Acasti Pharma Inc. (V:ACST)
Business Focus: Pharmaceuticals (NEC)
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Latest 10 SEDI filings for ACST within the last 6 months
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Company News
Feb 14, 2023 07:00 ET
Acasti Pharma Reports Third Quarter 2023 Operational Results
Acasti Pharma Inc. (“Acasti” or the “Company”) (Nasdaq: ACST and TSX-V: ACST), a late-stage, specialty pharma company advancing three clinical stage drug candidates addressing rare and orphan diseases, today announced financial and operational...
Jan 25, 2023 09:00 ET
Acasti Receives Extension to Regain Compliance with NASDAQ Minimum Bid Price Rule
Acasti Pharma Inc. (“Acasti” or the “Company”) (Nasdaq: ACST and TSX-V: ACST), a late-stage, specialty pharma company advancing three clinical stage drug candidates addressing rare and orphan diseases, announces that it has received notification...
Valuation Ratios
Industry
Sector
Beta
1.55
--
--
Price to Sales - TTM
--
3.49
3.64
Price to Book - most recent quarter
0.41
3.07
2.11
Price to Cash Flow per share - TTM
--
7.07
10.39
Price to Free Cash Flow per share - TTM
--
20.15
14.85
Short Report
| Date | Number of Shares Shorted | Net Change |
|---|---|---|
| Dec 31, 1969 | 0 | 0 |
| Dec 31, 1969 | 0 | 0 |
| Dec 31, 1969 | 0 | 0 |
Business Summary
| Sector: Healthcare | Industry: Pharmaceuticals |
Acasti Pharma Inc. is a Canada-based late-stage biopharma company with drug candidates addressing rare and orphan diseases. The Company is targeting three underserved orphan diseases: GTX-104, an intravenous infusion targeting subarachnoid hemorrhage (SAH), a rare and life-threatening medical emergency, in which bleeding occurs over the surface of the brain in the subarachnoid space between the brain and skull; GTX-102, an oral mucosal spray targeting ataxia-telangiectasia (A-T), a progressive, neurodegenerative genetic disease that primarily impacts children causing severe disability; and GTX-101, a topical spray, targeting postherpetic neuralgia, a persistent and often debilitating neuropathic pain caused by nerve damage from the varicella zoster virus (shingles). The Company's clinical assets have each been granted Orphan Drug Designation by the FDA, which provides seven years of marketing exclusivity post-launch in the United States, and additional intellectual property protection.
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