Remove 2021 Remove Immune Response Remove Pharmacokinetics Remove Small Molecule
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Antibody-drug conjugates payloads: then, now and next

Drug Target Review

Groundbreaking strategies like proteolysis-targeting chimeric molecules (PROTACs) are also being explored. 6 Combining the effect of payloads with different mechanisms of action – an approach that revolutionised small molecule chemotherapy – also holds the promise of enhanced therapeutic activity for ADCs.

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Organ-on-a-chip models in drug development

Drug Discovery World

Testing new modality drugs poses additional challenges The drug development pipeline is no longer predominantly composed of small molecule drugs. 2021) 6 evaluated the role of SPTBN1 in diet-induced liver diseases and cancer. Drug-induced liver injury (DILI) is the most common cause of acute liver failure in the western world 4.

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Organ-on-a-chip models in drug development

Drug Discovery World

Testing new modality drugs poses additional challenges The drug development pipeline is no longer predominantly composed of small molecule drugs. 2021) 6 evaluated the role of SPTBN1 in diet-induced liver diseases and cancer. Drug-induced liver injury (DILI) is the most common cause of acute liver failure in the western world 4.

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Analysis Life Sciences Thank You FDA finalizes new guidance on nonclinical assessment of potential immunotoxicity

Agency IQ

However, this guideline is primarily intended to provide recommendations on evaluating the immune system’s response to small molecule drugs. The guidance contains recommendations for small molecule drugs, as well as any biological products that fall within CDER’s purview.

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Advances in the Battle Against Autoimmune Disease

The Pharma Data

Small Molecule Inhibitors. NMD670 is a first-in-class small molecule inhibitor of the muscle specific chloride ion channel, the ClC-1 ion channel. The secondary outcome involves pharmacokinetic endpoints. The FDA has set an action date of July 7, 2021. Oral, Small Molecules.

Disease 52
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Pfizer Investor Day Features Significant Number of Pipeline Advances for COVID-19 Programs and Across Numerous Therapeutic Areas

The Pharma Data

Of note, The Phase 1b study is a double-blind, placebo-controlled clinical trial evaluating the safety, tolerability and pharmacokinetics of PF-07304814, a phosphate prodrug that when administered intravenously is metabolized to the active compound PF-00835321, shown to be a very potent inhibitor of the SARS-Cov2 3CL protease in preclinical studies.

Vaccine 52