SAE Media Group reports: The Ophthalmic Drugs Conference will be focusing on developments in Gene Therapy for Ocular Diseases.
- (1888PressRelease) August 26, 2022 – The Ophthalmic drugs industry continues to expand year on year, with an ageing population there is continual demand for advancements in ophthalmic treatments. This year’s Ophthalmic Drugs Conference will have a key focus on gene therapy and artificial intelligence with developments on the latest drug pipelines and clinical trials.
The conference will convene on 21 22 November 2022 in London, UK, this year attendees will hear from industry giants about the developments being made in the ophthalmics and gene therapy field.
Interested parties can register at http://ophthlamicdrugs.com/PR21888 – register by 30 September to save £100.
The 5th annual conference will have a more in-depth discussion about the Developments in Gene Therapy for Ocular Diseases, with presentations and keynote speakers.
Use of Antisense Oligonucleotides for the Treatment of Inherited Retinal Diseases
Antisense oligonucleotides have shown much promise in Ph1/2 Clinical Trials in LCA10 and Ushers Syndrome
Lessons learned from Ph 2/3 trial with Sepofarsen for LCA10
Latest trial data from Interim Analyses for Ultevursen for Ushers syndrome and non-syndromic Retinitis Pigmentosa
Led by: Aniz Girach, Chief Medical Officer, ProQR Therapeutics
Lumevoq Gene Therapy in Leber Hereditary Optic Neuropathy
LHON, a rare disease with high unmet medical need
Development of Lumevoq Gene Therapy to treat ND4 LHON patients Developments in Gene Therapy for Ocular Diseases Drug Delivery Regulatory pathways
Key learnings from recent data
Led by: Magali Taiel, Chief Medical Officer, Gensight Biologics
Ocular Inflammation associated with Gene and Cell Therapy
Immune privilege and the eye
Inflammation and gene therapy
Inflammation and cell-based therapy
What to look for .
Led by: Virginia Calder, Professor of Ocular Immunology, University College London
Strengthening the Therapeutic Landscape for Inherited Retinal Diseases Using Genome Editing with AAV Vectors & CRISPR/Cas9 Technologies
Expanding on the clinical development of novel gene therapies including SPVN06
The benefits of designing gene therapies to act independently of the causative gene mutation
An introduction to new clinical trials and future workings
Led by: Daniel Chung, Chief Medical Officer, Sparing Vision
To find out more about the line up of the esteemed speakers for the conference and to download a complimentary brochure please visit http://ophthlamicdrugs.com/PR21888
For sponsorship enquiries contact Andrew Gibbons on +44 (0) 20 7827 6156 or email: agibbons ( @ ) smi-online dot co dot uk
For media enquiries or a press pass contact Marketing, Simi Sapal on +44 (0) 20 7827 6162 or email ssapal ( @ ) smi-online dot co dot uk
21-22 November 2022
Sponsor: The Technology Partnership | Celanese
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