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Friday, February 17, 2017 8:11:44 AM
There are so many moving parts here, I think it's difficult to answer your question:
- Trial results: mild improvement? or significant improvement in > 50% of patients? Durable improvements?
- Long-term safety: if there are long-term safety issues, this will directly affect which AD population Bryostatin is prescribed for. Only for severe AD (low bar)? or also include mild-to-moderate (significantly increases patients treated and revenue)?
- Treatment duration: a lifetime of regular treatment, one-time treatment cycle, or 2-3 cycles of treatment per year? (I'm thinking the latter)
- COGS: how much it costs to synthesize in large quantities is an unknown.
- Are there other diseases (Fragile X, etc) that Bryostatin is effective in that bring in further revenue?
- Reimbursement: how will the insurance landscape change over the next few years, considering the drug pricing rhetoric among politicians?
- If results are positive and we aren't bought out, it's likely we will need a partner, which means our revs are no more than 30% (that's generous).
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My near-term expectations: In April if Bryostatin shows real improvement (signs of disease reversal) and no significant safety signals, conservatively gain 4-10x.
Long-term: If Bryostatin is SOC and widely prescribed by physicians in only moderate-to-severe disease cycling on and off for the rest of the patients' lives, improving cognition in > 50% of patients, without a Pharma partner, our market cap should conservatively be several billion.
Recent SNPX News
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- Form 10-Q - Quarterly report [Sections 13 or 15(d)] • Edgar (US Regulatory) • 05/15/2024 09:03:21 PM
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- Form SC 13G/A - Statement of acquisition of beneficial ownership by individuals: [Amend] • Edgar (US Regulatory) • 02/06/2024 03:16:19 PM
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- Form ARS - Annual Report to Security Holders • Edgar (US Regulatory) • 11/14/2023 10:05:18 PM
- Form DEF 14A - Other definitive proxy statements • Edgar (US Regulatory) • 11/13/2023 10:00:48 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 11/06/2023 10:00:23 PM
- Form PRE 14A - Other preliminary proxy statements • Edgar (US Regulatory) • 11/03/2023 09:00:19 PM
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- Synaptogenix Announces Peer-Reviewed Publication of NIH-Sponsored Phase 2 Clinical Trial Results Demonstrating Safe, Significant, and Persistent Benefits of Bryostatin-1 in Advanced Alzheimer's Disease • PR Newswire (US) • 09/26/2023 01:00:00 PM
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- Synaptogenix and Cleveland Clinic to Submit Investigational New Drug (IND) Application to FDA for Clinical Trial of Bryostatin-1 in Multiple Sclerosis • PR Newswire (US) • 07/19/2023 01:00:00 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 07/19/2023 12:55:57 PM
- Synaptogenix Abstract Highlighting Bryostatin-1 Benefits in Severe Alzheimer's Disease Accepted for Presentation at 11th International Brain Research Organization World Congress of Neuroscience • PR Newswire (US) • 07/13/2023 01:00:00 PM
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