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Beam Therapeutics/$BEAM

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About Beam Therapeutics

Beam Therapeutics Inc is a biotechnology company committed to creating a new class of precision genetic medicines based on its proprietary base editing technology, with a vision of providing lifelong cures to patients suffering from serious diseases. The company is focused on its programs in the hematology and genetic disease portfolios, which comprise different product candidates in its pipeline, such as BEAM-101, which is being developed to target Sickle Cell Disease, BEAM-302, a liver-targeting lipid nanoparticle, being developed to target Alpha-1 antitrypsin deficiency, and other drug candidates including BEAM-302, BEAM-103 & 104. The company operates and manages its business in one operating segment, United States.
Ticker
$BEAM
Sector
Health
Primary listing
NASDAQ
Employees
557
Website
beamtx.com

BEAM Metrics

BasicAdvanced
$2.6B
-
-$1.04
2.22
-

What the Analysts think about BEAM

Analyst ratings (Buy, Hold, Sell) for Beam Therapeutics stock.
Analyst projections of the future price of Beam Therapeutics stock.

Bulls say / Bears say

BEAM-301’s first six-patient readout offers early proof of concept: two of three patients at 40 mg fasted for the full 15 hours and no longer needed starch supplements. The result is preliminary, but it shows a potential meaningful benefit from a single treatment. (Beam Therapeutics)
BEAM-302 has produced durable rises in functional AAT above the protective threshold and an 84% reduction in mutant Z-AAT at 60 mg. Beam has started a roughly 50-patient pivotal cohort and plans to seek accelerated approval using 12-month biomarker data. (GlobeNewswire)
Risto-cel is approaching a key regulatory milestone in sickle cell disease: dosing is complete in the adult and adolescent BEACON trial, and Beam expects to submit its US application as early as year-end 2026. A successful filing would give the company a near-term route towards its first product launch. (Beam Therapeutics)
BEAM-301’s encouraging results come from only six patients, and treatment-related serious adverse events occurred in four, including three Grade 3 infusion reactions. The small, early study leaves both the safety profile and the apparent benefit uncertain. (Beam Therapeutics)
BEAM-302’s pivotal approval plan relies on AAT biomarkers rather than demonstrated improvement in how patients feel or function, with a confirmatory trial still to come. Its safety data are also not clean: 41% of patients had infusion reactions, and one patient with liver disease had a transient Grade 3 liver-enzyme rise. (GlobeNewswire)
Beam remains loss-making, with a $122.7 million net loss in the second quarter and management expecting operating losses and negative cash flow for the foreseeable future. It says its $1.2 billion cash balance should fund plans into mid-2029, but further financing may be needed and could dilute shareholders or add debt. (SEC)
Data summarised monthly by Lightyear AI. Last updated on 29 Oct 2026.

BEAM Financial Performance

Revenues and expenses
Income statement
QuarterlyAnnual
Q3 24
QoQ growth
Revenue
Net income
Profit margin

BEAM Earnings Performance

Company profitability
Earnings per share
QuarterlyAnnual
Q4 23
Q1 24
Q2 24
Q3 24
Q4 24
Actual
Expected
Surprise

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