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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
540
Website
beamtx.com

BEAM Metrics

BasicAdvanced
$2.5B
-
-$0.84
2.23
-

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

In Beam’s small Phase 1/2 readout, a single 60 mg dose raised functional AAT above the protective threshold for up to 18 months; corrected AAT made up 93% of circulating AAT and mutant Z-AAT fell by 84%. These are encouraging signs that BEAM-302 could address the cause of AATD. (GlobeNewswire)
Beam completed dosing in its BEACON sickle cell trial and expects to submit a biologics licence application for risto-cel as early as year-end 2026. That creates a near-term regulatory catalyst for its most advanced programme. (GlobeNewswire)
Beam reported $1.2 billion in cash and marketable securities and expects its cash, together with planned credit-facility draws, to fund operations into mid-2029. This runway gives it time to advance several programmes before it may need further capital. (GlobeNewswire)
BEAM-302’s safety data include a transient Grade 3 liver-enzyme rise in one patient with liver disease at the selected 60 mg dose; mild-to-moderate infusion reactions were also reported in 41% of patients. Larger trials are needed to clarify the risks. (Yahoo Finance)
The BEAM-302 results so far come from a small, open-label study and show changes in biomarkers, not yet slower lung decline or less liver damage. The accelerated-approval approach would still require a confirmatory study to verify clinical benefit. (Yahoo Finance)
Serapha Bio is developing SERP-01 for the same AATD mutation as BEAM-302, backed by $230 million and with a Phase 2/3 start targeted for late 2026 or early 2027. A well-funded rival could narrow Beam’s first-mover advantage. (BioPharma Dive)
Data summarised monthly by Lightyear AI. Last updated on 5 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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