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Accelerating Drug Development through Collaboration Molecules-to-Medicine: Accelerating Drug Development through Collaboration
Case Study
Case Study 4: Gatifloxacin - Crystalline Form Changes With A Licensed Compound Gatifloxacin (also known as AM-1155, CG5501, and BMS-206584) has been established as a fluoroquinoline broad-spectrum antibiotic (Fukuda et al. 1998) (Fig. 10). It was originally discovered by Kyorin ...
Stability and Solubility Studies Chemical and physical stability. The intent of the stability study is to evaluate the chemical and physical stability of the API in solution and solid-state. The solid-state evaluation will probe the pr...
Comprehensive Physicochemical Property Evaluation A comprehensive physicochemical property evaluation is an important premise for the development of formulation and process. It provides an important basis for the druggability evaluation of the compou...
CATUG and Crystal Bio Establish Strategic Partnership, Launching “CATUG-Crystal” Joint Lab Dedicated to Advanced Nucleic Acid Analytical Services CAMBRIDGE, Massachusetts & CRANBURY, New Jersey, February 21, 2024, – CATUG Inc. (CATUG) and Crystal Bio, a member of Crystal Pharmatech, announced today a long-term strategic partnership to prov...
Unlocking the Power of AI in Pharmaceutical Development Featuring co-speakers: Kevin Bittorf, Ph.D., and Keith Parent
Developability Assessment, Pre-formulation Study for IND Enabling Strategic designing and generating work package utilizing analytical and biophysical tools to study accelerated and stressed stability of lead candidate for risk assessment
Product Quality Analysis Rationally combined both analytical with various biophysical/chemical tools and bio-analytical with various bioassay tools for structure and structure-function characterization
Additional Capabilities Versatile with flexible adoption of existing methods to address different modalities such as ADC with novel conjugated combinations, mRNA & LNPStrong troubleshooting skills in resolving challengin...
Application of Compaction Simulation Technology in the Development of Oral Solid Dosage Forms Characterization of powder mechanical properties and systematic study of powder compression are critical for guiding formulation and process development, enabling tableting scale-up across product lif...
AAPS PharmSci 360 Crystal Pharmatech will be at AAPS Booth 3345 to share practical formulation work and approaches that keep early development on track. If you're building data packages for IND or optimizing a clin...
Determination and Control of Crystal Form in ASD Formulations: A Case Study on Everolimus Tablets
Solid Form Landscape to Formulation Strategy: The role of computational screening and risk assessment