$3.94-0.12 (-2.96%)
Larimar Therapeutics, Inc., a clinical-stage biotechnology company, focuses on developing treatments for rare diseases using its novel cell penetrating peptide technology platform.
Larimar Therapeutics, Inc. in the Healthcare sector is trading at $3.94. The stock is currently 39% below its 52-week high of $6.42, remaining 1.5% below its 200-day moving average. Technical signals show oversold RSI of 12 and bearish MACD signal, explaining why LRMR maintains its current current market pressure. The Whystock Score of 45/100 suggests a balanced risk-reward profile.
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Larimar Therapeutics, Inc., a clinical-stage biotechnology company, focuses on developing treatments for rare diseases using its novel cell penetrating peptide technology platform. Its lead product candidate is CTI-1601, which is in Phase 2 OLE clini...
Larimar Therapeutics, Inc. (NASDAQ:LRMR) is one of the 10 Small–Cap Stocks Insiders Are Buying Recently. On March 20, 2026, Wedbush raised the price target on Larimar Therapeutics, Inc. (NASDAQ:LRMR) to $13 from $12 previously and maintained an Outperform rating. Wedbush said the Q4 update was in line with expectations as the company prepares for its […]
BALA CYNWYD, Pa. AP) — Larimar Therapeutics, Inc. LRMR) on Thursday reported a loss of $62.5 million in its fourth quarter.
Larimar's stock jumps 55% in a month after the FDA grants breakthrough therapy status to its FA drug nomlabofusp and backs a potential accelerated path.
Wedbush raised the firm’s price target on Larimar Therapeutics (LRMR) to $12 from $11 and keeps an Outperform rating on the shares. The firm notes that last week, the company completed an upsized $100M offering following receipt of Breakthrough Therapy designation for nomlabofusp in Friedreich’s ataxia. After incorporating the raise, Wedbush is also increasing its Q4 spending to tie with year-end 2025 cash $137M. While the firm acknowledges recent FDA decisions have been a source of concern for
Larimar Therapeutics recently completed an upsized US$100,000,000 follow-on equity offering at US$5.00 per share, shortly after the FDA granted Breakthrough Therapy Designation to its lead Friedreich’s ataxia candidate, nomlabofusp. This combination of expedited regulatory status and fresh capital raises the company’s capacity to advance nomlabofusp toward planned late-stage development and potential approval milestones. Next, we’ll examine how Breakthrough Therapy Designation for...