La catena delle opzioni mostra i dati chiave delle opzioni azionarie di Longeveron a vari prezzi di esercizio e date di scadenza. I trader utilizzano queste informazioni per analizzare potenziali operazioni e valutare il sentiment del mercato per Longeveron..

Longeveron (NASDAQ:LGVN) Azioni, Catena delle Opzioni

LONGEVERON INC-A

Longeveron

Longeveron Inc is a clinical-stage biotechnology company developing regenerative medicines to address unmet medical needs for specific aging-related and life-threatening conditions. Its investigational product is Lomecel-B an stem cell formulation sourced from the bone marrow of young, healthy adult donors and has potential mechanisms of action that can promote tissue repair and healing. The company currently has three pipeline indications: Hypoplastic Left Heart Syndrome (HLHS), Alzheimer's disease (AD) and Aging-related Frailty.

WIIM

LGVN

Longeveron shares are trading higher after the company announced that the FDA approved its Investigational New Drug application for its stem cell therapy laromestrocel as a potential treatment for pediatric dilated cardiomyopathy.

<a href="https://s27.q4cdn.com/906368049/files/News/2025/Zacks_SCR_Research_07082025_LGVN_Sorensen.pdf" title="https://s27.q4cdn.com/906368049/files/News/2025/Zacks_SCR_Research_07082025_LGVN_Sorensen.pdf">https://s27.q4cdn.com/906368049/files/News/2025/Zacks_SCR_Research_07082025_LGVN_Sorensen.pdf</a>

News

Analyst Ratings

Trading Ideas

Watching Longeveron; Zacks Small-Cap Reiterates $9.55 Price Valuation, Originally Stated On June 24, 2025

<ul>
<li>Accepted IND application allows for development program to move directly to a Phase 2 pivotal registration clinical trial</li>
<li>Phase 2 clinical trial initiation anticipated in first half of 2026</li>
<li>Pediatric cardiomyopathies affect at least 100,000 children worldwide</li>
<li>Effective treatment options are limited, with nearly 40% of children with DCM requiring a heart transplant or dying within two years of diagnosis</li>
</ul>
MIAMI, July 08, 2025 (GLOBE NEWSWIRE) -- &nbsp;<a href="https://www.globenewswire.com/Tracker?data=DYnoFRstChOTa6jqFuAQm9hu7qAtPRK7WTUf3KYn6TEPGsV_2jkV8t-Q4ObWSyZUVFQH74m2YV039ppxYp2i9ePUzRyeriyyhqHXa5_5pFY=">Longeveron Inc.</a> (NASDAQ:<a class="ticker" href="https://www.benzinga.com/stock/LGVN#NASDAQ">LGVN</a>), a clinical stage regenerative medicine biotechnology company developing cellular therapies for life-threatening and chronic aging-related conditions, today announced that the U.S. Food and Drug Administration (FDA) has approved the Investigational New Drug (IND) application for its stem cell therapy <a href="https://www.globenewswire.com/Tracker?data=VCQ4uzOP67FljSm-u3Y8CqfuPh0fHmfpBXcAEKS6PPqXOwrVaCqagxHcTjyYnjb_1t7sYguGW9-T-My5o_m1zACTxaEyM1bauaskpDH8Hzc=">laromestrocel</a> as a potential treatment for pediatric dilated cardiomyopathy (DCM). The accepted IND application provides for moving directly to a single Phase 2 pivotal registration clinical trial.

Longeveron Announces FDA Approval Of IND Application For Stem Cell Therapy Laromestrocel As Potential Treatment For Pediatric Dilated Cardiomyopathy

<a href="https://scr.zacks.com/files/News/2025/Zacks_SCR_Research_06242025_LGVN_Sorensen.pdf" title="https://scr.zacks.com/files/News/2025/Zacks_SCR_Research_06242025_LGVN_Sorensen.pdf">https://scr.zacks.com/files/News/2025/Zacks_SCR_Research_06242025_LGVN_Sorensen.pdf</a>

Watching Longeveron; Zacks Small-Cap Research Gives Stock $9.55 Price Valuation

<ul>
<li>Top-line trial results are anticipated in the third quarter of 2026, after the final follow-up at 12-months</li>
<li>Laromestrocel Biological License Application (BLA) submission for full traditional approval for HLHS anticipated in 2026, if ELPIS II results are positive</li>
<li>U.S. FDA has awarded laromestrocel HLHS program Rare Pediatric Disease designation, Orphan drug designation, and Fast track designation</li>
<li>Laromestrocel HLHS program addresses unmet medical needs with U.S. market potential of up to $1 billion</li>
</ul>
MIAMI, June 24, 2025 (GLOBE NEWSWIRE) -- <a href="https://www.globenewswire.com/Tracker?data=LpTK0ohCzvSmm119iBVMPIVxBwZ0diUvbKgCWINgacLZ20PwHvC5wD8shoK1_ohH4Ag6He2-oYHxVyCsw8M5uW7Qb8DIjcevNN_kuFosDH4=">Longeveron Inc.</a> (NASDAQ:<a class="ticker" href="https://www.benzinga.com/stock/LGVN#NASDAQ">LGVN</a>), a clinical stage regenerative medicine biotechnology company developing cellular therapies for life-threatening and chronic aging-related conditions, today announced that it has achieved full enrollment of the Phase 2b clinical trial (ELPIS II) evaluating its investigational cellular therapy <a href="https://www.globenewswire.com/Tracker?data=W1AagQaXvhI3pJkdhPX1jXyKjbyW6TncdwGjarjHlIAS0RuTYWORZfdmzd04rShPW7gXz_YUKmp10p_xLg4AgEHSwLmznqrgmcGrRvSvRdc=">laromestrocel</a> as a potential adjunct treatment for <a href="https://www.globenewswire.com/Tracker?data=hMHj6cUdu2hH5iyehQ_VyJEsbhtBqH6MUSxmYKMl-e6R_XzS4uCyyAp896RgWxkbiAvB3HDT7ri7qaHbAErr0_Dm8vqQqORlAuZ8QV5LjxPJ8aQC2D2fRn9lTe9XLIA2bpiV6LkVzqPjpWm4z_lQDQ==">Hypoplastic Left Heart Syndrome (HLHS)</a>, a rare pediatric and orphan-designated disease. Top-line trial results are anticipated in the third quarter of 2026, after the final follow-up at 12-months. Laromestrocel is a proprietary, scalable, allogeneic cellular therapy being evaluated in multiple indications.

Longeveron Completes Enrollment Of Phase 2b Clinical Trial Evaluating Investigational Cellular Therapy Laromestrocel As Potential Adjunct Treatment For Hypoplastic Left Heart Syndrome

Longeveron (NASDAQ:<a class="ticker" href="https://www.benzinga.com/stock/LGVN#NASDAQ">LGVN</a>) reported quarterly losses of $(0.34) per share which missed the analyst consensus estimate of $(0.30) by 13.33 percent. This is a 78.88 percent increase over losses of $(1.61) per share from the same period last year. The company reported quarterly sales of $381.00 thousand which missed the analyst consensus estimate of $608.25 thousand by 37.36 percent. This is a 30.47 percent decrease over sales of $548.00 thousand the same period last year.

Earnings

Earnings Misses

Longeveron Q1 EPS $(0.34) Misses $(0.30) Estimate, Sales $381.00K Miss $608.25K Estimate

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Earnings Scheduled For May 8, 2025

Dear Fellow Shareholders,
Twenty twenty-four was a year of execution for Longeveron. We made significant progress advancing Longeveron's founding mission - developing cutting-edge cellular therapy research to impact patients' lives for the better by addressing unmet medical needs. We have come a long way pursuing that mission and now have clarity on the pathway to our first potential Biological License Application (BLA) submission.
Today, I am excited to update you on our overall strategy, progress, and key priorities and goals for 2025.
Strategic Overview and 2024 Progress: Over the past decade, stem cell therapy has seen remarkable strides, transforming from a promising field into one delivering tangible clinical outcomes. We've seen the solidification of cell therapy's role in regenerative medicine and its potential to treat a wide range of conditions, signaling an exciting future for both scientific innovation and patient care.
Longeveron has been at the forefront of this evolution in medicine. Our lead investigational product is laromestrocel (Lomecel-B&#x2122;), a stem cell therapy derived from culture-expanded mesenchymal stem cells (MSCs) that are sourced from bone marrow of young healthy adult donors. The number of functional MSCs in the body declines as we age, which has driven interest in their use for aging-related conditions. Their unique properties — including the ability to reduce inflammation, promote tissue repair and regeneration, modulate immune responses, and improve vascularization — also support their application in some rare cardiovascular diseases/conditions with high unmet medical need. We believe that by using the same cells that promote tissue repair, organ maintenance, and immune system function, we can develop safe and effective therapies for some of the most difficult diseases and conditions.
A decade ago, our stem cell therapy vision was an academic idea. Today, laromestrocel represents a pipeline in a product opportunity that has delivered positive results from multiple clinical trials: Phase 1 &amp; 2 in Alzheimer's disease, Phase 1 &amp; 2 in Aging-related Frailty, Phase 1 in Hypoplastic Left Heart Syndrome (HLHS), a rare pediatric disease. We are currently conducting a pivotal Phase 2b clinical trial for HLHS. Our development programs for these 3 initial indications address market opportunities of what we estimate to be approximately ~$5+ billion, ~$4+ billion and up to ~$1 billion, respectively. Earlier this year, the World Health Organization's International Nonproprietary Names (INN) Expert Committee approved "laromestrocel" as the non-proprietary name for Lomecel-B&#x2122; — a key milestone in the development and future commercialization of our stem cell therapy.
As we did this past year, in 2025, we will continue focusing our efforts on two of our most promising programs: HLHS and Alzheimer's disease.
Hypoplastic Left Heart Syndrome (HLHS):
HLHS is a rare pediatric disease in which the left ventricle (one of the pumping chambers of the heart) is either severely underdeveloped or missing. Because the left ventricle is the chamber that normally pumps blood to the body, infants born with this condition have a profound reduction in blood flow and thus cannot get the normal supply of oxygen to their organs. In order for the children to survive, they must undergo a complicated, three-stage heart reconstruction surgery over the course of the first 5 years of their lives. Despite this surgical reconstruction, only 50% of the affected children survive to age 15 without heart transplantation.
Our program is designed to boost/improve the heart function in these children with the goal of potentially enhancing their survival. In our Phase I clinical trial (ELPIS I) evaluating laromestrocel in 4-month-old infants with HLHS, we observed 100% transplant-free survival up to five years following treatment. This contrasts with an approximately 20% mortality rate observed in historical control data. Five-year post-treatment long-term survival data from the ELPIS I Phase 1 clinical trial was presented at the Congenital Heart Surgeons' Society (CHSS) 51st Annual Meeting in October 2024.
We are currently nearing completion of enrollment for our Phase 2b study, ELPIS II, which is evaluating laromestrocel as a potential adjunct treatment to the standard of care for HLHS. ELPIS II has achieved nearly 95% enrollment, and we expect to complete enrollment in the second quarter of this year.
In September 2024, we completed a Type C meeting with the U.S. FDA regarding our HLHS development program and the pathway toward a potential BLA submission. We reached foundational alignment on the primary endpoint and secondary endpoints for the ELPIS II trial. The FDA confirmed that, contingent on positive results, ELPIS II may be considered a pivotal trial and potentially acceptable for BLA submission seeking full traditional approval. With this regulatory clarity, we are now focused on BLA preparedness and enabling activities for the HLHS program. Notably, because this program has received Rare Pediatric Disease Designation, we may be eligible to receive a Priority Review Voucher (PRV) if our BLA is approved. We may use the PRV internally or sell to a third party. Historically, PRVs have commanded values exceeding $100 million.
Alzheimer's Disease:
The laromestrocel Alzheimer's disease (AD) program continues to garner important recognition and support. In 2024, data from the CLEAR MIND Phase 2a clinical trial evaluating laromestrocel in mild Alzheimer's disease were presented as a featured research oral presentation at the 2024 Alzheimer's Association International Conference held at the end of July and as a late breaking poster presentation at the 17th edition of the Clinical Trials on Alzheimer's Disease Conference (CTAD24) in October. We are very excited about the trial's positive results. The trial met its primary objective of demonstrating safety, with laromestrocel being well-tolerated. In addition, we observed encouraging trends suggesting a potential slowing or prevention of disease progression in patients treated with laromestrocel compared to placebo.
This program has received Regenerative Medicine Advanced Therapy (RMAT) and Fast Track designations, providing us with the opportunity for enhanced and frequent communication with the FDA to facilitate the development and review process. In March of this year, results from the trial were <a href="https://www.globenewswire.com/Tracker?data=q5z76BEDJ6-_BNlI7zxiW7bj7HH_JA6z2l_-sTbO61K_qKYtMQAMaF9FDMVXrEj3T_9nYmWCk-Lq0zdwrX4bx2qd5ntW3sf1N8Ytp1j1BkoTux4GUbqWzdOydRL9flts">published</a> in Nature Medicine.
Also in March of this year, we held a Type B meeting with the FDA to discuss the regulatory pathway for a potential BLA for laromestrocel in mild Alzheimer's disease. We reached foundational alignment on the overall study design for a proposed single, pivotal, seamless adaptive Phase 2/3 clinical trial. To support an accelerated path to potential approval, the FDA agreed to consider a BLA submission based on positive interim results from this planned single study.
With this regulatory clarity in hand, we are focused on seeking partnership opportunities and/or non-dilutive funding for the Alzheimer's disease program.
Our Core Business Objectives: Our strategic plan is built on the strength of the science underlying our stem cell therapy laromestrocel. For 2025, we are focused on four key objectives:
<ol>
<li>Advance HLHS Program as the Main Near-Term Value Driver:
<ul>
<li>Pivotal Phase 2 clinical trial (ELPIS II) is nearing enrollment completion.</li>
<li>Regulatory pathway clarified with U.S. FDA.</li>
<li>Potential to initiate rolling BLA submission in 2026.</li>
<li>Potential to receive a Rare Pediatric Disease priority review voucher associated with HLHS upon BLA approval which could have significant monetary value and further enhance our product's value proposition upon approval.</li>
</ul>
</li>
<li>HLHS BLA and Commercialization Readiness:
<ul>
<li>Successful meeting with FDA confirmed ELPIS II could be pivotal.</li>
<li>2025 will see significant focus on organizational readiness for potential BLA filing for HLHS in 2026. Our goal is to accomplish BLA readiness this year ahead of data readout to potentially shorten the timeline to BLA submission.</li>
<li>Emphasis on Chemistry, Manufacturing, and Controls (CMC) preparedness.</li>
<li>Hired industry veteran Chief Technology Officer to support BLA preparedness.</li>
<li>We are committed to helping HLHS patients worldwide. In 2025, we intend to take initial steps connecting with non-U.S. regulatory bodies, including EMA (European Union), MHRA (United Kingdom), PMDA (Japan) and HealthCanada.</li>
<li>Recognizing substantial revenue potential from worldwide commercialization, we anticipate capitalizing on recent rare disease pricing trends and the unique aspects of our treatment.</li>
</ul>
</li>
<li>Strategic Collaborations for Alzheimer's Disease:
<ul>
<li>We believe our Alzheimer's disease program holds immense potential. Due to the large size of the affected population, it involves larger-scale studies and commercialization requirements. This scale of development effort necessitates significant investment, prompting our focus on potential strategic partnerships with biotech/pharmaceutical companies and/or non-dilutive funding sources.</li>
<li>We believe the clarity on the pathway to potential BLA submission and the need for only a single pivotal clinical trial enhance the attractiveness and economic benefits of the program to potential partners.</li>
</ul>
</li>
<li>Efficient Resource Management and Capital Allocation:
<ul>
<li>We strive to be prudent stewards of shareholder capital and focus allocating it to the organization's top priorities to effectuate optimal resource utilization and alignment with strategic objectives.</li>
<li>We prudently manage expenses. In 2024, we reduced total operating expenses 13% while continuing to effectively advance our development programs.</li>
</ul>
</li>
</ol>
Financial Position and Capital Strategy: Longeveron is working diligently to effectively advance our development programs while managing expenses and our capital. We will need additional capital to achieve our business strategy and objectives.
We indicated in our recently filed Annual Report on Form 10K that we anticipated our existing cash and cash equivalents would fund our operating expenses and capital expenditure requirements into the fourth quarter of 2025. However, as we also indicated, as a result of our successful Type C meeting with the FDA in August 2024 with respect to the HLHS regulatory pathway, we have started to ramp up BLA enabling activities to prepare for a potential filing with the FDA in 2026 if the current ELPIS II trial is successful. We expect our operating expenses and capital expenditure requirements to accelerate this year as a result of these activities, including CMC (Chemistry, Manufacturing, and Controls) and manufacturing readiness. We intend to seek additional financing and non-dilutive funding options to support these activities, and additional non-dilutive funding and/or strategic partners to support the AD development program. We anticipate that our current cash projections may be impacted by these ramped up activities and any financing transactions we enter into.
2025 Goals and Priorities Our goals for 2025 center on efficient, effective execution of our strategic plan with an emphasis on three primary operational goals:
<ol>
<li>ELPIS II Completion: We anticipate completion of ELPIS II enrollment in the second quarter of 2025. We will then focus on supporting our investigative sites through completion of the 12-month primary endpoint follow-up period and preparation for data collection and analysis at the end of the study.</li>
<li>HLHS BLA Preparedness: We intend to accomplish the majority of BLA readiness in 2025 to support a potentially shortened time frame from clinical trial readout to BLA submission.</li>
<li>Alzheimer's Disease Program Partnering: We plan to leverage the strength of our Phase 2 data and clarity on the clinical pathway to a potential BLA for AD to engage with potential funding/commercialization partners. &nbsp;</li>
</ol>
Outlook Longeveron has made tremendous progress in two important stem cell development programs over the past 12 months, successfully delivering on our strategic plan. We are now approaching multiple potentially transformational milestones over the next 12 months including completion of enrollment in our pivotal Phase 2b clinical trial in HLHS which may establish the timeline for a potential BLA submission for HLHS, and potential partnering for the Alzheimer's disease program. Our team's expertise and industry experience enable the organization to accomplish so much with a small team and few resources. Generating several positive initial results across five clinical trials in three indications, continues to position Longeveron as a leader in stem cell therapy research and, potentially, commercialization of cellular therapeutics.
We believe Longeveron's demonstrated track record of successful clinical execution, strength of data generated to date and the potential size of addressable markets provide for a compelling investment opportunity.
We deeply appreciate the support of our stakeholders and look forward to continued collaboration and progress in the future.
Sincerely, Wa'el Hashad CEO, Longeveron

Longeveron Issues Letter To Shareholders

Offerings

Longeveron Files For Mixed Shelf Of Up To $70M

HC Wainwright &amp; Co. analyst Raghuram Selvaraju reiterates Longeveron (NASDAQ:<a class="ticker" href="https://www.benzinga.com/stock/LGVN#NASDAQ">LGVN</a>) with a Buy and maintains $10 price target.

Price Target

Reiteration

HC Wainwright & Co. Reiterates Buy on Longeveron, Maintains $10 Price Target

<a href="https://www.globenewswire.com/Tracker?data=CfDdIU-vUWn-uP7WHZnuaEMaCT_kqK23e2B2rnWSgQ5QTVFsFxDKp6KvoNJv4aIe5LwgelnDBkS8uQ2d1vFWv_zrjJe72SQMKwWgyt9sjno=">Longeveron Inc.</a> (NASDAQ:<a class="ticker" href="https://www.benzinga.com/stock/LGVN#NASDAQ">LGVN</a>), a clinical stage regenerative medicine biotechnology company developing cellular therapies for life-threatening and chronic aging-related conditions, today announced the positive outcome of a Type B meeting with the U.S. Food and Drug Administration (FDA), supporting the advancement of <a href="https://www.globenewswire.com/Tracker?data=vYENKpHkG8Q8TKtnRxrYYFtmm_mUPJS_XTwI5jShRSwA5Dr06tUzISpzZEL9NxPouMnJI0KUgXAnhKBQomWSBWMdIFwZsURvx6s39Xd4YDgljvier2cBsVb7vvOcmB2C">laromestrocel (Lomecel-B</a><a href="https://www.globenewswire.com/Tracker?data=H-H0Ucz0WPTEb36hcT-70z9e_WbFg-Z8bsgF9UaKGYDsTdENcA3nzIgYTf8iKQEYwAVwH-nb1iksUeViM8KA1Q==">TM</a>), a proprietary, scalable, allogeneic, investigational cellular therapy, as a potential treatment for <a href="https://www.globenewswire.com/Tracker?data=wZ5v0WKJTKNsAImVqEvVI5wS4Ce0JLoAGRVmvMihw6AXPD-OIwMKUX0v-4Cqp7P6jgGfR-1NN6SepnEXcg1bxn_PeVHqlbgbL8N4JlbAV4Y=">Alzheimer's</a> disease (AD).
The Company and the FDA reached foundational alignment on the overall study design for a proposed single, pivotal, seamless adaptive Phase 2/3 clinical trial, including proposed AD patient population, proposed placebo control, laromestrocel (Lomecel-BTM) dose selection and frequency, trial duration and trial endpoints. To accelerate the pathway to potential approval, the FDA agreed to consider a BLA based on positive interim trial results from the planned single study.

Longeveron Says Co. And FDA Reached Foundational Alignment On Overall Study Design Supporting Laromestrocel In Alzheimer's Disease

<ul>
<li>Phase 2a results demonstrated laromestrocel (Lomecel-B&#x2122;) improved cognitive function, quality of life, and brain volume in the treatment of mild Alzheimer's disease</li>
<li>This encouraging clinical trial data adds to the body of evidence supporting the safety of single and multiple doses of laromestrocel (Lomecel-B&#x2122;) treatment for mild Alzheimer's disease and provides indications of efficacy in combating decline of brain volume and potentially cognitive function</li>
<li>Laromestrocel (Lomecel-B&#x2122;) is, to Company's knowledge, the first cellular therapeutic candidate to receive U.S. FDA Regenerative Medicine Advanced Therapy (RMAT) designation for Alzheimer's disease</li>
</ul>

Biotech

General

Longeveron Publishes Results Of Phase 2a Clinical Trial Evaluating Laromestrocel In Alzheimer's Disease In Nature Medicine

Longeveron shares are trading higher after the company provided 2024 clinical updates and financial results.

Longeveron (NASDAQ:<a class="ticker" href="https://www.benzinga.com/stock/LGVN#NASDAQ">LGVN</a>) reported quarterly losses of $(2.62) per share which beat the analyst consensus estimate of $(3.53) by 25.78 percent. The company reported quarterly sales of $2.392 million which beat the analyst consensus estimate of $2.143 million by 11.63 percent.

Longeveron FY 2024 GAAP EPS $(2.62) Beats $(3.53) Estimate, Sales $2.392M Beat $2.143M Estimate

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• Chart Industries (NYSE:<a class="ticker" href="https://www.benzinga.com/stock/GTLS#NYSE">GTLS</a>) is expected to report quarterly earnings at $3.23 per share on revenue of $1.18 billion. 
• Alpha Metallurgical (NYSE:<a class="ticker" href="https://www.benzinga.com/stock/AMR#NYSE">AMR</a>) is estimated to report quarterly earnings at $1.12 per share on revenue of $683.10 million. 
• Docebo (NASDAQ:<a class="ticker" href="https://www.benzinga.com/stock/DCBO#NASDAQ">DCBO</a>) is expected to report quarterly earnings at $0.27 per share on revenue of $56.24 million. 
• Northwest Natural Hldg (NYSE:<a class="ticker" href="https://www.benzinga.com/stock/NWN#NYSE">NWN</a>) is expected to report quarterly earnings at $1.49 per share on revenue of $395.05 million. 
<h3>Companies Reporting After The Bell</h3>
• BIT Mining (NYSE:<a class="ticker" href="https://www.benzinga.com/stock/BTCM#NYSE">BTCM</a>) is estimated to report earnings for its fourth quarter. 
• Monroe Cap (NASDAQ:<a class="ticker" href="https://www.benzinga.com/stock/MRCC#NASDAQ">MRCC</a>) is expected to report quarterly earnings at $0.27 per share on revenue of $14.99 million. 
• Longeveron (NASDAQ:<a class="ticker" href="https://www.benzinga.com/stock/LGVN#NASDAQ">LGVN</a>) is projected to report quarterly loss at $0.36 per share on revenue of $660 thousand. 
• Middlesex Water (NASDAQ:<a class="ticker" href="https://www.benzinga.com/stock/MSEX#NASDAQ">MSEX</a>) is likely to report quarterly earnings at $0.37 per share on revenue of $45.00 million. 
This article was generated by Benzinga's automated content engine and reviewed by an editor.

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Earnings Scheduled For February 28, 2025

Longeveron Announces WHO Approval Of Non-Proprietary Name Laromestrocel For Cellular Therapy Lomecel-B In Alzheimer's And HLHS Treatment

<a href="https://scr.zacks.com/files/News/2024/Zacks_SCR_Research_11132024_LGVN_Sorensen-pdf.pdf" title="https://scr.zacks.com/files/News/2024/Zacks_SCR_Research_11132024_LGVN_Sorensen-pdf.pdf">https://scr.zacks.com/files/News/2024/Zacks_SCR_Research_11132024_LGVN_Sorensen-pdf.pdf</a>

Watching Longeveron; Zacks Small-Cap Research Sets $9.50 Price Valuation

Longeveron (NASDAQ:<a class="ticker" href="https://www.benzinga.com/stock/LGVN#NASDAQ">LGVN</a>) reported quarterly losses of $(0.34) per share which beat the analyst consensus estimate of $(0.44) by 22.73 percent. This is a 87.81 percent increase over losses of $(2.79) per share from the same period last year. The company reported quarterly sales of $773.000 thousand which beat the analyst consensus estimate of $397.000 thousand by 94.71 percent. This is a 415.33 percent increase over sales of $150.000 thousand the same period last year.

Earnings Beats

Longeveron Q3 2024 GAAP EPS $(0.34) Beats $(0.44) Estimate, Sales $773.000K Beat $397.000K Estimate

Health Care

Press Releases

Longeveron® Announces Positive Type B Meeting with U.S. FDA Regarding Pathway to BLA for Laromestrocel (Lomecel-BTM) in Alzheimer's Disease

Longeveron® Issues Letter to Shareholders Highlighting Corporate Strategy, Recent Progress and Key Priorities and Goals for 2025

Longeveron® to Report First Quarter 2025 Financial Results and Host Conference Call on May 8, 2025

Longeveron® Announces First Quarter 2025 Financial Results and Provides Business Update

Longeveron® Named XPRIZE Healthspan Semifinalist and Top 40 Milestone 1 Award Recipient

Longeveron® to Attend BIO International Convention 2025

Longeveron® to Participate in the H.C. Wainwright 6th Annual Neuro Perspectives Hybrid Conference

Longeveron® Announces Completion of Enrollment of Pivotal Phase 2b Clinical Trial Evaluating Laromestrocel as a Treatment for Hypoplastic Left Heart Syndrome (HLHS)

Management

Longeveron® Appoints Than Powell as Chief Business Officer

Longeveron® Announces U.S. FDA Approval of IND Application for a Phase 2 Pivotal Registration Study Evaluating Laromestrocel as a Treatment of Pediatric Dilated Cardiomyopathy (DCM)

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