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Primmune aims to advance the development of their novel orally-administered, smallmolecule toll-like receptor 7 agonists as therapeutic-adjuvants for acute viral diseases and cancer. Primmune’s early data shows the potential for PRTX007 to drive the natural innate immuneresponse to combat systemic diseases. .
SmallMolecule Inhibitors. NMD670 is a first-in-class smallmolecule inhibitor of the muscle specific chloride ion channel, the ClC-1 ion channel. The secondary outcome involves pharmacokinetic endpoints. Oral, SmallMolecules. The primary outcome includes safety and tolerability endpoints.
However, this guideline is primarily intended to provide recommendations on evaluating the immune system’s response to smallmolecule drugs. The guidance contains recommendations for smallmolecule drugs, as well as any biological products that fall within CDER’s purview.
Developing Antimicrobial Peptides and Biomolecules In addition to traditional small-molecule antibiotics, researchers are exploring the potential of antimicrobial peptides (AMPs) and other biomolecules. AMPs disrupt bacterial membranes, making them less susceptible to resistance development.
Conversely, conjugation involves chemically attaching the drug to the nanoparticle surface, allowing for targeted delivery and improved pharmacokinetics. These ligands can be antibodies, peptides, aptamers, or smallmolecules.
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 smallmolecule chemotherapy – also holds the promise of enhanced therapeutic activity for ADCs.
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.
The MC4R-based ConfoGen was used to immunize llamas, resulting in an immuneresponse that generated a highly diverse panel of MC4R-specific agonists. In addition to generating agonistic antibodies, Confo is also successfully applying the ConfoBody/ConfoChimer technology to drugging GPCR with smallmolecules.
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