Tetra Bio-Pharma Provides Additional Information on CAUMZ Following Type B Meeting with USA FDA
OTTAWA, Feb. 25, 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 additional information on the drug development program for CAUMZ following the previously announced Type B meeting with the US Food and Drug Administration (FDA).
- OTTAWA, Feb. 25, 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 additional information on the drug development program for CAUMZ following the previously announced Type B meeting with the US Food and Drug Administration (FDA).
- The highly purified cannabinoid molecules are also an important element in the future success of CAUMZ.
- CAUMZ-kit results in the inhalation of cannabinoid molecules and not any compounds such as excipients, preservatives or oils.
- As CAUMZ shares similarities to QIXLEEF, the FDA confirmed in the Type B meeting that CAUMZ would be eligible for waivers of some of the standard nonclinical toxicology studies.