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项与 Shreya Life Sciences Pvt Ltd. 相关的临床试验

CTRI/2012/09/003033

/ Completed临床3期

A 12 Week Open Label, Parallel Group, Comparative, Multicentric Phase III Study to Assess Efficacy and Safety of Metered Dose Buccal Insulin Spray versus Rapid Insulin s.c. on subjects with type II Diabetes who are inadequately controlled i.e. HbA1C 6.5 to 8.5 while on Oral Anti- Diabetic Agents - BUCLAR

开始日期2010-08-17

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Shreya Life Sciences Pvt Ltd.

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100 项与 Shreya Life Sciences Pvt Ltd. 相关的临床结果

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0 项与 Shreya Life Sciences Pvt Ltd. 相关的专利（医药）

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9

项与 Shreya Life Sciences Pvt Ltd. 相关的文献（医药）

2023-03-28·Indian Journal of Pharmacy and Pharmacology

A prospective, post-marketing surveillance (PMS) study to monitor the safety of fixed dose combination of Triprolidine Hydrochloride IP 2.5 mg and Phenylephrine Hydrochloride IP 5 mg [Recofast Tablets] for the symptomatic relief in patients with upper respiratory tract infections

作者: Patil, Preksha Pramod ; Kadoo, Sachin Madhukar

Upper Respiratory Tract Infection (URTI) is the most frequent illness in humans. The vast majority of acute upper respiratory tract infections are caused by viruses. These cause a variety of patient diseases including acute bronchitis, common cold, influenza, and respiratory distress syndromes.The study was conducted in patients with upper respiratory tract infections to see if the medication provides symptomatic relief in these conditions. Other conditions like allergic rhinitis and influenza were also included in the study for symptomatic relief.This is an open label, multicentric, active Post Marketing Surveillance (PMS) study with an objective to assess safety of fixed dose combination regarding Recofast tablets (Triprolidine Hydrochloride IP 2.5 mg and Phenylephrine Hydrochloride IP 5 mg) which was evaluated in 150 participants from different geographical regions. And then results were documented. A total of 19 (13%) patients recorded minor adverse event from these regions. Out of 150 patients 95 were male & 55 were female. All the patients were in the range of 18-80 years.No significant adverse events were observed during the course of the study, only 13% patients recorded minor adverse events from all regions. Thus this formulation is completely safe and effective in the management of Upper Respiratory Tract Infections and allergies.

2012-12-13·ISRN Pharmaceutics

Itraconazole Niosomes Drug Delivery System and Its Antimycotic Activity against Candida albicans

Article

作者: Wagh, Vijay D. ; Deshmukh, Onkar J.

Niosomes have potential applications in topical drug delivery system. The objective of the study was to formulate and evaluate the niosome of Itraconazole. Surfactant : cholesterol ratio and quantity of ethanol used were studied by applying factorial design. Formulated niosomes were evaluated for vesicle size, entrapment efficiency, drug release, skin permeation, and antimycotic activity. Vesicle size, entrapment efficiency, and drug release were markedly dependent on surfactant : cholesterol ratio and quantity of ethanol used. Permeation of the drug through the skin was affected by cholesterol content in formulation. Itraconazole niosome were having larger zone of inhibition than marketed formulation when activity was checked against C. albicans. Niosomes may be a promising carrier for topical delivery of Itraconazole especially due to their simple production.

World Journal of Pharmaceutical Research

Spectrophotometric method for the estimation of Clopidogrel bisulphate residue in swab samples

作者: Ghadlinge, Shyam V. ; Rajendra, Vivek B. ; Khushwaha, Shailendrasingh ; Deshmukh, Onkar J. ; Gulecha, Bhushan S. ; Rawat, Pavan Kumar

A simple, sensitive, rapid, precise, cost effective, and reproducible UV spectrophotometric method was developed for determination of clopidogrel residue in swab samples to validate cleaning procedure.The swabbing procedure was optimized to obtain suitable recovery from stainless steel surface using Tex wipe polyurethane swab stick.A mean recovery of 94.9733% was obtained when swab dipped in methanol were used.Beer's law is valid in concentration range of 2.5-20 μg/mL and UV detection was done at 217nm.The proposed method was validated in terms of linearity, precision, accuracy, limit of detection, limit of quantification.The proposed method was found to be accurate and precise for routine determination of clopidogrel in quality control laboratories

100 项与 Shreya Life Sciences Pvt Ltd. 相关的药物交易

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100 项与 Shreya Life Sciences Pvt Ltd. 相关的转化医学

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