BEAM

Beam Therapeutics Inc
NASDAQHEALTHCAREBIOTECHNOLOGY

Key Statistics

Market Cap
$2.58B
P/E Ratio
EPS
$-0.49
Beta
2.18
52W High
$38.26
52W Low
$15.60
50-Day MA
$30.86
200-Day MA
$28.11
Dividend Yield
Profit Margin
-40.20%
Forward P/E
PEG Ratio

About Beam Therapeutics Inc

Beam Therapeutics Inc., a biotechnology company, develops precision genetic drugs for patients with serious illnesses in the United States. The company is headquartered in Cambridge, Massachusetts.

Official WebsiteUSAFY End: December

Fundamentals

Revenue (TTM)$164.01M
Gross Profit (TTM)$-240.93M
EBITDA$-349.25M
Operating Margin-337.80%
Return on Equity-5.77%
Return on Assets-15.80%
Revenue/Share (TTM)$1.60
Book Value$11.71
Price-to-Book2.22
Price-to-Sales (TTM)15.73
EV/Revenue9.88
EV/EBITDA-7.03
Quarterly Earnings Growth (YoY)0.00%
Quarterly Revenue Growth (YoY)324.90%
Shares Outstanding$102.88M
Float$87.94M
% Insiders1.40%
% Institutions106.75%

Historical Volatility

HV 10-Day
60.54%
HV 20-Day
65.32%
HV 30-Day
67.69%
HV 60-Day
72.72%
HV Rank
26.2%

Volatility is currently contracting

Analyst Ratings

Consensus ($52.31 target)
1
Strong Buy
14
Buy
2
Hold

Latest News

Beam 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) Congress 2026

CAMBRIDGE, Mass., July 23, 2026 (GLOBE NEWSWIRE) -- Beam Therapeutics Inc. (Nasdaq: BEAM), a biotechnology company developing precision genetic medicines through base editing, today announced that the company will present updated clinical data from the Phase 1/2 trial evaluating BEAM-302 for alpha-1 antitrypsin deficiency (AATD) at the European Respiratory Society (ERS) Congress 2026, taking place September 5–9, 2026, in Barcelona, Spain.

GlobeNewsWire7/23/2026Neutral
Prime Medicine Beats Beam Therapeutics In Patent Dispute - But Both Are Investable

Prime Medicine, Inc. secured a favorable arbitration ruling against Beam Therapeutics, allowing continued development of its PM647 gene editing program for AATD. PRME's Prime Editing platform offers precise, versatile gene correction using LNP delivery, but remains preclinical with IND/CTA filings for PM647 expected mid-2026 and initial clinical data in 2027. PRME lags competitors like Beam, Sanofi, and Arrowhead in the AATD development race, facing significant funding needs and clinical risks.

Seeking Alpha7/9/2026Positive
Beam 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 Administration

BEAM-304 Development Approach Has Potential to Create Transformative, One-time Therapies for the Majority of Patients with PKU  BEAM-304 Program Designed as Platform-based Approach Reflecting Emerging FDA Guidance for Accelerated Development of Genome Editing Therapies New Preclinical Data for BEAM-304 to be Presented at FASEB Genome Engineering: Research and Applications Conference CAMBRIDGE, Mass., June 18, 2026 (GLOBE NEWSWIRE) -- Beam Therapeutics Inc. (Nasdaq: BEAM), a biotechnology company developing precision genetic medicines through base editing, today announced that the United States (U.S.) Food and Drug Administration (FDA) has cleared the investigational new drug (IND) application for BEAM-304 for the treatment of phenylketonuria (PKU).

GlobeNewsWire6/18/2026Neutral
The Healthcare M&A Wave

In this week's edition of InnovationRx, we look at biotech M&A, the rise of India's Anthem Biosciences, and more. To get it in your inbox, subscribe here.

Forbes6/17/2026Neutral
Beam Therapeutics Eyes Sickle Cell BLA as Alpha-1 Gene-Editing Program Advances

Beam Therapeutics NASDAQ: BEAM Chief Executive Officer John Evans said the company is advancing its base-editing platform across hematology and liver disease programs, with a potential biologics license application for its sickle cell disease candidate possible as early as the end of this year.

MarketBeat5/20/2026Neutral

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Data last updated: 7/29/2026