The history of electroCore
Co-founded 2005
2005
We were co-founded in 2005 by JP Errico, Thomas J. Errico, MD, former president of the North American Spine Society, Charles Theofilos, MD, and Peter Staats, MD, former president of the North American Neuromodulation Society. The founders shared a mutual belief that neuromodulation represented a tremendous opportunity for safer and more effective treatments across a variety of conditions.
Initial Studies
2008
Our first human studies were completed in emergency room patients and tested the ability of VNS to treat asthma.
Pivotal Cluster Headache Studies
2014-2015
We completed our first cluster headache study in 2014. Soon after, in 2015, we announced that we would be initiating two pivotal studies in the acute treatment of cluster headache.
FDA Clearance
2017
In April 2017, we received FDA clearance for the acute treatment of pain associated with episodic cluster headache. We began commercial distribution in the US shortly after.
FDA Clearance
2018
In January 2018, we received FDA clearance for the acute treatment of pain associated with migraine headache.
Initial Public Offering
2018
In June 2018, we announced an IPO with the Nasdaq Global Select Market and began trading under ECOR.
FDA Clearance
2018
In November 2018, we received FDA clearance for the adjunctive use for the preventive treatment of cluster headache.
FDA Clearance
2020
In March 2020, we received FDA clearance for the preventive treatment of migraine headache in adult patients.
EUA
2020
In July 2020, gammaCore Sapphire™ CV (nVNS) receives EUA to treat patients with known or suspected COVID-19 who are experiencing exacerbation of asthma-related dyspnea and reduced airflow.
FDA Clearance
2021
In February 2021, we received FDA clearance for the acute and preventive treatment of migraine in adolescents 12 to 17 years of age.
FDA Clearance
2021
In September 2021, we received FDA clearance to treat Paroxysmal Hemicrania and Hemicrania Continua
Breakthrough Device Designation for PTSD
2022
gammaCore was granted Breakthrough Device Designation for PTSD by the US Food and Drug Administration in January 2022.