Beam Therapeutics
Market cap $2.73B 103.5M shares (10-Q, Oct 27, 2026) × $26.41 close Nov 6, 2026
Most recent annual filing: 2026-02-24
- BEAM-304 IND filing2026BEAM-304 IND filing, 2026, notable
- risto-cel BLA filingYear-End 2026risto-cel BLA filing, Year-End 2026, major
- risto-cel manufacturing updateas early as year-end 2026risto-cel manufacturing update, as early as year-end 2026, notable
Bar width shows how precise the guidance is — a pin is a stated date, a wide band a six-month window. Deeper blue means more of the thesis rides on the event; it is not a view on the stock.
Pipeline (6 active programs)
BEAM-302
BEAM-304
BEAM-301
BEAM-103
- Undisclosed indication
BEAM-102
- Undisclosed indication
Technology platforms
ESCAPE
Engineered Stem Cell Antibody Paired Evasion — non-genotoxic conditioning platform combining antibody-based conditioning with multiplex gene edited HSCs; applicable ex vivo or in vivo including for sickle cell disease
Targets: CD117
Base Editing Platform
Proprietary base editing technology enabling precision genetic medicines that target a single base in the genome without double-stranded DNA breaks, using CRISPR-guided deaminase enzymes. Supports ex vivo and in vivo delivery modalities across hematology and other disease areas including sickle cell disease and beta-thalassemia.
Apellis Complement Base Editing Collaboration · Apellis Pharmaceuticals
Research collaboration using Beam's base editing technology to discover treatments for complement system-driven diseases across six programs targeting specific genes in the complement system in various organs including the eye, liver, and brain. Apellis holds exclusive option rights to license any or all programs.
Capital (as filed)
- Cash
- $213M cash and cash equivalents · Sep 30, 2026 (10-Q)
- Short-term investments
- $831M Sep 30, 2026
- Operating cash flow
- −$111M quarter Jun 30, 2026 → Sep 30, 2026, year-to-date difference (10-Q)
- As stated in coverage
- $1.15B cash, runway mid-2029 per the update of Sep 8, 2026 — the company's own words as read there, not the filed figure
Cash, investments and operating cash flow are the company's own XBRL facts as filed with the SEC, each shown with its period end and tag. As-stated figures come from the company's own words as read in Biotech Distilled coverage, dated, and routinely count securities and planned financing that a balance sheet does not. Offering rows are the SEC cover pages as filed. Not investment advice. Figures as of Nov 7, 2026.
Biotech Distilled coverage (6)
- 2026-10-28 UPDATE: Beam Therapeutics (BEAM) - Off the Cornstarch 🔒 Paid
- 2026-10-14 UPDATE: Beam Therapeutics (BEAM) - The Second Liver Bet Shows Its Hand 🔒 Paid
- 2026-09-08 UPDATE: Beam Therapeutics (BEAM) - Barcelona Answers the Liver Question 🔒 Paid
- 2026-08-04 UPDATE: Beam Therapeutics (BEAM) - The Pivotal Cohort Opens, The Stock Doesn’t Care 🔒 Paid
- 2026-06-18 UPDATE: Beam Therapeutics (BEAM) - The Third Liver Bet Goes Clinical 🔒 Paid
- 2026-04-24 Beam Therapeutics (BEAM) - Scientific Deep Dive for Risto-cel and Pipeline Products 🔒 Paid
Articles open on Substack. Some are subscriber-only; those marked ★ Distilled Pro are for Distilled Pro members.
Verdict history (6 calls)
Every verdict Biotech Distilled has published on Beam Therapeutics, oldest first — the full history, never a selection. How calls are scored: the track record.
- 2026-04-24 Watch core Beam Therapeutics (BEAM) - Scientific Deep Dive for Risto-cel and Pipeline Products Base editing science is undeniable and the balance sheet is a fortress, but the smart move is to wait for FDA reaction to Grade 4 ALT elevations in BEAM-302 multi-dose cohort before taking a heavy position.
- 2026-06-18 Watch UPDATE: Beam Therapeutics (BEAM) - The Third Liver Bet Goes Clinical PKU IND clearance is a checkpoint not a re-rating event; the binding constraint of LNP hepatotoxicity in BEAM-302's multi-dose cohort remains unresolved, so the position stays on watch until hepatic safety reads out in 2H 2026.
- 2026-08-04 Watch UPDATE: Beam Therapeutics (BEAM) - The Pivotal Cohort Opens, The Stock Doesn't Care Pivotal cohort is dosing and the ERS late-breaker in five weeks is now a defined-event setup, but the therapeutic window of the LNP is still unproven at scale and the runway now leans on milestone-gated debt; waiting for Barcelona hepatic safety data before deploying heavily.
- 2026-09-08 Speculative buy speculative UPDATE: Beam Therapeutics (BEAM) - Barcelona Answers the Liver Question The single dominant failure mode — LNP hepatotoxicity — read out clean at n=29 with no Grade 4 events and 18-month durability covering the 12-month approval endpoint; remaining risks are regulatory and commercial rather than existential-biological, warranting a starter position sized for the reality that a biomarker accelerated approval is a negotiation, not a formality.
- 2026-10-14 Speculative buy speculative UPDATE: Beam Therapeutics (BEAM) - The Second Liver Bet Shows Its Hand A second liver program on the same LNP showed no transaminase elevation above Grade 2 and tangible efficacy at 40 mg, reinforcing the vehicle de-risking from Barcelona, though n=5 and thin follow-up keep conviction at speculative.
- 2026-10-28 Speculative buy speculative UPDATE: Beam Therapeutics (BEAM) - Off the Cornstarch Two of three 40 mg GSDIa patients achieved full starch independence with the liver staying quiet in a second dataset on the shared LNP, deepening the vehicle de-risking case, but n=3 at the active dose with one non-responder and serious IRRs dependent on an untested premedication fix keep the call speculative.
- Long call · opened Sep 9, 2026 at $25.18 · +4.9% vs XBI -4.5% (Nov 6, 2026)
Every verdict Biotech Distilled has published on this company, in order, with the post it came from — the full history, never a selection. Position figures are the same ones shown on /track-record, computed by the same method. Editorial opinion, not investment advice.
Timing, in the company's words (1 quote from 1 filing)
Sentences quoted verbatim from the company's SEC filings, newest filing first. Each sits under the filing it appeared in; the "matched to" tag names the calendar row it was read for.
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““We are approaching a potential first BLA filing with risto-cel as early as the end of this year, and the pivotal cohort for BEAM-302 is rapidly advancing with completion of dosing expected in the first half of 2027.”
matched to risto-cel · regulatory submission · read as first half of 2027
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Timing sentences quoted from the company's own SEC filings, each under the filing it appeared in. The 'matched to' tag is the calendar row the sentence was read for; the filing is the source. Not investment advice.
Filings & releases (24)
SEC filings from EDGAR and press releases captured from the company's investor-relations site, newest first. Releases captured from May 7, 2026; filings from March 2026. Summaries come from the BD update that read the document; "BD extracted" counts point at the pipeline table above. All companies →
- Nov 4, 2026ReleaseBeam Therapeutics to Present Updated Clinical Data from BEACON Phase 1/2 Trial of Risto-cel in Sickle Cell Disease in an Oral Presentation at American Society of Hematology (ASH) Annual MeetingThe BEACON risto-cel data earns an oral slot at ASH and lands in the press program — with patient-reported outcomes data showing real-world functional improvements now added to the efficacy story, and the BLA timeline locked to year-end 2026.
- Nov 3, 2026ReleaseBeam Therapeutics Reports Third Quarter 2026 Financial Results and Highlights Clinical Progress Across Base Editing PortfolioSummary on the 8-K
- Nov 3, 20268-KCurrent report: results of operations · EX-99.1Q3 earnings arrive as BEAM enters its most critical execution quarter: risto-cel BLA filing expected by year-end, BEAM-302 pivotal cohort dosing set to complete 1H 2027, and $1.0B on hand — but the runway math is now explicitly milestone-gated, and the Apellis collaboration has quietly unraveled.
- Nov 3, 202610-QQuarterly reportSummary on the 8-K
- Oct 27, 2026ReleaseBeam Therapeutics Reports Initial Clinical Data from Phase 1/2 Trial of BEAM-301, Demonstrating Proof of Concept for Genetic Correction in Glycogen Storage Disease Type Ia (GSDIa) at ESGCT 33rd Annual→ BD updateBEAM-301's ESGCT poster delivers the answers the October 13 update asked for: two 40 mg patients are now completely off cornstarch, the non-responder has a mechanistic explanation, the 60 mg cohort is enrolling, and Beam is engaging the FDA on an approval path — all on the same clean-liver-enzyme story that has anchored the platform thesis.BD extracted 1 program update from this document → BEAM pipeline
- Oct 13, 2026ReleaseBeam Therapeutics to Present Initial Data from Phase 1/2 Trial of BEAM-301 in Glycogen Storage Disease Type Ia (GSDIa) at the ESGCT 33rd Annual Congress→ BD updateBEAM-301's first-in-human data in GSDIa delivers a genuine functional proof of concept — 40 mg patients achieved ≥15 hours of controlled fasting from a 2.5-hour baseline, with ~80-92% starch reductions — and the LNP safety profile held, extending the platform de-risking story that Barcelona started in September.BD extracted 1 program update from this document → BEAM pipeline
- Sep 8, 2026ReleaseBeam Therapeutics Presents Updated Clinical Data from the Phase 1/2 Trial of BEAM-302 in Alpha-1 Antitrypsin Deficiency (AATD) at the European Respiratory Society (ERS) Congress 2026→ BD updateThe ERS late-breaker landed: BEAM-302's single-dose data held clean across 29 patients and up to 18 months of follow-up — the hepatotoxicity overhang that defined the bear case looks materially narrower than it did five weeks ago, and the pivotal cohort is already dosing.
- Sep 1, 2026ReleaseBeam Therapeutics Appoints Eric Foster as Chief Commercial OfficerBeam just hired Eric Foster — the exec who helped build Horizon Therapeutics' rare-disease machine into a $2.75B franchise — as CCO, five weeks before ERS and with a year-end BLA on the clock. It's a direct answer to the commercial execution bear case.
- Aug 31, 2026ReleaseBeam Therapeutics to Participate in Upcoming September 2026 Investor Conferences
- Aug 4, 2026ReleaseBeam Therapeutics Reports Second Quarter 2026 Financial Results and Announces First Patient Dosed in Global Pivotal Cohort of BEAM-302 Trial in Alpha-1 Antitrypsin Deficiency (AATD)BD extracted 2 program updates from this document → BEAM pipeline
- Aug 4, 20268-KCurrent report: results of operations · EX-99.1
- Aug 4, 202610-QQuarterly report
- Jul 23, 2026ReleaseBeam Therapeutics to Present Updated Data from Phase 1/2 Trial of BEAM-302 in Alpha-1 Antitrypsin Deficiency (AATD) in Late-Breaking Oral Presentation at the European Respiratory Society (ERS) CongresBD extracted 1 program update from this document → BEAM pipeline
- Jun 18, 2026ReleaseBeam Therapeutics Announces Clearance of Investigational New Drug Application for BEAM-304 for the Treatment of Phenylketonuria (PKU) by the United States (U.S.) Food and Drug AdministrationBD extracted 1 program update from this document → BEAM pipeline
- Jun 8, 20268-KCurrent report: shareholder vote
- May 18, 2026ReleaseBeam Therapeutics Presents Recently Reported Topline Clinical Data for BEAM-302 in Alpha-1 Antitrypsin Deficiency (AATD) at the American Thoracic Society (ATS) 2026 International Conference
- May 13, 2026ReleaseBeam Therapeutics to Present at 2026 RBC Capital Markets Global Healthcare Conference
- May 12, 2026ReleaseBeam Therapeutics to Present Updated Biomarker Data from Phase 1/2 BEACON Trial Further Underscoring Risto-cel’s Ability to Restore Red Blood Cell Health and Function in Sickle Cell Disease at EHA2026
- May 7, 2026ReleaseBeam Therapeutics Reports First Quarter 2026 Financial Results and Recent Business Updates
- May 7, 20268-KCurrent report: results of operations · EX-99.1
- May 7, 202610-QQuarterly report
- Apr 17, 2026DEFA14AProxy soliciting material
- Apr 17, 2026DEF 14AProxy statement
- Mar 5, 20268-KCurrent report: agreement terminated
5 more filings (13G holder notices, S-8, proxy material, SEC correspondence …)
- Aug 14, 2026SCHEDULE 13G/A13G amendment
- Aug 13, 2026SCHEDULE 13G/A13G amendment
- Apr 29, 2026SCHEDULE 13GPassive >5% holder (13G)
- Apr 17, 2026ARSAnnual report to shareholders
- Mar 26, 2026SCHEDULE 13G/A13G amendment