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The Role of Scientific Expertise in Generic Drug Development

Drug Patent Watch

The Importance of Scientific Expertise Generic drug development involves a deep understanding of the scientific principles underlying drug development, including pharmacology, pharmacokinetics, and bioequivalence. Retrieved from [link] East Street Pharmacy. For instance, the U.S. ” References : BioPharma Services. Johnson, W.

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Scalable precision design targeting complex product profiles

Drug Target Review

Given the relevance of brain metastases in cancer patients, what are the pharmacokinetic properties that enable CNS penetration of LSD1 inhibitors? To date, other LSD1 inhibitors in development have failed to achieve the combination of appropriate pharmacokinetics, required brain penetrance and a reversible mechanism of action.

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Regeneron’s BCMAxCD3 Bispecific Antibody (REGN5458) Shows Deep and Durable Responses in Patients with Heavily-pretreated Multiple Myeloma in Phase 1

The Pharma Data

Additionally, Regeneron bispecifics are manufactured using similar approaches used for human monoclonal antibody medicines, yielding similar properties and pharmacokinetics. These allow for the creation of bispecific antibodies that closely resemble natural human antibodies with no linkers or artificial sequences.

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United Therapeutics Corporation Reports Third Quarter 2020 Financial Results

The Pharma Data

We commenced launch activities for the Remunity Pump for Remodulin, including shipping training devices to specialty pharmacies and certain health care practitioners, and entering into agreements with specialty pharmacies to purchase Remunity Pumps and accessories and to pre-fill the Remunity cartridges exclusively with Remodulin.

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Analysis Life Sciences Thank You The FDA and oncology: 2023 year in review

Agency IQ

The data used to generate a control arm may be derived from prior clinical trial data (individual or pooled), or observational, real-world data (RWD), such as from registries, electronic health records (EHRs), and medical or pharmacy claims. In July, a new contract notice indicated that this is an area of interest for FDA as well.

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Analysis Life Sciences Thank You FDA’s nonprescription advisors find no efficacy for phenylephrine

Agency IQ

The committee also made recommendations regarding pharmacokinetic and safety assessments. Other comments from the American College of Clinical Pharmacy (ACCP) and American Association of Colleges of Pharmacy (AACP) also endorsed the actions sought in the Citizen Petition. hours, the drug is no longer physiologically active.

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Top 10 Life Science Resources

Alta Sciences

34: Toxicokinetics, Pharmacokinetics, and Pharmacodynamics Take a closer look at the collection and use of pharmacokinetic (PK) and pharmacodynamic (PD) data in early phase drug development, as well as the critical role of nonclinical toxicokinetic (TK) studies in guiding early phase clinical trials. Listen here. Watch it now.

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