공시 • May 02
EHAVE, Inc. announced delayed 20-F filing On 05/01/2026, EHAVE, Inc. announced that they will be unable to file their next 20-F by the deadline required by the SEC. 공시 • Sep 09
EHAVE, Inc. has filed a Follow-on Equity Offering in the amount of $200 million. EHAVE, Inc. has filed a Follow-on Equity Offering in the amount of $200 million.
Security Name: Common Shares
Security Type: Common Stock
Securities Offered: 2,000,000,000
Price\Range: $0.0005 to $0.1
Discount Per Security: $0 공시 • Dec 17
FDA Grants EHAVE, Inc. Consent to Proceed with Its Clinical Study on Intravenous Ketamine Infusion for Major Depressive Disorder Ehave, Inc. announced that it received confirmation from the U.S. Food and Drug Administration that its review of Investigational New Drug application is complete. The FDA authorized Ehave to proceed with its clinical study, "An open label study of electrographic responses pre, during and post, a low dose, weekly intravenous ketamine infusion for 4 weeks, in a study population with major depression disorder submitted under section 505 of the Federal Food, Drug, and Cosmetic Act for Ketamine HCl. The objective of this study is to characterize the change in EEG response of patients with MDD, during and 4 weeks after a course of IV ketamine infusions. The clinical study includes 35 participants with Major Depression Disorder. It will include subjects with an inadequate response to at least two FDA-approved antidepressant therapies, including the current course of antidepressant therapy, at a sufficient dose and duration for the current episode. An electroencephalography machine measures the brain’s activity at baseline and after four weekly low-dose IV ketamine study treatments. The purpose of the study is to learn about the neurological responses seen on EEGs of participants receiving low-dose IV ketamine therapy. Dr. Jeffrey Kamlet and Tristar Wellness will complete the study. Dr. Kamlet has served as the principal investigator on more than 20 major pharmaceutical trials. More than 264 million people across the globe suffer from depression. As a pervasive and often chronic health condition, depression is a global health burden and a significant source of disability. While depression might be considered a non-fatal health burden, severe depressive symptoms can lead to suicide, which is the second most common cause of death in people aged 15-29 years. Common treatments for depression include pharmacological interventions such as selective serotonin reuptake inhibitors, serotonin-norepinephrine reuptake inhibitors, monoamine oxidase inhibitors and tricyclic antidepressants and psychotherapy; however, the efficacy of these interventions often fails in severe cases. Ketamine is a dissociative anesthetic, used most frequently in veterinary medicine and pediatrics, that has been repurposed as an off-label analgesic and antidepressant. Extensive investigation of its rapid antidepressive effects have been a breakthrough offering a potential reprieve to those suffering from MDD. Ketamine has also been shown to reduce suicidal ideation in depressed patients at risk for suicide. Similarly, the administration of ketamine was effective at reducing depressive symptoms, acute suicidal behavior, and mood lability in the youth with treatment-resistant depression and bipolar disease. Intranasal esketamine is the only form of ketamine that has been FDA-approved as a treatment for TRD. However, clinical research and real-world feasibility have established significant drawbacks to intranasal ketamine, including patient discomfort with administration, greater risk of diversion to the illicit market, and potentially serious adverse reactions. Intravenous use of racemic ketamine is the more established route of administration as it has long been used as an anesthetic at much higher doses. Ehave management believes intravenous administration of ketamine includes benefits which include greater dose control and reduced cost of drug acquisition. This belief is the fundamental premise that has led to many dedicated outpatient clinics offering intravenous ketamine therapy for MDD across the United States. 공시 • May 03
EHAVE, Inc. announced delayed 20-F filing On 05/02/2022, EHAVE, Inc. announced that they will be unable to file their next 20-F by the deadline required by the SEC. 공시 • Apr 20
Ehave, Inc. Announces MetaHealthU Will Enter The Market With A Focus On HPPD Ehave, Inc. announced its MetaHealthU mobile application platform will focus on determining the cause and finding a possible cure for hallucinogen-persisting perception disorder (HPPD). Ehave has pioneered HPPD research efforts by launching a series of studies through its partnership with the University of Melbourne to gather data and bio-markers to target the condition. HPPD, (HPPD) or “flashbacks” is the only recognized long-term complication of hallucinogen use. It can cause a person to keep reliving the visual element of an experience caused by hallucinogenic drugs. As psychedelics become more widely accepted, the data and biomarkers from Ehave’s MetaHealthU will enhance research into HPPD, which will assist medical and mental health professionals diagnose if an individual is genetically predisposed to suffer from the condition. MetaHealthU is a mobile application platform that empowers individuals to take complete control of their health and their healthcare data. One component of MetaHealthU is its digital wallet connectivity with blockchain, which enables users to bundle and share their health records in a secure and seamless way. Ehave chose blockchain for its MetaHealthU platform since it increases trust, security, transparency, and the traceability of data shared across a business network — and delivers cost savings with new efficiencies. Ehave has partnered with BurstIQ, the leading provider of blockchain-based data solutions for the healthcare industry, to use its privacy-protecting technology to protect the personal information of MetaHealthU users. With MetaHealthU, users can securely track their health data from wearables, Electronic Health Records Systems (EHRs), Doctors and Medical Labs. It includes a “digital file cabinet” for medical records, which is ideal for research into HPPD. Users can log into their patient portals on various healthcare systems and medical labs and download their medical records in the digital file cabinet, which empowers individuals to take complete control of their health and their healthcare data. As Ehave progresses in its partnership with the University of Melbourne, the Company plans to create bio lines and a testing revenue model, as well as screening products based on MetaHealthU that are capable of indicating HPPD. Currently, researchers at the University of Melbourne have completed the necessary documents required for university ethics approval for online study of HPPD. The pilot study will begin sometime late in the second quarter, or the beginning of the third quarter. The researchers have also submitted a full ethics application, and are awaiting a decision on minimal risk accreditation. They have received preliminary approval for the pilot project to be considered “low or negligible risk,” and received ethics board review feedback on the submission seeking clarification on the role of funders regarding data, as well as minor clarifications on surveys/tasks being used. Individuals with HPPD have recurring visual disturbances that only recall the part of the psychedelic experience that involved visions, which can cause anxiety and affect a person’s vision. HPPD is most commonly caused by LSD and Mushrooms, but also can be caused by MDMA, Cannabis, and even SSRIs. As many as 5% of LSD users report some version of HPPD and serious cases could be as frequent as 1 in every 100 users of psychedelics. The market for an HPPD cure extends far beyond simple psychedelics. 공시 • Feb 10
EHAVE, Inc. (OTCPK:EHVV.F) acquired Rejuv IV Inc. EHAVE, Inc. (OTCPK:EHVV.F) acquired Rejuv IV Inc. on February 9, 2022. Rejuv IV will become KetaDASH, a wholly owned subsidiary of Ehave, Inc.
EHAVE, Inc. (OTCPK:EHVV.F) completed the acquisition of Rejuv IV Inc. on February 9, 2022 