Tetra Bio Pharma Inc TBPMQ

Healthcare Cannabis

Tetra Bio-Pharma Inc. is a Canada-based cannabinoid-derived drug discovery and development company. The Company has developed a pipeline of cannabinoid-based drug products for a range of medical conditions, including pain, inflammation, and oncology. The Company has a pipeline of formulations and drug delivery systems with a portfolio of assets from the early research and development phase to advanced stage clinical programs. Its products include QIXLEEF, CAUMZ, PPP004, REDUVO, and REBORN 1. QIXLEEF is a botanical therapy with a fixed dosage of tetrahydrocannabinol (THC) and cannabidiol (CBD). CAUMZ is its inhaled cannabinoid-derived drug candidate. PPP004 is a topical preparation containing either a standardized amount of CBD or a defined ratio of THC and CBD. REDUVO is a soft gel capsule used to treat chemotherapy-induced nausea and vomiting (CINV) and weight loss and severe nausea in people living with human immunodeficiency virus (HIV) infection. REBORN 1 is in phase II trial.

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Tetra Bio Pharma Inc > Tetra is FAR From Over! Wake-up everyone

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Comment by Viceroy77on Mar 18, 2023 12:05pm

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RE:RE:RE:RE:Tetra is FAR From Over! Wake-up everyone

Davesnothere wrote: SamV21

Can we believe this so called news , or is it just smoke & mirrors ?

Montreal, QC - TheNewswire - March 10, 2023 - Tetra Bio-Pharma Inc. ("Tetra" or the "Company") (TSX:TBP) (OTC:TBPMF) (FRA:JAM1), a leader in cannabinoid-derived drug discovery and development is pleased to announce Health Canada has issued the Company a No Objection Letter (NOL) to proceed with its first in human clinical trial using oral ARDS-003 to treat various immunomodulatory conditions, in Canada.

Tetra Bio-Pharma receives approval from Health Canada of its Phase 1 Clinical Trial with oral ARDS-003.

Oral ARDS-003 is a new therapeutic positioned to modulate acute systemic inflammation and prevent sepsis, acute respiratory distress syndrome (“ARDS”), and organ damage.

The NOL provides the acknowledgement of drug candidacy and authority to proceed with Tetra’s Phase 1 clinical trial to assess the safety, tolerability, and pharmacokinetics of a single ascending dose of oral ARDS-003 in healthy volunteers. The results will guide further development of the drug for patients with hyper inflammatory conditions such as Acute Respiratory Distress Syndrome (ARDS).

Tetra received $4.5M in support from the Government of Quebec for the clinical development of ARDS-003 in the indication of acute respiratory distress syndrome, whether or not it is caused by COVID-19, as well as in patients with sepsis. The receipt of the NOL was one of the last conditions to be met to allow the company to draw on this investment.

Dr. Guy Chamberland, CEO and Chief Regulatory Officer at Tetra, commented, “We are excited to see our novel drug candidate, oral ARDS-003, moving forward in a clinical setting. As few as 1 out of 1,000 compounds make it into Phase 1 human trials. The development of effective, out-patient, oral therapies that either directly address viral infection or treat associated complications such as inflammation, organ damage, or fibrosis, is important in a national response to future pandemics or health emergencies. With over 12 years of preclinical efficacy research in sepsis and cytokine hyperinflammatory reactions, we are very confident that oral ARDS-003 will be an effective drug with strong commercial potential.”