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NEW YORK, January 5, 2017 /PRNewswire/ — Neurotrope, Inc. (OTCQB: NTRP), a clinical-stage biopharmaceutical company developing novel therapies for neurodegenerative diseases, including Alzheimer’s disease, announced today that Dr. Susanne Wilke, Ph.D., Neurotrope’s Chief Executive Officer, will be presenting a corporate overview at two investor conferences:



Event: 10th Annual One Med Forum Conference – Two Presentations
Date: January 9, 2017
Time: 4:15 PM PT
Date: January 10, 2017
Time: 2:00 PM PT
Location: 450 Post Street, San Francisco CA (room to be announced)


Event: 9th Annual Biotech Showcase Conference
Date: January 11, 2017
Time: 8:30 AM PT
Location: Room 2, Hilton San Francisco Union Square Hotel, San Francisco, CA



“Neurotrope has a unique neuro-regenerative mechanism of action with the potential to reverse Alzheimer’s disease by replacing lost synaptic networks that are so consistently associated with the breakdown of human cognitive functions,” stated Dr. Wilke, Neurotrope’s Chief Executive Officer. “Top line results of our double-blinded, placebo-controlled Phase 2 study in 148 moderate to severe Alzheimer’s patients at 26 U.S. sites, is expected to be announced in April 2017.


Company management will be available to participate in one-on-one meetings with investors who are registered to attend the conferences. Meetings may also be scheduled outside of the conferences by contacting Neurotrope Bioscience investor relations.


For more information on NeurotropeBioscience, please visit:
For more information on Biotech Showcase 2017, please visit:
For more information on OneMedMarketSF 2017, please visit:



About Neurotrope BioScience, Inc:


Neurotrope BioScience, Inc., a wholly owned subsidiary of Neurotrope, Inc., is at the forefront of biotechnology companies having a focus on developing a novel therapy for the treatment of moderately severe to severe Alzheimer’s disease. The scientific basis of our treatment is activation of Protein Kinase C isozymes ε and α by bryostatin, a natural product, which in mouse AD models was demonstrated to result in repair of damaged synapses as well as synaptogenesis, the induction of new neuronal networks, reduction of toxic beta-amyloid generation, prevention of neuronal death, and enhancement of memory and learning, thus having the potential to improve cognition and behavior in Alzheimer’s disease.


Neurotrope is also conducting preclinical studies of bryostatin-1 as a treatment for Fragile X Syndrome and Niemann-Pick Type C disease, two rare genetic diseases for which only symptomatic treatments are currently available. The FDA has granted Orphan Drug Designation to Neurotrope for bryostatin-1 as a treatment for Fragile X Syndrome. Bryostatin-1 has undergone testing in over 1,500 people establishing a large safety database.


Neurotrope has exclusively licensed technology from Cognitive Research Enterprises (formerly named the Blanchette Rockefeller Neurosciences Institute) for Alzheimer’s disease therapeutics and Fragile X Syndrome and has a world-wide, exclusive license with the Icahn School of Medicine at Mt. Sinai for Niemann-Pick Type C disease.


Forward-Looking Statements


Any statements contained in this press release that do not describe historical facts may constitute forward-looking statements. These forward-looking statements include statements regarding the proposed study and timing of initiation, and continued development of use of bryostatin for Alzheimer’s disease and other cognitive diseases, and the Company’s ability to list its common shares on a major stock exchange. Such forward-looking statements are subject to risks and uncertainties and other influences, many of which the Company has no control over. Actual results and the timing of certain events and circumstances may differ materially from those described by the forward-looking statements as a result of these risks and uncertainties. Factors that may influence or cause actual results to differ materially from expected or desired results may include, without limitation, the Company’s inability to obtain adequate financing, the significant length of time associated with drug development and related insufficient cash flows and resulting illiquidity, the Company’s patent portfolio, the Company’s inability to expand the Company’s business, the Company’s inability to meet listing requirements for major stock exchanges, significant government regulation of pharmaceuticals and the healthcare industry, lack of product diversification, availability of the Company’s raw materials, existing or increased competition, stock volatility and illiquidity, and the Company’s failure to implement the Company’s business plans or strategies. These and other factors are identified and described in more detail in the Company’s filings with the SEC, including the Company’s Annual Report on Form 10-K for the year ended December 31, 2015 and its Quarterly Report on Form 10-Q for the quarter ended September 30, 2016. The Company does not undertake to update these forward-looking statements.



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For additional information, please contact:
Neurotrope Bioscience
Jeffrey Benison, Investor Relations
212.334.8709 or 516.286.6099