First UK patient enrolled onto Novartis retinal vascular disease study

Article

Luminous, a program created to develop the understanding of retinal vascular diseases, has enrolled its first patient this month.

Luminous, a program created to develop the understanding of retinal vascular diseases, has enrolled its first patient this month.

Novartis Pharmaceuticals has launched Luminous for wet age-related macular degeneration (AMD), diabetic macular oedema (DME) and visual impairment due to macular oedema secondary to retinal vein occlusion (RVO).

The program, in conjunction with leading ophthalmologists and the AMD Alliance International, will gather prospective data from 30,000 patients worldwide and will also include information from existing ranibizumab registries.

Christopher Brand, Royal Hallamshire Hospital, Sheffield, is the leading consultant ophthalmologist involved in the enrolment of the first UK patient. He said: "This programme will enable us to facilitate real-time comparisons between the results seen in the UK with different ranibizumab treatment regimens in clinics around the world. The information we receive could help us provide better care for our patients and identify the best course of therapy for each individual.”

Dr Timothy Cave, Chief Scientific Officer, Novartis Pharmaceutcals, explained: "A wealth of data is already available on the safety and efficacy of ranibizumab from clinical trials, but we hope Luminous will further support this data and provide information on the long-term outcomes in clinical practice. Novartis is committed to ophthalmology and improving understanding and treatment of vascular diseases.”

Recent Videos
Patrick C. Staropoli, MD, discusses clinical characterisation of Hexokinase 1 (HK1) mutations causing autosomal dominant pericentral retinitis pigmentosa
Richard B. Rosen, MD, discusses his ASRS presentation on illuminating subclinical sickle cell activities using dynamic OCT angiography
ASRS 2024: Socioeconomic barriers and visual outcomes in patients with rhegmatogenous retinal detachments, from Sally S. Ong, MD
Ashkan Abbey, MD, speaks about his presentation on the the CALM registry study, the 36-month outcomes of real world patients receiving fluocinolone acetonide 0.18 mg at the annual ASRS meeting in Stockholm, Sweden.
Nikoloz Labauri, MD, FVRS, speaks at the 2024 ASRS meeting about suspensory macular buckling as a novel technique for addressing myopic traction maculopathy
Jordana Fein, MD, MS, speaks with Modern Retina about the IOP outcomes with aflibercept 8 mg and 2 mg in patients with DME through week 48 of the phase 2/3 PHOTON trial at the annual ASRS meeting in Stockholm, Sweden.
John T. Thompson, MD, discusses his presentation at ASRS, Long-Term Results of Macular Hole Surgery With Long-Acting Gas Tamponade and Internal Limiting Membrane Peeling
ASRS 2024: Michael Singer, MD, shares 100-week results from the RESTORE trial
© 2024 MJH Life Sciences

All rights reserved.