Beam Therapeutics Inc. (BEAM) Earnings

Beam Therapeutics Inc. is expected to report next earnings on August 4, 2026 (in NaN days), with a consensus EPS estimate of $-1.11. BEAM has beaten EPS estimates in 4 of its last 9 reported quarters (average surprise +86.4% over the last four).

Next earnings
Aug 4, 2026in NaN days
EPS est $-1.11 · Revenue est $15M
Track record
Beat EPS in 4 of 9 quarters
Avg surprise +86.4% (last 4 quarters)
Earnings history
Report dateEPS estEPS actualSurpriseRevenueRev. surprise
May 7, 2026$-0.87$-0.91-4.6%$32M+189.1%
Feb 24, 2026$-1.13$-0.10+91.2%$114M+970.0%
Nov 4, 2025$-0.98$-1.10-12.2%$10M-26.6%
Feb 27, 2024$-1.01$1.73+271.3%$316M+1593.6%
Feb 28, 2023$-1.32$-0.54+59.1%$20M+57.6%
Feb 28, 2022$-1.02$-0.85+16.7%$51M+496.4%
Aug 10, 2021$-0.58$-0.95-63.8%$6000+11.6%
Mar 15, 2021$-0.70$-0.72-2.9%$6000
Aug 12, 2020$-0.56$-0.69-23.2%$6000+30.2%
Feb 7, 2020$-0.54$6000
Jun 29, 2019$-0.51$6000

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

Earnings call summary

Q4 FY2025 · February 24, 2026

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

Management highlights

John Evans introduced Beam's vision of providing lifelong cures using base editing. Beam is expanding its pipeline with a new development program for PKU (BEAM-304) leveraging base editing and LNP delivery. Amy Simon detailed PKU's clinical manifestations and unmet needs. Gopi Shanker discussed the base editing approach for BEAM-304 and early preclinical data. Kiran Musunuru shared insights on PKU variants and regulatory interactions. Sravan Emany announced a strategic financing agreement to support risto-cel's commercialization and strengthen the balance sheet.

Guidance

Anticipate filing IND for BEAM-304 in 2026, report initial BEAM-301 data in GSDIa, complete BEAM-103 healthy volunteer study, and continue advancing in vivo HSC editing. Look forward to submitting risto-cel BLA as early as year-end and accelerating the path to approval for lead programs.

Analyst Q&A

  • Q: Talked about regulatory path forward and addressing multiple mutations in PKU, and strategic financing impact on reallocating capital.

    A: Gopi mentioned research underway for other mutations with fast timelines, Amy spoke about FDA collaboration and adaptive trial design, Sravan said financing provides flexibility for commercial launch and pipeline growth.

  • Q: Questions on IP for R408W and LNP delivery in 304.

    A: John said Beam has access to necessary IP, and 304 uses similar LNP approaches as 302, 301 with internal ionizable lipids.

  • Q: Questions on FDA draft guidance for individualized therapy and PKU mutations, 304 guide RNAs and bystander editing.

    A: Kiran discussed FDA interactions and plausible mechanism framework, Gopi talked about unique guide RNAs for mutations and confident bystander profile.

  • Q: Question on sickle cell market share assumptions for risto-cel.

    A: Giuseppe Ciaramella talked about market demand, risto-cel's manufacturing process optimization.

  • Q: Questions on AATD upcoming readout and pivotal.

    A: John talked about data update on 302, dosing schedule, efficacy, safety, and durability.

  • Q: Questions on PKU patient responses to current options and Phase I/II age range.

    A: Amy said R408W patients don't respond well to current options, and FDA collaborative on age range recruitment.

  • Q: Questions on A1AT, GSK returning rights, and U.S. enrollment for pivotal.

    A: John didn't comment on GSK but said BEAM-302 has best-in-class data, and U.S. enrollment part is premature.

  • Q: Question on PKU patient mutation copies and Phase I/II design.

    A: Gopi said one copy correction sufficient, and Amy talked about age range recruitment.

  • Q: Questions on PKU editing rate vs other diseases and OpEx for PKU program.

    A: Gopi explained low threshold for PKU editing, Sravan said PKU is in runway guidance and cost balanced across portfolio.

  • Q: Questions on plausible mechanism pathway for AATD and LNP safety for PKU.

    A: John said plausible mechanism not necessary for AATD traditional path, and Beam has expertise in LNP for PKU.

  • Q: Question on next-gen sickle cell program prioritization.

    A: Giuseppe Ciaramella talked about in vivo program's ease of delivery and progress.

  • Q: Question on 103 healthy volunteers and in vivo editing efficiencies.

    A: Giuseppe Ciaramella talked about 103's antibody component and comparable editing efficiencies