Larimar Therapeutics, Inc. (LRMR) Earnings

Larimar Therapeutics, Inc. is expected to report next earnings on August 13, 2026 (in NaN days), with a consensus EPS estimate of $-0.39. LRMR has beaten EPS estimates in 6 of its last 12 reported quarters (average surprise -17.0% over the last four).

Next earnings
Aug 13, 2026in NaN days
EPS est $-0.39 · Revenue est
Track record
Beat EPS in 6 of 12 quarters
Avg surprise -17.0% (last 4 quarters)
Earnings history
Report dateEPS estEPS actualSurpriseRevenueRev. surprise
May 14, 2026$-0.53$-0.31+41.5%
Mar 19, 2026$-0.44$-0.73-65.9%
Nov 5, 2025$-0.39$-0.61-56.4%
Aug 14, 2025$-0.47$-0.41+12.8%
Apr 30, 2025$-0.42$-0.46-9.5%
Mar 24, 2025$-0.29$-0.45-55.2%$241000
Oct 30, 2024$-0.37$-0.24+35.1%
May 9, 2024$-0.24$-0.27-12.5%
Mar 14, 2024$-0.25$-0.30-20.0%
Nov 14, 2023$-0.23$-0.21+8.7%
Aug 10, 2023$-0.21$-0.19+9.5%
May 15, 2023$-0.25$-0.15+40.0%

Source: company filings + earnings calendar. For informational purposes only — not investment advice.

Earnings call summary

Q1 FY2023 · September 29, 2025

AI summary of management’s prepared remarks and analyst Q&A. For informational purposes only — not investment advice.

Management highlights

- Positive 25-milligram and 50-milligram data from the long-term open-label study for Friedreich's ataxia patients, showing increased tissue frataxin and clinical outcome improvements. - Safety: 7 participants had anaphylaxis, most on initial administration day; dosing regimen modified with 5-milligram test dose, antihistamines, and EpiPen for participants. - Development program: Amending open-label study protocol to include adolescents and adults not in prior studies; global Phase III study in progress, qualifying sites globally. - Clinical outcomes: Compared to FACOMS reference population, observed 2.25 point improvement in mFARS over 1 year vs. 1 point worsening in reference, and improvements in other measures.

Guidance

- Targeting BLA submission in the second quarter of 2026, seeking accelerated approval. - Confident in nomlabofusp's potential as a disease-modifying therapy for Friedreich's ataxia.

Segment performance

The company's lead program is nomlabofusp for Friedreich's ataxia. Positive data from a long-term open-label study showed consistent directional improvements in key clinical outcome measures like mFARS, FARS ADL, 9-hole PEG test, and MFIS. Skin frataxin levels increased, with 100% of participants at 6 months achieving over 50% of healthy volunteer levels. No traditional product segment revenue contribution discussed as it's a clinical stage biotech focused on one program.

Risks & headwinds

- Anaphylaxis events in 7 participants, with most occurring on initial administration; risk of allergic reactions and need to consider in context of the disease. - Uncertainties in clinical trial data interpretation, success, cost, and timing of product development activities; ability to raise capital.

Analyst Q&A

  • Q: How does the data at 14 patients 6 months compare to historical control?

    A: Can't compare at 6 months as FACOMS data is annual; best comparison at 1 year.

  • Q: Color on severity of anaphylaxis?

    A: Treatment is standard of care (epinephrine, antihistamines, steroids), patients respond quickly.

  • Q: Confidence in titration dosing strategy?

    A: Confident, with test dose and expert consultants; data shows patients still willing to enroll despite events.

  • Q: Details on 7 anaphylaxis events?

    A: Most in previously dosed patients, not age-related; FDA agreed with new dosing regimen.

  • Q: Benefit of prophylactic antihistamines?

    A: Test dose may help tie up receptors on mast cells.

  • Q: Rate and severity of anaphylaxis vs other ERTs?

    A: Benign safety profile except anaphylaxis; differences in baseline characteristics of those who had vs didn't have anaphylaxis.

  • Q: Patient number data and anaphylaxis with urticaria?

    A: Patient numbers related to those who received at least 1 dose; 3 urticaria cases discontinued early.

  • Q: mFARS data and baseline values?

    A: Baselines similar to reference population; updates to be provided closer to BLA submission.

  • Q: Impact on confirmatory study powering?

    A: Ambulatory patients have more change potential, but conservative approach to powering in Phase III.