
LYNO AI Reports Strong Momentum in Early Bird Presale Ahead of Price Increase to $0.055
ROAD TOWN, British Virgin Islands, Aug. 13, 2025 (GLOBE NEWSWIRE) — LYNO AI is progressing at a rapid pace during its Early Bird presale period, attracting attention from traders and investors. The project's autonomous AI-powered cross-chain arbitrage engine operates across more than 15 EVM-compatible blockchains, contributing to the growing participation in the presale.
At this stage, LYNO tokens are priced at $0.050 per token, with a total of 16 million tokens available. More than 265,000 tokens have already been sold, reflecting heightened interest ahead of the upcoming price adjustment to $0.055 per token.
Presale Details Highlight Limited-Time Opportunity
The Early Bird stage provides participants with the chance to acquire LYNO tokens at the current rate before the planned increase. Key presale data include: Current token price: $0.050
Next stage token price: $0.055
Tokens sold so far: 265,879.247
Total tokens allocated: 16 million
Payments can be made via ETH, USDT, or USDC, using supported wallets such as MetaMask and Trust Wallet.
Additionally, buyers who purchase more than $100 in LYNO tokens will be entered into the LYNO AI Giveaway for a chance to win one of ten 10,000-token prizes from a 100,000-token pool.
Technology Designed for Cross-Chain Arbitrage
LYNO AI is an open-source, decentralized protocol that applies advanced machine learning to identify and execute arbitrage opportunities across blockchain networks, including Ethereum, BNB Chain, Polygon, Arbitrum, and Optimism. Its automated system incorporates: Real-time market data aggregation
AI-driven scoring and routing of profitable arbitrage opportunities
Automated trade execution using flash loans and cross-chain bridges
Continuous profit distribution and AI model updates
Holders of the $LYNO token have governance rights, enabling participation in protocol-related decisions. Staking options are available, with up to 60 percent of protocol fees distributed to the community. The system includes a buyback and burn mechanism to help manage token supply.
Security measures include multi-signature wallets, slippage controls, and zero-knowledge proofs to help prevent front-running and MEV attacks. The protocol has been audited by Cyberscope.
Early Participation Encouraged Before Price Change
With the Early Bird stage advancing toward its allocation limit, participants have a short window to secure tokens at $0.050 before the next pricing level of $0.055. This presale period offers early access to a decentralized finance protocol integrating AI technology with cross-chain arbitrage capabilities.
Additional Information
Website: https://lyno.ai/Buy Presale: https://lyno.ai/#presaleWhitepaper: https://lyno.ai/whitepaper.pdfTwitter/X: https://x.com/Lyno_AITelegram: https://t.me/lyno_ai
Win 100k: https://gleam.io/KCCV3/lyno-ai-giveaway
Contact DetailsLYNO AI
[email protected]
Disclaimer: This content is provided by LYNO AI. The statements, views, and opinions expressed in this content are solely those of the content provider and do not necessarily reflect the views of this media platform or its publisher. We do not endorse, verify, or guarantee the accuracy, completeness, or reliability of any information presented. We do not guarantee any claims, statements, or promises made in this article. This content is for informational purposes only and should not be considered financial, investment, or trading advice.Investing in crypto and mining-related opportunities involves significant risks, including the potential loss of capital. It is possible to lose all your capital. These products may not be suitable for everyone, and you should ensure that you understand the risks involved. Seek independent advice if necessary. Speculate only with funds that you can afford to lose. Readers are strongly encouraged to conduct their own research and consult with a qualified financial advisor before making any investment decisions. However, due to the inherently speculative nature of the blockchain sector—including cryptocurrency, NFTs, and mining—complete accuracy cannot always be guaranteed.Neither the media platform nor the publisher shall be held responsible for any fraudulent activities, misrepresentations, or financial losses arising from the content of this press release. In the event of any legal claims or charges against this article, we accept no liability or responsibility. Globenewswire does not endorse any content on this page.
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Key presentations and posters featured at major scientific meetings included: Oral presentation highlighting QTORIN™ rapamycin for the treatment of microcystic LMs was presented by Amy Paller, M.S., M.D., Chair of Dermatology at Northwestern University's Feinberg School of Medicine, at the 15th World Congress of Pediatric Dermatology; the presentation highlighted the Phase 3 SELVA trial design and reviewed Phase 2 results. Poster highlighting the estimated diagnosed U.S. prevalence and U.S. annual incidence of lymphatic malformations was presented at the 82nd Annual Meeting of the Society for Investigative Dermatology. The United States Patent and Trademark Office (USPTO) issued patent No. 12,268,673 with claims to QTORIN™ rapamycin for the treatment of microcystic LMs with anticipated patent life extending into 2038. Top-line results from SELVA are on track for the first quarter of 2026. 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(Nasdaq: PVLA) is a clinical-stage biopharmaceutical company focused on developing and commercializing novel therapies to treat patients suffering from serious, rare genetic skin diseases for which there are no FDA-approved therapies. Palvella is developing a broad pipeline of product candidates based on its patented QTORIN™ platform, with an initial focus on serious, rare genetic skin diseases, many of which are lifelong in nature. Palvella's lead product candidate, QTORIN™ 3.9% rapamycin anhydrous gel (QTORIN™ rapamycin), is currently being evaluated in the Phase 3 SELVA clinical trial in microcystic lymphatic malformations and the Phase 2 TOIVA clinical trial in cutaneous venous malformations. For more information, please visit or follow Palvella on LinkedIn or X (formerly known as Twitter). QTORIN™ rapamycin is for investigational use only and has not been approved or cleared by the FDA or by any other regulatory agency for any indication. Forward-Looking Statements This press release contains forward-looking statements (including within the meaning of Section 21E of the Securities Exchange Act of 1934, as amended, and Section 27A of the Securities Act of 1933, as amended (Securities Act)). These statements may discuss goals, intentions, and expectations as to future plans, trends, events, results of operations or financial condition, or otherwise, based on current beliefs of the management of Palvella, as well as assumptions made by, and information currently available to, the management of Palvella. Forward-looking statements generally include statements that are predictive in nature and depend upon or refer to future events or conditions, and include words such as 'may,' 'will,' 'should,' 'would,' 'expect,' 'anticipate,' 'plan,' 'likely,' 'believe,' 'estimate,' 'project,' 'intend,' and other similar expressions or the negative or plural of these words, or other similar expressions that are predictions or indicate future events or prospects, although not all forward-looking statements contain these words. Statements that are not historical facts are forward-looking statements. Forward-looking statements include, but are not limited to, statements regarding the expected timing of the presentation of data from ongoing clinical trials, Palvella's clinical development plans and related anticipated development milestones, Palvella's cash and financial resources and expected cash runway, and the potential of, and expectations regarding, Palvella's programs, including QTORIN™ rapamycin, and its research-stage opportunities and any additional indications or platform candidates, including its expected therapeutic potential and market opportunity. Forward-looking statements are based on current beliefs and assumptions that are subject to risks and uncertainties and are not guarantees of future performance. Actual results could differ materially from those contained in any forward-looking statement as a result of various factors, including, without limitation: the ability to raise additional capital to finance operations; the ability to advance product candidates through preclinical and clinical development; the ability to obtain regulatory approval for, and ultimately commercialize, Palvella's product candidates, including QTORIN™ rapamycin; the outcome of early clinical trials for Palvella's product candidates, including the ability of those trials to satisfy relevant governmental or regulatory requirements; the fact that data and results from clinical studies may not necessarily be indicative of future results; Palvella's limited experience in designing clinical trials and lack of experience in conducting clinical trials; the ability to identify and pivot to other programs, product candidates, or indications that may be more profitable or successful than Palvella's current product candidates; the substantial competition Palvella faces in discovering, developing, or commercializing products; the negative impacts of global events on operations, including ongoing and planned clinical trials and ongoing and planned preclinical studies; the ability to attract, hire, and retain skilled executive officers and employees; the ability of Palvella to protect its intellectual property and proprietary technologies; reliance on third parties, contract manufacturers, and contract research organizations; and the risks and uncertainties described in the filings made by Palvella with the Securities and Exchange Commission (SEC), including the annual report on Form 10-K, quarterly reports on Form 10-Q and current reports on Form 8-K, filed with or furnished to the SEC and available at The events and circumstances reflected in our forward-looking statements may not be achieved or occur, and actual results could differ materially from those projected in the forward-looking statements. New risk factors and uncertainties may emerge from time to time, and it is not possible for management to predict all risk factors and uncertainties that Palvella may face. Except as required by applicable law, Palvella does not plan to publicly update or revise any forward-looking statements contained herein, whether as a result of any new information, future events, changed circumstances or otherwise. This press release contains hyperlinks to information that is not deemed to be incorporated by reference into this press release. Contact Information Investors Wesley H. Kaupinen Founder and CEO, Palvella Therapeutics Media Marcy Nanus Managing Partner, Trilon Advisors LLC mnanus@ PALVELLA THERAPEUTICS, INC. CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS (in thousands, except share and per share amounts) Three Months EndedJune 30, Six Months EndedJune 30, 2025 2024 2025 2024 Operating expenses: Research and development $ 5,118 $ 1,442 $ 9,192 $ 2,426 General and administrative 4,132 1,466 7,929 2,241 Total operating expenses 9,250 2,908 17,121 4,667 Loss from operations (9,250 ) (2,908 ) (17,121 ) (4,667 ) Total other income (expense), net (221 ) (1,264 ) (535 ) (2,041 ) Net loss $ (9,471 ) $ (4,172 ) $ (17,656 ) $ (6,708 ) Less: Cumulative Series D preferreddividends — (194 ) — (388 ) Net loss attributable to commonstockholders $ (9,471 ) $ (4,366 ) $ (17,656 ) $ (7,096 ) Net loss per share — basic and diluted $ (0.86 ) $ (2.47 ) $ (1.60 ) $ (4.01 ) Weighted-average number of commonshares used in computing net loss per share— basic and diluted 11,052,741 1,770,167 11,033,327 1,770,167 PALVELLA THERAPEUTICS, INC. CONDENSED CONSOLIDATED BALANCE SHEET INFORMATION (in thousands) June 30,2025 December 31,2024 Assets Cash and cash equivalents $ 70,433 $ 83,602 Other current assets 3,314 4,632 Total current assets 73,747 88,234 Total assets $ 73,747 $ 88,234 Liabilities and Stockholders' Equity Current liabilities $ 9,616 $ 12,038 Non-current liabilities 16,351 13,589 Total liabilities 25,967 25,627 Total stockholders' equity 47,780 62,607 Total liabilities and stockholders' equity $ 73,747 $ 88,234 Sign in to access your portfolio