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Aura Biosciences’ novel treatment for uveal melanoma receives US FDA orphan drug designation
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The US Food and Drug Administration (FDA) granted Orphan Drug Designation to Aura Biosciences’ drug AU-011 for the treatment of uveal melanoma.

The FDA’s Orphan Drug Designation programme provides orphan status to drugs and biologics, which demonstrate promise for the diagnosis and/or treatment of rare diseases or conditions in the US. In addition, the first oral presentation of Aura Biosciences’ pre-clinical research, ‘Evaluating the in vivo efficacy of a first-in-class drug for the treatment of primary uveal melanoma’, was recently delivered by McGill University Health Centre researchers at the ARVO (Association for Research in Vision and Ophthalmology) Annual Meeting.

“There are currently no approved drug therapies for the treatment of uveal melanoma which is a rare but life threatening disease. We are thrilled to receive this Orphan Drug Designation that, together with the positive preclinical data, is enabling us to move this drug one step closer to the clinic,” said Elisabet de los Pinos, founder and CEO of Aura Biosciences.

Uveal melanoma, also referred to as ocular melanoma (OM), is an aggressive form of cancer that develops in the uvea, or uveal tract, of the eye. The primary tumour is diagnosed when it is still in the eye but has no targeted therapies available and is usually treated with an invasive radioactive plaque placed against the exterior of the eye near the tumour. This treatment requires multiple surgeries and can lead to cataracts, retinopathy and loss of vision. The alternative is enucleation, a surgery to remove the eye.

“There is an unmet medical need in the rare cancer patient community with which we work to have access to treatments that target the primary tumour and spare vision, forgoing risky and invasive surgical intervention. Aura’s novel approach has the potential to dramatically improve the outcomes, and hope, for patients with uveal melanoma,” said Grant Allen, Co-founder and chairman of the Ocular Melanoma Foundation. “The Orphan Drug Designation for AU-011 is a huge step forward, enabling Aura to potentially bring this drug to patients in an expedited manner.”

“The Melanoma Research Foundation’s CURE OM initiative leads the field in OM research support. We appreciate partners who are also working to advance the OM field and applaud efforts to develop new treatments with the goal of saving lives. Today’s news about a treatment that could potentially eliminate OM tumours early in the eye brings hope for improved outcomes for patients,” said Sara Selig, MD, CURE OM Co-Founder and Director, Melanoma Research Foundation.

AU-011 consists of Viral-like Nanoparticles that demonstrate highly selective targeting of solid tumours while leaving normal epithelium untouched. Aura’s lead product incorporates its viral-like nanoparticle conjugated with a potent cell-killing laser-activated molecule that is delivered efficiently and selectively to cancerous cells, thereby reducing or eliminating the risk of non-specific activity and undesirable toxicity. The molecule is activated by a standard ophthalmologic laser and treatment will be administered in an outpatient visit. A video explaining how Aura’s technology is applied to uveal melanoma can be accessed at the Aura Biosciences website at aurabiosciences.com.

Aura Biosciences is applying nanotechnology to the fight against cancer. Its novel viral-like nanoparticle technology, developed in partnership with the National Cancer Institute (NCI), harnesses the potential of viral evolution and tumour targeting for the treatment of cancer.

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