Abstract Categories
You can present research in the following categories at the Annual Meeting

ASGCT Annual Meeting Abstract Categories

When submitting an abstract, authors will select one topic from the list below that best describes their abstract:

A - Viral Vector Development

  • A1 - Viral Vectors (excluding AAV – including lentivirus and other RNA viruses, adenovirus, herpesvirus, bocavirus, and chimetic vectors)
  • A2 - AAV Vectors - Virology and Vectorology (Excluding CNS)
  • A3 - AAV Vectors - Capsid Engineering
  • A4 - AAV Vectors - Preclinical and Proof-of-Concept In-Vivo Studies (Excluding Non-Human Primates)
  • A5 - AAV Vectors - Non-Human Primates and Large Animal Models
  • A6 - AAV Vectors - Manufacturing New Technologies
  • A7 - AAV Vectors - Immune Modulation 

B - Disease Models and Clinical Applications

  • B1 - Metabolic Diseases (including Diabetes)
  • B2 - Liver Genetic Diseases (including Hemophilia)
  • B3 - Lysosomal Storage Diseases
  • B4 - Heart, Lung, and Kidney Diseases
  • B5 - Neurologic Diseases - Vectorology (excluding Ophthalmic and Auditory Diseases) 
  • B6 - Neurological Disease Models (excluding Ophthalmic, auditory, and vectorology)
  • B7 - Ophthalmic and Auditory Diseases
  • B8 - Musculo-skeletal Diseases
  • B9 - Genetic Disorders of the Blood and Immune System (Including hemoglobinopathies, hematopoietic lineages, and inherited immune deficiencies)  
  • B10 - Organoids and Induced Pluripotent Stem Cells (iPSCs) Models of Disease

C - Gene Targeting and Gene Correction

  • C1 - Base Editing and Prime Editing
  • C2 - Epigenetic Editing and RNA Editing 
  • C3 - Genome Editing (including disruption, excision, and insertion – HDR)
  • C4 - On- and Off-Target Method Development
  • C5 - Gene Targeting and Gene Correction New Technologies 

D - Oligonucleotides

  • D - Oligonucleotide Therapeutics (including siRNAs, aptamers, antagomirs, miRNAs, shRNA, antisense, splice switching oligos, plasmids)  

E - Nonviral Delivery

  • E1 - Lipid nanoparticles (including Engineering, therapeutic delivery, Manufacturing, CMC considerations)
  • E2 - Physical delivery methods and DNA/RNA drug dvelopment (including electroporation, ultrasound, other enhanced physical methods of delivery, DNA/RNA modifications, and RNPs) 
  • E3 - Exosomes, VLPs and Nanoagents (including extracellular vesicles, microvesicles, synthetic polymers, but excluding LNPs) 

F - Cancer

  • F1 - Cancer - Immunotherapy and Cancer Vaccines
  • F2 - Cancer - Oncolytic Viruses
  • F3 - Cancer - Targeted Gene and Cell Therapy 
  • F4 - Cancer – CAR/TCR in T/NK and other immune cell types for Solid Tumors 
  • F5 - Cancer – CAR/TCR in T/NK and other immune cell types for Hematologic Malignancies 

G - Immunology

  • G1 - Challenges to Immunological Responses to Therapeutic Interventions (Includes host responses, therapy/prevention of infectious diseases, nucleic acid therapy, RNA-based Therapies; excludes cancer immunotherapy and cancer vaccines) 
  • G2 - CAR/TCR in T/NK and other immune cell types for Autoimmune and Infectious Diseases (Including immune targeting) 

H - Cell Therapy

  • H1 - Cell Therapies with or without Ex-Vivo Genetic Manipulation
  • H2 - In-Vivo Editing of HSPCs and Immune Cells

I – CMC & Clinical Translation

  • I1 - Vector Product Engineering, Development and Manufacturing (excluding AAV) 
  • I2 - Cell Therapy Product Engineering, Development and Manufacturing
  • I3 - Pharmacology/Toxicology Studies and Analytics/Assay Development
  • I4 - Molecular and Cellular Methods (Including assess vector integration, genome integrity, and outcomes) 
  • I5 - Chemistry, Manufacturing, and Controls (INCLUDING Vector & Cell Therapy, Formulation, Supply Chain)  

J - Clinical Trials

  • J1 - Gene Therapy Trials - In-Vivo Gene Therapy Modification
  • J2 - Cell Therapy and Cell-Based Gene Therapy Trials 

Submit an abstract

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