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Litecoin is a peer-to-peer cryptocurrency created by Charlie Lee. It was created based on the Bitcoin protocol but differs in terms of the hashing algorithm used. Litecoin uses the memory intensive Scrypt proof of work mining algorithm. Scrypt allows consumer-grade hardware such as GPU to mine those coins.  Why Litecoin? Litecoin is a cryptocurrency that has evolved from Bitcoin after its own popularity in the industry, this alternative, or ‘altcoin’ has emerged to allow investors to diversify their digital currency package, according to Investopedia. Litecoin is one of the most prominent altcoins and was created by former Google employee and Director of Engineering at Coinbase, Charlie Lee. Litecoin was the first to alter Bitcoin and the most significant difference is that it takes 2.5 minutes for Litecoin to generate a block, or transaction, in comparison to Bitcoin's 10 minutes.  ‘While this matters little to traders, miners who use hardware to run Bitcoin's network cannot switch over to Litecoin. This keeps bigger mining conglomerates away from Litecoin because they cannot easily optimize their profits by swapping to another coin, contributing to a more decentralized experience. Litecoin also has bigger blocks, and more coins in circulation, making it more affordable and swift when transacting,’ Investopedia explained.  As explained above, Litecoin can transact a lot faster than Bitcoin, but there are also a number of other characteristics that investors need to know before trading. Litecoin can handle higher volumes of transactions because of the capability of transacting faster and if Bitcoin attempted to transact on the scale of its altcoin, a code update would be needed. However, Litecoin’s blocks would be larger, but with more ‘orphaned blocks'. The faster block time of litecoin reduces the risk of double spending attacks - this is theoretical in the case of both networks having the same hashing power.  Litecoin Technical Details: The transaction confirmation time taken for Litecoin is about 2.5 minutes on average (as compared to Bitcoin's 10 minutes). The Litecoin network is scheduled to cap at 84 million currency units.   Litecoin has inspired many other popular alternative currencies (eg. Dogecoin) because of its Scrypt hashing algorithm in order to prevent ASIC miners from mining those coins. However it is said that by the end of this year, Scrypt ASIC will enter the mass market.

Litecoin

Litecoin is trending as the crypto community debates its potential amidst broader market movements, particularly in relation to Bitcoin's performance. Discussions revolve around whether LTC can break free from BTC's influence and if it's poised for a significant rally, with some eyeing potential price targets.

Internet Computer (IC) is the world’s first blockchain that is capable of running at web speed at unrestrictive capacities. Built by the DFINITY Foundation, IC aims to recreate the web by supporting smart contract development at scale and changing the way people can interact using web services. Internet Computer aims to extend the public internet, so that it can be the world’s computing platform, in a decentralized manner. Internet Computer sets to revolutionalize the design of the crypto economy, with an aim to overhaul traditional software services.   The project was founded in October 2016 by Dominic WIllams and have raised a total of $121 million from investors such as Adreessen Horowitz, Polychain Capital, Multicoin Capital and such. On May 10, 2021, DFINITY launched the Internet Computer into the public domain, marking it a major milestone for ICP as it means the internet now functions as a decentralised global computer. This is marked by the release of all of the Internet Computer’s source code into the public domain, as well as ICP utility token that allows tens of thousands of community members to govern the Internet Computer network.  ICP is Internet Computer's native token. It plays three prominent roles:  1. Network Governance: Users that participate in the governance will be rewarded with ICPI 2. Production of Cycles for Compute: ICP can be converted into cycles where it is used as the transaction fee to access the network. Cycles are burned after used. 3. Rewarding Users: ICP is used as the rewards to incentivize users to participate in the network such as securing the network.

Internet Computer

Internet Computer (ICP) is trending as community members discuss its potential for decentralized applications and its unique technology, with some drawing comparisons to early-stage tech giants. Talk centers on its recent price surge and whether it can sustain its momentum, while others point to its long-term potential and growing ecosystem. Bullish sentiment seems to be fueled by the belief that ICP is undervalued and poised for significant growth.

Intuitive Machines, Inc. is a space exploration, infrastructure, and services company, which engages in contributing to the establishment of cislunar infrastructure and helping to develop cislunar and deep space commerce. It offers space products and services. The company was founded by Stephen J. Altemus, Kam Ghaffarian, and Timothy P. Crain in 2013 and is headquartered in Houston, TX.

Intuitive Machines Inc - Ordinary Shares - Class A

Intuitive Machines Inc

Intuitive Machines ($LUNR) is trending as the community discusses its recent acquisition of Lanteris Space Systems and potential implications for future contracts, including the Lunar Terrain Vehicle (LTV) project. Community members are weighing the impact of potential dilution against the benefits of expanding capabilities in the space sector. Optimism persists regarding $LUNR's long-term growth and strategic positioning within the evolving space economy.

NEAR Protocol is the blockchain for AI. A high-performance, AI-native platform built to power the next generation of decentralized applications and intelligent agents. It provides the infrastructure AI needs to transact, operate, and interact across Web2 and Web3. NEAR combines three core elements: User-Owned AI, which ensures agents act in users’ best interests; Intents and Chain Abstraction, which eliminate blockchain complexity for seamless, goal-driven transactions across chains; and a sharded blockchain architecture that delivers the scalability, speed, and low-cost execution needed for real-world AI and Web3 use. This integrated stack makes NEAR the foundation for building secure, user-owned, AI-native applications at internet scale.

Near

NEAR is trending as community members discuss its potential and recent price action. Some suggest user growth is driving the rally, while others await further upward movement. Bullish sentiment remains with many noting its AI capabilities and potential for long-term growth.

Klarna Group Plc operates as an investment holding company. It provides an e-commerce payment solutions for merchants and shoppers. The firm connect an array of different financial services and commerce organizations, from PSPs, traditional banks, card networks and open banking providers, to commerce enablers, technology partners, in-store payments providers and shipping and return logistics providers. The company was founded by Gustav Erik Niklas Adalberth, Karl Anders Victor Jacobsson, and Sebastian Marcin Siemiatkowski in 2005 and is headquartered in London, the United Kingdom.

Klarna Group plc

Klarna ($KLAR) is trending as investors discuss its recent IPO performance and future catalysts. Community chatter revolves around its AI integration and potential to disrupt traditional banking, while some express concerns about short selling and market manipulation. The stock is also being compared to competitors like Affirm ($AFRM) within the Buy Now, Pay Later sector, with discussions on market share and growth strategies.

CRISPR Therapeutics AG is a gene editing company, which engages in the development of transformative gene-based medicines for serious diseases using its proprietary CRISPR/Cas9 platform. Its CRISPR/Cas9 platform is a gene editing technology that allows for precise, directed changes to genomic DNA. The firm offers a portfolio of therapeutic programs across a broad range of disease areas including hemoglobinopathies, oncology, regenerative medicine, and rare diseases. The company was founded by Rodger Novak, Emmanuelle Charpentier, Shaun Patrick Foy, Matthew Porteus, Daniel Anderson, Chad Cowan, and Craig Mellow on October 31, 2013 and is headquartered in Zug, Switzerland.

CRISPR Therapeutics AG

CRSP is trending due to positive Phase 1 clinical data for its CTX310 in vivo gene-editing therapy, which showed significant lipid reductions and no serious safety issues. Community members are excited about the potential for this treatment to address heart disease and validate CRSP's in vivo LNP delivery platform, while some are discussing analyst price target adjustments and upcoming catalysts.

Centene Corp. is a healthcare enterprise, which engages in the provision of programs and services to government sponsored healthcare programs. It operates through the following segments: Medicaid, Medicare, Commercial, and Other. The Medicaid segment includes the Temporary Assistance for Needy Families program, Medicaid Expansion programs, the Aged, Blind or Disabled program, the Children's Health Insurance Program, Long-Term Services and Supports, Foster Care, Medicare-Medicaid Plans, which cover beneficiaries who are dually eligible for Medicaid and Medicare, and other state-based programs. The Medicare segment consists of Medicare Advantage, Medicare Supplement, Dual Eligible Special Needs Plans, and Medicare Prescription Drug Plans. The Commercial segment is involved in the Health Insurance Marketplace product along with individual, small group, and large group commercial health insurance products. The Other segment refers to pharmacy operations, Envolve Benefit Options’ vision and dental services, clinical healthcare, behavioral health, the TRICARE program, and corporate management companies. The company was founded in 1984 and is headquartered in St. Louis, MO.

Centene Corp.

Centene Corp. is trending amid discussions around potential ACA subsidy extensions and government shutdown negotiations, with community members weighing the potential impacts on the healthcare sector. Trump's stance on sending federal health insurance money directly to individuals is also fueling debate, with some viewing it as potentially beneficial for insurers like CNC. Traders are actively discussing potential entry and exit points, as well as the stock's technical strength in a volatile market.

Innodata, Inc. is a data engineering company, which engages in providing artificial intelligence software platforms and management of its services. It operates through the following business segments: Digital Data Solutions (DDS), Synodex, and Agility. The DDS segment combines deep neural networks and human expertise in multiple domains to make unstructured information useable. The Synodex segment enables clients in the insurance and healthcare sectors to transform medical records into useable digital data and to apply technologies to the digital data to augment decision support. The Agility segment provides tools and related professional services that enable public relations and communications professionals to discover influencers, amplify messages, monitor coverage, and measure the impact of campaigns. The company was founded by Todd H. Solomon in 1988 and is headquartered in Ridgefield Park, NJ.

Innodata Inc

Innodata is trending amid speculation about upcoming strategic partnerships, particularly regarding sovereign AI programs and potential deals in the Middle East, which could be revealed in 2026. Community discussions focus on the potential for significant contract wins with Saudi Arabia and the UAE and the possibility of new big tech clients. Some investors suggest Microsoft is increasing its contract with Innodata, and bullish sentiment is bolstered by Innodata's position in the AI data sector, though bearish sentiment remains due to INOD's position relative to its moving averages.

Braintrust is the first decentralized talent network that connects skilled, vetted knowledge workers with the world’s most reputable brands. The community that relies on Braintrust to find work are the same people who own and build it, ensuring the network always serves the needs of its users, instead of a centrally-controlled corporation. Unlike other marketplaces that take 20% to 50% of talent earnings, Braintrust allows talent to keep 100% of earnings and enables clients to make their budgets go further by cutting out the unnecessary middle men.  The community expands beyond 50,000 members across 100+ countries. Braintrust partners with global enterprises including Nestle, Porsche, Atlassian, Goldman Sachs, and Nike. Braintrust is backed by Tiger Global, Coinbase Ventures, Pantera and Multicoin Capital along with a contingent of individual investors.

Braintrust

Braintrust (BTRST) is experiencing increased attention, with community members pointing to a recent price surge and potential connections to AI developments as possible catalysts. Chatter includes speculation about partnerships, comparisons to "sister cryptos," and discussions around entry and exit points. Some users are also referencing the token's limited supply and previous all-time highs, while others are calling it a "shitcoin pump and dump."

Pfizer Inc. is a research-based global biopharmaceutical company, which engages in the discovery, development, manufacture, marketing, sales and distribution of biopharmaceutical products worldwide. The firm works across developed and emerging markets to advance wellness, prevention, treatments and cures that challenge the most feared diseases. The company was founded by Charles Pfizer Sr. and Charles Erhart in 1849 and is headquartered in New York, NY.

Pfizer Inc.

Pfizer Inc

Pfizer ($PFE) is trending due to a heated bidding war with Novo Nordisk ($NVO) for Metsera, a company developing obesity drugs, with the community debating if Pfizer is overpaying. Some investors believe Pfizer's pursuit of Metsera highlights its commitment to growth in the weight-loss market, while others are concerned about potential overspending and the impact on the company's reputation. Overall, the community is closely watching the outcome of the acquisition and its potential effects on Pfizer's future earnings and market position.

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Lexeo Therapeutics (NASDAQ:LXEO) Earns Buy Rating from Chardan Capital

Chardan Capital reiterated a "buy" rating and issued a $17.00 price objective on shares of Lexeo Therapeutics in a research report on Wednesday...

Wall Street Analysts See a 108.23% Upside in Lexeo Therapeutics, Inc. (LXEO): Can the Stock Really Move This High?

The consensus price target hints at a 108.2% upside potential for Lexeo Therapeutics, Inc. (LXEO). While empirical research shows that this sought-after metric is hardly effective, an upward trend in earnings estimate revisions could mean that the stock will witness an upside in the near term.

Beyond Traditional Drugs: Novel Platforms Targeting Hard-to-Treat Conditions

Beyond Traditional Drugs: Novel Platforms Targeting Hard-to-Treat Conditions Beyond Traditional Drugs: Novel Platforms Targeting Hard-to-Treat Conditions PR Newswire VANCOUVER, Oct. 21, 2025 Equity...

Lexeo Therapeutics shares rose to an 11-month high on Tuesday following a series of analyst upgrades that have rekindled investor interest in the biotech’s gene therapy LX2006 for heart problems associated with Friedreich’s ataxia.The rally came after Lexeo said the U.S. Food and Drug Administration has expressed willingness to consider an accelerated approval pathway for LX2006. Such a move would allow Lexeo to combine data from its current early-stage studies with results from an ongoing pivotal trial, potentially reducing the time to commercialization.Leerink Partners lifted the firm’s price target to $20 from $9 and reiterated an 'Outperform' rating, noting that the FDA’s willingness to pool data from the ongoing Phase I/II SUNRISE-FA and pivotal studies represents “regulatory flexibility and a relatively straightforward path to approval.”&nbsp;The brokerage stated that the FDA’s decision to assess the left ventricular mass index (LVMI), the therapy’s key cardiac endpoint, earlier than planned could accelerate timelines. Additionally, further clinical data show dose-dependent, durable LVMI reductions and clean safety profiles.H.C. Wainwright raised its price target to $15 from $9 and maintained a 'Buy' rating, saying the FDA feedback improves the probability of approval to 50% from 40%. The firm also advanced its expected commercial launch to 2028 from 2030, pointing to a faster and smaller pivotal trial.Chardan followed with an increase to $17 from $15, also keeping a 'Buy' rating. The firm stated that the FDA’s decision to allow the pooling of Phase I/II and pivotal data supports the potential for accelerated approval, while updated results showed “sustained and dose-dependent improvements” in cardiac measures.The bullish revisions followed Lexeo’s announcement that the FDA was open to a Biologics License Application (BLA) that combines data from its Phase I/II studies with new pivotal data to support accelerated approval. The agency also agreed to assess LVMI improvements earlier than 12 months.Interim results from the ongoing LX2006 trials showed encouraging efficacy, with participants who had abnormal heart mass at baseline achieving an average 18% reduction in LVMI at six months and 23% at 12 months, well above the FDA’s 10% improvement threshold.&nbsp;Neurological function also improved as measured by patients' scores on the modified Friedreich Ataxia Rating Scale (mFARS) and reductions in cardiac biomarkers, including troponin I and lateral wall thickness. The therapy was well tolerated, with no serious adverse events. The company plans to initiate the pivotal study in the first half of 2026, pending completion of final protocol and manufacturing comparability reviews.LX2006 has received Breakthrough Therapy, Regenerative Medicine Advanced Therapy (RMAT), Orphan Drug, and Fast Track designations, among others, and is part of the FDA’s CMC Development and Readiness Pilot (CDRP) program. The company expects the therapy to advance into its pivotal stage within the next year and believes the new framework could bring approval two years earlier than previously projected.On Stocktwits, retail sentiment for Lexeo was ‘extremely bullish’ amid a 6,200% surge in 24-hour message volume.One user called the FDA update a major win but warned of a dilution risk, noting that Lexeo’s $75 million shelf registration and recent $80 million private placement could lead to a share sale if the stock continues to rise. They said it’s a typical biotech setup with big news, big move, then dilution.<stembedurl>https://stocktwits.com/Jamesnewbie/message/631275401</stembedurl>Another user took a more upbeat tone, suggesting a rapid rally ahead, stating that a swift move to $20 could be on the way.&nbsp;<stembedurl>https://stocktwits.com/kpop1/message/631309344</stembedurl><a href="https://stocktwits.com/symbol/LXEO">Lexeo’s stock</a> has risen 27% so far in 2025.For updates and corrections, email newsroom[at]stocktwits[dot]com.

Lexeo’s stock (LXEO) has risen 27% so far in 2025. (Photo credit: Getty Images)

Lexeo Therapeutics Stock Hits 11-Month High On Bullish Analyst Calls For Friedreich’s Ataxia Gene Therapy — Retail Traders Join In

Analysts raised price targets and boosted approval odds after the FDA signaled support for a faster review process, citing strong safety and efficacy data in early trials of Lexeo’s treatment for Friedreich’s ataxia–related heart disease.

Equity

Lexeo Therapeutics (LXEO) announced on Tuesday that the company is considering a smaller pivotal study for LX2006 in the treatment of Friedreich's ataxia (FA) cardiomyopathy, scheduled to begin in the first half of 2026, pending finalization of the study protocol.The <a class="st-link-external" target="_blank" rel="noopener noreferrer nofollow" href="https://ir.lexeotx.com/news-releases/news-release-details/lexeo-therapeutics-announces-progress-fda-discussions">data</a> from the planned pivotal study will be pooled with data from the ongoing Phase I/II studies of LX2006 to support an approval application to the U.S. Food and Drug Administration for the therapy, the company stated after discussions with the agency.Lexeo will submit enhanced manufacturing comparability data and meet an additional nonclinical requirement before the initiation of the planned pivotal study to enable pooling, the company added.Lexeo is continuing to engage with the agency regarding the protocol of the pivotal study, it stated, adding that it believes this regulatory feedback has the potential to reduce the size and duration of the planned pivotal study. The company is also optimistic that the feedback may accelerate the overall timeline to an application submission.Updated interim clinical data from both ongoing Phase I/II studies of LX2006 show sustained or deepening improvements in the majority of participants across both cardiac and neurologic measures of Friedreich’s ataxia, the company said.FA cardiomyopathy is the leading cause of death in individuals with Friedreich’s ataxia (FA), a rare, inherited neurodegenerative disorder causing progressive damage to the nervous system, leading to impaired balance, muscle coordination, and sensory loss, often beginning in childhood. It is estimated to affect approximately 5,000 people in the U.S.Shares of the company rallied 24% at the time of writing. On Stocktwits, retail sentiment around <a href="https://stocktwits.com/symbol/LXEO">LXEO stock</a> jumped from ‘bearish’ to ‘extremely bullish’ territory over the past 24 hours, while message volume rose from ‘low’ to ‘extremely high’ levels.<figure class="image"><img style="aspect-ratio:1368/120;" src="https://news.stocktwits-cdn.com/Screenshot_2025_10_07_at_9_19_18_AM_png_3d23b7c692.webp" alt="LXEO's Sentiment Meter and Message Volume as of 9:19 a.m. ET on Oct. 07, 2025 | Source: Stocktwits" width="1368" height="120"><figcaption>LXEO's Sentiment Meter and Message Volume as of 9:19 a.m. ET on Oct. 07, 2025 | Source: Stocktwits</figcaption></figure>LXEO stock has risen 22% this year and but fallen by approximately 6% over the past 12 months.&nbsp;Read also:&nbsp;<a href="https://stocktwits.com/news-articles/markets/equity/novo-nordisk-reportedly-slashes-workforce-at-its-us-wegovy-manufacturing-plant/ch6PBqJR3WD">Novo Nordisk Reportedly Slashes Workforce At Its US Wegovy Manufacturing Plant</a>For updates and corrections, email newsroom[at]stocktwits[dot]com.

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Lexeo Therapeutics Stock Rallies On Discussions With FDA To Expedite Friedreich’s Ataxia Drug Approval Process

The company stated that data from a planned pivotal study will be pooled with data from the ongoing Phase I/II studies of LX2006 to support an approval application to the U.S. Food and Drug Administration for the therapy. 

Biotech stocks jump as Makary outlines FDA vision, RBC comments

Investing.com -- Biotech stocks climbed Monday after new FDA Commissioner Dr. Marty Makary laid out a clear and collaborative regulatory strategy that analysts say bodes well for drug developers. In his first major interview since taking office, Makary emphasized pragmatic reforms, faster drug approvals, and modernized use of real-world data across the agency.

Shares of clinical-stage genetic medicine company Lexeo Therapeutics, Inc. soared over 50% on Monday, marking their best day on record. The rally extended into after-hours trading following the company's latest quarterly results, which largely pleased investors.Lexeo specializes in therapies for hereditary and acquired diseases, with a focus on genetically defined cardiovascular conditions and a subset of Alzheimer's disease.&nbsp;Its pipeline includes LX2006 for treating Friedreich's ataxia cardiomyopathy and LX1001 for APOE4 homozygous Alzheimer's patients.According to Stocktwits data, the company reported an adjusted fourth-quarter loss of $0.78 per share, beating expectations for a $0.81 loss. The early-stage biotech firm is still in a pre-revenue stage.CEO R. Nolan Townsend highlighted regulatory progress on LX2006, noting ongoing collaboration with the FDA for an accelerated approval pathway.&nbsp;He also announced promising early safety data for LX2020, a treatment for arrhythmogenic cardiomyopathy (PKP2-ACM).&nbsp;The company expects to share additional clinical updates later in 2025, with the second cohort of a Phase 1/2 trial now fully enrolled.Despite the stock's sharp rally, Leerink lowered its price target from $19 to $18, which still implies a potential fourfold gain from current levels.&nbsp;The research firm remains bullish, citing positive registrational design elements in the LX2006 pivotal trial and interim data for LX2020.Lexeo ended 2024 with $128.5 million in cash and investments, which management believes will sustain operations into 2027.On Stocktwits, Lexeo's following surged 13% — the largest jump among biotech stocks.&nbsp;The stock, however, remains down over 39% year-to-date, with short interest creeping up from 6.2% to 7.3%.Traders on Stocktwits are watching technical patterns closely.&nbsp;"Nice breakout. I could see this running for a while," one user noted.<stembedurl>https://stocktwits.com/Sillyspuh/message/609105298</stembedurl>Another speculated that a cup-and-handle formation was forming.<stembedurl>https://stocktwits.com/Marcobucks/message/609063542</stembedurl>According to Koyfin, seven Wall Street analysts cover Lexeo. Four rate it a 'buy,' while three assign a 'strong buy' or equivalent rating.For updates and corrections, email newsroom[at]stocktwits[dot]com.

Lexeo Therapeutics Sees Biggest Retail Follower Surge Among Biotech Stocks After Record-Breaking Rally: What's The Big Draw?

The company reported an adjusted Q4 loss of $0.78 per share, beating expectations for a $0.81 loss.  

Satellos to Participate in Duchenne KOL Investor Webinar on December 4, 2024

Satellos Bioscience Inc. (TSX:MSCL, OTCQB:MSCLF) ('Satellos' or the 'Company'), a public biotech company developing new small molecule therapeutic approaches to improve the treatment of muscle...

Lexeo Down Despite Upbeat Rare Disease Gene Therapy Data

Shares of Lexeo Therapeutics (NASDAQ: LXEO) lost 26% on Monday after it reported positive interim data from two cohorts of the phase I/II SUNRISE-FA study evaluating LX2006, an investigational gene...

Buy Rating Affirmed for Lexeo Therapeutics Amid Promising Clinical Trial Results for FA-CM Treatment

Geulah Livshits, an analyst from Chardan Capital, reiterated the Buy rating on Lexeo Therapeutics, Inc. (LXEO Research Report). The associated pr...

Lexeo Therapeutics, Inc. is a clinical stage genetic medicine company, which engages in the development of therapies for hereditary and acquired diseases. The firm focuses on the medication of genetically defined cardiovascular diseases and sub-group of Alzheimer’s disease. It offers LX2006 for the treatment of patients with Friedreich's ataxia, cardiomyopathy, and LX1001 for APOE4 homozygous patients with Alzheimer's disease. The company was founded by Ronald G. Crystal in February 2017 and is headquartered in New York, NY.

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