Table 2.
The SCN9A is a Gene Which Belongs to a Gene Family That is Involved in the Development of Sodium Channels
Status | Study Title | Conditions | Interventions | Phase | Sponsor/Collaborators | Locations |
---|---|---|---|---|---|---|
Completed Has results |
The impact of SCN9A gene polymorphism on individual pain perception in the general population | Pain Surgery |
Xianwei Zhang Huazhong University of Science and Technology |
Department of Anesthesiology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology Wuhan, Hubei, China |
||
Recruiting | fMRI-study in patients with small fiber neuropathy | Small fiber neuropathy | Diagnostic test: functional MRI |
Harvard University |
Maastricht University Medical Center Maastricht, Netherlands |
|
Completed | The impact of the SCN9A gene polymorphism on postoperative pain |
Pregnancy |
Drug: Opioid Tramadol |
Tokat Gaziosmanpasa University | Gaziosmanpasa University Medical School Hospital Tokat, Turkey |
|
Completed | Safety and tolerability of lacosamide in patients with gain-of-function Nav1.7 mutations related small fiber neuropathy | Small fiber neuropathy |
Drug: Placebo |
Phase 3 | Academisch Ziekenhuis Maastricht | Maastricht University Medical Center Maastricht, Netherlands |
Active, not recruiting | Evaluation and risk assessment for persistent postsurgical pain after breast surgery |
Depression, anxiety |
Other: Pain threshold assessment |
Duke University |
KK Women’s and Children’s Hospital Singapore, Singapore |
|
Unknown † | Painful channelopathies study |
Chronic pain |
Other: Observation |
Neuroscience Technologies S.L.P |
Nuffield Department of Clinical Neurosciences Oxford, Oxfordshire, United Kingdom |
Notes: The positively charged sodium ions are transmitted through these channels generating and transmitting electrical signals. The SCN9A gene is involved in the making of the alpha subunit of its protein expression which assembles into the sodium channel called Nav1.7. Nav1.7 is found in key locations within the peripheral nervous system and is involved in the transmission of pain signals. There is presently six human clinical trials studies that are associated with the understanding of SCN9A that are listed on http://www.clinicaltrials.gov as of December 2022. Of the several studies listed, only one indicated a human clinical phase III study completion. That study looked at small fiber neuropathy treated by the therapeutics lacosamide. Lacosamide is a therapeutic that is used to control seizure, namely partial onset seizures, in both adults and children from the age of one month and older. The results were in conclusion. Therefore, there is a presently no Food and Drug Administration (FDA) approval of a small molecule that can be used to treat chronic pain no matter the source of pain. The small lack of therapeutic studies could indicate the challenges of a moving a small molecule through human clinical trials targeting SCN9A. Yet, there is significant evidence that the targeting of the gene has the potential bring to bear hope to millions that suffering from chronic pain. A success treatment targeting SCN9A could be the answer to the opioid crisis by presenting a viable therapeutic alternative.