Thursday, September 30, 2021 11:41:05 AM
MyMD's 6th Path To Success
This Path relates to the Akers Biosciences / Premas Biotech Covid 19 vaccine!
History - When Akers was an independent company it contracted with Premas Biotech of India for a Covid 19 vaccine, and Premas delivered with a trivalent Covid 19 vaccine. With the merger of MyMD and Akers the vaccine became a part of the new public MyMD Pharmaceuticals Inc. MyMD then joined with Oramed Pharmaceuticals to form Oravax Medical, a company focussed on vaccines in pill form, owned 13% by MyMD and 87% by Oramed, and assigned to it the RIGHTS to the Premas vaccine.
The Covid 19 vaccine developed by Premas is a trivalent vaccine, targeting 3 proteins on the Covid molecule, unlike the Pfizer and Moderna vaccines which target only the "spike" protein. This makes the Premas vaccine a much stronger vaccine against any variants that may develope.
Oravax has since licensed Premas to develope a injectable version of the vaccine for use in India. Sales of the injectable there, and sales of the pill form which is easily shipped anywhere, needs only normal refridgeration, and does not require medical personnel to administer it, would likely be a huge seller producing huge royalties.
Recent MYMD News
- Form 8-K - Current report • Edgar (US Regulatory) • 03/07/2024 09:30:39 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 03/05/2024 04:00:19 PM
- MyMD Pharmaceuticals Regains Compliance with Nasdaq Minimum Bid Price Requirement for Continued Listing • Business Wire • 03/05/2024 02:15:00 PM
- Form SC 13G - Statement of acquisition of beneficial ownership by individuals • Edgar (US Regulatory) • 02/14/2024 08:13:35 PM
- Form SC 13G/A - Statement of acquisition of beneficial ownership by individuals: [Amend] • Edgar (US Regulatory) • 02/14/2024 04:27:33 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 02/13/2024 09:57:03 PM
- MyMD Pharmaceuticals Announces Reverse Stock Split to Maintain Nasdaq Listing • Business Wire • 02/13/2024 04:45:00 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 12/06/2023 02:15:12 PM
- MyMD Pharmaceuticals Plans FDA-Cleared Phase 2 Clinical Trial of MYMD-1 in Rheumatoid Arthritis • Business Wire • 12/06/2023 02:15:00 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 10/19/2023 01:00:10 PM
- MyMD Announces Preclinical Study Results Showing Novel Cannabidiol Analog, Supera-CBD™, Reduced Acute Inflammatory Pain • Business Wire • 10/19/2023 01:00:00 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 10/13/2023 09:00:16 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 10/04/2023 08:30:23 PM
- MyMD Pharmaceuticals to Present Updated Statistically Significant Phase 2 Data for MYMD-1, Potential TNF-α Market Disrupter, at BioFuture 2023 • Business Wire • 10/04/2023 11:30:00 AM
- Form 8-K - Current report • Edgar (US Regulatory) • 09/08/2023 09:24:39 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 08/24/2023 09:58:33 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 08/18/2023 08:21:49 PM
- Form 10-Q - Quarterly report [Sections 13 or 15(d)] • Edgar (US Regulatory) • 08/14/2023 09:00:57 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 08/14/2023 12:30:38 PM
- FDA Accepts MyMD Pharmaceuticals’ Investigational New Drug Application (IND) for Phase 2 Study of oral TNF-α inhibitor MYMD-1® in Rheumatoid Arthritis (RA) • Business Wire • 08/14/2023 12:30:00 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 08/03/2023 08:30:47 PM
- MyMD Pharmaceuticals to Hold Conference Call Today to Discuss Phase 2 Trial Results • Business Wire • 08/02/2023 12:30:00 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 08/01/2023 08:30:32 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 07/31/2023 01:00:09 PM
- MyMD Pharmaceuticals Reports Statistically Significant Positive Topline Phase 2 Results for Next Generation Oral TNF-α Inhibitor MYMD-1® in Sarcopenia/Age-Related Frailty • Business Wire • 07/31/2023 01:00:00 PM
NanoViricides Reports that the Phase I NV-387 Clinical Trial is Completed Successfully and Data Lock is Expected Soon • NNVC • May 2, 2024 10:07 AM
ILUS Files Form 10-K and Provides Shareholder Update • ILUS • May 2, 2024 8:52 AM
Avant Technologies Names New CEO Following Acquisition of Healthcare Technology and Data Integration Firm • AVAI • May 2, 2024 8:00 AM
Bantec Engaged in a Letter of Intent to Acquire a Small New Jersey Based Manufacturing Company • BANT • May 1, 2024 10:00 AM
Cannabix Technologies to Deliver Breath Logix Alcohol Screening Device to Australia • BLO • Apr 30, 2024 8:53 AM
Hydromer, Inc. Reports Preliminary Unaudited Financial Results for First Quarter 2024 • HYDI • Apr 29, 2024 9:10 AM