Clinical Trial Support Services - GMP Clinical Trial Manufacturing of APIs - Piramal Pharma Solutionns
Piramal Pharma Solutions offer specialized services in the area of Clinical Trial Supply management. We provideprovide a range of clinical trial services that include clinical trial manufacturing, packaging and supply of APIs and Formulations. The services are offered for molecules in Phase I-III clinical trials
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Piramal Pharma Solutions offers wide range of clinical analytical support services, including analytical method development, validation and transfer and also API chemical and physical properties.
Pharmaceutical Development Services - Piramal Pharma Solutions
Piramal Pharma offers pharmaceutical development services for various dosage forms like Oral solids, Semi-Solids, Sterile and Non-Sterile in US, UK and India.
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Piramal Pharma Solutions experts offers pre-formulation studies in drug formulation with valuable information and suggestions to handle a wide range of compounds.
Process R&D and API Development Services | Piramal Pharma Solutions
Piramal Pharma R&D services provide pharmaceutical intermediated and API development for new drug discovery and development solutions to the clients worldwide.
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Non-GMP Kilo Lab Services | Rapid Drug Development
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ADC Process Development & Scale-up | Piramal Pharma Solutions
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Custom API Manufacturing Services | Piramal Pharma Solutions
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HPAPI (Highly Potent APIs) Development & Contract Manufacturing Services
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Pharmaceutical Development Services - Piramal Pharma Solutions
Piramal Pharma offers pharmaceutical development services for various dosage forms like Oral solids, Semi-Solids, Sterile and Non-Sterile in US, UK and India.
ADC Proof of Concept Studies | Bioconjugation Manufacturing
Piramal Pharma Solutions offers early stage development service for ADC Program. Its cost-effective service to demonstrate the viability of cytotoxic drugs or monoclonal antibodies for use of therapeutic ADCs.
Contract Development & Manufacturing Pharmaceutical company (CDMO) - Piramal Pharma Solutions, one of the leading pharmaceutical manufacturing companies in India established in 1984, offering contract manufacturing services covering drug life cycle from drug discovery to development. Contact us for further details.
A Comparison of Ceftriaxone and Cefuroxime for the Treatment of Bacterial Meningitis in Children | NEJM
Original Article from The New England Journal of Medicine — A Comparison of Ceftriaxone and Cefuroxime for the Treatment of Bacterial Meningitis in Children
pharmacokinetics of once-daily dosing of ceftriaxone in critically ill patients | Journal of Antimicrobial Chemotherapy | Oxford Academic
Abstract. The aim of this study was to determine the pharmacokinetic profile of the normal recommended dose of ceftriaxone in critically ill patients and to est
1g versus 2 g daily intravenous ceftriaxone in the treatment of community onset pneumonia – a propensity score analysis of data from a Japanese multicenter registry | BMC Infectious Diseases | Full Text
Background Community-onset pneumonia (COP) is a combined concept of community acquired pneumonia and the previous classification of healthcare-associated pneumonia. Although ceftriaxone (CRO) is one of the treatment choices for COP, it is unclear whether 1 or 2 g CRO daily has better efficacy. We compared the effectiveness of 1 g with 2 g of CRO for COP treatment. We hypothesized that 1 g CRO would show non-inferiority over 2 g CRO. Methods This study was an analysis of prospectively registered data of the patients with COP from four Japanese hospitals (the Adult Pneumonia Study Group-Japan: APSG-J). We included subjects who were initially treated solely with 1 or 2 g of CRO. The propensity score was estimated from the 33 pre-treatment variables, including age, sex, weight, pre-existing comorbidities, prescribed drugs, risk factors for aspiration pneumonia, vital signs, laboratory data, and a finding from chest xrays. The primary endpoint was the cure rate, for which a non-inferiority analysis was performed with a margin of 0.05. In addition, we performed three sensitivity analyses; using data limited to the group in which CRO solely was used until the completion of treatment, using data limited to inpatient cases, and performing a generalized linear mixed-effect logistic regression analysis to assess the primary outcome after adjusting for random hospital effects. Results Of the 3817 adult subjects with pneumonia who were registered in the APSG-J study, 290 and 216 were initially treated solely with 1 or 2 g of CRO, respectively. Propensity score matching was used to extract 175 subjects in each group. The cure rate was 94.6 and 93.1% in the 1 and 2 g CRO groups, respectively (risk difference 1.5%; 95% confidence interval − 3.1 to 6.0; p = 0.009 for non-inferiority). The results of the sensitivity analyses were consistent with the primary result. Conclusions The propensity score-matched analysis of multicenter cohort data from Japan revealed that the cure rate for COP patients treated with 1 g daily CRO was non-inferior to that of patients treated with 2 g daily CRO.