(TBPMF) – Accesswire
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Health Canada Accepts New Drug Submission for REDUVO(TM) as a Treatment for Patients with Chemotherapy-induced Nausea and Vomiting
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Tetra Bio-Pharma Accelerates PLENITUDE(C) Clinical Trial to Evaluate the Effect of Cannabis for Use in Managing Uncontrolled Cancer Pain
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Tetra Bio-Pharma Announces Start of the REBORN1(C) Clinical Trial
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Tetra Bio-Pharma Signs a Definitive Distribution Agreement with DanCann Pharma to Monetize Its Dronabinol and Botanical Product Portfolios
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Tetra Bio-Pharma Re-activates Veterinary Clinical Study in Companion Animals
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Tetra Bio-Pharma Granted a Drug Establishment License to Distribute REDUVO Soft Gel Capsules in Canada
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Tetra Bio-Pharma Submits Request for Scientific Advice to Malta Medicines Authority
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Tetra Bio-Pharma Provides an Update on its U.S. REBORN1 Clinical Trial
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Tetra Bio-Pharma Announces Granting of U.S. Patent for Treatment of Interstitial Cystitis
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Tetra Bio-Pharma Provides Update on Its New Drug Submission Application in Canada
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FDA Provides Positive Feedback on Tetra Bio-Pharma's Application for ARDS-003 Clinical Development in COVID-19 Patients
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Tetra Bio-Pharma Receives Second Compliant Rating on Inspection from Health Canada
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Health Canada Provides Positive Feedback on Tetra Bio-Pharma’s Application for ARDS-003 to be Studied in COVID-19 Patients at Risk of Developing Acute Respiratory Distress Syndrome
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Tetra Bio-Pharma Initiates Additional Studies on Leading Drug Candidate ARDS-003
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Tetra Bio-Pharma Receives Compliant Rating on Inspection from Health Canada
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Tetra Bio-Pharma Provides Status of Its New Drug Submission Application in Canada
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Correction To Tetra Bio-Pharma News Release Dated February 25th
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Tetra Bio-Pharma to Present at the H.C. Wainwright Global Life Sciences Virtual Conference
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Tetra Bio-Pharma To Monetize Its Dronabinol And Botanical Product Portfolios
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Tetra Bio-Pharma Creates the ENJOUCA Business Unit
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Tetra Bio-Pharma Announces FDA Clearance on IND, allowing U.S. Reborn1(TM) Clinical Trial to Commence
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Tetra Bio-Pharma Files New Drug Submission for REDUVO(TM) in Canada
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Tetra Bio-Pharma Confirms it is on Track to Receive Government Funding
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Tetra Bio-Pharma Hits Another Milestone Before Year End
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Tetra Bio-Pharma Provides Update on Market Potential for QIXLEEF(TM)
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Tetra Bio-Pharma Completes Major Milestone for COVID-19 Therapeutic
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Tetra Bio-Pharma Provides Update on Recent Milestones
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Tetra Bio-Pharma Provides Update on Market Potential of ARDS-003
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Tetra Bio Pharma Announces Divestiture of Lumiera Health Innovation Inc.
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Tetra Bio-Pharma, Targeted Pharmaceutical & the George Mason University Partner on ARDS-003 to Prevent & Treat COVID-19
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Tetra Bio-Pharma Acquires Exclusive Global Technology Rights to a Mucoadhesive Delivery Technology Called Adversa(R) for its PPP-002 (dronabinol) drug candidate from IntelGenx
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Tetra Bio-Pharma Announces Positive Results in Animal Studies for Treatment of Hyperinflammatory Lung Injury
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Tetra Bio-Pharma Unveils its Commercial Vision on a Robust Chemotherapy Induced Nausea and Vomiting Portfolio
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Tetra Bio-Pharma to Present at Alpha Bronze Virtual Town Hall
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Tetra Bio-Pharma (TBP) Acquires Dronabinol Soft Gel Capsules Exclusive Canadian Distribution Rights to Establish a Strong Commercial Presence in Canada and Accelerate its Profitability
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Tetra Bio-Pharma Adds Two Board Members and Appoints New COO
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Tetra Bio-Pharma Appoints Chief Financial Officer
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Dania Scott Joins Tetra Bio-Pharma as Senior Vice President Commercial Strategy
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Tetra Bio-Pharma Announces Plenitude Clinical Trial is Initiated
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Tetra Bio-Pharma Announces Data on its CBD Metabolite Study in Humans
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Tetra Bio-Pharma Engages Dalton Pharma for GMP Manufacturing of ARDS-003
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Tetra Bio-Pharma and Mondias Enter Into Final Agreement For The Purchase Of Lumiera Health Innovation Inc.
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Tetra Bio-Pharma Virtually Opens the Market
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CORRECTION FROM SOURCE: Tetra Bio-Pharma Provides Update on QIXLEEF(TM)'s European Activities
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CORRECTION FROM SOURCE: Tetra Bio-Pharma Provides Update on QIXLEEF(TM)'s European Activities
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Tetra Bio-Pharma Provides Update on QIXLEEF(TM)'s European Activities
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Tetra Bio-Pharma’s Management Provides Corporate Update on QIXLEEF(TM) & CAUMZ(TM) Drug Development Activities
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Tetra Bio-Pharma Provides Management Update on Pharma Focus
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FDA Provides Positive Feedback on Tetra Bio-Pharma's Pre-Investigational New Drug Application for ARDS-003 to Be Studied in COVID-19 Patients at Risk of Developing Acute Respiratory Distress Syndrome
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Tetra Bio-Pharma Receives Conditional Approval to Graduate to the TSX
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