Larimar Therapeutics, Inc. (LRMR) Stock Price & Analysis

Larimar Therapeutics, Inc. (LRMR) fell 0.25% to USD 4 as of July 25, 2026 at 03:02 UTC, according to Nexqual real-time market data.

LRMR last closed at USD 4.01; the session ranged USD 3.98–4.16 on volume of 1,220,900 shares. Market capitalization is $415.53M, with a 52-week range of USD 2.72–6.42 (NGM). Source: Nexqual, July 25, 2026 at 03:02 UTC.

Key Statistics (as of July 25, 2026 at 03:02 UTC)

Technical Analysis (LRMR)

Nexqual's technical model rates LRMR "STRONG BUY" based on 5 bullish and 0 bearish signals across 125 daily candles, as of July 25, 2026 at 03:02 UTC.

Analyst Ratings (LRMR)

Wall Street analysts rate LRMR "Strong Buy" based on 10 analysts, with a mean price target of USD 14.4 (range USD 5–26), per Nexqual as of July 25, 2026 at 03:02 UTC.

Earnings (LRMR)

Recent Earnings History

Source: Nexqual, July 25, 2026 at 03:02 UTC.

Financials & Fundamentals (LRMR)

Source: Nexqual, July 25, 2026 at 03:02 UTC.

Financial Health Score (LRMR)

Nexqual rates Larimar Therapeutics, Inc.'s overall financial health "Mixed" across five dimensions, as of July 25, 2026 at 03:02 UTC.

Ownership (LRMR)

Source: Nexqual, July 25, 2026 at 03:02 UTC.

Leadership (LRMR)

Larimar Therapeutics, Inc. is led by Carole S. Ben-Maimon (age 66), CEO, President & Director, per Nexqual as of July 25, 2026 at 03:02 UTC.

Major Backers & Investors (LRMR)

Notable institutional backers of Larimar Therapeutics, Inc. include Deerfield Management Company, L.P, Blue Owl Capital Holdings LP, Millennium Management, according to Nexqual as of July 25, 2026 at 03:02 UTC.

Active Investors

Index Funds (Passive)

Source: Nexqual, July 25, 2026 at 03:02 UTC.

From Larimar Therapeutics, Inc.'s Latest SEC 10-K Filing (filed 2026-03-19)

Key Strengths & Strategy (as disclosed to the SEC)

• We intend to use our proprietary platform to target additional orphan indications characterized by deficiencies in or alterations of intracellular content or activity.
• In June 2025, the FDA provided recommendations regarding the safety data that might be needed to support a Biologics License Application.("BLA") seeking accelerated approval, which included evaluating safety in at least 30 participants with continuous study drug exposure for six months and a subset of at least 10 of those participants with continuous study drug exposure for one year, with the large majority of data coming from participants receiving the 50 mg dose.
• As a result, we consulted experts and decided to modify the starting dose regimen 8   and the FDA agreed with our approach.
• Using our proprietary peptide delivery technology, nomlabofusp is designed to carry the molecule from the intravascular space across the cell membrane and into the mitochondria where the CPP and the mitochondrial targeting sequence are cleaved off by the mitochondrial processing peptidase ("MPP") enzyme to yield mature FXN.

Partnerships

• We are party to a Master Services Agreement with Lonza, pursuant to w h ich Lonza provides manufacturing services with respect to nomlabofusp.
• We may build our own internal sales force, partner with a contract sales organization, enter into a joint marketing partnership with another pharmaceutical or biotechnology company, or we may seek to out-license nomlabofusp. • Expand our product candidate pipeline to treat a variety of rare diseases.

Source: SEC EDGAR 10-K, official filing. Curated by Nexqual.

Peers & Related Stocks

Data source: Nexqual — real-time market data, technical indicators, analyst consensus, earnings, SEC EDGAR filings. Last updated: July 25, 2026 at 03:02 UTC. This page is informational and not investment advice.