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Case Studies & WhitepapersMar 24, 2025

Preformulation Strategy- Inception to Completion

Drug discovery is an exceedingly complex process. Discovering a new chemical entity is in itself a huge accomplishment, which is often possible only after almost two decades of hard experimental work as well as advanced simulation efforts. Therefore, the next stage of the process, determination of toxicity becomes even more crucial as most new chemical entities (NCE) are disqualified if the NCE shows a potential toxic effect, despite any possible therapeutic effect.

Small MoleculesMar 13, 2025

Facilitating PROTAC Drugs Development with Innovative Processes

The PROTAC technology, through an innovative mechanism of "degradation rather than inhibition," provides a new pathway for targeting traditionally undruggable proteins and addressing resistance issues.

Biologics and ConjugatesFeb 10, 2025

Efficacy and Safety - Guidelines for Clinical In-use Stability Studies of ADCs

Antibody-drug conjugates (ADCs) consist of three parts: antibody, linker, and payload. This special combination enables ADCs to selectively target tumor cells and release cytotoxic drugs, but they face many stability challenges during manufacture, storage, and clinical use. In this paper, the drug product development team at Porton (hereinafter referred to as "we") discusses the necessary clinical in-use stability studies for ADCs.

Case Studies & WhitepapersJan 06, 2025

Molecular Modeling and Data Science for De-risking and Cost- saving of Pharmaceutical Development

Molecular Modeling and Data Science for De-risking and Cost- saving of Pharmaceutical Development

Small MoleculesJan 06, 2025

Continuous Improvement of Project Life Cycle Management, Benefiting Customers by Reducing Total Cost

Continuous Improvement of Project Life Cycle Management, Benefiting Customers by Reducing Total Cost

Case Studies & WhitepapersJan 03, 2025

Agile and Fast:Enabling Rapid Market Launch of Innovative Drugs from Preclinical to Commercialization in 18 Months

Enabling Rapid Market Launch of Innovative Drugs from Preclinical to Commercialization in 18 Months

Overview and Case Study of Antibody Oligonucleotide Conjugates (AOC)

Biologics and ConjugatesNov 27, 2024

Overview and Case Study of Antibody Oligonucleotide Conjugates (AOC)

In the field of biomedical science, technological changes are common and constantly evolving. In recent years, antibody oligonucleotide conjugates (AOCs) have attracted considerable attention in the industry as an innovative and advanced biomedical method, and more and more domestic and foreign biopharmaceutical companies have participated in the research and application of AOCs. Because AOC combines the advantages of oligonucleotide technology and antibodies, it is considered to have the potential to provide precise targeted therapy and is expected to bring about a revolution in the biomedical field.

Small MoleculesNov 25, 2024

Co-processing: Co-Precipitation Technology (CPT) for the Enhancement of Flowability and Bulk Density

Formulating compressed tablets is one of the most widely used oral solid form dosages. However, a vital first step is choosing a suitable manufacturing approach and the right excipients to support the desired therapeutic effect.

Biologics and ConjugatesNov 18, 2024

An ADC's Path to Market-Analysis of Difficulties and Key Points in ADC Process Scale up

An Antibody-Drug Conjugate (ADC) is a novel therapeutic agent which can deliver a highly-potent traditional small molecule drug to a specific site or cell within the body. It is formed when an active drug (the payload) is connected to an antibody using a linker. The complex is referred to as an ADC and it uses the cellular specificity of antibodies to direct the payload and deliver to the active disease site within the cell. This enables ADCs to selectively treat cancer cells, tumor microenvironments, or other target cells, while reducing systemic, off-target toxicity. This targeted delivery of ADC agents has shown great promise and explosive growth in recent years.

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