NVG-291 for Spinal Cord Injury

(RESTORE Trial)

Not yet recruiting at 17 trial locations
ST
AR
Overseen ByAdam Rogers MD, Chief Executive Officer, NervGen Pharma
Pivotal Trial (Near Approval)This treatment is in the last trial phase before FDA approval
Prior Safety DataThis treatment has passed at least one previous human trial

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial tests a new treatment called NVG-291, an experimental therapy, to determine if it can improve hand function and daily activities in individuals with a spinal cord injury in the neck area. Researchers aim to assess the safety and effectiveness of this treatment compared to a placebo, which resembles the treatment but lacks the active ingredient. Participants will receive daily injections for 12 weeks and attend regular checkups. The trial suits adults who experienced a cervical spinal cord injury 1 to 10 years ago and still retain some movement in their arms or legs. As a Phase 3 trial, this study represents the final step before FDA approval, offering participants a chance to contribute to potentially groundbreaking treatment advancements.

Is there any evidence suggesting that NVG-291 is likely to be safe for humans?

In a previous study, patients generally tolerated NVG-291 well, meaning most did not experience serious side effects. Common side effects included mild headaches and slight nausea, typical for many medications and not severe enough to halt treatment. Since this trial is in a late stage, NVG-291 has already undergone earlier testing and demonstrated sufficient safety for broader testing. This is encouraging for potential participants, as it indicates NVG-291 has been safe for human use so far.12345

Why do researchers think this study treatment might be promising for spinal cord injury?

Unlike the standard treatments for spinal cord injury, which often focus on rehabilitation and managing symptoms, NVG-291 is unique because it targets a specific pathway in the body to promote nerve repair. This new mechanism of action is designed to enhance the body's natural ability to heal by modulating a protein involved in nerve growth and repair. Researchers are excited about NVG-291 because it offers a novel approach that could potentially improve recovery outcomes for patients with spinal cord injuries, providing hope for more effective healing.

What evidence suggests that NVG-291 might be an effective treatment for spinal cord injury?

Research has shown that NVG-291, which participants in this trial may receive, may help people with long-term spinal cord injuries improve their abilities. In various studies, this treatment led to noticeable improvements in movement, self-care, and quality of life. For instance, patients using NVG-291 gained better control over their arms and legs and became more active daily. It also calmed overactive nerve signals, which is important for improved movement. Overall, NVG-291 has shown potential in helping patients regain some lost abilities.678910

Are You a Good Fit for This Trial?

This trial is for adults with a chronic spinal cord injury in the neck area (cervical), who still have some movement below their injury. Participants should be generally healthy aside from their spinal cord injury.

Inclusion Criteria

Have chronic cervical spinal cord injury resulting from acute traumatic injury occurring 1 to 10 years prior to randomization
I have some hand grasp ability but not full function in at least one hand.
Be willing and able to comply with study visits, assessments, procedures, and drug administration requirements
See 6 more

Exclusion Criteria

I rely on a machine to help me breathe due to chronic respiratory failure.
I have severe nerve pain that is not well controlled by medication.
History of substance abuse within 12 months prior to screening
See 16 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive NVG-291 or placebo by subcutaneous injection once daily for 12 weeks

12 weeks
Weekly clinic visits for checkups and safety tests

Follow-up

Participants are monitored for safety and effectiveness after treatment

4 weeks
1 visit (in-person) within 14 days after Week 12

Open-label extension (optional)

Participants may opt into continuation of treatment long-term with NVG-291

What Are the Treatments Tested in This Trial?

Interventions

  • NVG-291

Trial Overview

The study tests NVG-291, given as a daily injection under the skin for 12 weeks, to see if it improves hand function and daily activities compared to a placebo. Participants are randomly assigned to either NVG-291 or placebo groups.

How Is the Trial Designed?

2

Treatment groups

Experimental Treatment

Placebo Group

Group I: NVG-291 ArmExperimental Treatment1 Intervention
Group II: Placebo ArmPlacebo Group1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

NervGen Pharma

Lead Sponsor

Trials
2
Recruited
110+

Citations

NervGen Pharma Announces Expanded CONNECT SCI ...

NVG-291 treatment produced a statistically significant reduction of hyperactive reticulospinal signaling in both the upper and lower limbs, as ...

Corporate Presentation

Preclinical efficacy in >15 models of nervous system damage demonstrating independent and validated evidence of neural repair and functional recovery. (1) ...

nervgen presenting interim phase 1 clinical trial data for ...

NVG-291 dose administered in the first cohort is already above the highest corresponding dose found to be efficacious in animal models and is substantially ...

504292-SPINAL CORD INJURY Canadian clinical trial search ...

A Trial Investigating the Efficacy and Safety of NVG-291 in Subjects With Chronic Spinal Cord Injury. MIZED, DOUBLE-BLIND, Phase data displayed ...

NervGen's NVG-291 Shows Clinically Meaningful ...

NVG-291 demonstrated clinically meaningful improvements in function, independence and quality of life … week study period compared to placebo.

6.

sci-corp.com

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Service Corporation International: Home

Service Corporation International is proud to be North America's leading provider of funeral, cremation and cemetery services. Since 1962, SCI has been serving ...

Injury | Journal | ScienceDirect.com by Elsevier

Topics covered include: trauma systems and management; surgical procedures; epidemiological studies; surgery (of all tissues); resuscitation; biomechanics; ...

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Commit to protect hunting for future generations. Safari Club International (SCI) is the leader in defending the freedom to hunt and promoting sustainable-use ...

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Injuries can be caused in many ways, including mechanical trauma, toxins, interactions with other organisms, or abiotic factors in the environment. In many ...

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injuryjournal.com

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Injury: Home Page

Our primary aim is to facilitate the exchange of ideas, techniques and information among all members of the trauma team. Read More. Companion Journal.