guido Gembillo, Valeria Cernaro, Elisa Longhitano, Vincenzo Calabrese, Chiara Casuscelli, Luigi Peritore, Domenico Santoro

Introduction: Chronic kidney disease (CKD) is widespread throughout the world, with a high social and health impact. It is considered a 'silent killer' for its sudden onset without symptoms in the early stages of the disease. The main goal of nephrologists is to slow the progression of kidney disease and treat the associated symptoms with a range of new medications.

Areas covered: The aim of this systematic review is to analyze the new investigational drugs for the treatment of chronic renal failure. Data were obtained from the available scientific literature and from the ClinicalTrials.gov website.

Expert opinion: Among the drugs currently being researched, SGLT2 inhibitors appear to be the most promising drugs for the treatment of CKD, has they have slower progression of CKD and protection of cardiorenal function. An important role in the future of CKD treatment is played by autologous cell-therapy, which appears to be a new frontier in the treatment of CKD. Other therapeutic strategies are currently being investigated and have been shown to slow the progression of CKD. However, further studies are needed to determine whether these approaches may offer benefits in slowing the progression of CKD in the near future.

导言:慢性肾脏病(CKD)在全世界范围内广泛存在,对社会和健康造成了严重影响。肾病学家的主要目标是通过一系列新药延缓肾病的进展并治疗相关症状:本系统综述旨在分析治疗慢性肾功能衰竭的新研究药物。数据来自现有的科学文献和ClinicalTrials.gov网站:在目前正在研究的药物中,SGLT2 抑制剂似乎是最有希望治疗慢性肾功能衰竭的药物,因为它们能减缓慢性肾功能衰竭的进展并保护心肾功能。自体细胞疗法在未来的慢性肾功能衰竭治疗中扮演着重要角色,它似乎是治疗慢性肾功能衰竭的一个新领域。目前正在对其他治疗策略进行研究,这些策略已被证明可以减缓慢性肾功能衰竭的进展。然而,要确定这些方法是否能在不久的将来为减缓慢性肾功能衰竭的进展带来益处,还需要进一步的研究。
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引用次数: 0
Microbiome modulators for atopic eczema: a systematic review of experimental and investigational therapeutics. 治疗特应性湿疹的微生物组调节剂:实验性和研究性疗法的系统综述。
IF 4.9 2区 医学 Q1 PHARMACOLOGY & PHARMACY Pub Date : 2024-04-01 Epub Date: 2024-03-06 DOI: 10.1080/13543784.2024.2326625
Jonathan D Greenzaid, Lina J Chan, Brittany M Chandani, Nicholas R Kiritsis, Steven R Feldman

Introduction: Atopic dermatitis (AD) is a common inflammatory cutaneous disease that arises due to dysregulation of the Th2 immune response, impaired skin barrier integrity, and dysbiosis of the skin and gut microbiota. An abundance of Staphylococcus aureus biofilms in AD lesions increases the Th2 immune response, and gut bacteria release breakdown products such as Short Chain Fatty Acids that regulate the systemic immune response.

Areas covered: We aim to evaluate therapies that modulate the microbiome in humans and discuss the clinical implications of these treatments. We performed a review of the literature in which 2,673 records were screened, and describe the findings of 108 studies that were included after full-text review. All included studies discussed the effects of therapies on the human microbiome and AD severity. Oral probiotics, topical probiotics, biologics, and investigational therapies were included in our analysis.

Expert opinion: Oral probiotics demonstrate mixed efficacy at relieving AD symptoms. Topical probiotics reduce S. aureus abundance in AD lesional skin, yet for moderate-severe disease, these therapies may not reduce AD severity scores to the standard of biologics. Dupilumab and tralokinumab target key inflammatory pathways in AD and modulate the skin microbiome, further improving disease severity.

简介:特应性皮炎(AD)是一种常见的皮肤炎症性疾病:特应性皮炎(AD)是一种常见的皮肤炎症性疾病,是由于Th2免疫反应失调、皮肤屏障完整性受损以及皮肤和肠道微生物群失调而引起的。AD 病变中大量的金黄色葡萄球菌生物膜会增加 Th2 免疫反应,肠道细菌会释放短链脂肪酸等分解产物,从而调节全身免疫反应:我们旨在评估调节人体微生物组的疗法,并讨论这些疗法的临床意义。我们对 2,673 条记录进行了文献综述,并描述了经全文审阅后纳入的 108 项研究的结果。所有纳入的研究都讨论了治疗方法对人类微生物组和注意力缺失症严重程度的影响。我们的分析包括口服益生菌、局部益生菌、生物制剂和研究疗法:口服益生菌在缓解AD症状方面的疗效参差不齐。外用益生菌可减少 AD 病变皮肤中金黄色葡萄球菌的数量,但对于中重度疾病,这些疗法可能无法达到生物制剂的标准,从而降低 AD 的严重程度。杜匹鲁单抗和曲妥珠单抗以AD的关键炎症通路为靶点,调节皮肤微生物组,从而进一步改善疾病的严重程度。
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引用次数: 0
Early investigational agents for the treatment of benign prostatic hyperplasia'. 治疗良性前列腺增生症的早期研究药物"。
IF 6.1 2区 医学 Q1 PHARMACOLOGY & PHARMACY Pub Date : 2024-04-01 Epub Date: 2024-03-04 DOI: 10.1080/13543784.2024.2326023
Stamatios Katsimperis, Konstantinos Kapriniotis, Ioannis Manolitsis, Themistoklis Bellos, Panagiotis Angelopoulos, Patrick Juliebø-Jones, Bhaskar Somani, Andreas Skolarikos, Lazaros Tzelves

Introduction: Benign prostatic hyperplasia (BPH), as a clinical entity that affects many people, has always been in the forefront of interest among researchers, pharmaceutical companies, and physicians. Patients with BPH exhibit a diverse range of symptoms, while current treatment options can occasionally cause adverse events. All the aforementioned have led to an increased demand for more effective treatment options.

Areas covered: This review summarizes the outcomes of new medications used in a pre-clinical and clinical setting for the management of male lower urinary tract symptoms (LUTS)/BPH and provides information about ongoing trials and future directions in the management of this condition. More specifically, sheds light upon drug categories, such as reductase‑adrenoceptor antagonists, drugs interfering with the nitric oxide (NO)/cyclic guanosine monophosphate (GMP) signaling pathway, onabotulinumtoxinA, vitamin D3 (calcitriol) analogues, selective cannabinoid (CB) receptor agonists, talaporfin sodium, inhibitor of transforming growth factor beta 1 (TGF-β1), drugs targeting the hormonal control of the prostate, phytotherapy, and many more.

Expert opinion: Clinical trials are being conducted on a number of new medications that may emerge as effective therapeutic alternatives in the coming years.

简介良性前列腺增生症(BPH)作为一种影响许多人的临床实体,一直是研究人员、制药公司和医生关注的焦点。良性前列腺增生症患者的症状多种多样,而目前的治疗方案偶尔会引起不良反应。综上所述,人们越来越需要更有效的治疗方案:本综述总结了在临床前和临床环境中用于治疗男性下尿路症状(LUTS)/良性前列腺增生症的新药的疗效,并提供了有关正在进行的试验和未来治疗方向的信息。更具体地说,它揭示了各类药物,如还原酶-肾上腺素受体拮抗剂、干扰一氧化氮(NO)/单磷酸环鸟苷(GMP)信号通路的药物、onabotulinumtoxinA、维生素 D3(钙三醇)类似物、选择性大麻素(CB)受体激动剂、他拉泊芬钠、转化生长因子β1(TGF-β1)抑制剂、针对前列腺激素控制的药物、植物疗法等等。专家意见目前正在对一些新药进行临床试验,它们可能在未来几年内成为有效的替代治疗药物。
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引用次数: 0
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Expert opinion on investigational drugs
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