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Meeting report: DMDG peptide and oligonucleotide ADME workshop 2022
Jesper Kammersgaard Christensen1, Inga Bjørnsdottir1, Anders Sonesson2
1Development ADME, Novo Nordisk A/S, Måløv, Denmark.
Summary
This report summarizes the 2022 Drug Metabolism and Discussion Group workshop on peptide and oligonucleotide ADME. Experts discussed challenges and solutions for drug absorption, distribution, metabolism, and elimination.
Area of Science:
- Pharmacokinetics and Drug Metabolism
- Medicinal Chemistry
- Biotechnology
Background:
- Peptides and oligonucleotides represent promising therapeutic modalities.
- Significant challenges exist in understanding and optimizing their absorption, distribution, metabolism, and elimination (ADME).
- The Drug Metabolism and Discussion Group (DMDG) convened a workshop to address these issues.
Purpose of the Study:
- To summarize key discussions and insights from the DMDG Peptide and Oligonucleotide ADME Workshop 2022.
- To highlight current challenges and proposed solutions in peptide and oligonucleotide ADME.
- To provide an overview of the topics covered, including drug modality landscape, metabolism, analytical methods, drug-drug interactions, and regulatory considerations.
Main Methods:
- The report is based on presentations and discussions from the DMDG workshop.
- Key topics were synthesized from expert contributions.
- Industry working group reports were incorporated.
Main Results:
- The workshop covered the current drug modality landscape for peptides and oligonucleotides.
- Discussions addressed metabolism and modeling strategies.
- Analytical challenges and drug-drug interaction reports were presented.
- Regulatory interactions concerning these drug classes were explored.
Conclusions:
- Addressing ADME challenges is crucial for the successful development of peptide and oligonucleotide therapeutics.
- Collaboration and discussion among experts are vital for advancing the field.
- The workshop provided valuable insights into overcoming hurdles in peptide and oligonucleotide drug development.
Keywords:
ADMEHRMSLC-MS/MSPBPK modellingPeptidesdrug-drug interactionsin vitro assaysoligonucleotidesplasma protein binding
