The Phase 1B/2A Connect SCI study found a 9.3x improvement in hand function compared to placebo and a 2x improvement in upper limb function compared to placebo. Specifically, improvements were noted in "grasp," which measures fine hand movements like putting a key in a lock or picking up a glass of water, and in coarse upper arm movements.
NervGen Pharma's mission is to bring NVG291 to market to improve the lives of individuals with spinal cord injury. The company anticipates starting a large Phase 3 clinical trial next year for chronic spinal cord injury patients (injuries from one to ten years old). Their focus for the next 6 to 12 months is ensuring a successful launch of this Phase 3 study.
The video mentions that the company has an FDA meeting coming up at some point. While the specific outcomes or details of this meeting are not elaborated on, it indicates interaction with the FDA regarding the development of NVG291.
The Phase 1B/2A Connect SCI study showed a 9.3x improvement in hand function compared to placebo and a 2x improvement in upper limb function compared to placebo. These improvements were specifically noted in "grasp," which measures fine hand movements, and in more general upper arm movements.
This video features a discussion with Dr. Adam Rogers, CEO of NervGen Pharma, about their innovative treatments for nervous system repair. The conversation highlights the company's lead candidate, NVG291, currently in clinical trials for spinal cord injury, and explores the underlying science of nervous system repair, drawing parallels to Dr. Rogers' past work in ophthalmology. They also touch upon the broader applications of NervGen's technology for other neurological conditions.
| Topic | Tags |
|---|---|
| Nervous System Repair | Nerve regeneration, Spinal cord injury, Neurotrauma, CNS repair |
| NervGen Pharma | NVG291, Clinical trials, Pharmaceutical, Biotechnology |
| Ophthalmology | Macular degeneration (AMD), Gene therapy, Anti-VEGF, Retinal diseases |
| Spinal Cord Injury (SCI) | Traumatic injury, Rehabilitation, Neurological deficit, Functional recovery |
| Neurological Conditions | Stroke, Traumatic Brain Injury (TBI), ALS, Hearing loss |
| Drug Development | Pre-clinical studies, Phase 1, Phase 2, Phase 3 trials, FDA |
| Scar Tissue Inhibition | CSPGs, PTP sigma, Inhibitory signals, Neuroplasticity |
| Department of Defense Collaboration | Blast injury, Defense Health Agency, Military medicine |
| Patient Advocacy & Unmet Medical Needs | Independence, Quality of life, Functional improvement, Unserved population |
| CEO Vision & Strategy | Company growth, Market expansion, Patient focus, Future outlook |
NVG291 works by inhibiting the protein tyrosine phosphatase sigma (PTP sigma) receptor. This receptor interacts with chondroitin sulfate proteoglycans (CSPGs) in the extracellular matrix of the central nervous system, which form scar tissue. By inhibiting PTP sigma, NVG291 is intended to block these inhibitory signals, allowing neurons to sprout and grow, thus enabling regeneration and repair of the nervous system.
Yes, the drug, NVG291, is designed to help nerves grow through scar tissue. Dr. Silver discovered that chondroitin sulfate proteoglycans (CSPGs) in the scar tissue, through interaction with the PTP sigma receptor, inhibit nerve regeneration. NVG291 inhibits the PTP sigma receptor, thereby blocking these inhibitory signals and allowing neurons to sprout and grow through or around the scar tissue.
The transcript mentions lower extremity functions in the context of what is not yet being discussed in detail. Dr. Rogers states, "And we're not even talking about, and I I can't even get into the lower extremity functions as far as improvements there, which we can talk about at a later date." This indicates that while there might be potential for improvements in lower extremity function, the current discussion is focused on other aspects and these details are reserved for a future conversation.