最新色情影片

Skip to Main ContentSkip to FooterSkip to Search
Main menu
Regional Sites
  1. Home
  2.  » OptiForm庐 Solution Suite
Icon of a water droplet with a beaker inside of it

OptiForm庐 Solution Suite

When developing a new therapy, challenges often arise during the early stages of development: outcome of preclinical assessments, timing of the project, funding, and patient needs.聽 The path to first-in-human needs to be as fast and efficient as possible, but improper candidate selection, poor formulations, and gaps in clinical dose strategy can lead to inadequate preclinical and clinical data; often extending timelines and increasing cost.

最新色情影片 has a long history of early phase development and understands these challenges and has developed OptiForm庐 Solution Suite, a comprehensive program that seamlessly integrates for candidate selection, optimal form assessment, bioavailability enhancement, and cGMP clinical materials delivery.

最新色情影片 helps its partners turn promising molecules into better treatments with its 鈥淔ollow the Molecule庐鈥 contract manufacturing and drug development services that provides accelerated integrated solutions from development to commercial supply.

OptiForm庐 Solution Suite was designed to help you get it right the first time.聽 At each step in the process, 最新色情影片 has developed ways to accelerate your project鈥檚 progress, reduce risks, and get you to the key decision points quickly.聽 Based on our experience, 最新色情影片 has designed this service around five critical areas of development:

  1. Candidate Selection: 最新色情影片 helps you select your most viable candidate with services that provide insight on developability and solubility tools designed to maximize exposure with minimal material usage.
  2. Preformulation: Backed by a range of expert testing and release capabilities, our preformulation team provides expert support from preclinical stages of drug development through regulatory filing for oral solid dosage forms.
  3. Formulation Selection: This includes parallel screening of proven bioavailability enhancement technologies for challenging molecules.
  4. Formulation Development for GLP Toxicology Studies
  5. Formulation & cGMP Manufacturing for Phase 1

Let’s look at each in detail.

Back to top

CANDIDATE SELECTION

Don鈥檛 let your molecule meet the same fate as the hundreds of discovery molecules shelved each year due to poor solubility, or the estimated 40% of drugs that fail in development due to not having an appropriate DMPK profile1. 最新色情影片 helps you select your聽most viable candidate with services that inform on developability, and solubility tools designed to maximize exposure with minimal material usage.

翱耻谤听OptiForm庐聽Select formulation screening聽tool allows you to quickly obtain initial PK data using our laboratory service or an in-house kit you can order. Combined with expert聽in silico聽DMPK modeling, you get a full understanding of human PK and critical formulation parameters early so you can advance your molecule.聽Read more

1 Alavijeh, Mohammad S., Palmer, Alan M.; The Pivotal Role Of Drug Metabolism And Pharmacokinetics In The Discovery And Development Of New Medicines, Drugs: the investigational drugs journal 7(8):755-63 路 September 2004

Back to top

PREFORMULATION

Characterizing your molecule is critical in understanding potential challenges and gaining insight into formulation strategies. By applying proven high throughput screening tools, 最新色情影片 provides detailed pre-formulation data to help characterize your molecule. A dedicated OptiForm庐 Solution Suite scientific advisor will then recommend a development and formulation path based on preformulation and solid-state screening data. If your molecule has bioavailability challenges, the next phase of OptiForm庐 Solution Suite will screen it against proven bioavailability enhancing technologies to keep your program moving forward.

Back to top

BIOAVAILABILITY ENHANCEMENT SCREENING

Your molecule may be one of the many with bioavailability challenges because according to industry reports1聽only “1 in 10 new molecules in active clinical development are readily bioavailable2“, and even those may not be sufficiently absorbed when dosed at escalated levels. OptiForm庐 Solution Suite is your answer. By utilizing the Developability Classification System3 we consider both dissolution and solubility for poorly soluble drugs, and combined with a parallel screening approach, 最新色情影片鈥檚 formulation experts efficiently determine the feasibility of multiple bioavailability enhancement technologies, test short-term stability, and ship prototypes to your facility of PK testing. Once you鈥檝e obtained your PK data, your dedicated OptiForm庐 Solution Suite adviser will provide formulation options based on physical, chemical, and processing stability risks to provide directional ranges of dose escalation limits (exposure and Acceptable Daily Intake driven), and recommend a path forward based on rigorous data so you can make an informed decision on your formulation strategy for Phase I studies. Whether your molecule benefits from a lipid-based formulation, amorphous dispersion, or even particle size reduction, OptiForm Solution Suite will keep you moving forward.

2 R. Lipp; The Innovator Pipeline: Bioavailability Challenges and Advanced Oral Drug Delivery Opportunities, Am. Pharm. Rev., 2013

3 Butler JM1, Dressman JB.; The developability classification system: application of biopharmaceutics concepts to formulation development.; J Pharm Sci. 2010 Dec;99(12):4940-54. doi: 10.1002/jps.22217.

Back to top

FORMULATIONS FOR GLP STUDIES

With a handle on formulation, testing your drug for toxicity is a critical next step. Avoid getting tripped up by suboptimal formulations that don鈥檛 provide proper exposure, leading to potential costly delays. OptiForm庐 Solution Suite uses rigorous preformulation data and guidance and allows you to test with confidence due to our ability to develop intravenous and either conventional or bioavailability enhanced oral formulations for cGLP studies that can provide maximum exposure of your molecule during toxicity studies.

Back to top

PHASE I DOSE FORM DEVELOPMENT & GMP MANUFACTURING

When you鈥檙e ready for Phase 1, the invaluable data generated quickly in your OptiForm庐 Solution Suite program allows your 最新色情影片 adviser to collaborate to develop a dosage form strategy for first-in-human clinical studies. Whether you need a powder-in-capsule or an enhanced formulation, 最新色情影片 can manufacture your clinical trial material under cGMP conditions to get you into clinic and beyond. Your Molecule has so much potential. We share your passion to unlock it with OptiForm庐 Solution Suite.

Back to top

WEBINARS

A number of recent webinars provided more details to the structured approach for parallel formulation feasibility assessment that is designed to reveal the most suitable pathway to enhance bioavailability and accelerate development. Learn more by viewing:

Back to top

AFTER YOUR OPTIFORM庐 SOLUTION SUITE PROGRAM

With 最新色情影片鈥檚 extensive network of聽Clinical Supply Services聽and Manufacturing Solutions, we can stay with you every step of the way, offering expert dose design guidance, advanced聽drug delivery technologies, and even聽regulatory support聽for your submission. Continue the journey with 最新色情影片 to achieve an optimized therapeutic profile and dose form which meets patient, payer, and provider needs.

By using this website you understand and accept that 最新色情影片 tracks your website activities to be able to offer you a more tailored response or information to meet your requirements, and that your personal data will be held in accordance with our聽听触听听触听Cookies Settings.