May 2024
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00 issues in this vol.

AI-POWERED PATIENT EDUCATION: EVALUATING CHATGPT 4.0 AS A RESOURCE FOR UVEITIS

UVEITIS

A study led by scientists at Stanford University presented at ARVO 2024evaluated ChatGPT 4.0 as an online education resource for patients with uveitis.Standard ChatGPT responses were compared against information from topwebsites including the National Health Service, Cleveland Clinic, and Healthline,and specialists deemed the AI-generated responses to be comprehensive andaccurate, with additional flexibility to tailor information to the education level ofeach patient.

Equitable access to information in healthcare has been a challenge for the field, and evidence of AI's efficacy as an educational tool presents a potential solution to make reliable information accessible to patients regardless of their existing knowledge

DEEP LEARNING MODEL ESTABLISHED TO SEGMENT GA DATA

GEOGRAPHIC ATROPHY

Technological innovation in healthcare was a major topic atARVO 2024, highlighted by the presentation of a deeplearning model for geographic atrophy segmentationadaptable to swept-source optical coherence tomography(SS-OCT) and spectral domain OCT (SD-OCT) data. Throughanalysis of OCT images, the model achieved high sensitivity(99%) and specificity (93%), with a differential scanningcalorimetry of 0.92 compared to ground truth data,demonstrating promise as a tool to segment, monitor anddetect GA.

While deep-learning models have demonstrated efficacy in segmenting images of GA in patients to streamline studies, the adaptability of this tool to a variety of image types will allow it to be more effective in the real-world as a means for detection and diagnosis in new patients.

APELLIS' SYFOVRE (PEGCETACOPLAN) PRESENTS POSITIVE STUDY DATA AT ARVO 2024

GEOGRAPHIC ATROPHY

Apellis presented the 36-month results of the GALEstudy on SYFOVRE for geographic atrophy, a followon to the DERBY and OAKS clinical trials. The resultsdemonstrated a 42% reduction in non-subfoveallesions with monthly treatments at 3 years. The study also demonstrated a 38% risk reductionfor progression of visual impairment through monthlytreatments, a significant reduction compared to the2-year data previously released.

The study results support the real-world efficacy of SYFOVRE to slow GA progression, likely to bolster the drug's usage in the US market, where it has been available for over a year, and international markets where the new data will support regulatory approvals.

POST-HOC ANALYSIS OF BIOGEN’S SB15 SUPPORTS SWITCH TO AFLIBERCEPT BIOSIMILAR

AGE-RELATED MACULAR DEGENERATION

The post-hoc analysis of a Phase 3 trial on SB15, anaflibercept biosimilar, regarding the efficacy and safetyof switching in neovascular age-related maculardegeneration patients was presented at ARVO 2024.The study showed that switching to the biosimilarmaintained visual and anatomic outcomes relative to thebrand name (LUCENTIS), supporting its clinical use inproviding more affordable anti-VEGF therapy forpatients.

The indication of efficacy for the aflibercept biosimilar will provide patients a more alternative to the brand-name treatment, which was previously believed to be the only effective long-term treatment in its class.

REGENERON PRESENTS IMPROVED OUTCOMES IN EYLEA STUDY

DIABETIC MACULAR EDEMA

The results of Regeneron's Phase 2 BOULEVARDstudy for EYLEA were presented at ARVO 2024, whichused a new deep-learning based retina segmentationtool to show that patients with diabetic macularedema (DME) experienced improved outcomes withgreater reductions in intraretinal fluid (IRF) volumes,linked to improved vision at one year. Specificstatistical comparisons between IRF volumereductions (<20%, 20-50%, >50%) showed that agreater reduction in fluid after treatment led to agreater reduction in total retinal thickness, innerretinal thickness and ultimately better vision.

Not only did the study present promising results for the treatment of diabetic macular edema, but also demonstrated the utility of a new deep-learning based retina segmentation tool that significantly reduced the manual workload required to conduct the study.

MERCK ACQUIRES EYEBIO AND DME PIPELINE TO ENHANCE OPHTHALMOLOGY PORTFOLIO

DIABETIC MACULAR EDEMA

Separate from ARVO, Merck has acquired EyeBio to expandits pipeline with a novel late-phase candidate and preclinicaloptions for retinal diseases. The acquisition involves a $1.3billion upfront payment and up to $1.7 billion in milestonepayments, reflecting a potential total value of $3 billion.EyeBio's Restoret is set to enter a pivotal study for diabeticmacular edema in the latter half of 2024, following up on thepositive results from the AMARONE Phase II clinical trialreleased in February, which demonstrated a meanimprovement in best-corrected visual acuity and a meanreduction in retinal thickness.

The acquisition aims to enhance Merck's ophthalmology presence, expected to close in Q3 of 2024, and has the potential to impact financials by approximately $0.50 per share.

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