Q BioMed Inc. (OTCMKTS:QBIO) Files An 8-K Regulation FD Disclosure
Item 7.01
On November 20, 2019, we issued a press release announcing that the U.S. Food and Drug Administration (the “FDA”) approved our contract manufacturer, IsoTherapeutics Group LLC (“ITG”). ITG is now cleared to manufacture our FDA approved non-opioid cancer bone pain drug Strontium-89 Chloride USP. A copy of the press release is furnished herewith as Exhibit 99.1. On November 14, 2019, the Department of Health and Human Services notified the Company that its supplemental abbreviated new drug application for a new drug product manufacturing site, IsoTherapeutics Group, LLC, has been approved as of November 4, 2019.
The information in this Item 7.01 of this Form 8-K is being furnished and shall not be deemed “filed” for the purposes of Section 18 of the Securities Exchange Act of 1934, or otherwise subject to the liabilities of that section. The information in this Item 7.01 of this Form 8-K also shall not be deemed to be incorporated by reference into any filing under the Act or the Securities Exchange Act of 1934, except to the extent that we specifically incorporate it by reference.
Exhibits.
| 99.1 | Press Release entitled “Q BioMed Announces FDA Approval. Company Gets Green Light for Manufacturing FDA Approved Non-Opioid Cancer Palliation Drug”, dated November 20, 2019. |
Q BioMed Inc. Exhibit
EX-99.1 2 tm1923562d1_ex99-1.htm EXHIBIT 99.1 Exhibit 99.1 Q BioMed Announces FDA Approval Company Gets Green Light for Manufacturing FDA Approved Non-Opioid Cancer Palliation Drug NEW YORK,…
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About Q BioMed Inc. (OTCMKTS:QBIO)
Q BioMed, Inc., formerly ISMO Tech Solutions, Inc., is a biomedical acceleration and development company. The Company is focused on licensing, acquiring and providing strategic resources to life sciences and healthcare companies. The Company intends to acquire multiple assets over time and across a spectrum of healthcare related products, companies and sectors. The Company intends to develop these assets to provide returns through organic growth, out-licensing, sale or spin-off into new public companies. The Company holds license for a generic drug, Strontium Chloride (SR89). SR89 is a radiopharmaceutical agent and indicated for the treatment of pain associated with metastatic bone cancer. Its asset, MAN-01, is indicated for the treatment of glaucoma. MAN-01 is in pre-clinical stage. The Company is assessing multiple biomedical assets in various areas of healthcare and drug development. It is pursuing a pipeline of therapeutics, diagnostics and orphan drug candidates.
