Editas Medicine (EDIT)


Market Price (7/20/2026): $2.99 | Market Cap: $292.7 MilSector: Health Care | Industry: Biotechnology

Editas Medicine (EDIT)


Market Price (7/20/2026): $2.99
Market Cap: $292.7 Mil
Sector: Health Care
Industry: Biotechnology

Investment Highlights Why It Matters Detailed financial logic regarding cash flow yields vs trend-riding momentum.

0

Cash is significant % of market cap
Net D/ENet Debt/Equity. Debt net of cash. Negative indicates net cash. Equity is taken as the Market Capitalization is -36%

Megatrend and thematic drivers
Megatrends include Biotechnology & Genomics, and Precision Medicine. Themes include Gene Editing & Therapy, and Targeted Therapies.

Weak multi-year price returns
2Y Excs Rtn is -79%, 3Y Excs Rtn is -134%

Not profitable at operating income level
Op Inc LTMOperating Income, Last Twelve Months is -89 Mil, Op Mgn LTMOperating Margin = Operating Income / Revenue Reflects profitability before taxes and before impact of capital structure (interest payments). is -230%

Weak revenue growth
Rev Chg QQuarterly Revenue Change % is -39%

Significant share based compensation
SBC/Rev LTMShare Based Compensation / Revenue (Sales), Last Twelve Months (LTM) is 24%

Not cash flow generative
CFO/Rev LTMCash Flow from Operations / Revenue (Sales), Last Twelve Months (LTM) is -363%, FCF/Rev LTMFree Cash Flow / Revenue (Sales), Last Twelve Months (LTM) is -365%

Valuation getting more expensive
P/S 6M Chg %Price/Sales change over 6 months. Declining P/S indicates valuation has become less expensive. is 53%

Yield minus risk free rate is negative
ERPEquity Risk Premium (ERP) = Total Yield - Risk Free Rate, Reflects the premium above risk free assets offered by the investment. is -42%

Significant short interest
Short Interest % of Basic SharesShort Interest % of Basic Shares = (Short Interest Quantity) / (Basic Shares Outstanding). A high fraction of short interest can indicate potential risk of a short squeeze. is 23%

Key risks
EDIT key risks include [1] significant technical and regulatory hurdles for its unproven in vivo gene-editing approach, Show more.

0 Cash is significant % of market cap
Net D/ENet Debt/Equity. Debt net of cash. Negative indicates net cash. Equity is taken as the Market Capitalization is -36%
1 Megatrend and thematic drivers
Megatrends include Biotechnology & Genomics, and Precision Medicine. Themes include Gene Editing & Therapy, and Targeted Therapies.
2 Weak multi-year price returns
2Y Excs Rtn is -79%, 3Y Excs Rtn is -134%
3 Not profitable at operating income level
Op Inc LTMOperating Income, Last Twelve Months is -89 Mil, Op Mgn LTMOperating Margin = Operating Income / Revenue Reflects profitability before taxes and before impact of capital structure (interest payments). is -230%
4 Weak revenue growth
Rev Chg QQuarterly Revenue Change % is -39%
5 Significant share based compensation
SBC/Rev LTMShare Based Compensation / Revenue (Sales), Last Twelve Months (LTM) is 24%
6 Not cash flow generative
CFO/Rev LTMCash Flow from Operations / Revenue (Sales), Last Twelve Months (LTM) is -363%, FCF/Rev LTMFree Cash Flow / Revenue (Sales), Last Twelve Months (LTM) is -365%
7 Valuation getting more expensive
P/S 6M Chg %Price/Sales change over 6 months. Declining P/S indicates valuation has become less expensive. is 53%
8 Yield minus risk free rate is negative
ERPEquity Risk Premium (ERP) = Total Yield - Risk Free Rate, Reflects the premium above risk free assets offered by the investment. is -42%
9 Significant short interest
Short Interest % of Basic SharesShort Interest % of Basic Shares = (Short Interest Quantity) / (Basic Shares Outstanding). A high fraction of short interest can indicate potential risk of a short squeeze. is 23%
10 Key risks
EDIT key risks include [1] significant technical and regulatory hurdles for its unproven in vivo gene-editing approach, Show more.

EDIT in ETFs

Weight = EDIT's share of each fund

VTI0.00%
IWM0.01%
IBB0.03%
IWO0.02%
VTWO0.01%
VHT0.01%
SCHA0.01%
IWN0.00%
+2 more covered ETFs

Valuation & Metrics

Price Chart

Why The Stock Moved

Qualitative Assessment

AI Analysis | Feedback

Updated on 7/16/2026

Editas Medicine (EDIT) stock has gained about 20% since 3/31/2026 because of the following key factors:

1. Positive Preclinical Data and Advancement of Lead Candidate EDIT-401.

Editas Medicine consistently released encouraging preclinical data for its lead in vivo gene editing candidate, EDIT-401, designed to treat hyperlipidemia. The company reported that EDIT-401 demonstrated approximately 90% or greater mean reductions in key atherogenic lipoproteins, including LDL-C, Lp(a), and ApoB, in non-human primates. This strong efficacy data, coupled with positive pre-IND feedback from the U.S. FDA, supported the company's plans to submit a Clinical Trial Notification by mid-2026 and initiate a first-in-human clinical trial later in 2026, with early human proof-of-concept data expected by year-end.

2. Strong Financial Position and Strategic Capital Raise.

Editas Medicine reported a solid cash position with cash and cash equivalents totaling $123.6 million as of March 31, 2026 (fiscal Q1 2026), providing a projected cash runway into fiscal Q3 2027. Further strengthening its financial outlook, the company announced the pricing of an up to $319.4 million public offering in May 2026, which is expected to support ongoing operations and the advancement of its pipeline.

Show more
Updated on 7/16/2026

Editas Medicine (EDIT) stock has gained about 20% since 3/31/2026 because of the following key factors:

1. Positive Preclinical Data and Advancement of Lead Candidate EDIT-401.

Editas Medicine consistently released encouraging preclinical data for its lead in vivo gene editing candidate, EDIT-401, designed to treat hyperlipidemia. The company reported that EDIT-401 demonstrated approximately 90% or greater mean reductions in key atherogenic lipoproteins, including LDL-C, Lp(a), and ApoB, in non-human primates. This strong efficacy data, coupled with positive pre-IND feedback from the U.S. FDA, supported the company's plans to submit a Clinical Trial Notification by mid-2026 and initiate a first-in-human clinical trial later in 2026, with early human proof-of-concept data expected by year-end.

2. Strong Financial Position and Strategic Capital Raise.

Editas Medicine reported a solid cash position with cash and cash equivalents totaling $123.6 million as of March 31, 2026 (fiscal Q1 2026), providing a projected cash runway into fiscal Q3 2027. Further strengthening its financial outlook, the company announced the pricing of an up to $319.4 million public offering in May 2026, which is expected to support ongoing operations and the advancement of its pipeline.

3. Better-than-Expected Fiscal Q1 2026 Earnings Per Share.

On May 5, 2026, Editas Medicine announced its fiscal Q1 2026 earnings, reporting a net loss of $0.26 per share, which exceeded analysts' consensus estimates of a $0.30 loss per share by $0.04. This earnings beat, despite revenue of $2.83 million falling below estimates, contributed positively to investor sentiment and the stock's performance, which gained 1.3% the day after the announcement and drifted 20.1% higher in the subsequent 58 days.

4. Favorable Analyst Sentiment and Price Targets.

Throughout the period, Wall Street analysts maintained a generally positive outlook on Editas Medicine. As of July 15, 2026, the stock held a "Moderate Buy" to "Buy" consensus rating from analysts. The average twelve-month price target was approximately $5.40, representing a significant forecasted upside of 87.50% from the stock's price of $2.88 at that time.

Show less
Holding a concentrated position? Know your true downside before the momentum shifts.
Protect Your Wealth →

Stock Movement Drivers

Fundamental Drivers

The 20.6% change in EDIT stock from 3/31/2026 to 7/19/2026 was primarily driven by a 27.0% change in the company's P/S Multiple.
(LTM values as of)33120267192026Change
Stock Price ($)2.472.9820.6%
Change Contribution By: 
Total Revenues ($ Mil)4139-4.5%
P/S Multiple5.97.527.0%
Shares Outstanding (Mil)9798-0.5%
Cumulative Contribution20.6%

LTM = Last Twelve Months as of date shown

Market Drivers

3/31/2026 to 7/19/2026
ReturnCorrelation
EDIT20.6% 
Market (SPY)14.3%28.2%
Sector (XLV)9.9%22.8%

Fundamental Drivers

The 45.4% change in EDIT stock from 12/31/2025 to 7/19/2026 was primarily driven by a 89.3% change in the company's P/S Multiple.
(LTM values as of)123120257192026Change
Stock Price ($)2.052.9845.4%
Change Contribution By: 
Total Revenues ($ Mil)4639-16.6%
P/S Multiple4.07.589.3%
Shares Outstanding (Mil)9098-8.0%
Cumulative Contribution45.4%

LTM = Last Twelve Months as of date shown

Market Drivers

12/31/2025 to 7/19/2026
ReturnCorrelation
EDIT45.4% 
Market (SPY)9.3%35.6%
Sector (XLV)4.5%33.1%

Fundamental Drivers

The 35.5% change in EDIT stock from 6/30/2025 to 7/19/2026 was primarily driven by a 47.8% change in the company's P/S Multiple.
(LTM values as of)63020257192026Change
Stock Price ($)2.202.9835.5%
Change Contribution By: 
Total Revenues ($ Mil)36398.0%
P/S Multiple5.17.547.8%
Shares Outstanding (Mil)8398-15.1%
Cumulative Contribution35.5%

LTM = Last Twelve Months as of date shown

Market Drivers

6/30/2025 to 7/19/2026
ReturnCorrelation
EDIT35.5% 
Market (SPY)21.3%29.8%
Sector (XLV)21.1%28.7%

Fundamental Drivers

The -63.8% change in EDIT stock from 6/30/2023 to 7/19/2026 was primarily driven by a -69.7% change in the company's P/S Multiple.
(LTM values as of)63020237192026Change
Stock Price ($)8.232.98-63.8%
Change Contribution By: 
Total Revenues ($ Mil)233969.8%
P/S Multiple24.97.5-69.7%
Shares Outstanding (Mil)6998-29.6%
Cumulative Contribution-63.8%

LTM = Last Twelve Months as of date shown

Market Drivers

6/30/2023 to 7/19/2026
ReturnCorrelation
EDIT-63.8% 
Market (SPY)73.6%30.7%
Sector (XLV)27.1%28.1%

Return vs. Risk

Price Returns Compared

 202120222023202420252026Total [1]
Returns
EDIT Return-62%-67%14%-87%61%40%-96%
Peers Return10%-39%9%-36%7%8%-46%
S&P 500 Return27%-19%24%23%16%10%101%

Monthly Win Rates [3]
EDIT Win Rate17%33%50%17%67%57% 
Peers Win Rate37%42%47%40%57%51% 
S&P 500 Win Rate75%42%67%75%67%57% 

Max Drawdowns [4]
EDIT Max Drawdown-71%-70%-46%-89%-69%-34% 
Peers Max Drawdown-47%-55%-45%-56%-52%-30% 
S&P 500 Max Drawdown-5%-25%-10%-8%-19%-9% 


[1] Cumulative total returns since the beginning of 2021
[2] Peers: CRSP, NTLA, BEAM, VRTX, CRBU. See EDIT Returns vs. Peers.
[3] Win Rate = % of calendar months in which monthly returns were positive
[4] Max drawdown represents maximum peak-to-trough decline within a year
[5] 2026 data is for the year up to 7/17/2026 (YTD)

How Low Can It Go

EventEDITS&P 500
2025 US Tariff Shock
  % Loss-69.4%-18.8%
  % Gain to Breakeven226.5%23.1%
  Time to Breakeven105 days79 days
Summer-Fall 2023 Five Percent Yield Shock
  % Loss-27.8%-9.5%
  % Gain to Breakeven38.6%10.5%
  Time to Breakeven15 days24 days
2023 SVB Regional Banking Crisis
  % Loss-36.3%-6.7%
  % Gain to Breakeven57.1%7.1%
  Time to Breakeven27 days31 days
2020 COVID-19 Crash
  % Loss-43.9%-33.7%
  % Gain to Breakeven78.4%50.9%
  Time to Breakeven56 days140 days
Q4 2018 Fed Policy Error / Growth Scare
  % Loss-39.8%-19.2%
  % Gain to Breakeven66.1%23.8%
  Time to Breakeven343 days105 days
2016-2017 Trump Reflation Bond Selloff
  % Loss-10.5%-3.7%
  % Gain to Breakeven11.7%3.9%
  Time to Breakeven6 days6 days

Compare to CRSP, NTLA, BEAM, VRTX, CRBU

In The Past

Editas Medicine's stock fell -69.4% during the 2025 US Tariff Shock. Such a loss loss requires a 226.5% gain to breakeven.

Preserve Wealth

Limiting losses and compounding gains is essential to preserving wealth.

Asset Allocation

Actively managed asset allocation strategies protect wealth. Learn more.

EventEDITS&P 500
2025 US Tariff Shock
  % Loss-69.4%-18.8%
  % Gain to Breakeven226.5%23.1%
  Time to Breakeven105 days79 days
Summer-Fall 2023 Five Percent Yield Shock
  % Loss-27.8%-9.5%
  % Gain to Breakeven38.6%10.5%
  Time to Breakeven15 days24 days
2023 SVB Regional Banking Crisis
  % Loss-36.3%-6.7%
  % Gain to Breakeven57.1%7.1%
  Time to Breakeven27 days31 days
2020 COVID-19 Crash
  % Loss-43.9%-33.7%
  % Gain to Breakeven78.4%50.9%
  Time to Breakeven56 days140 days
Q4 2018 Fed Policy Error / Growth Scare
  % Loss-39.8%-19.2%
  % Gain to Breakeven66.1%23.8%
  Time to Breakeven343 days105 days
2015-2016 China Devaluation / Global Growth Scare
  % Loss-29.6%-12.2%
  % Gain to Breakeven42.1%13.9%
  Time to Breakeven10 days62 days
2014-2016 Oil Price Collapse
  % Loss-29.6%-6.8%
  % Gain to Breakeven42.1%7.3%
  Time to Breakeven10 days15 days

Compare to CRSP, NTLA, BEAM, VRTX, CRBU

In The Past

Editas Medicine's stock fell -69.4% during the 2025 US Tariff Shock. Such a loss loss requires a 226.5% gain to breakeven.

Preserve Wealth

Limiting losses and compounding gains is essential to preserving wealth.

Asset Allocation

Actively managed asset allocation strategies protect wealth. Learn more.

About Editas Medicine (EDIT)

Editas Medicine (EDIT) is a clinical-stage biotechnology company dedicated to developing transformative genomic medicines using its proprietary gene editing platform, primarily based on CRISPR technology. The company's core focus is on precisely editing genes to correct the underlying genetic causes of a range of serious diseases, aiming to provide novel therapeutic solutions where current treatments are insufficient.

The company's pipeline features several key product candidates. EDIT-101 is currently in Phase 1/2 clinical trials for Leber Congenital Amaurosis 10, a leading cause of inherited childhood blindness. They are also developing EDIT-102 for other retinal conditions like Usher Syndrome 2A and autosomal dominant retinitis pigmentosa. Beyond ocular disorders, Editas is advancing EDIT-301 to address severe blood disorders such as sickle cell disease and transfusion-dependent beta-thalassemia.

Additionally, Editas Medicine is exploring the application of gene-edited immune cell therapies, including Natural Killer cell, alpha-beta T cell, and gamma delta T cell medicines, for various solid tumor cancers and other malignancies. The company strategically collaborates with pharmaceutical partners like Allergan and Juno Therapeutics to broaden its research and development scope. Editas primarily serves patients with severe genetic and oncological diseases, offering potential breakthrough treatments for conditions with high unmet medical needs.

AI Analysis | Feedback

Moderna for genetic diseases, but using CRISPR gene-editing technology.

An early-stage Intel for the human genome, building foundational CRISPR tools to repair DNA.

The Adobe of human DNA, developing powerful CRISPR tools to precisely edit and correct disease-causing genes.

AI Analysis | Feedback

  • EDIT-101: A gene-editing therapy in clinical trials for Leber Congenital Amaurosis 10, an inherited childhood blindness.
  • EDIT-102: A gene-editing therapy in development for Usher Syndrome 2A and autosomal dominant retinitis pigmentosa, both affecting vision and sometimes hearing.
  • EDIT-301: A gene-editing therapy designed to treat sickle cell disease and transfusion-dependent beta-thalassemia.
  • Gene-edited Natural Killer (NK) cell medicines: Therapies under development that modify NK cells to treat solid tumor cancers.
  • Alpha-beta T cell therapies: Gene-edited T cell therapies being developed for various cancers.
  • Gamma delta T cell therapies: Gene-edited T cell therapies in development for treating different types of cancer.
  • Neurological disease therapy (Early Discovery): A therapy in early discovery stages aimed at treating a specific neurological disease.

AI Analysis | Feedback

Editas Medicine (EDIT) is a clinical-stage genome editing company focused on developing genomic medicines. As such, it does not currently sell approved products directly to individuals (patients). Instead, its primary "customers" are other companies with which it forms strategic alliances and research collaborations for the development and potential commercialization of its therapies. These collaborations often involve upfront payments, milestone payments, and future royalties, which represent Editas Medicine's revenue streams from these partners.

Based on the provided information, Editas Medicine's major corporate partners (customers) include:

  • Juno Therapeutics, Inc.
  • Allergan Pharmaceuticals International Limited
  • Asklepios BioPharmaceutical, Inc. (AskBio)

AI Analysis | Feedback

null

AI Analysis | Feedback

Gilmore O'Neill, President and Chief Executive Officer

Gilmore O'Neill joined Editas Medicine as President and Chief Executive Officer in June 2022. He brings over 20 years of experience in genetic medicine, neurobiology, and clinical development. Prior to Editas, Dr. O'Neill served as Executive Vice President of Research & Development and Chief Medical Officer at Sarepta Therapeutics from 2018 to 2021. He also spent 15 years at Biogen, where his roles included Senior Vice President, Late Stage Clinical Development. He has a track record of driving successful clinical programs and achieving marketing approvals for several medicines, including Amondys®, Vyondys®, Spinraza®, Plegridy®, and Tecfidera®. He currently serves as a Director at Unity Biotechnology.

Amy Parison, Chief Financial Officer

Amy Parison was appointed Chief Financial Officer of Editas Medicine in March 2025, succeeding Erick J. Lucera. She joined Editas Medicine in August 2022 and has held multiple roles of increasing responsibility within the company, including Senior Vice President of Finance, Vice President of Finance, and Corporate Controller. Prior to her tenure at Editas, Ms. Parison was the Corporate Controller at Rubius Therapeutics, Inc., and held various financial roles at Vertex Pharmaceuticals.

Linda C. Burkly, Ph.D., Chief Scientific Officer

Linda C. Burkly joined Editas Medicine as Chief Scientific Officer in July 2023. She is responsible for leading the company's drug discovery team and activities across all therapeutic areas. Dr. Burkly brings more than 35 years of experience in biotechnology as a research leader, with expertise spanning drug discovery and development in immunological, neurological, and rare genetic disorders. She spent 37 years at Biogen, where she contributed to the foundations of approved medicines and late-stage programs, including the multiple sclerosis treatment Tysabri.

Brieana Buckley, Senior Vice President, Development and Program Leadership

Brieana Buckley serves as the Senior Vice President, Development and Program Leadership at Editas Medicine. She is a member of the executive leadership team responsible for advancing the company's experimental medicines.

Frank Panaccio, Senior Vice President and Chief Business Officer

Frank Panaccio is the Senior Vice President and Chief Business Officer at Editas Medicine. He is part of the executive leadership team responsible for business development and strategic initiatives for the company.

AI Analysis | Feedback

```html

  1. Clinical Development and Regulatory Approval Risk: As a clinical-stage genome editing company, Editas Medicine's success is critically dependent on the successful outcome of its ongoing and future clinical trials for drug candidates such as EDIT-101, EDIT-102, and EDIT-301. Failure to achieve favorable results in these trials, significant delays, or unforeseen safety concerns would severely impact the company's ability to develop and commercialize its medicines. Even with successful clinical data, there is a substantial risk of not obtaining the necessary regulatory approvals from health authorities for these novel gene editing therapies.
  2. Intellectual Property and Patent Disputes: Editas Medicine's proprietary gene editing platform is based on CRISPR technology. The field of CRISPR technology is characterized by complex and often contentious intellectual property landscape, with numerous ongoing patent disputes and litigation among various entities. The company's ability to operate, develop, and commercialize its products hinges on its ability to maintain and defend its intellectual property rights and navigate potential challenges from competitors regarding patent infringement or ownership.

```

AI Analysis | Feedback

null

AI Analysis | Feedback

Addressable Markets for Editas Medicine's Main Products

Editas Medicine, Inc. focuses on developing genomic medicines for serious diseases. The addressable markets for their main products and services are as follows:

  • Leber Congenital Amaurosis 10 (LCA10) - EDIT-101: The global market for Leber Congenital Amaurosis is estimated to be valued at approximately USD 1.29 billion in 2025 and is projected to reach USD 1.78 billion by 2032. North America is expected to account for an estimated 39.8% of this market in 2025. EDIT-101 specifically targets the IVS26 CEP290 mutation, which affects about 1,500 patients in the U.S.
  • Usher Syndrome 2A - EDIT-102: The global Usher Syndrome market is estimated to be valued at approximately USD 2.29 billion in 2025 and is expected to reach USD 3.20 billion by 2032. North America is projected to lead this market, holding a 38.2% share in 2025. More specifically for Usher Syndrome Type 2, the global market size was valued at USD 1.35 billion in 2024 and is expected to reach USD 2.15 billion by 2032, with North America dominating at approximately 39.6% of the global market share in 2025.
  • Autosomal Dominant Retinitis Pigmentosa: The global Retinitis Pigmentosa market size is projected to grow from approximately USD 14.27 billion in 2024 to USD 30.69 billion by 2035. In 2022, between 82,500 and 110,000 individuals in the United States were affected by retinitis pigmentosa. The total Retinitis Pigmentosa treatment market size in the U.S. was estimated to be nearly USD 260 million in 2023. Autosomal dominant retinitis pigmentosa accounts for 20-25% of nonsyndromic retinitis pigmentosa cases.
  • Sickle Cell Disease - EDIT-301: The global sickle cell disease treatment market size was estimated at approximately USD 2.75 billion in 2023 and is projected to reach USD 7.42 billion by 2030. Other estimates place the global market size at USD 3.94 billion in 2025, reaching USD 20.47 billion by 2034. North America dominated the global market with a 37.87% share in 2023, and the United States alone held a 63.35% market share in 2025.
  • Transfusion-Dependent Beta-Thalassemia - EDIT-301: The global thalassemia market size was valued at approximately USD 850.0 million in 2023 and is projected to grow at a CAGR of 7.8% from 2024 to 2030. The beta-thalassemia segment constituted 71.2% of the revenue share in 2023, and its market size is expected to reach USD 822.5 million by 2034 from USD 340.3 million in 2023. North America held the largest share of the global thalassemia market, at 42.8% in 2023.
  • Gene-Edited Natural Killer (NK) Cell Medicines for Solid Tumor Cancers: The global natural killer (NK) cell therapeutics market size was estimated at USD 340.25 million in 2024 and is predicted to increase to approximately USD 9,997.65 million by 2034. The cancer segment held the largest share in the NK cell therapeutics market in 2024. The CAR-NK cell therapy market was valued at USD 2.16 billion in 2024 and is projected to reach USD 3.10 billion by 2032, with the U.S. currently dominating.
  • Alpha-Beta T Cells for Multiple Cancers: The global T-cell immunotherapy market size was approximately USD 8.43 billion in 2025 and is predicted to increase to USD 26.53 billion by 2034. Another estimate places the T-cell immunotherapy market at USD 3.94 billion in 2025, rising to USD 32.75 billion by 2030. North America held the largest share of the T-cell therapy market, at 63.88% in 2022. The cancer gene therapy market, which includes T-cell therapies, was valued at USD 24.96 billion in 2025 and is estimated to grow to USD 67.11 billion by 2031, with solid tumors projected to advance at a 27.29% CAGR between 2026 and 2031.
  • Gamma Delta T Cell Therapies to Treat Cancer: The gamma delta T cell cancer therapy market size was USD 2.11 billion in 2025 and is projected to reach USD 4.94 billion by 2030. North America was the largest region in this market in 2025.
  • Therapy to Treat a Neurological Disease (Early Discovery Program): The gene therapy market for neurological diseases was valued at USD 3.13 billion in 2024 and is expected to grow to USD 5.76 billion in 2029. The Gene Therapy in CNS Disorder Market is projected to reach USD 13.86 billion by 2025 and USD 191.04 billion by 2035. The United States is a leading region for gene therapy in CNS disorders.

AI Analysis | Feedback

Editas Medicine (EDIT) is a clinical-stage genome editing company primarily focused on developing transformative genomic medicines. Over the next 2-3 years, the company's revenue growth is expected to be driven by a combination of its lead clinical programs and strategic collaborations. Here are 3-5 expected drivers of future revenue growth for Editas Medicine: * Advancement and Potential Commercialization of EDIT-401 for Heterozygous Familial Hypercholesterolemia (HeFH): Editas Medicine has designated EDIT-401 as its lead *in vivo* development candidate, targeting heterozygous familial hypercholesterolemia (HeFH). Preclinical studies for EDIT-401 have shown significant reduction in LDL cholesterol levels. The company anticipates submitting an Investigational New Drug (IND) or Clinical Trial Application (CTA) by mid-2026, with plans to initiate the first-in-human clinical trial in HeFH patients later in 2026. Early human proof-of-concept data is targeted by year-end 2026, and topline dose-finding results are expected in 2027. Successful progression through these clinical milestones could pave the way for future product revenue or significant partnership deals. * Growth in Collaboration and Licensing Revenue from Strategic Partnerships: As a pre-commercial biotechnology company, Editas Medicine relies on revenue generated from collaboration agreements and licensing its proprietary CRISPR technology. The company has recognized revenue from milestone achievements in existing collaborations, such as with Bristol Myers Squibb (BMS). Furthermore, a non-exclusive license agreement with Vertex Pharmaceuticals for Editas's Cas9 gene editing technology, which includes Vertex's CASGEVY™ for sickle cell disease and beta-thalassemia, provides for upfront payments, a contingent upfront payment, and annual license fees through 2034. Continued and expanded strategic alliances are crucial for sustained revenue growth. * Continued Clinical Progress and Potential Milestone Payments from EDIT-101 for Leber Congenital Amaurosis 10 (LCA10): EDIT-101, an experimental CRISPR-based medicine for Leber Congenital Amaurosis 10 (LCA10), remains in a Phase 1/2 clinical trial. Editas Medicine has a strategic alliance with Allergan Pharmaceuticals International Limited (now part of AbbVie) for the discovery, development, and commercialization of new gene editing medicines for ocular disorders. Under this agreement, Editas is eligible to receive development and commercial milestones, as well as royalty payments. Further positive clinical trial data and the achievement of development milestones for EDIT-101 could contribute to revenue growth in the next 2-3 years.

AI Analysis | Feedback

Capital Allocation Decisions (2021-2025)

Share Issuance

  • Editas Medicine generated $17.3 million in proceeds from sales of common stock under an at-the-market (ATM) facility after September 30, 2025.
  • As of February 27, 2026, the company had 97,871,999 shares of common stock outstanding.

Inbound Investments

  • Collaboration and other research and development revenues increased to $40.5 million for the full year 2025, up from $32.3 million in 2024. This increase was primarily due to the recognition of deferred revenue from a concluded collaboration agreement with a strategic partner and a milestone achieved in 2025 under a collaboration with Bristol Myers Squibb (BMS).
  • In the third quarter of 2025, the company recognized $7.5 million in collaboration and other research and development revenues, largely attributed to a milestone payment from its agreement with Bristol Myers Squibb.
  • A milestone payment was triggered in the second quarter of 2025 from the collaboration agreement with Bristol Myers Squibb, following the acceptance of the first Investigational New Drug (IND)/Clinical Trial Application (CTA) for the CD19 HD Allo CAR T program.

Outbound Investments

  • Editas Medicine has made one investment in Nomad Health.
  • The company has not made any acquisitions.

Capital Expenditures

  • Editas Medicine expects its existing cash, cash equivalents, and marketable securities to fund its operating expenses and capital expenditure requirements into the third quarter of 2027.
  • Capital expenditures are an ongoing requirement for the company, supporting the advancement of its in vivo gene editing programs, including lead candidate EDIT-401, through preclinical and clinical development.

Better Bets vs. Editas Medicine (EDIT)

Latest Trefis Analyses

Recent Active Movers

Peer Comparisons

Peers to compare with:

Financials

EDITCRSPNTLABEAMVRTXCRBUMedian
NameEditas M.CRISPR T.Intellia.Beam The.Vertex P.Caribou . 
Mkt Price2.9847.7811.3827.53485.651.6519.45
Mkt Cap0.34.61.32.8123.40.22.1
Rev LTM3916616412,2181152
Op Inc LTM-89-646-421-3724,662-120-246
FCF LTM-141-426-364-3843,710-102-252
FCF 3Y Avg-169-301-388-3051,977-120-235
CFO LTM-141-400-363-3704,241-101-252
CFO 3Y Avg-165-289-382-2872,401-114-226

Growth & Margins

EDITCRSPNTLABEAMVRTXCRBUMedian
NameEditas M.CRISPR T.Intellia.Beam The.Vertex P.Caribou . 
Rev Chg LTM8.0%-97.1%45.0%158.0%10.1%13.0%11.5%
Rev Chg 3Y Avg54.7%-5.0%10.0%148.7%9.9%23.4%16.7%
Rev Chg Q-39.2%--9.5%324.9%7.8%1.9%1.9%
QoQ Delta Rev Chg LTM-4.5%--2.3%17.4%1.8%0.4%0.4%
Op Inc Chg LTM57.0%-36.3%22.2%13.7%1,214.0%26.9%24.6%
Op Inc Chg 3Y Avg21.1%-16.1%-1.3%-24.5%364.1%-3.4%-2.3%
Op Mgn LTM-230.1%-64,639.5%-636.6%-226.6%38.2%-1,067.2%-433.3%
Op Mgn 3Y Avg-358.4%-22,035.2%-935.8%-318.1%24.1%-1,036.0%-647.1%
QoQ Delta Op Mgn LTM15.1%-15.1%48.0%0.2%153.3%15.1%
CFO/Rev LTM-363.1%-39,996.4%-549.5%-225.4%34.7%-903.8%-456.3%
CFO/Rev 3Y Avg-385.0%-13,643.7%-715.9%-272.2%21.5%-866.5%-550.5%
FCF/Rev LTM-364.6%-42,617.6%-550.2%-234.0%30.4%-909.2%-457.4%
FCF/Rev 3Y Avg-394.3%-14,519.9%-727.1%-282.9%17.7%-896.2%-560.7%

Valuation

EDITCRSPNTLABEAMVRTXCRBUMedian
NameEditas M.CRISPR T.Intellia.Beam The.Vertex P.Caribou . 
Mkt Cap0.34.61.32.8123.40.22.1
P/S7.54,589.320.417.310.114.115.7
P/Op Inc-3.3-7.1-3.2-7.626.5-1.3-3.2
P/EBIT-2.8-7.1-3.2-7.624.4-1.3-3.0
P/E-2.7-8.1-3.4-43.728.4-1.2-3.0
P/CFO-2.1-11.5-3.7-7.729.1-1.6-2.9
Total Yield-37.4%-12.4%-29.3%-2.3%3.5%-84.2%-20.8%
Dividend Yield0.0%0.0%0.0%0.0%0.0%0.0%0.0%
FCF Yield 3Y Avg-102.2%-7.6%-30.5%-14.3%1.8%-83.1%-22.4%
D/E0.10.20.10.10.00.20.1
Net D/E-0.4-0.4-0.2-0.3-0.0-0.6-0.3

Returns

EDITCRSPNTLABEAMVRTXCRBUMedian
NameEditas M.CRISPR T.Intellia.Beam The.Vertex P.Caribou . 
1M Rtn10.8%-11.7%-27.4%-19.4%7.5%0.6%-5.5%
3M Rtn-14.6%-17.6%-23.9%-12.3%10.1%-25.0%-16.1%
6M Rtn46.8%-10.7%-9.0%-11.8%10.0%13.0%0.5%
12M Rtn8.0%-26.6%-5.7%32.7%5.6%-19.5%-0.0%
3Y Rtn-66.0%-15.5%-73.7%-11.1%34.2%-75.1%-40.8%
1M Excs Rtn27.0%-7.4%-21.1%-10.5%7.9%-1.7%-4.5%
3M Excs Rtn-17.0%-20.2%-25.6%-15.1%5.6%-29.2%-18.6%
6M Excs Rtn26.6%-23.7%-13.0%-29.9%0.4%-5.2%-9.1%
12M Excs Rtn-14.1%-32.4%-24.0%18.1%-15.6%-28.9%-19.8%
3Y Excs Rtn-133.9%-83.6%-141.9%-81.1%-26.4%-145.5%-108.8%

Financials

Segment Financials

Revenue by Segment
$ Mil20252024202320222021
Developing and commercializing genome editing technology4132782026
Total4132782026


Net Income by Segment
$ Mil20252024
Developing and commercializing genome editing technology-160-237
Total-160-237


Price Behavior

Price Behavior
Market Price$2.98 
Market Cap ($ Bil)0.3 
First Trading Date02/03/2016 
Distance from 52W High-28.2% 
   50 Days200 Days
DMA Price$2.94$2.69
DMA Trendindeterminateindeterminate
Distance from DMA1.5%10.9%
 3M1YR
Volatility91.7%92.1%
Downside Capture92.04223.24
Upside Capture1.41186.48
Correlation (SPY)27.3%30.3%
EDIT Betas & Captures as of 6/30/2026

 1M2M3M6M1Y3Y
Beta1.832.302.442.502.342.06
Up Beta4.444.143.173.802.312.00
Down Beta3.934.143.432.332.461.76
Up Capture-5%122%223%338%408%904%
Bmk +ve Days11244067140429
Stock +ve Days10203561116328
Down Capture65%95%148%154%163%113%
Bmk -ve Days10172358112321
Stock -ve Days11212859128406

[1] Upside and downside betas calculated using positive and negative benchmark daily returns respectively
Based On 1-Year Data
Annualized
Return
Annualized
Volatility
Sharpe
Ratio
Correlation
with EDIT
EDIT4.9%92.7%0.45-
Sector ETF (XLV)21.6%15.8%1.0529.2%
Equity (SPY)20.2%12.6%1.1829.6%
Gold (GLD)19.6%28.0%0.6323.7%
Commodities (DBC)30.0%19.0%1.25-8.6%
Real Estate (VNQ)15.7%14.0%0.8122.1%
Bitcoin (BTCUSD)-46.3%42.8%-1.3331.5%

Smart multi-asset allocation framework can stack odds in your favor. Learn How
Based On 5-Year Data
Annualized
Return
Annualized
Volatility
Sharpe
Ratio
Correlation
with EDIT
EDIT-42.7%93.7%-0.19-
Sector ETF (XLV)6.2%15.0%0.2330.7%
Equity (SPY)12.8%17.1%0.5737.9%
Gold (GLD)16.9%18.4%0.749.3%
Commodities (DBC)8.7%19.5%0.342.0%
Real Estate (VNQ)2.9%18.9%0.0533.3%
Bitcoin (BTCUSD)13.6%53.5%0.4426.9%

Smart multi-asset allocation framework can stack odds in your favor. Learn How
Based On 10-Year Data
Annualized
Return
Annualized
Volatility
Sharpe
Ratio
Correlation
with EDIT
EDIT-19.3%83.9%0.11-
Sector ETF (XLV)10.1%16.6%0.4933.0%
Equity (SPY)15.3%17.9%0.7337.6%
Gold (GLD)11.0%16.1%0.557.1%
Commodities (DBC)7.0%17.9%0.318.6%
Real Estate (VNQ)5.3%20.7%0.2226.9%
Bitcoin (BTCUSD)58.5%66.2%0.9918.6%

Smart multi-asset allocation framework can stack odds in your favor. Learn How

Short Interest

Short Interest: As Of Date6302026
Short Interest: Shares Quantity22.5 Mil
Short Interest: % Change Since 615202622.0%
Average Daily Volume3.1 Mil
Days-to-Cover Short Interest7.2 days
Basic Shares Quantity97.9 Mil
Short % of Basic Shares23.0%

Earnings Returns History

Updated 6/18/2026
Expand for More
 Forward Returns
Earnings Date1D Returns5D Returns21D Returns
5/5/20261.3%2.0%-7.3%
3/9/202616.0%22.0%37.0%
11/10/20252.0%5.3%5.3%
8/12/202534.5%14.8%18.3%
5/12/2025-2.6%-3.2%31.8%
3/5/2025-13.2%-26.3%-45.4%
1/13/2025-7.9%-3.2%-6.3%
11/4/2024-1.0%7.2%-32.0%
...
SUMMARY STATS   
# Positive161410
# Negative91115
Median Positive9.7%8.2%27.6%
Median Negative-7.9%-11.9%-17.3%
Max Positive34.5%45.1%58.3%
Max Negative-13.2%-26.3%-45.4%
Collapse to Preview
 Forward Returns
Earnings Date1D Returns5D Returns21D Returns
5/5/20261.3%2.0%-7.3%
3/9/202616.0%22.0%37.0%
11/10/20252.0%5.3%5.3%
8/12/202534.5%14.8%18.3%
5/12/2025-2.6%-3.2%31.8%
3/5/2025-13.2%-26.3%-45.4%
1/13/2025-7.9%-3.2%-6.3%
11/4/2024-1.0%7.2%-32.0%
8/7/2024-12.2%-14.7%-25.4%
5/8/2024-11.4%0.0%-4.4%
2/28/202424.9%3.2%-16.0%
11/3/202318.2%11.9%57.2%
8/2/20235.7%2.9%4.5%
5/5/202312.0%9.6%8.3%
2/22/20236.2%-1.5%-20.5%
11/2/20221.1%-12.0%-21.1%
8/3/202213.4%9.2%-10.8%
5/4/202211.5%-20.6%-18.6%
2/24/202210.1%19.0%31.5%
11/8/20218.2%1.1%-17.4%
8/4/20219.4%45.1%58.3%
5/5/20210.2%-5.4%-3.8%
2/25/2021-9.9%-13.2%-15.1%
11/5/2020-3.4%-11.9%23.8%
8/6/2020-5.8%-4.1%-17.3%
SUMMARY STATS   
# Positive161410
# Negative91115
Median Positive9.7%8.2%27.6%
Median Negative-7.9%-11.9%-17.3%
Max Positive34.5%45.1%58.3%
Max Negative-13.2%-26.3%-45.4%

SEC Filings

Expand for More
Report DateFiling DateFiling
03/31/202605/05/202610-Q
12/31/202503/09/202610-K
09/30/202511/10/202510-Q
06/30/202508/12/202510-Q
03/31/202505/12/202510-Q
12/31/202403/05/202510-K
09/30/202411/04/202410-Q
06/30/202408/07/202410-Q
03/31/202405/08/202410-Q
12/31/202302/28/202410-K
09/30/202311/03/202310-Q
06/30/202308/02/202310-Q
03/31/202305/05/202310-Q
12/31/202202/22/202310-K
09/30/202211/02/202210-Q
06/30/202208/03/202210-Q
Collapse to Preview
Report DateFiling DateFiling
03/31/202605/05/202610-Q
12/31/202503/09/202610-K
09/30/202511/10/202510-Q
06/30/202508/12/202510-Q
03/31/202505/12/202510-Q
12/31/202403/05/202510-K
09/30/202411/04/202410-Q
06/30/202408/07/202410-Q
03/31/202405/08/202410-Q
12/31/202302/28/202410-K
09/30/202311/03/202310-Q
06/30/202308/02/202310-Q
03/31/202305/05/202310-Q
12/31/202202/22/202310-K
09/30/202211/02/202210-Q
06/30/202208/03/202210-Q
03/31/202205/04/202210-Q
12/31/202102/24/202210-K
09/30/202111/09/202110-Q
06/30/202108/05/202110-Q
03/31/202105/06/202110-Q
12/31/202002/26/202110-K
09/30/202011/06/202010-Q
06/30/202008/07/202010-Q
03/31/202005/08/202010-Q
12/31/201902/26/202010-K
09/30/201911/12/201910-Q
06/30/201908/07/201910-Q

Insider Activity

Updated 6/5/2026
Expand for More
#OwnerTitleHoldingActionFiling DatePriceSharesTransacted
Value
Value of
Held Shares
Form
1Parison, AmySVP, Chief Financial OfficerDirectSell60520262.704641,25340,434Form
2O'Neill, Gilmore NeilCEODirectSell60520262.7015,38041,543670,718Form
3Burkly, LindaEVP, CHIEF SCIENTIFIC OFFICERDirectSell60520262.707311,975181,776Form
4O'Neill, Gilmore NeilCEODirectSell30420262.025,39410,894532,581Form
5Parison, AmySVP, Chief Financial OfficerDirectSell30420262.0247495731,177Form
Collapse to Preview
#OwnerTitleHoldingActionFiling DatePriceSharesTransacted
Value
Value of
Held Shares
Form
1Parison, AmySVP, Chief Financial OfficerDirectSell60520262.704641,25340,434Form
2O'Neill, Gilmore NeilCEODirectSell60520262.7015,38041,543670,718Form
3Burkly, LindaEVP, CHIEF SCIENTIFIC OFFICERDirectSell60520262.707311,975181,776Form
4O'Neill, Gilmore NeilCEODirectSell30420262.025,39410,894532,581Form
5Parison, AmySVP, Chief Financial OfficerDirectSell30420262.0247495731,177Form
6Burkly, LindaEVP, CHIEF SCIENTIFIC OFFICERDirectSell30420262.027491,513137,389Form
7Burkly, LindaEVP, CHIEF SCIENTIFIC OFFICERDirectSell120420252.157131,535148,084Form
8O'Neill, Gilmore NeilCEODirectSell120420252.155,60312,064579,371Form
9Parison, AmySVP, Chief Financial OfficerDirectSell120420252.1546199334,252Form
10Burkly, LindaEVP, CHIEF SCIENTIFIC OFFICERDirectSell90420252.607101,843180,403Form
11Parison, AmySVP, Chief Financial OfficerDirectSell90420252.604581,18942,496Form
12O'Neill, Gilmore NeilCEODirectSell90420252.605,59214,517713,123Form
13Parison, AmySVP, Chief Financial OfficerDirectSell80820252.586791,75243,414Form
14Burkly, LindaEVP, CHIEF SCIENTIFIC OFFICERDirectSell80420252.495,12112,757160,422Form
15Parison, AmySVP, Chief Financial OfficerDirectSell60420251.7244676930,180Form
16Burkly, LindaEVP, CHIEF SCIENTIFIC OFFICERDirectSell60420251.727261,252119,872Form
17O'Neill, Gilmore NeilCEODirectSell60420251.7215,19226,196483,290Form
Core Cache Last Updated: 7/19/2026