A total of 109 volunteers participated in the two studies. In both studies, BPN14770 was shown to be orally bioavailable, safe, and well-tolerated. In the elderly, high dose group, headaches were the most frequently reported adverse event (5 of 10 subjects) and were observed in the one subject who withdrew by choice midway in the trial. In the cognitive portion of the multiple dose study, analysis of the low, mid and high dose cohorts revealed impaired reaction times in the high dose group with no change in the low and mid dose groups. Therefore the high dose group was excluded from a pooled exploratory analysis of elderly volunteers receiving drug in comparison to placebo. This post hoc analysis of the elderly subjects in the low and mid dose groups (20 subjects received drug and 15 subjects received placebo) demonstrated significant improvements (p<0.05, effect size >0.70) in two measures of working memory at doses of 10 and 20 mg bid. No detectable effect was observed on other cognitive domains, however, inference is limited by the small sample size.
Working memory is a system for temporarily storing and managing the information required to carry out complex cognitive tasks such as learning, reasoning, and comprehension. The part of the brain responsible for working memory is also responsible for focus and concentration. Working memory is a domain of cognition that is impacted by Alzheimer's disease.
The Phase 1 single-ascending and multiple-ascending dose studies of BPN14770 were conducted with the support of the National Institute of Health through a grant from the National Institute on Aging (AG054243) and funding from the Alzheimer's Drug Discovery Foundation. BPN14770 was developed through a cooperative research agreement with the Blueprint Neurotherapeutics Program (NS078034). The company plans full disclosure of the clinical trial data at future medical conference presentations and through peer-reviewed journal publication.
BPN14770 is a novel therapeutic agent that selectively inhibits phosphodiesterase-4D (PDE4D). PDE4D works through the PKA‐CREB pathway to enhance synaptic action of the brain neurons involved in memory and cognition. This unique mechanism of action has the potential to improve cognitive and memory function in devastating disorders including Alzheimer's disease, schizophrenia, and learning/developmental disabilities such as Fragile X syndrome.
About Tetra Discovery Partners
Tetra Discovery Partners is a clinical stage biotechnology company developing a portfolio of therapeutic products that will bring clarity of thought to people suffering from Alzheimer's disease and other brain disorders. Tetra uses structure-guided drug design to discover mechanistically novel, allosteric inhibitors of phosphodiesterase 4 (PDE4), an enzyme family that plays key roles in memory formation, learning, neuroinflammation, and traumatic brain injury. Tetra was a recipient of an NIH Blueprint Neurotherapeutics Program cooperative research agreement, and also receives major funding from the National Institute on Aging and the National Institute of Mental Health through the Small Business Innovation Research (SBIR) program. Tetra Discovery Partners is headquartered in Grand Rapids, Michigan. For more information, please visit the company's website at http://www.tetradiscovery.com.
This press release does not constitute an offer to sell or the solicitation of an offer to buy any securities in a Tetra Discovery Partners stock offering. There will not be any sale of these securities in any state or jurisdiction in which such offering, sale, or solicitation would be unlawful prior to registration or qualification under the securities laws of any such state or jurisdiction.
Statements made in this press release that look forward in time or that express beliefs, expectations or hopes regarding future occurrences or anticipated outcomes or benefits are forward-looking statements. A number of risks and uncertainties, such as risks related to product development and commercialization efforts, results of clinical trials, ultimate clinical outcomes, and benefit of Tetra Discovery Partners' products to patients, market, and physician acceptance of Tetra Discovery Partners' products, intellectual property protection, and competitive product offerings, could cause actual events to differ from the expectations indicated in these forward-looking statements. You are cautioned not to put any undue reliance on any forward-looking statement. This press release is neither an offer to sell nor a solicitation of an offer to purchase any particular securities. Any such offer or solicitation will be made only pursuant to definitive legal agreements prepared specifically for such purpose. Tetra Discovery Partners does not assume any obligation to publicly update or revise any forward-looking statements, whether as a result of new events or information, future otherwise.
Mark Gurney, Ph.D., Chief Executive Officer
Tetra Discovery Partners
Joan Kureczka, Kureczka/Martin Associates
To view the original version on PR Newswire, visit:http://www.prnewswire.com/news-releases/tetra-discovery-partners-announces-positive-results-from-phase-1-studies-of-cognition-drug-candidate-bpn14770-300379985.html
SOURCE Tetra Discovery Partners