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Traxion Sab De Cv Ord Shs GRPOF

Grupo Traxion SAB de CV is a Mexico-based company engaged in the transportation sector. The Company provides logistics services within eight business areas: Fright, including intermodal and multimodal services, door-to-door, national and cross-border distribution, among others; Integrated logistics, including logistics management, aerial and maritime services and custom transportation support services; Warehousing, including dedicated storage, shared warehouses, packing and value-added services, such as labeling and products assembly; Logistics systems, including software for logistics management; Passenger transportation, including transportation of personnel and students; Special services, including rental of bus and vans; Moving, including national and international moving services, and Advertising, including custom transportation services during marketing campaigns. The Company operates through a number of group companies.


PINL:GRPOF - Post by User

Post by monarkaon Jan 28, 2020 8:10am
207 Views
Post# 30607615

Tetra Bio-Pharma Provides an Update on Its Veterinary Ophtha

Tetra Bio-Pharma Provides an Update on Its Veterinary Ophtha

Tetra’s sterile cannabinoid manufacturing facility fully validated and operational

Tetra’s subsidiary, Panag Pharma, ready to initiate the treatment phase of clinical trial of PPP003 for treatment of eye pain

OTTAWA, Jan. 28, 2020 (GLOBE NEWSWIRE) -- Tetra Bio-Pharma Inc. (“Tetra” or the “Company”) (TSX-V:TBP) (OTCQB:TBPMF), a leader in cannabinoid-derived drug discovery and development, is pleased to provide an update on its veterinary clinical trial to evaluate the safety, tolerability and potential efficacy of its PPP003 ophthalmic drug in the treatment of eye pain in companion animals with indolent corneal ulcers.

Following the authorization from Health Canada in 2019, Tetra has invested in the setup of a sterile cannabinoid drug manufacturing suite at the facility in New Brunswick which has been used to manufacture validated batches of sterile PPP003 drug for use in its ophthalmic drug development program. The design of the sterile suite, implementation of cGMPs, and validation of the sterile process was performed by Tetra’s manufacturing and quality compliance staff. The validated batches of sterile drug will be used in the planned clinical trial in companion animals with indolent corneal ulcers, which is expected to begin in 2020. A similar manufacturing process is required for the clinical trials in human patients with eye diseases such as painful dry eye and uveitis.    

“We are thrilled to have successfully created and validated a facility to manufacture batches of sterile drugs for our ophthalmic drug development program.  In June 2019, the U.S. FDA validated our ophthalmic research program and with this significant milestone achieved, we are in an excellent position to bring PPP003 to human clinical trials later this year," said Dr. Guy Chamberland, CEO and Chief Regulatory Officer of Tetra Bio-Pharma.  “Along with our PPP011 and PPP001 drug development programs, this drug development program is one of Tetra’s corporate priorities, since there is a significant unmet medical need for ophthalmic drugs in both companion animals and humans. PPP003 was selected because it is a non-controlled cannabinoid and will favor global market penetration.”

According to a 2019 report by Market® Research Reports report, the global companion animal healthcare market reached a value of approximately $46 billion USD in 2018 and is expected to reach an estimated $67 billion USD by the end of 2025.  This market has an estimated growth at a CAGR of 5.56% over the period of 2019-2025.

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