● Annual Assembly | November 11–12, 2027 | San Francisco

Annual Colloquium on Cell & Gene Therapy and Advanced Biotherapeutics

Convening academic principal investigators, clinical trialists, and molecular vector engineers to evaluate high-fidelity gene editing, synthetic cellular immunology, and non-viral nucleic acid delivery pipelines.

📅 November 11–12, 2027
📍 San Francisco, CA, USA
🎓 14.5 Educational Contact Hours
🌐 Hybrid: On-Site & Synchronous Virtual
14.5
Accredited Contact Hours
4
Scientific Tracks
100%
Double-Blind Peer Review
35+
Plenary & Poster Defenses

Bridging Preclinical Precision with Clinical Scalability

While viral and cellular engineering breakthroughs continue to transform rare disease and oncology landscapes, major clinical bottlenecks persist across vector manufacturing, off-target detection, in vivo immunogenicity, and solid tumor microenvironment suppression.

CellGene 2027 operates as a rigorous translational forum designed to accelerate laboratory findings into audited Phase I/II trial designs, matching academic faculty with bioprocessing engineers and clinical investigators.

Participating Delegate Profiles

The colloquium brings together specialized stakeholders across the advanced biotherapeutics ecosystem:

  • Academic Lab Heads & PIs: Directing functional genomics, synthetic biology, and vector development laboratories.
  • Clinical Trialists & Oncologists: Leading autologous and allogeneic cellular trials across university medical centers.
  • Bioengineers & Process Developers: Optimizing closed-system automated cell processing, LNP encapsulation, and viral titer yields.
  • Regulatory & CMC Directors: Auditing vector purity, cGMP release testing, and IND-enabling safety packages.

Four Core Tracks in Advanced Therapeutics

Peer-reviewed abstract evaluations are organized across dedicated scientific domains to connect clinical faculty with molecular engineering breakthroughs.

Track 01

CAR-T, CAR-NK & Engineered Cellular Immunotherapy

Next-generation cell architectures combating antigen escape, allogeneic off-the-shelf platforms, and solid tumor microenvironment infiltration.

  • Dual-targeting & tandem CAR architectures
  • Allogeneic iPSC-derived CAR-NK cells
  • T-cell exhaustion reversal & metabolic conditioning
Track 02

CRISPR, Base Editing & In Vivo Genomic Engineering

High-fidelity precision nucleases, prime editing optimizations, and rigorous protocols for measuring and mitigating off-target mutagenesis.

  • Epigenetic editing without double-strand DNA breaks
  • High-throughput GUIDE-seq & off-target screening
  • In vivo targeted tissue editing pipelines
Track 03

Viral (AAV/Lentivirus) & Non-Viral (LNP) Delivery Systems

Engineering enhanced tropism, reducing immunogenicity, and optimizing scalable manufacturing for viral and non-viral delivery modalities.

  • Novel synthetic AAV capsid directed evolution
  • Lipid nanoparticle (LNP) extrahepatic targeting
  • Electroporation & biomembrane mechanical delivery
Track 04

Regenerative Medicine & Stem Cell Therapeutics

Pluripotent stem cell-derived organ models, in vivo tissue regeneration, GMP compliance, and translational safety in human clinical trials.

  • GMP-compliant autologous & allogeneic bioprocessing
  • Exosome and extracellular vesicle therapeutic cargo
  • Clinical biodistribution & long-term tumorigenicity audits

Presentation Formats & Proceedings Indexing

All accepted proffered abstracts are indexed in the serialized colloquium compendium with permanent citable DOIs.

Podium Defense

Plenary Oral Presentation

15-minute podium presentation delivered in the primary colloquium amphitheater, followed by a 5-minute moderated discussion with panel discussants.

Visual Exhibition

Moderated Poster Defense

Dedicated physical poster board allocation across Day 1 and Day 2 exhibition intervals with designated evaluation defense windows for scientific appraisal.

Remote Access

Synchronous Virtual Defense

Live interactive digital presentation stream accommodating overseas faculty unable to travel to the United States due to institutional or visa restrictions.

Submission & Registration Milestones

Abstracts are accepted on a rolling basis with committee decisions returned within 14 business days.

Jan 31, 2027
Tier 1 Early-Bird Cutoff
Maximum registration savings for academic faculty & fellows.
Rolling
Abstract Decision Window
14-day turnaround for travel grant applications.
Aug 15, 2027
Late-Breaking Abstract Cutoff
Final deadline for late-stage clinical trial readouts.
Nov 11–12, 2027
Colloquium Assembly
Two full days of plenary podium & poster defenses in San Francisco.

Tiered Delegate Registration Rates

Early-bird rates valid through January 31, 2027. Proforma wire invoices available for university procurement.

Postdoc & Fellow Pass
$499
Standard: $649 | Verified ID Required
  • Full 2-Day Plenary & Poster Access
  • 14.5 Educational Contact Hours Certificate
  • Catered Luncheons & Evening Receptions
  • Compendium Proceedings Access
Register Fellow Pass
Biopharma & Corporate
$1,199
Standard: $1,499 | Industry Pass
  • Complete 2-Day Conference & Floor Access
  • Commercial Partnering Suite Access
  • Full Delegate Directory with Direct Contact
  • Company Listing in Printed Compendium
Register Corporate Pass

Need Proforma Invoicing or a Visa Support Letter?

The Secretariat Desk coordinates departmental purchase orders, wire transfers, and expedited invitation documentation for international research groups.

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