CURRICULUM ARCHITECTURE TAXONOMY REFERENCE GUIDE • ADC-RadCon 2027 Paris Directorate

Scientific Tracks & Subject Taxonomy

Comprehensive academic classification for proffered abstracts, podium defenses, and clinical symposia. Proffered manuscripts are evaluated under double-blind peer review and categorized across five primary translational disciplines.

TRACK CODE: TC-01

Novel Bioconjugation Chemistries & Cleavable Linker Design

Focuses on bioorthogonal conjugation reactions, structural linker stabilization, and controlled Drug-to-Antibody Ratio (DAR) engineering to maximize systemic circulation half-life while preventing premature payload detachment in human plasma.

TC-01.1

Site-Specific Conjugation Platforms

Enzymatic transglutaminase labeling, engineered unnatural amino acids, and cysteine-rebridging architectures achieving homogenous DAR 2, 4, and 8 profiles.

TC-01.2

Hydrophilicity & Pharmacokinetic Modulators

Polyethylene glycol (PEG) branches, polar carbohydrate shields, and polysarcosine spacers overcoming payload-induced aggregation and rapid hepatic clearance.

TC-01.3

Enzyme- & Lysosome-Cleavable Mechanisms

Cathepsin B-cleavable valine-citrulline (Val-Cit) and valine-alanine (Val-Ala) linkers, glucuronide-cleavable designs, and self-immolative spacer kinetics.

TC-01.4

Conditional Microenvironment Release

Tumor microenvironment-activated linkers responding to acidic intratumoral pH, hypoxia gradients, and extracellular matrix metalloproteinases (MMPs).

Review Directive for Track 01: Authors submitting synthetic chemistry datasets must include HPLC/LC-MS DAR characterization, in vitro plasma stability profiles (minimum 96 hours), and in vivo rodent pharmacokinetic parameters.
Submit Under Track 01 →
TRACK CODE: TC-02

Next-Gen Warheads & Payload Modalities

Addresses the transition beyond classic tubulin inhibitors (MMAE/DM1) toward high-potency Topoisomerase I inhibitors, targeted degradation actuators, immune-modulating warheads, and dual-targeted bispecific conjugates.

TC-02.1

Topoisomerase I Inhibitors & Camptothecins

Deruxtecan (DXd) and SN-38 derivatives, optimizing intracellular retention, bystander killing kinetics, and overcoming multi-drug resistance (MDR1) efflux pumps.

TC-02.2

Degrader-Antibody Conjugates (DACs)

Targeted delivery of PROTACs and molecular glues via antibody scaffolds to selectively degrade undruggable oncogenic transcription factors and kinases.

TC-02.3

Immune-Stimulating Payloads (ISACs)

STING agonists, TLR7/8 agonists, and RIG-I modulators conjugated to turn immunologically "cold" solid tumors "hot" without inducing systemic cytokine release storms.

TC-02.4

Bispecific & Biparatopic ADC Architectures

Dual-antigen targeting to enhance internalization velocity, overcome single-target downregulation, and achieve high solid-tumor selectivity over normal tissue.

Review Directive for Track 02: Manuscripts describing cytotoxic or immune warheads must report IC50 comparison values against established benchmarks, bystander killing assays, and off-target cytotoxicity controls.
Submit Under Track 02 →
TRACK CODE: TC-03

Targeted Alpha Therapies (TAT) & Radioligand Engineering

Dedicated to high linear energy transfer (LET) alpha-emitting radionuclides. Covers stable cage macrocycles, recoil daughter retention, small-molecule and peptide pharmacokinetic matching, and double-strand DNA cluster break radiobiology.

TC-03.1

Actinium-225 (225Ac) Chelation Platforms

DOTA modifications, crown ethers (Macropa), and novel eighteen-membered chelating rings achieving rapid radiolabeling kinetics at mild ambient temperatures.

TC-03.2

Lead-212 (212Pb) & In Vivo Alpha Generators

TCMC and cyclen-based chelator chemistry, managing Bismuth-212 daughter emissions, and exploiting Lead-212's favorable 10.6-hour therapeutic half-life.

TC-03.3

Astatine-211 (211At) & Halogen Chemistry

Aromatic Astato-demetalation reactions, neopentyl glycol stabilizers, and mitigating in vivo deastatination to prevent thyroid and stomach radiation uptake.

TC-03.4

Peptide & Nanobody Carrier Optimization

Designing low-molecular-weight carriers for rapid tumor infiltration and fast renal transit to avoid alpha-induced bone marrow exposure.

Review Directive for Track 03: Research must include radiochemical yield (RCY), radiochemical purity (RCP > 95%), daughter radionuclide release tracking, and renal clearance quantification.
Submit Under Track 03 →
TRACK CODE: TC-04

Clinical Theranostics & Dual-Action Imaging

Bridges the clinic and the imaging suite. Evaluates diagnostic stratification paired with beta and alpha therapy (e.g., Gallium-68/Lutetium-177, Copper-64/Copper-67), patient-tailored dosimetry, and multicenter solid tumor trial designs.

TC-04.1

68Ga / 177Lu Theranostic Pairs in Solid Tumors

Clinical response metrics in PSMA, FAPI, and SSTR-expressing tumors; optimizing administration intervals, pre-treatment imaging criteria, and salvage therapy protocols.

TC-04.2

Quantitative 3D Voxel-Based Dosimetry

SPECT/CT and PET/CT internal radiation dose calculations, assessing individual biological effective doses (BED) to avoid arbitrary standard-activity administration.

TC-04.3

Renal & Bone Marrow Radioprotection

Basic amino acid co-infusion strategies, gelatin-plasma expanders, and pharmacological nephroprotective adjuvants to widen the maximum tolerated activity (MTA).

TC-04.4

Combination Protocols: Radioligands + ADCs / IO

Evaluating radiation-induced antigen upregulation, synergy between targeted radionuclide radiation and immune checkpoint blockade, and sequence-dependent trial outcomes.

Review Directive for Track 04: Clinical reports must disclose ethical review board (IRB) approval, Declaration of Helsinki compliance, quantitative RECIST 1.1 or PERCIST response metrics, and Grade 3/4 toxicity incidence.
Submit Under Track 04 →
TRACK CODE: TC-05

Radioisotope Supply Chain, GMP Production & Safety Toxicology

Addresses the acute manufacturing bottlenecks confronting radiopharmaceutical expansion: isotope supply security, hot-cell automation, GMP quality release, regulatory CMC validation, and clinical translation toxicology.

TC-05.1

Actinium-225 Production Routes

Thorium-229 generator milking, high-energy proton spallation of Thorium-232, and cyclotron irradiation of Radium-226; addressing isotopic purity and Actinium-227 contamination limits.

TC-05.2

Automated Hot-Cell Radiosynthesis & QC

Microfluidic cassettes, robotic dispensing systems, rapid analytical release methods for short-lived radioisotopes, and compliance with Annex 1 sterile manufacturing regulations.

TC-05.3

Radiolytic Degradation & Formulation Stability

Radical scavengers (ascorbic acid, gentisic acid, ethanol) and carrier protein stabilizers to prevent self-radiolysis and linker fragmentation during cold-chain shipping.

TC-05.4

Radiation Safety, Waste Management & Regulatory CMC

Hospital radioactive waste storage, patient release clearance criteria, and harmonized cross-border radiopharmaceutical transportation regulations (IAEA / Euratom / US NRC).

Review Directive for Track 05: Submissions in CMC and manufacturing must highlight scalable process parameters, batch-to-batch radiochemical purity validation, and compliance with international pharmacopeia monographs.
Submit Under Track 05 →
ACADEMIC GOVERNANCE

Proffered Abstract Submission Standards

Every submission must adhere to the editorial guidelines established by the Review Directorate to qualify for double-blind peer review and conference proceedings indexing.

Double-Blind Formatting

Abstract texts must omit author names, institutional affiliations, and commercial brand identifiers within the abstract body to preserve blind evaluation integrity.

Word Count & Structure

Maximum 350 words structured into four distinct headings: Background & Aim, Methods & Chemistries, Results & Data, and Conclusions & Translational Impact.

10-Day Rolling Review

Manuscripts are assigned to collegiate review teams immediately upon intake, with formal editorial determinations delivered within 10 business days.

Presentation Allocation

Top-ranked submissions are designated for 15-minute Plenary Podium Defenses; all approved scientific studies are allocated to the Dedicated Poster Walk.

Review Directorate & Editorial Abstract Desk Convened by: Catalyst Colloquia Network • Central Inquiries: [email protected] • Direct Abstract Desk: [email protected] • Paris, France (Hybrid Convening)
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