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Registration
Event
Hybrid Event

Accelerate Ideas, Partnerships and Opportunities

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  • Start 9:00am - 6:00pm
  • Rome, Italy
 

About Conference

Sciinov Group is proud to announce the Oligonucleotide Therapeutics and Delivery ConferenceSeptember 09-10, 2024 in Rome, Italy. This year OTDC 2024 annual Oligonucleotide Therapeutics and Delivery conference will showcase recent advances in oligonucleotide development, regulatory requirements and CMC considerations, strategies to enhance oligonucleotide discovery and targeting and optimised delivery techniques for oligonucleotide-based therapies, in the hope to continue to drive forward the field of oligonucleotide drug development. Join us on the September 09-10, 2024 at Rome, Italy.

Industry and academic experts deliver detailed case studies on ...

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Abstract Tracking Tool

ask & questions

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We are always looking for new industry leaders to join our speaker faculty to deliver presentations, lead panel discussions and moderate sessions or roundtables. 
If you are interested in being considered as a speaker, submit your proposal/abstract Online

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We let speakers propose the topic they want to talk about. This process allows speakers to propose sessions that speak from their expertise and passion.
Speaker can choose the topic of your choice in related to the conference subject or any of their recent research work to present at our conference.
For details of scientific sessions covered please visit [not limited to, you can propose]  

 

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Please visit the page here

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Yes, as our conference is scheduled in Hybrid Mode, you can present and listen to full program virtually connecting via ZOOM live stream


Recent Updates

16 JAN
2024

New RNA Therapeutics Core Facility to Drive Cutting-Edge Research

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21 FEB
2024

A new RNA editing tool could enhance cancer treatment

The new study found that an RNA-targeting CRISPR platform could tune immune cell metabolism without permanent genetic changes, potentially unveiling a relatively low-risk way to upgrade existing cell therapies for cancer.Readmore

9th JAN
2024

New CRISPR Center Brings Hope for Rare and Deadly Genetic Diseases

CRISPR collaboration combines expertise from three UC schools to scale treatment for diseases that industry has largely passed by – until now.Readmore

21 Aug
2023

Qalsody is an antisense oligonucleotide that targets SOD1 mRNA

FDA approved Qalsody (tofersen) to treat patients with amyotrophic lateral sclerosisReadmore


08:00-09:00

Registration

09:00-09:30

Opening Ceremony and Introduction

09:30-10:10

Keynote Session I

10:10-10:50

Keynote Session II

10:50-11:00

Refreshment Break

11:00-15:00

Break Out Session I

15:00-15:10

Refreshment Break

15:10-18:00

Break Out Session II

09:30-10:10

Keynote Session III

10:10-10:50

Keynote Session IV

10:50-11:00

Refreshment Break

11:00-15:00

Break Out Session III

15:00-15:10

Refreshment Break

15:10-18:00

Break Out Session IV

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