Tearsheet

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

0

Megatrend and thematic drivers
Megatrends include Precision Medicine. Themes include Targeted Therapies, and Biopharmaceutical R&D.

Weak multi-year price returns
2Y Excs Rtn is -66%, 3Y Excs Rtn is -101%

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 109%

Key risks
COAG key risks include [1] the potential failure of its novel and unproven product candidates to complete development and commercialization, Show more.

0 Megatrend and thematic drivers
Megatrends include Precision Medicine. Themes include Targeted Therapies, and Biopharmaceutical R&D.
1 Weak multi-year price returns
2Y Excs Rtn is -66%, 3Y Excs Rtn is -101%
2 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 109%
3 Key risks
COAG key risks include [1] the potential failure of its novel and unproven product candidates to complete development and commercialization, Show more.

Valuation & Metrics

Price Chart

Why The Stock Moved

Qualitative Assessment

AI Analysis | Feedback

Updated on 6/4/2026

Hemab Therapeutics (COAG) stock has lost about 25% since it went public on 5/1/2026 because of the following key factors:

1. Post-IPO Valuation Correction Following Initial Surge: Hemab Therapeutics experienced a significant initial price surge on its Nasdaq debut on May 1, 2026, closing at $34.00 per share, an increase of nearly 90% from its $18.00 IPO price. This strong opening was followed by a subsequent market correction, a common occurrence for newly public companies as valuations adjust after initial enthusiasm. The stock's current trading levels reflect this adjustment from its post-IPO peak, resulting in an approximate 25% decline from its first-day closing high.

2. Wider Net Loss in First Quarter 2026 Financial Results: The company reported a net loss of $22.7 million for the first quarter of 2026, widening from a net loss of $15.3 million in Q1 2025. This increased loss was primarily driven by higher research and development expenses, which rose to $19.5 million, and increased general and administrative costs as the company advanced its clinical programs. While the successful IPO provided approximately $317.2 million in net proceeds, extending the cash runway into 2029, the expanding operational losses may have contributed to investor caution.

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

Stock Movement Drivers

Fundamental Drivers

null
null

Market Drivers

2/28/2026 to 6/13/2026
ReturnCorrelation
COAG  
Market (SPY)8.4%26.3%
Sector (XLV)-3.6%8.3%

Fundamental Drivers

null
null

Market Drivers

11/30/2025 to 6/13/2026
ReturnCorrelation
COAG  
Market (SPY)9.2%26.3%
Sector (XLV)-1.6%8.3%

Fundamental Drivers

null
null

Market Drivers

5/31/2025 to 6/13/2026
ReturnCorrelation
COAG  
Market (SPY)27.3%26.3%
Sector (XLV)18.0%8.3%

Fundamental Drivers

null
null

Market Drivers

5/31/2023 to 6/13/2026
ReturnCorrelation
COAG  
Market (SPY)84.5%26.3%
Sector (XLV)26.5%8.3%

Return vs. Risk

Price Returns Compared

 202120222023202420252026Total [1]
Returns
COAG Return------21%-21%
Peers Return8%5%-39%42%0%17%16%
S&P 500 Return27%-19%24%23%16%8%97%

Monthly Win Rates [3]
COAG Win Rate-----0% 
Peers Win Rate50%47%22%42%43%46% 
S&P 500 Win Rate75%42%67%75%67%50% 

Max Drawdowns [4]
COAG Max Drawdown------ 
Peers Max Drawdown-30%-30%-52%-37%-40%-34% 
S&P 500 Max Drawdown-5%-25%-10%-8%-19%-9% 


[1] Cumulative total returns since the beginning of 2021
[2] Peers: PFE, BMRN, QURE, CBIO.
[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 6/12/2026 (YTD)

How Low Can It Go

COAG has limited trading history. Below is the Health Care sector ETF (XLV) in its place.

EventXLVS&P 500
2025 US Tariff Shock
  % Loss-11.7%-18.8%
  % Gain to Breakeven13.3%23.1%
  Time to Breakeven142 days79 days
2022 Inflation Shock & Fed Tightening
  % Loss-13.8%-24.5%
  % Gain to Breakeven15.9%32.4%
  Time to Breakeven166 days427 days
2020 COVID-19 Crash
  % Loss-27.9%-33.7%
  % Gain to Breakeven38.8%50.9%
  Time to Breakeven77 days140 days
Q4 2018 Fed Policy Error / Growth Scare
  % Loss-15.0%-19.2%
  % Gain to Breakeven17.6%23.8%
  Time to Breakeven191 days105 days
2015-2016 China Devaluation / Global Growth Scare
  % Loss-15.9%-12.2%
  % Gain to Breakeven18.9%13.9%
  Time to Breakeven165 days62 days
2011 US Debt Ceiling Crisis & European Contagion
  % Loss-15.8%-17.9%
  % Gain to Breakeven18.8%21.8%
  Time to Breakeven153 days123 days

Compare to PFE, BMRN, QURE, CBIO

In The Past

State Street Health Care Select Sector SPDR ETF's stock fell -11.7% during the 2025 US Tariff Shock. Such a loss loss requires a 13.3% 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.

COAG has limited trading history. Below is the Health Care sector ETF (XLV) in its place.

EventXLVS&P 500
2020 COVID-19 Crash
  % Loss-27.9%-33.7%
  % Gain to Breakeven38.8%50.9%
  Time to Breakeven77 days140 days
2008-2009 Global Financial Crisis
  % Loss-37.9%-53.4%
  % Gain to Breakeven61.1%114.4%
  Time to Breakeven767 days1085 days

Compare to PFE, BMRN, QURE, CBIO

In The Past

State Street Health Care Select Sector SPDR ETF's stock fell -11.7% during the 2025 US Tariff Shock. Such a loss loss requires a 13.3% 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 Hemab Therapeutics (COAG)

We are a clinical-stage biotechnology company developing therapies that reimagine the treatment of blood coagulation disorders to sustain life and human resilience. Our mission is to build the leading coagulation company by discovering, developing, and commercializing innovative therapies for the millions of patients worldwide suffering from serious bleeding and thrombotic diseases. Coagulation disorders encompass a broad and heterogeneous group of conditions, and many patients experience significant life-long disease burden due to either a lack of available prophylactic therapies or limitations associated with existing treatment approaches. Our lead asset, sutacimig (HMB-001), is a bispecific antibody currently in Phase 1/2 clinical development for the prophylactic treatment of Glanzmann thrombasthenia and Phase 2 clinical development for the prophylactic treatment of Factor VII deficiency. Our second clinical-stage asset, HMB-002, is a monovalent antibody in Phase 1/2 clinical development for the subcutaneous prophylactic treatment of Von Willebrand Disease. We are also advancing multiple preclinical and discovery-stage assets. We estimate that there are approximately an aggregate of 10,000 patients with Glanzmann thrombasthenia and Factor VII deficiency and an aggregate of 120,000 patients with Von Willebrand Disease in the geographies where we intend to commercialize our assets, including the United States, the European Union, Japan, the Gulf Cooperation Council countries and other select regions. With greater disease burden awareness, potential regulatory approvals of new prophylactic options and expanding global reach of these options, we believe the overall number of addressable patients for our clinical-stage assets, and preclinical and discovery stage programs could be greater than we currently estimate. We aim to establish the industry’s leading coagulation franchise through the execution of our “Hemab 2x3 by 2030” strategic roadmap, which is designed to build a franchise consisting of 2 commercial medicines, 2 new late-stage clinical programs, and 2 new early-stage clinical programs by 2030. We have not yet initiated pivotal trials for any of our product candidates, and due to the novel and unproven nature of our programs, their current stage of development and the lack of approved prophylactic therapies to inform endpoint selection and trial design, we may not be able to achieve our strategic goals on the timeline we expect or at all. Our principal executive offices are located in Cambridge, MA.

AI Analysis | Feedback

Here are a few analogies to describe Hemab Therapeutics (COAG):

  • Vertex Pharmaceuticals for blood coagulation disorders.

  • Intuitive Surgical for blood coagulation therapies.

AI Analysis | Feedback

  • sutacimig (HMB-001): A bispecific antibody currently in clinical development for the prophylactic treatment of Glanzmann thrombasthenia and Factor VII deficiency.
  • HMB-002: A monovalent antibody in clinical development for the subcutaneous prophylactic treatment of Von Willebrand Disease.

AI Analysis | Feedback

Hemab Therapeutics (COAG) is a clinical-stage biotechnology company. As described in the background information, the company's product candidates are currently in Phase 1/2 and Phase 2 clinical development and have not yet received regulatory approval or been commercialized. Therefore, Hemab Therapeutics does not currently have major customers, as it is not selling any products.

AI Analysis | Feedback

null

AI Analysis | Feedback

Benny Sorensen, MD, PhD, Chief Executive Officer
Benny Sorensen co-founded Hemab Therapeutics in 2020. He joined Hemab as CEO from Codiak Biosciences, where he served as Senior Vice President, Strategic Projects, and was involved in building the company and advancing its first engineered exosome therapeutics from idea to clinical proof of concept. Prior to Codiak, he was Senior Director of Clinical Research at Alnylam Pharmaceuticals, leading the development of fitusiran and other hematology products. He also served as a Global Medical Director at Baxter Healthcare Corporation, advancing the pivotal development of Adynovate® and Vonvendi®. Hemab has secured funding from private equity firms such as Novo Holdings, HealthCap, RA Capital Management, Access Biotechnology, Deep Track Capital, Avoro Ventures, Invus, Rock Springs Capital, and Maj Invest Equity.

Mads Behrndt, Chief Financial Officer
Mads Behrndt was appointed Chief Financial Officer of Hemab in September 2021. He brings over 14 years of financial experience in international capital markets and business development. Before joining Hemab, he was a Partner at PwC's Corporate Finance team, where he led and executed private and public company financings and M&A transactions. Hemab is backed by a syndicate of top-tier investors.

Kate Madigan, MD, Chief Medical Officer
Kate Madigan was appointed Chief Medical Officer of Hemab in January 2025. Previously, she served as Chief Medical Officer at Syndax Pharmaceuticals, where she led the U.S. Food and Drug Administration (FDA) approvals of Revuforj and Niktimvo. Her extensive leadership experience also includes roles as Senior Medical Director at Alnylam Pharmaceuticals and Medical Director within Biogen's Rare Disease Innovation Unit.

Anant Murthy, PhD, Chief Operating Officer
Anant Murthy was appointed Chief Operating Officer of Hemab in September 2025. In this role, he is responsible for leading the company's global efforts in market access, launch, and commercialization of Hemab's pipeline.

Caroline Rasmussen, DVM, PhD, Vice President, Nonclinical Development
Caroline Rasmussen serves as Vice President, Nonclinical Development at Hemab, bringing over a decade of experience in nonclinical development, from early drug development to marketing authorization. She began her career at Novo Nordisk A/S, focusing primarily on the hemostasis portfolio. Most recently, she was Director of Toxicology and Safety Pharmacology at Ascendis Pharma A/S.

AI Analysis | Feedback

The key risks for Hemab Therapeutics (COAG) are:

  1. The risk that its novel and unproven product candidates may not successfully complete clinical development, receive regulatory approval, or be effectively commercialized. This is due to the early stage of development, the lack of established prophylactic therapies to inform endpoint selection and trial design, and the inherent uncertainties of clinical trials.
  2. The risk of failing to achieve its strategic goals outlined in the "Hemab 2x3 by 2030" roadmap, which aims to build a franchise consisting of two commercial medicines, two new late-stage clinical programs, and two new early-stage clinical programs by 2030.

AI Analysis | Feedback

```html null ```

AI Analysis | Feedback

The addressable markets for Hemab Therapeutics' main products are:

  • Glanzmann thrombasthenia and Factor VII deficiency: approximately 10,000 patients. This market size is for the United States, the European Union, Japan, the Gulf Cooperation Council countries, and other select regions.
  • Von Willebrand Disease: approximately 120,000 patients. This market size is for the United States, the European Union, Japan, the Gulf Cooperation Council countries, and other select regions.

AI Analysis | Feedback

Hemab Therapeutics (NASDAQ: COAG) is a clinical-stage biotechnology company focused on developing therapies for blood coagulation disorders. As a pre-revenue company, its future revenue growth over the next two to three years will be primarily driven by the successful advancement and potential commercialization of its pipeline assets.

The key expected drivers of future revenue growth for Hemab Therapeutics include:

  1. Successful progression of sutacimig (HMB-001) through late-stage clinical trials for Glanzmann thrombasthenia and Factor VII deficiency. sutacimig is the company's lead asset, poised to enter a Phase 3 clinical trial for Glanzmann thrombasthenia in the second half of 2026. It is being developed as the first prophylactic treatment for Glanzmann thrombasthenia, a severe bleeding disorder. Additionally, Phase 2 clinical data for sutacimig in Factor VII deficiency is anticipated in late 2026 or early 2027. Positive outcomes from these trials are crucial steps toward regulatory approval and eventual commercial launch.
  2. Advancement of HMB-002 into late-stage clinical development for Von Willebrand Disease. HMB-002, a monovalent antibody, is currently in Phase 1/2 clinical development for the subcutaneous prophylactic treatment of Von Willebrand Disease, the most common inherited bleeding disorder. Hemab aims to advance HMB-002 towards a registration study. Successful progression through clinical development for this asset could unlock access to a significantly larger patient population and represent a substantial future revenue stream.
  3. Expansion of the pipeline with new clinical-stage assets, such as HMB-003. Hemab's strategic roadmap, "Hemab 2x3 by 2030," includes building a franchise with two new early-stage clinical programs by 2030. The company expects to announce HMB-003, another novel drug candidate, in the first half of 2026. The successful advancement of these new programs into clinical development could broaden Hemab's portfolio and establish additional platforms for future revenue generation, potentially through milestone payments from partnerships or eventual product commercialization.

AI Analysis | Feedback

Share Repurchases

Hemab Therapeutics has not reported any share repurchases for the trailing twelve months ending December 2025, with a reported value of $0.00 million. As a recently public, clinical-stage biotechnology company, it has not engaged in share buyback programs.

Share Issuance

  • Hemab Therapeutics completed its Initial Public Offering (IPO) on May 1, 2026, raising $302 million by offering 16.8 million shares at $18 per share.
  • The IPO was upsized to 16.75 million shares and priced at $18.00 per share, raising $301.5 million.
  • The underwriters fully exercised their option to purchase an additional 2,512,500 shares, bringing the total shares issued in the IPO to 19,262,500 at $18.00 per share.

Inbound Investments

  • In October 2025, Hemab Therapeutics closed a $157 million Series C financing round, led by Sofinnova Partners with participation from new and existing investors including Novo Holdings, RA Capital Management, and Avoro Capital Advisors.
  • The company secured a $135 million Series B financing round in 2023, with participation from investors such as Novo Holdings.
  • Hemab Therapeutics raised $55 million in a Series A financing round in 2021, co-led by Novo Holdings.

Capital Expenditures

  • Hemab Therapeutics reported minimal capital expenditures, with -$0.02 million for the year ending December 2025 and -$0.28 million for December 2024.

Recent Active Movers

Peer Comparisons

Peers to compare with:

Financials

COAGPFEBMRNQURECBIOMedian
NameHemab Th.Pfizer BioMarin.uniQure Crescent. 
Mkt Price24.9826.2155.9527.5717.9226.21
Mkt Cap-149.210.81.70.56.3
Rev LTM-63,3143,24218121,630
Op Inc LTM-15,508315-188-16376
FCF LTM-9,483759-173-151304
FCF 3Y Avg-8,603514-161-514
CFO LTM-11,984874-172-70402
CFO 3Y Avg-11,517618-156-618

Growth & Margins

COAGPFEBMRNQURECBIOMedian
NameHemab Th.Pfizer BioMarin.uniQure Crescent. 
Rev Chg LTM-1.4%9.9%-10.4%-1.4%
Rev Chg 3Y Avg--9.2%14.3%-29.0%--9.2%
Rev Chg Q-5.4%2.8%127.3%-5.4%
QoQ Delta Rev Chg LTM-1.2%0.7%12.4%9.6%5.4%
Op Inc Chg LTM-3.1%-49.1%-13.8%--13.8%
Op Inc Chg 3Y Avg-203.9%93.5%-12.2%-93.5%
Op Mgn LTM-24.5%9.7%-1,039.8%-1,372.9%-515.1%
Op Mgn 3Y Avg-17.3%13.5%-1,079.8%-13.5%
QoQ Delta Op Mgn LTM--0.7%-3.0%86.0%34.7%17.0%
CFO/Rev LTM-18.9%27.0%-951.2%-585.9%-283.5%
CFO/Rev 3Y Avg-18.9%20.7%-816.3%-18.9%
FCF/Rev LTM-15.0%23.4%-954.1%-1,266.9%-469.6%
FCF/Rev 3Y Avg-14.0%17.0%-845.4%-14.0%

Valuation

COAGPFEBMRNQURECBIOMedian
NameHemab Th.Pfizer BioMarin.uniQure Crescent. 
Mkt Cap-149.210.81.70.56.3
P/S-2.43.395.645.824.6
P/Op Inc-9.634.2-9.2-3.33.1
P/EBIT-14.126.4-12.2-3.45.3
P/E-19.940.1-8.3-3.48.3
P/CFO-12.412.3-10.1-7.82.2
Total Yield-11.6%2.5%-12.1%-29.8%-4.8%
Dividend Yield-6.6%0.0%0.0%0.0%0.0%
FCF Yield 3Y Avg-5.7%4.2%-33.9%-4.2%
D/E-0.40.10.00.00.1
Net D/E-0.3-0.1-0.3-0.3-0.2

Returns

COAGPFEBMRNQURECBIOMedian
NameHemab Th.Pfizer BioMarin.uniQure Crescent. 
1M Rtn-11.9%1.8%5.1%-0.6%-15.6%-0.6%
3M Rtn-26.5%0.2%-4.4%77.5%60.3%0.2%
6M Rtn-26.5%4.8%5.0%41.3%27.2%5.0%
12M Rtn-26.5%14.3%-0.5%79.7%13.5%13.5%
3Y Rtn-26.5%-19.7%-40.7%42.3%13.5%-19.7%
1M Excs Rtn-12.4%1.1%4.7%-5.3%-8.4%-5.3%
3M Excs Rtn-38.6%-11.8%-16.4%65.5%48.2%-11.8%
6M Excs Rtn-34.4%-2.8%-3.7%29.0%15.8%-2.8%
12M Excs Rtn-49.9%-8.9%-25.5%46.6%-9.9%-9.9%
3Y Excs Rtn-100.7%-92.9%-112.7%-39.1%-60.7%-92.9%

Comparison Analyses

null

Financials

Segment Financials

Revenue by Segment
$ Mil20252024
Research and development of prophylactic therapeutics for bleeding disorders00
Total00


Net Income by Segment
$ Mil20252024
Research and development of prophylactic therapeutics for bleeding disorders-49-64
Total-49-64


Short Interest

Short Interest: As Of Date5292026
Short Interest: Shares Quantity1.0 Mil
Short Interest: % Change Since 515202635.3%
Average Daily Volume0.2 Mil
Days-to-Cover Short Interest6.5 days
Basic Shares Quantity0.9 Mil
Short % of Basic Shares108.5%

Earnings Returns History

Updated 6/2/2026
Expand for More
 Forward Returns
Earnings Date1D Returns5D Returns21D Returns
5/21/2026-0.6%5.8% 
SUMMARY STATS   
# Positive010
# Negative100
Median Positive 5.8% 
Median Negative-0.6%  
Max Positive 5.8% 
Max Negative-0.6%  

SEC Filings

Expand for More
Report DateFiling DateFiling
03/31/202605/21/202610-Q
12/31/202505/01/2026424B4

Insider Activity

Updated 5/21/2026
Expand for More
#OwnerTitleHoldingActionFiling DatePriceSharesTransacted
Value
Value of
Held Shares
Form
1Ra, Capital Management, LPSee footnotesBuy521202624.9499624,840159,041,582Form
2Ra, Capital Management, LPSee footnotesBuy521202624.973,80294,936159,208,021Form
3Ra, Capital Management, LPSee footnotesBuy514202624.906,387159,036158,667,033Form
4Ra, Capital Management, LPSee footnotesBuy511202624.8139,869989,226157,947,233Form
5Ra, Capital Management, LPSee footnotesBuy511202624.981,48337,045158,021,332Form
Core Cache Last Updated: 6/13/2026