Upperton is a leading contract development and manufacturing organisation (CDMO) with capabilities to develop across multiple dosage forms, including OSD Capsules. Speak to our experts about developing your molecule today.
Capsule formulations are often the favoured dosage form for initial clinical studies as they offer a fast, convenient way to deliver the API to the pharmacy. Capsules may contain simple unformulated API or more advanced formulations, such as amorphous spray-dried dispersions designed to enhance bioavailability.
Whether your project is early stage R&D or late stage manufacturing, speak to our team about how we can support your capsule needs.
Filling spray dried powders and other API’s into hard shell HPMC or gelatin capsules enables projects to move more quickly into FIH or POC studies. In many cases, it is possible to fill capsules manually. As the trial progresses through the clinical stages. Scale up of batch size is managed through automation, into semi-automated capsules fillers (Profill range) and then onto fully automated capsule filling machines capable of producing several thousand capsules per hour. When developing the approach to capsule filling, consideration should be given to the target formulation, powder properties and the dose required.
Drugs that have short half-lives or are rapidly metabolized often require dosing three or four times a day to maintain drug levels in the required therapeutic range. In such cases, sustained-release dosage forms can reduce the frequency of dosing.
We provide fully integrated services across every stage of drug product development:
We provide fully integrated services across every stage of drug product development: