Glow LifeTech Corp. reported positive preliminary results from a clinical study into the influence of ArtemiC Support® on patients with Post-Acute COVID Syndrome, also known as Long COVID. Long COVID refers to the ongoing health problems that people can experience four or more weeks after being infected with SARS-COV-2[2], the virus responsible for COVID-19.

Long COVID is believed to affect more than 50% of all COVID-19 patients. The study, undertaken in conjunction with primary care clinicals in Barcelona, CAP Can Bou and Sardenya EAP Spain, was an open label, single arm study, consisting of six-weeks of treatment with ArtemiC Support®. The objectives of the study were to provide an initial assessment of the safety and efficacy of ArtemiC Support® in Long COVID patients.

The clinical study was sponsored by Swiss PharmaCan AG and co-sponsored by Glow and MGC Pharmaceuticals Ltd. The study enrolled 150 patients suffering from Long COVID who were administered ArtemiC Support®, under the supervision of their doctor, with their progress being measured using a Post-COVID Functional Scale (PCFS) and symptoms on a 10-point Likert scale at 1, 2, 3 and 6 weeks after treatment initiation. Symptoms measured include: Dyspnea - shortness of breath Asthenia - abnormal physical weakness or lack of energy, Anosmia - loss of senses of smell, Ageusia - loss of sense of taste, Cough, Headache, Mental confusion. The results of the study demonstrated a statistically significant reduction in the severity of several Long COVID symptoms, including Dyspnea, Cough, Asthenia, Headache and Mental Confusion over the course of the protocol.

The graphs below show the Emmeans (Estimated Marginal Mean) observed results from data collected during the Artemic Support® Long COVID study: · Dyspnea: a significant difference was seen in reported symptom severity (intensity) (visit 1 to visit 5), with a higher emmean indicating higher severity and a lower enmean indicating a lower severity. Cough: a significant difference was seen in reported symptom severity (intensity) (visit 1 to visits 4 & 5), with a higher emmeans indicating higher severity and a lower emmeans indicating a lower severity. Asthenia: a significant difference was seen in reported symptom severity (intensity) (visit 1 to visit 3, 4 and 5), with a higher emmeans indicating higher severity and a lower emmeans indicating a lower severity.

Headache: a significant difference was seen in reported symptom severity (intensity) (visit 1 to visit 3, 4 and 5), with a higher emmeans indicating higher severity and a lower enmeans indicating a lower. Mental confusion: a significant difference was seen in reported symptom intensity (visit 1 to visit 5), with a higher emmeans indicating higher severity and a lower emmeans indicating a lower severity.