The overall aim of this project is to implement a non-invasive method of measuring quantitative regional cerebral blood flow (rCBF) on the UAB hybrid PET/MRI scanner to allow conducting such [O-15]water based scans with relative ease and safety in a large variety of important clinical and research applications. Participants will undergo imaging at baseline and after administration of a drug to increase cerebral blood flow to evaluate perfusion estimates during low and high flow states. The goal of this study is to generate data that will justify eliminating invasive arterial sampling in most [O-15]water-based PET protocols.

开始日期2025-02-01

申办/合作机构

The University of Alabama at Birmingham

NCT06273397 / Not yet recruitingN/A

Acetazolamide or Metolazone in Acute Heart Failure

Impact of Acute Heart Failure:
According to the World Health Organization (WHO), approximately 26 million people suffer from Heart Failure (HF), with a mortality rate of up to 50% within five years of diagnosis. Acute Heart Failure (AHF) exacerbations, leading to hospitalization, are common and represent the primary cause of hospital admissions in those over 65. Effective decongestion during hospitalization is crucial, as failure to achieve it doubles the risk of rehospitalization and mortality, incurring significant healthcare costs.
Use of Diuretics in Acute Heart Failure:
Diuretics, particularly loop diuretics like furosemide, are a cornerstone in managing AHF by inducing natriuresis and achieving decongestion. Clinical experience supports their use, though limited clinical trials exist. Pharmacological concepts guide their administration, emphasizing intravenous delivery in high doses and adjusting subsequent doses based on decongestive efficacy. Additionally, sequential tubular blockade with other diuretics like metolazone and acetazolamide is explored to enhance decongestion.
Use of Metolazone and Acetazolamide:
Sequential tubular blockade, using metolazone and acetazolamide in conjunction with furosemide, aims to achieve rapid and effective decongestion. While metolazone targets the distal tubule, inhibiting sodium-chloride channels, acetazolamide affects proximal tubular function. Studies like ADVOR (acetazolamide) and CLOROTIC (thiazide-like diuretic) demonstrate the potential benefits of combining these diuretics for quicker decongestion but with potential risks (in the case of Hydrochlorothiazide).
Outcomes Measured by Major Studies:
Recent studies assessing decongestion in AHF reveal a lack of uniformity in outcome selection. The primary focus should be on reducing rehospitalizations and post-discharge mortality by achieving effective decongestion. The ADVOR study, using a simple congestion score based on clinical and imaging criteria, underscores the importance of reaching a congestion score of 0 or 1 promptly.
Congestion Monitoring:
Monitoring diuretic treatment solely based on clinical aspects may not capture subclinical congestion, necessitating biochemical and imaging parameters. The ACME-AHF trial proposes a diagnostic score integrating clinical and imaging aspects to evaluate congestion status. Secondary outcomes include cumulative diuresis, weight loss, diuretic efficiency, and natriuresis, with a focus on natriuresis as a reliable physiological parameter for decongestion.
Aim of the study:
The ACME-AHF trial is designed to compare the efficacy and safety of two diuretic combination strategies: acetazolamide with furosemide and metolazone with furosemide. The primary objective is to relieve congestion, assessed using a congestion score, within the first three days of treatment during an hospitalization for acute heart failure.

开始日期2024-05-01

申办/合作机构

Clínica Alemana de Santiago SA

NCT06166654 / Not yet recruiting临床4期IIT

Optimal Diuretic Therapies for Acute Heart Failure With Volume Overload - A Randomized Clinical Trial

Aim to identify the best strategy for treating acute heart failure (AHF) with volume overload, particularly focusing on patients resistant to standard loop-diuretics. The trial is a double-blinded, randomized, controlled, multicenter study. Its primary objective is to compare the efficacy of loop-diuretics combined with either Metolazone or Acetazolamide, against loop-diuretics alone. The trial will also determine the optimal type of loop-diuretic to use.
Eligible participants include adults over 18 years hospitalized with AHF and volume overload, showing signs of congestion and at risk of diuretic resistance. Exclusions apply to those with acute coronary syndrome, low systolic blood pressure, prior renal therapy, or previous treatment with Acetazolamide or Metolazone.
The primary outcome is the number of days alive and out-of-hospital by day 30. Secondary outcomes include a composite clinical benefit at 30 days, Kansas City Cardiomyopathy Questionnaire (KCCQ) scores, and successful decongestion 72 hours post-inclusion.
The trial aims to enroll about 1,041,939 patients across three treatment arms over three years. The minimal important difference is set as a reduction in out-of-hospital days by at least two days, with an anticipated low dropout rate. The study's power is calculated to be 80% with an adjusted alpha level for comparing the three diuretic groups.

开始日期2024-04-01

申办/合作机构

Copenhagen University Hospital

100 项与乙酰唑胺相关的临床结果

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100 项与乙酰唑胺相关的转化医学

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100 项与乙酰唑胺相关的专利（医药）

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项与乙酰唑胺相关的文献（医药）

2024-12-31·Journal of Enzyme Inhibition and Medicinal Chemistry

Acetazolamide and human carbonic anhydrases: retrospect, review and discussion of an intimate relationship

Review

作者: Tsikas, Dimitrios

Acetazolamide (AZM) is a strong pharmacological sulphonamide-type (R-SO₂-NH₂, pK_a 7.2) inhibitor of the activity of several carbonic anhydrase (CA) isoforms, notably of renal CA II (K_i, 12 nM) and CA IV (K_i, 74 nM). AZM is clinically used for about eighty years in various diseases including epilepsy and glaucoma. Pharmacological AZM increases temporarily the urinary excretion of bicarbonate (HCO₃^-) and sodium ions (Na⁺) and sustainably the urinary pH. AZM is excreted almost unchanged over several hours at high rates in the urine. Closely parallel concentrations of circulating and excretory AZM are observed upon administration of therapeutical doses of AZM. In a proof-of-principle study, we investigated the effects of the ingestion of a 250-mg AZM-containing tablet by a healthy volunteer on the urinary excretion of organic and inorganic substances over 5 h (range, 0, 0.5, 1, 1.5, 2, 3, 4, 5 h). Measured analytes included: AZM, amino acids and their metabolites such as guanidinoacetate, i.e. the precursor of creatine, of asymmetrically (ADMA) and symmetrically (SDMA) dimethylated arginine, nitrite (O = N-O^-, pK_a 3.4) and nitrate (O₂N-O^-, pK_a -1.37), the major metabolites of nitric oxide (NO), the C-H acidic malondialdehyde (MDA; (CHO)₂CH₂, pK_a 4.5), and creatinine for correction of analytes excretion. All analytes were measured by validated isotopologues using gas chromatography-mass spectrometry (GC-MS) methods. AZM excretion in the urine reached its maximum value after 2 h and was fairly stable for the next 3 h. Time series analysis by the ARIMA method was performed. AZM ingestion increased temporarily the urinary excretion of the amino acids Leu + Ile, nitrite and nitrate, decreased temporarily the urinary excretion of other amino acids. AZM decreased sustainably the urinary excretion of MDA, a biomarker of oxidative stress (i.e. lipid peroxidation). Whether this decrease is due to inhibition of the excretion of MDA or attenuation of oxidative stress by AZM is unknown. The acute and chronic effects of AZM on the urinary excretion of electrolytes and physiological substances reported in the literature are discussed in depth in the light of its extraordinary pharmacokinetics and pharmacodynamics. Tolerance development/drug resistance to AZM in chronic use and potential mechanisms are also addressed.

2024-07-01·American Journal of Ophthalmology

Clinical Course and Visual Outcomes of Papilledema in Pediatric Cerebral Venous Sinus Thrombosis

Article

作者: Gise, Ryan ; Sun, Jessica A ; Estrela, Tais

PURPOSECerebral venous sinus thrombosis (CVST) is a rare but life-threatening event with significant neurologic and visual morbidity. In this study, we report on the natural history and visual outcomes of papilledema in children with CVST.DESIGNRetrospective case series.METHODSPatients with CVST evaluated by the Department of Ophthalmology between 2000 and 2023 were included. Records were reviewed for presence and course of papilledema, treatment, and final visual outcomes following papilledema resolution.RESULTSThe study included 35 patients with a mean age of 9 ± 5 years and 40% were female. The most common risk factors for CVST were infection (69%), dehydration (26%), and hypercoagulability (23%). 31 patients (89%) had papilledema. Of these patients, 9 (29%) had progression of papilledema despite treatment, 17 patients (55%) did not have progression, and 5 patients (16%) lacked follow-up records. Initial Frisén grade among all cases was 2 ± 1, and cases with progression reached a grade of 4 ± 1 between 10 and 32 days following initial identification. Most patients (97%) were treated with anticoagulation and 100% required acetazolamide and/or lumbar puncture. Among 26 patients with follow-up, papilledema resolved in 107 ± 128 days. Fifty-four percent of patients had permanent ophthalmic sequelae. An initial Frisén grade ≥3 (odds ratio 7.54, 95% confidence interval 6.53-8.70, P< .001) was significantly associated with eventual optic atrophy.CONCLUSIONSChildren with CVST are at high risk for ophthalmologic sequelae. Papilledema can progress despite appropriate therapy. Our results highlight the importance of ophthalmologic follow-up during treatment course to prevent irreversible vision loss.

2024-07-01·Magnetic Resonance Imaging

A mathematical model for temporal cerebral blood flow response to acetazolamide evaluated in patients with Moyamoya disease

Article

作者: Svedung Wettervik, Teodor ; Fahlström, Markus ; Sousa, Joao M ; Berglund, Johan ; Wikström, Johan ; Lewén, Anders ; Enblad, Per

BACKGROUNDPaired cerebral blood flow (CBF) measurement is usually acquired before and after vasoactive stimulus to estimate cerebrovascular reserve (CVR). However, CVR may be confounded because of variations in time-to-maximum CBF response (t_max) following acetazolamide injection. With a mathematical model, CVR can be calculated insensitive to variations in t_max, and a model offers the possibility to calculate additional model-derived parameters. A model that describes the temporal CBF response following a vasodilating acetazolamide injection is proposed and evaluated.METHODSA bi-exponential model was adopted and fitted to four CBF measurements acquired using arterial spin labelling before and initialised at 5, 15 and 25 min after acetazolamide injection in a total of fifteen patients with Moyamoya disease. Curve fitting was performed using a non-linear least squares method with a priori constraints based on simulations.RESULTSGoodness of fit (mean absolute error) varied between 0.30 and 0.62 ml·100 g^-1·min^-1. Model-derived CVR was significantly higher compared to static CVR measures. Maximum CBF increase occurred earlier in healthy- compared to diseased vascular regions.CONCLUSIONSThe proposed mathematical model offers the possibility to calculate CVR insensitive to variations in time to maximum CBF response which gives a more detailed characterisation of CVR compared to static CVR measures. Although the mathematical model adapts generally well to this dataset of patients with MMD it should be considered as experimental; hence, further studies in healthy populations and other patient cohorts are warranted.

项与乙酰唑胺相关的新闻（医药）

2024-05-07

·赛柏蓝

19个品种首家过评！4个品种有新剂型报产

编者按：本文来自米内网，作者菜小白；赛柏蓝授权转载，编辑凯西2024年4月，3个1类新药首次获批上市，9个品种获批新适应症；19个品种首家过评，其中7个为首仿。01创新药品种申报情况2024年4月，116个创新药品种（药品注册分类为“1”的品种）获CDE承办。9个品种申请上市：艾本那肽注射液(常山凯捷健生物药物研发(河北))、达希替尼片(轩竹生物)、莫米司特片(赣州和美药业)、苹果酸司妥吉仑片(上药信谊药厂)、昂戈瑞西单抗注射液(上海君实生物医药)、司普奇拜单抗注射液(成都康诺行生物医药科技)、注射用金纳单抗(长春金赛药业)、龙七胶囊(江苏康缘药业)、珍珠滴丸(贵州民族药业)。2024年4月创新药上市申请承办情况2024年4月创新药临床申请承办情况02改良型新药品种申报情况2024年4月，40个改良型新药品种获CDE承办，氟唑帕利胶囊(江苏恒瑞医药)、甲磺酸阿帕替尼片(江苏恒瑞医药)、利多卡因凝胶贴膏(北京泰德制药)、卡度尼利单抗注射液(康方药业)、纳武利尤单抗注射液(施贵宝)、信迪利单抗注射液(信达生物制药(苏州))、伊匹木单抗注射液(施贵宝)等7个品种申报新适应症；磷酸奥司他韦口崩片(北京星昊医药)、水合氯醛糖浆(成都倍特得诺药业)、盐酸普萘洛尔滴剂(四川奥邦古得药业)、注射用醋酸曲普瑞林微球(长春金赛药业)等4个品种为新剂型。2024年4月改良型新药上市申请承办情况2024年4月改良型新药临床申请承办情况03新分类仿制药品种申报情况2024年4月，221个品种仿制申请获CDE承办，41个品种目前暂无国内仿制药获批。申报硫酸镁钠钾口服用浓溶液的企业最多，有5家：大冢制药、河北华晨药业集团、山东如至生物医药、浙江凯润药业、珠海横琴国研医药科技。目前国内有3家企业的硫酸镁钠钾口服用浓溶液获批上市，济川药业在2022年首仿获批。2024年4月新分类仿制药品种申报情况04存量品种一致性评价申报情况2024年4月，31个品种的一致性评价补充申请获CDE承办。别嘌醇缓释胶囊、茶碱缓释片、对乙酰氨基酚缓释片、复方甘草酸苷胶囊、甲磺酸酚妥拉明注射液、盐酸米诺环素片、盐酸维拉帕米注射液、乙酰唑胺片等8个品种首次有企业申报。2024年4月存量品种一致性评价申报情况05获批情况2024年4月有3款1类新药首次获批上市：恩替司他片(泰州亿腾景昂药业)、富马酸安奈克替尼胶囊(正大天晴药业集团)、盐酸伊普可泮胶囊(诺华)。9个品种获批新适应症。148个品种按新分类仿制申请获批，66个品种按存量品种一致性评价补充申请过评。其中，20个品种首家过评，奥卡西平口服混悬液(广州一品红制药)、比索洛尔氨氯地平片(成都硕德药业)、醋酸钠林格葡萄糖注射液(安徽丰原药业)、二甲双胍恩格列净片(Ⅲ)(江苏德源药业)、来特莫韦片(南京正大天晴制药)、利伐沙班颗粒(江西施美药业)、利奈唑胺干混悬剂(石家庄四药)等7个品种为国内首仿。2024年4月主要注册类型品种获批情况数据来源：米内网中国申报进度数据库（MED）、CDE、NMPA；相关统计字段按药品名称统计，时间截至2024年4月30日；获批品种按NMPA发布时间统计；药物作用靶点以及适应症整理自公开资料。END内容沟通：13810174402医药代表交流群扫描下方二维码加入银发经济市场机遇交流群扫描下方二维码加入左下角「关注账号」，右下角「在看」，防止失联

上市批准一致性评价

2024-05-05

·米内网

4月19个品种首家过评，4个品种有新剂型报产，这款口服溶液仿制企业最多

摘要abstract2024年4月，9个1类新药、4个新剂型改良型新药申报上市，7个品种申报新适应症；221个品种按新分类仿制申请申报，其中41个品种暂无国内仿制获批，硫酸镁钠钾口服用浓溶液的申报企业最多；31个存量品种有企业申报一致性评价，其中8个品种为首次申报；3个1类新药首次获批上市，9个品种获批新适应症；19个品种首家过评，其中7个为首仿。创新药品种申报情况2024年4月，116个创新药品种（药品注册分类为“1”的品种）获CDE承办。9个品种申请上市：艾本那肽注射液(常山凯捷健生物药物研发(河北))、达希替尼片(轩竹生物)、莫米司特片(赣州和美药业)、苹果酸司妥吉仑片(上药信谊药厂)、昂戈瑞西单抗注射液(上海君实生物医药)、司普奇拜单抗注射液(成都康诺行生物医药科技)、注射用金纳单抗(长春金赛药业)、龙七胶囊(江苏康缘药业)、珍珠滴丸(贵州民族药业)。2024年4月创新药上市申请承办情况2024年4月创新药临床申请承办情况改良型新药品种申报情况2024年4月，40个改良型新药品种获CDE承办，氟唑帕利胶囊(江苏恒瑞医药)、甲磺酸阿帕替尼片(江苏恒瑞医药)、利多卡因凝胶贴膏(北京泰德制药)、卡度尼利单抗注射液(康方药业)、纳武利尤单抗注射液(施贵宝)、信迪利单抗注射液(信达生物制药(苏州))、伊匹木单抗注射液(施贵宝)等7个品种申报新适应症；磷酸奥司他韦口崩片(北京星昊医药)、水合氯醛糖浆(成都倍特得诺药业)、盐酸普萘洛尔滴剂(四川奥邦古得药业)、注射用醋酸曲普瑞林微球(长春金赛药业)等4个品种为新剂型。2024年4月改良型新药上市申请承办情况2024年4月改良型新药临床申请承办情况新分类仿制药品种申报情况2024年4月，221个品种仿制申请获CDE承办，41个品种目前暂无国内仿制药获批。申报硫酸镁钠钾口服用浓溶液的企业最多，有5家：大冢制药、河北华晨药业集团、山东如至生物医药、浙江凯润药业、珠海横琴国研医药科技。目前国内有3家企业的硫酸镁钠钾口服用浓溶液获批上市，济川药业在2022年首仿获批。2024年4月新分类仿制药品种申报情况存量品种一致性评价申报情况2024年4月，31个品种的一致性评价补充申请获CDE承办。别嘌醇缓释胶囊、茶碱缓释片、对乙酰氨基酚缓释片、复方甘草酸苷胶囊、甲磺酸酚妥拉明注射液、盐酸米诺环素片、盐酸维拉帕米注射液、乙酰唑胺片等8个品种首次有企业申报。2024年4月存量品种一致性评价申报情况获批情况2024年4月有3款1类新药首次获批上市：恩替司他片(泰州亿腾景昂药业)、富马酸安奈克替尼胶囊(正大天晴药业集团)、盐酸伊普可泮胶囊(诺华)。9个品种获批新适应症。148个品种按新分类仿制申请获批，66个品种按存量品种一致性评价补充申请过评。其中，20个品种首家过评，奥卡西平口服混悬液(广州一品红制药)、比索洛尔氨氯地平片(成都硕德药业)、醋酸钠林格葡萄糖注射液(安徽丰原药业)、二甲双胍恩格列净片(Ⅲ)(江苏德源药业)、来特莫韦片(南京正大天晴制药)、利伐沙班颗粒(江西施美药业)、利奈唑胺干混悬剂(石家庄四药)等7个品种为国内首仿。2024年4月主要注册类型品种获批情况数据来源：米内网中国申报进度数据库（MED）、CDE、NMPA；相关统计字段按药品名称统计，时间截至2024年4月30日；获批品种按NMPA发布时间统计；药物作用靶点以及适应症整理自公开资料。本文为原创稿件，转载请注明来源和作者，否则将追究侵权责任。投稿及报料请发邮件到872470254@qq.com稿件要求详询米内微信首页菜单栏商务及内容合作可联系QQ：412539092【分享、点赞、在看】点一点不失联哦

一致性评价上市批准

2024-04-04

·Pharmaceutical Technology

Obsidian raises $160.5m to advance TIL cell therapy programme

TIL therapy uses naturally occurring immune cells that detect and attack cancer cells. Image credit: Shutterstock/Christoph Burgstedt. Obsidian Therapeutics has raised $160.5m in a Series C financing round, with plans for the funds to be injected into the biotech’s tumour-infiltrating lymphocyte (TIL) cell therapy programme. Obsidian, already backed by Bristol Myers Squibb (BMS), added Novo Nordisk Foundation’s investment arm Novo Holdings to its arsenal of investors in this latest round. US investment firm Wellington Management led the oversubscribed Series C. The US biotech previously raised $115m in a Series B round in 2021. Obsidian’s lead asset is OBX-115 , which is part of its TIL programme. OBX-115 is a TIL cell therapy – which expands and enhances the patient’s own immune cells extracted from around and within the tumour itself. Unlike the emerging chimeric antigen receptor (CAR) T cell therapies , TILs already have multiple tumour target recognition. The T cell immunotherapy is in a Phase I clinical trial for the treatment of melanoma and a Phase I/II clinical trial for the treatment of non-small cell lung cancer (NSCLC). In the melanoma trial (NCT05470283), which is being sponsored by the MD Anderson Cancer Centre, OBX-115 is being administered in combination with the diuretic acetazolamide. Data from the study will inform dose levels for a Phase II trial. The company reported an objective response rate of 50% and a complete response rate of 33% in topline data released in December 2023. See Also: Seaport emerges after $100m raise with ex-Karuna team at helm Pluri launches manufacturing division as cell therapy pipeline progresses The NSCLC trial (NCT06060613) is investigating OBX-115 as a monotherapy, with endpoints assessing the drug’s safety and efficacy in treating advanced solid tumours. Obsidian said the Series C proceeds will go towards clinical trial activities and manufacturing scale-up with a view to conducting pivotal trials. Obsidian has engineered OXB-115 such that it produces the membrane-bound interleukin 15 (IL-15). Interleukin-2 (IL-2) co-administration is usually needed with traditional TIL cell therapies to act as an immunostimulatory agent. Obsidian states that the membrane-bound IL-15 could widen patient access by reducing potential toxicities associated with high-dose IL-2. Vertex and BMS have seen the potential in Obsidian’s platform, both signing multi-year partnerships with the biotech to discover and develop new cell therapies. Last month, Iovance Biotherapeutics ’ Amtagvi (lifileucel) became the first TIL cell therapy to get regulatory backing in the US, winning a US Food and Drug Administration (FDA) accelerated approval. Obsidian’s OBX-115 will face competition from Iovance, with Amtagvi indicated for the treatment of metastatic or unresectable melanoma. Iovance has priced its immunotherapy at $515,000 in a market where there are currently no other FDA-approved cell therapies for the treatment of solid tumours. Amtagvi is forecast to generate sales of $846m by 2029, according to GlobalData’s Pharma Intelligence Centre. GlobalData is the parent company of Pharmaceutical Technology. Cell & Gene Therapy coverage on Pharmaceutical Technology is supported by Cytiva. Editorial content is independently produced and follows the highest standards of journalistic integrity. Topic sponsors are not involved in the creation of editorial content. Free Whitepaper Cell and gene therapies: Pipe dream to pipeline The cell and gene industry is gaining momentum, with a new wave of therapies promising to transform the way doctors treat, and even cure, disease. In this report, Cytiva and GlobalData have collaborated to explore the rise of the cell and gene therapy industries, the current state of the market, present and future opportunities for advancement, and the challenges that lie ahead. By Cytiva Thematic By downloading this case study, you acknowledge that GlobalData may share your information with Cytiva Thematic and that your personal data will be used as described in their Privacy Policy

细胞疗法临床1期免疫疗法临床结果基因疗法

100 项与乙酰唑胺相关的药物交易

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外链

KEGG	Wiki	ATC	Drug Bank
D00218	乙酰唑胺	S01EC01	DB00819

研发状态

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适应症	国家/地区	公司	日期
先兆子痫	日本	Sanwa Kagaku Kenkyusho Co., Ltd.	1994-06-02
睡眠呼吸暂停综合征	日本	Sanwa Kagaku Kenkyusho Co., Ltd.	1988-03-29
高眼压症	中国	天津力生制药股份有限公司	1983-01-01
呼吸性酸中毒	日本	Sanwa Kagaku Kenkyusho Co., Ltd.	1955-03-29
水肿	日本	Sanwa Kagaku Kenkyusho Co., Ltd.	1955-03-29
癫痫	日本	Sanwa Kagaku Kenkyusho Co., Ltd.	1955-03-29
青光眼	日本	Sanwa Kagaku Kenkyusho Co., Ltd.	1955-03-29
梅尼埃病	日本	Sanwa Kagaku Kenkyusho Co., Ltd.	1955-03-29
经前综合征	日本	Sanwa Kagaku Kenkyusho Co., Ltd.	1955-03-29

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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


ESPE2023	N/A	家族性高钙尿症性低钙血症	-	Oral calcitriol	(衊構衊顧獵鑰艱淵獵願) = 網範築襯願艱窪鹽憲淵蓋構選觸鏇齋憲膚窪衊 (夢範範襯範遞繭構鹽築 ) 更多	积极	2023-09-21
				Phenobarbital	(衊構衊顧獵鑰艱淵獵願) = 壓繭鬱衊積鬱簾衊繭餘蓋構選觸鏇齋憲膚窪衊 (夢範範襯範遞繭構鹽築 ) 更多
ADVOR trial (ESC2023)	N/A	-	519	Acetazolamide	鹹築鬱糧艱夢鑰憲憲遞(襯鑰醖膚鏇膚鑰顧網淵) = 網觸獵鑰獵鹽廠願遞觸觸製衊淵膚遞獵齋製窪 (糧襯襯淵構鏇築願廠憲 ) 更多	-	2023-05-21
				Placebo	鹹築鬱糧艱夢鑰憲憲遞(襯鑰醖膚鏇膚鑰顧網淵) = 範窪夢襯蓋醖憲衊鏇製觸製衊淵膚遞獵齋製窪 (糧襯襯淵構鏇築願廠憲 ) 更多
NCT03505788 (ADVOR, Pubmed)	临床4期	音量过载 \| 急性失代偿性心力衰竭	519	Acetazolamide	選衊鹽網廠鹽衊顧壓艱(範網餘醖廠鹽鑰鏇蓋鬱) = 膚遞壓積夢憲膚夢衊鏇鹽願壓艱觸觸艱觸積網 (鏇選襯艱鹽鬱淵鏇積壓 ) 更多	-	2023-05-23
ADVOR (Pubmed)	N/A	急性失代偿性心力衰竭	519	Acetazolamide	壓夢鹽鹽襯鹽壓觸鹹窪(遞衊鏇鏇鹽襯構蓋遞鬱): OR = 1.77 (95% CI, 1.18 ~ 2.63)	积极	2022-11-06
				Placebo
AAIC2022	N/A	阿尔茨海默症	-	Acetazolamide 125 mg	襯齋襯積廠齋鏇鹹顧壓(積艱壓選構壓憲簾襯鹹) = 襯獵衊繭夢製遞襯繭鬱繭範鑰遞壓獵艱鑰廠夢 (鹹願艱繭網襯醖簾壓獵 ) 更多	积极	2022-12-20
Pubmed	N/A	-	86	Acetazolamide	(鑰蓋積鑰憲膚繭簾淵餘) = 鏇繭夢衊網遞觸糧鹽淵範構獵窪繭獵憲壓艱獵 (艱顧鏇艱鹽窪鬱齋顧顧 ) 更多	-	2022-11-10
				Placebo	(簾窪衊廠餘築夢顧窪獵) = 憲網鏇製觸廠艱選願鏇齋鹹選蓋鹽願簾餘淵鹽 (壓淵遞憲餘積積蓋鏇觸 ) 更多
NCT03505788 (ADVOR Trial, Pubmed)	临床4期	急性失代偿性心力衰竭	519	Acetazolamide	鑰衊簾繭廠壓製鹽選憲(夢積選廠構鑰積築願鹽) = 夢繭鹽積繭選憲淵繭製艱製鑰蓋窪鹹顧廠鹹糧 (鹹艱壓夢製網鏇膚憲顧 )	-	2023-08-25
				Placebo	鑰衊簾繭廠壓製鹽選憲(夢積選廠構鑰積築願鹽) = 鏇淵齋願顧壓襯簾淵鏇艱製鑰蓋窪鹹顧廠鹹糧 (鹹艱壓夢製網鏇膚憲顧 )
NCT02755298 (Pubmed)	临床2/3期	肺血管疾病	28	Acetazolamide	(蓋膚顧餘夢鏇鬱構鏇觸) = 糧簾憲鏇繭網膚鏇顧憲鏇鏇憲積淵鏇醖鹽網簾 (糧積鏇廠顧鏇範觸夢艱 )	不佳	2023-01-11
NCT03505788 (ADVOR, Pubmed \| Br Dent J) 人工标引	临床4期	急性失代偿性心力衰竭	515	Acetazolamide	艱選觸蓋齋齋願鹽憲繭(餘齋選鏇範壓醖鑰構鬱) = 積繭衊艱襯選鹽鏇築襯廠餘繭遞遞願鬱襯醖遞 (齋醖餘蓋製積鬱鏇製製 ) 更多	积极	2022-08-27
				placebo	艱選觸蓋齋齋願鹽憲繭(餘齋選鏇範壓醖鑰構鬱) = 夢遞鬱糧繭積膚淵鹹積廠餘繭遞遞願鬱襯醖遞 (齋醖餘蓋製積鬱鏇製製 ) 更多
ANA2022	N/A	testosterone levels \| hypothalamic-pituitary-testicular axis \| hemoglobin ... 更多	-	Testosterone cypionate	艱構範糧糧範製齋繭製(憲襯襯觸蓋膚繭範憲齋) = 網鏇壓艱壓鑰糧鹹積衊簾鑰衊觸襯構鏇選鑰顧 (構淵願艱鑰繭齋膚構醖 ) 更多	不佳	2022-09-14
				Acetazolamide	艱構範糧糧範製齋繭製(憲襯襯觸蓋膚繭範憲齋) = 願遞憲鑰獵繭網積齋觸簾鑰衊觸襯構鏇選鑰顧 (構淵願艱鑰繭齋膚構醖 )