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RARE US​
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RARE US​
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Ultragenyx Pharmaceutical Inc.(RARE US)

$16.09-0.181.11%(Market Open · 18:46:03 UTC)
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Ultragenyx Pharmaceutical Inc.(RARE US)

$16.09-0.181.11%(Market Open · 18:46:03 UTC)
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Doc SearchProfileEntity StructureFinancialsChartingShort InterestEmployees

Overview

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Ultragenyx Pharmaceutical Inc. — Company Profile

Ultragenyx Pharmaceutical Inc. is a biopharmaceutical firm dedicated to discovering, developing, and commercializing innovative treatments for rare and ultra-rare genetic conditions. Its operations span North America, Europe, and other international markets. The company's portfolio of marketed biologic products addresses several serious diseases. This includes Crysvita (burosumab), an antibody that targets fibroblast growth factor 23, used to treat X-linked hypophosphatemia and tumor-induced osteomalacia. Mepsevii offers enzyme replacement therapy for both pediatric and adult patients suffering from Mucopolysaccharidosis VII. Dojolvi is available for individuals with long-chain fatty acid oxidation disorders, while Evkeeza (evinacumab) provides a treatment option for homozygous familial hypercholesterolemia. Ultragenyx also boasts a robust pipeline of investigational therapies. Notable candidates include DTX401, an adeno-associated virus 8 (AAV8) gene therapy for glycogen storage disease type Ia, and DTX301, another AAV8 gene therapy aimed at ornithine transcarbamylase deficiency. Other promising developments feature UX143, a human monoclonal antibody for osteogenesis imperfecta; GTX-102, an antisense oligonucleotide designed for Angelman syndrome; UX701, targeting Wilson disease; and UX053, in development for glycogen storage disease type III. To advance its research and development efforts, Ultragenyx Pharmaceutical Inc. maintains strategic collaboration and licensing agreements with numerous partners, such as Kyowa Kirin Co., Ltd., Saint Louis University, REGENXBIO Inc., Bayer Healthcare LLC, GeneTx, Mereo, University of Pennsylvania, Arcturus Therapeutics Holdings Inc., Solid Biosciences Inc., and Daiichi Sankyo Co., Ltd. The company was founded in 2010 and operates from its headquarters in Novato, California.

Sector
Health Care
Industry
Pharmaceuticals
Exchange
UQ
CEO
Emil D. Kakkis
Headquarters
Novato, CA, US
IPO Date
Jan 31, 2014
Employees
1,371
Website
www.ultragenyx.com

Key Metrics

Price
$15.22
Market Cap
$1.50B
Revenue (TTM)
$136.00M
Net Income (TTM)
$-185000000.00
EPS (TTM)
-1.84
P/E (TTM)
-2.46
P/B (TTM)
-6.35
Dividend Yield
0.00%

Ultragenyx Pharmaceutical Inc. — Company Profile

Ultragenyx Pharmaceutical Inc. is a biopharmaceutical firm dedicated to discovering, developing, and commercializing innovative treatments for rare and ultra-rare genetic conditions. Its operations span North America, Europe, and other international markets. The company's portfolio of marketed biologic products addresses several serious diseases. This includes Crysvita (burosumab), an antibody that targets fibroblast growth factor 23, used to treat X-linked hypophosphatemia and tumor-induced osteomalacia. Mepsevii offers enzyme replacement therapy for both pediatric and adult patients suffering from Mucopolysaccharidosis VII. Dojolvi is available for individuals with long-chain fatty acid oxidation disorders, while Evkeeza (evinacumab) provides a treatment option for homozygous familial hypercholesterolemia. Ultragenyx also boasts a robust pipeline of investigational therapies. Notable candidates include DTX401, an adeno-associated virus 8 (AAV8) gene therapy for glycogen storage disease type Ia, and DTX301, another AAV8 gene therapy aimed at ornithine transcarbamylase deficiency. Other promising developments feature UX143, a human monoclonal antibody for osteogenesis imperfecta; GTX-102, an antisense oligonucleotide designed for Angelman syndrome; UX701, targeting Wilson disease; and UX053, in development for glycogen storage disease type III. To advance its research and development efforts, Ultragenyx Pharmaceutical Inc. maintains strategic collaboration and licensing agreements with numerous partners, such as Kyowa Kirin Co., Ltd., Saint Louis University, REGENXBIO Inc., Bayer Healthcare LLC, GeneTx, Mereo, University of Pennsylvania, Arcturus Therapeutics Holdings Inc., Solid Biosciences Inc., and Daiichi Sankyo Co., Ltd. The company was founded in 2010 and operates from its headquarters in Novato, California.

Sector
Health Care
Industry
Pharmaceuticals
Exchange
UQ
CEO
Emil D. Kakkis
Headquarters
Novato, CA, US
IPO Date
Jan 31, 2014
Employees
1,371
Website
www.ultragenyx.com

Key Metrics

Price
$15.22
Market Cap
$1.50B
Revenue (TTM)
$136.00M
Net Income (TTM)
$-185000000.00
EPS (TTM)
-1.84
P/E (TTM)
-2.46
P/B (TTM)
-6.35
Dividend Yield
0.00%
ROE (TTM)
78.39%
ROA (TTM)
-14.27%
Operating Margin
-124.26%
Beta
1.16

Dividends

Last Dividend
$0.00
Last Yield
0.00%

Summary

Ultragenyx Pharmaceutical Inc. is a biopharmaceutical firm dedicated to discovering, developing, and commercializing innovative treatments for rare and ultra-rare genetic conditions. Its operations span North America, Europe, and other international markets. The company's portfolio of marketed biologic products addresses several serious diseases. This includes Crysvita (burosumab), an antibody that targets fibroblast growth factor 23, used to treat X-linked hypophosphatemia and tumor-induced osteomalacia. Mepsevii offers enzyme replacement therapy for both pediatric and adult patients suffering from Mucopolysaccharidosis VII. Dojolvi is available for individuals with long-chain fatty acid oxidation disorders, while Evkeeza (evinacumab) provides a treatment option for homozygous familial hypercholesterolemia. Ultragenyx also boasts a robust pipeline of investigational therapies. Notable candidates include DTX401, an adeno-associated virus 8 (AAV8) gene therapy for glycogen storage disease type Ia, and DTX301, another AAV8 gene therapy aimed at ornithine transcarbamylase deficiency. Other promising developments feature UX143, a human monoclonal antibody for osteogenesis imperfecta; GTX-102, an antisense oligonucleotide designed for Angelman syndrome; UX701, targeting Wilson disease; and UX053, in development for glycogen storage disease type III. To advance its research and development efforts, Ultragenyx Pharmaceutical Inc. maintains strategic collaboration and licensing agreements with numerous partners, such as Kyowa Kirin Co., Ltd., Saint Louis University, REGENXBIO Inc., Bayer Healthcare LLC, GeneTx, Mereo, University of Pennsylvania, Arcturus Therapeutics Holdings Inc., Solid Biosciences Inc., and Daiichi Sankyo Co., Ltd. The company was founded in 2010 and operates from its headquarters in Novato, California.

Website
www.ultragenyx.com
Location
Novato, CA, US
Phone415 483 8800
Employees1,371
CEOEmil D. Kakkis
Sector
Health Care
Industry
Pharmaceuticals
IPO DateJan 31, 2014

Ask AI

Company overview
Business model, segments, and competition.
Peer comparison
Metrics vs closest competitors.
Guidance & outlook
Forward guidance and assumptions.
Bull vs bear case
Upside drivers and key risks.
Valuation snapshot
Multiples vs history and peers.
Competitive moat
Defensibility and market position.
Management track record
Leadership and capital allocation history.
How it makes money
A short diagram of the business model.

Latest Documents

SEC Filings(1.1K)

Expand
  • SC 13G/AUltragenyx Pharmaceutical Inc.08:51AM
  • SC 13GUltragenyx Pharmaceutical Inc.10 Nov
  • 10-QQ3ended 30 Sept 20263 Nov
  • 8-KCompletion of Acquisition or Disposition of Assets3 Nov
  • SC 13G/AUltragenyx Pharmaceutical Inc.30 Oct
  • SC 13GUltragenyx Pharmaceutical Inc.20 Oct
  • Form 4Horn Howard19 Oct
  • 8-KOther Events19 Oct
  • 8-KEntry into a Material Definitive Agreement14 Oct
  • 8-KEntry into a Material Definitive Agreement7 Oct
  • 8-KOther Events17 Sep
  • Form 4Huizenga Theodore Alan15 Sep
  • Form 144Huizenga Theodore Alan15 Sep
  • Form 4Huizenga Theodore Alan8 Sep
  • 8-KOther Events2 Sep
  • 8-KOther Events19 Aug
  • SC 13GUltragenyx Pharmaceutical Inc.14 Aug
  • SC 13GUltragenyx Pharmaceutical Inc.13 Aug
  • 8-KOther Events11 Aug
  • SC 13GUltragenyx Pharmaceutical Inc.7 Aug

News

  • Ultragenyx: Gene Therapies Must Show, Not Tell, Initiating Hold12 Nov
  • Ultragenyx to Participate at Investor Conferences in London11 Nov
  • Ultragenyx Announces the Marketing Authorisation Application (MAA) for its Investigational Gene Therapy for MPS IIIA (Sanfilippo syndrome Type A) is Under Review with the UK Medicines and Healthcare Products Regulatory Agency (MHRA)6 Nov
  • Ultragenyx: Still Lacking Appeal Despite 'Commercial-First' Pivot4 Nov
  • Ultragenyx Pharmaceutical Inc. (RARE) Q3 2026 Earnings Call Transcript4 Nov
  • What Ultragenyx Pharmaceutical (RARE) Said on Its Q3 Earnings Call3 Nov
  • Ultragenyx (RARE) Reports Q3 Loss, Lags Revenue Estimates3 Nov
  • Compared to Estimates, Ultragenyx (RARE) Q3 Earnings: A Look at Key Metrics3 Nov
  • Ultragenyx Reports Third Quarter 2026 Financial Results, Announces Substantial Expense Reductions, and Reaffirms Profitability in 20273 Nov
  • Ultragenyx to Host Conference Call for Third Quarter 2026 Financial Results and Corporate Update27 Oct
  • AMGEN TO PRESENT NEW DATA ACROSS RARE AND OTHER SERIOUS AUTOIMMUNE DISEASES AT ACR CONVERGENCE 202627 Oct
  • Ultragenyx (RARE) May Report Negative Earnings: Know the Trend Ahead of Q3 Release27 Oct
  • Ultragenyx Pharmaceutical (NASDAQ:RARE) CFO Howard Horn Sells 7,066 Shares of Company Stock20 Oct
  • RARE's Fayuvi Approval Spurs Second PRV Sale Worth $203M in a Week15 Oct
  • Can RARE's Approved Product Portfolio Drive Its Next Growth Phase?14 Oct
  • Ultragenyx Enters into Agreement to Sell Rare Pediatric Disease Priority Review Voucher for $203 Million14 Oct
  • Rep. Gilbert Ray Cisneros, Jr. Acquires Shares of Taiwan Semiconductor Manufacturing Company Ltd. (NYSE:TSM)14 Oct
  • Analyzing Atara Biotherapeutics (NASDAQ:ATRA) & Ultragenyx Pharmaceutical (NASDAQ:RARE)12 Oct
  • Ultragenyx to Sell Rare Pediatric Disease PRV for $210M to Boost Cash8 Oct
  • Ultragenyx shares rise after agreeing to sell FDA priority review voucher for $210 million7 Oct

Mentions in Filings

  • On May 16, 2022, the Company and <strong>Ultragenyx Pharmaceutical Inc.</strong> (“Ultragenyx”) entered into an exclusive license agreement (the “License Agreement”) for AAV gene therapy, ABO-102, for the treatment of Sanfilippo syndrome type A (MPS IIIA). Under the License Agreement, Ultragenyx assumed responsibility for the ABO-102 program from the Company, with the exclusive right to develop, manufacture, and commercialize ABO-102 worldwide. Also pursuant to t …
    ABEONA THERAPEUTICS INC.Ultragenyx Pharmaceutical Inc.·10-Q - Quarterly report Q3·Q3 26·9 Nov
  • … f September 30, 2026 and December 31, 2025. 17 --- Table of Contents Manufacturing and supply agreement with Ultragenyx In December 2024, the Company entered into a manufacturing and supply agreement with <strong>Ultragenyx Pharmaceutical Inc.</strong> (“Ultragenyx”) under which Ultragenyx is responsible for the manufacture and supply of setrusumab to the Company in its territories. The Company is also required to reimburse Ultragenyx for a portion of the ma …
    Mereo BioPharma Group plcUltragenyx Pharmaceutical Inc.·10-Q - Quarterly report Q3·Q3 26·9 Nov
  • … e treatment of alpha-1 antitrypsin deficiency-associated lung disease (AATD-LD); and vantictumab for the treatment of autosomal dominant osteopetrosis type 2 (ADO2). The Company and its partner for setrusumab, <strong>Ultragenyx Pharmaceutical Inc.</strong>, have reported top-line results from two Phase 3 studies for setrusumab in OI in patients aged 2 to 25 years old. Ultragenyx is funding and leading global development and Mereo has retained EU and UK commercia …
    Mereo BioPharma Group plcUltragenyx Pharmaceutical Inc.·EX-10.1 - 10-Q - Quarterly report Q3·Q3 26·9 Nov
  • … nticipated Milestones Setrusumab (UX143) for osteogenesis imperfecta (OI) • Following the results of the Orbit and Cosmic Phase 3 studies of setrusumab in OI, reported in December 2025, Mereo and its partner, <strong>Ultragenyx Pharmaceutical</strong>, Inc. (Ultragenyx), have engaged with regulatory agencies to determine a potential path forward for setrusumab in pediatric OI patients. These interactions have focused on understanding the necessary data to supp …
    Mereo BioPharma Group plcUltragenyx Pharmaceutical Inc.·EX-99.1 - 8-K - Results of Operations and Financial Condition·Q4 26·9 Nov
  • … urposes, including funding the development of the Company’s product candidate pipeline and supporting commercialization efforts for ZEVASKYN. **Ultragenyx secures U.S. FDA approval of FAYUVI™.** In September, <strong>Ultragenyx Pharmaceutical Inc.</strong> received FDA approval of FAYUVI (rebisufligene etisparvovec-hopf) gene therapy for Sanfilippo Syndrome Type A (MPS IIIA). Abeona previously advanced the program before licensing it to Ultragenyx in May 2022. P …
    ABEONA THERAPEUTICS INC.Ultragenyx Pharmaceutical Inc.·EX-99.1 - 8-K - Results of Operations and Financial Condition·Q4 26·9 Nov
  • … onsideration payable to the Company under specified license agreements (collectively, the Royalty Interest), including (i) the Novartis License for Zolgensma and Itvisma, (ii) the collaboration and license agreement with Nippon Shinyaku for RGX-121 and RGX-111, and (iii) NAV Technology Platform license agreements with Rocket Pharmaceuticals, Inc. and <strong>Ultragenyx Pharmaceutical Inc.</strong> Zolgensma and Itvisma royalties earned 14 --- Table of Contents
    REGENXBIO Inc.Ultragenyx Pharmaceutical Inc.·10-Q - Quarterly report Q3·Q3 26·5 Nov

Key Stats

Trading

Px/Chg 1D$15.22 / +3.19%
Avg Volume2.04M
Beta1.16
Mkt Cap1.50B
FD Mkt Cap2.45B

Float

Shrs Out/Float98.49M / 94.61M
Short Float0.17%
Days to Cover3.60
Stock Repurchased$0.00

Current Valuation

EV2.53B
EV/EBITDA-5.03
EV/Sales3.78
P/B-6.35
P/S2.24
FCF Yield-13.21%
ROE78.39%
ROA-14.27%
Current Ratio2.02

Estimates

P/E-2.46
Est P/E0.00
Est EPS-1.49
Est PEG0.00

Valuation

Metric5Yr AvgMay '23May '24May '25May '26Oct '26
PRICE-BASED RATIOS
Price / Earnings-8.56-4.53-5.24-5.58-19.37-8.10
Price / Sales8.988.827.325.6712.0711.02
Price / Book Value-0.919.0911.5412.43-31.23-6.35
Price / Free Cash Flow-10.41-6.08-6.09-7.53-24.79-7.57
ENTERPRISE VALUE METRICS
Enterprise Value3,006.93,101.43,006.73,047.93,347.52,531.0
Enterprise Value / Sales11.148.546.925.4416.1718.61
Enterprise Value / EBITDA-13.38-4.84-5.82-6.50-33.40-16.33
Enterprise Value / EBIT-12.51-4.71-5.54-6.04-30.71-15.53

Financials

Full Financials
Millions USD5Yr CAGR (%)Dec '21Dec '22Dec '23Dec '24Dec '25
INCOME STATEMENT
Revenue17.6%351.4363.3434.2560.2673.0
Gross Income13.9%335.4335.0389.0483.5564.0
EBITDA3.7%-410.3-640.5-516.5-469.0-474.0
EBIT4.7%-423.6-658.7-542.5-504.5-509.0
Net Income6.1%-454.0-707.4-606.6-569.2-575.0
EPS (Diluted)-3.4%-6.70-10.12-8.25-6.29-5.83
BALANCE SHEET
Cash & ST Inv-1.6%740.2747.8577.2610.0693.0
Total Assets15.7%1,522.41,545.41,491.01,503.51,532.0
Total Liabilities27.9%599.81,193.01,215.61,241.21,605.0
Total Shareholder Equity—922.6352.5275.4255.3-80.0
CASH FLOW
Net Operating Cash Flow8.3%-338.7-380.5-474.8-414.2-466.0
Cap Ex-46.5%-73.1-146.1-46.8-7.5-6.0
Free Cash Flow3.5%-411.8-526.6-521.6-421.7-472.0

Enterprise Value Bridge

Millions USD13 Nov '26
Price (As of 13 Nov '26)16.10
Basic Shares98.49
Market Cap1,585.7
Diluted Shares102.10
Fully Diluted Shares Outstanding102.10
Fully Diluted Market Cap1,643.8
+Consolidated Debt1,186.0
−In-the-Money Convertible Debt—
+Capital Leases-
+Operating Leases—
−Cash & Equivalents-150.0
−Short-term Investments-116.0
+Total Preferred-
−In-the-Money Convertible Preferred—
−Investments in Unconsolidated Subs—
+Non-Controlling Interest7.0
+Pension Liabilities—
Enterprise Value2,628.7

Segment data

Revenue

by Products and services

  • Product55%
  • Royalty45%

Revenue

by Geography

  • North America56%
  • Latin America25%
  • Emea16%
  • Asia Pacific3%

Related companies

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JNJ US

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ABBV US

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MRK US

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NVS US

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AZN US

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ABT US

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NVO US

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VRTX US

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ROE (TTM)
78.39%
ROA (TTM)
-14.27%
Operating Margin
-124.26%
Beta
1.16

Dividends

Last Dividend
$0.00
Last Yield
0.00%

Summary

Ultragenyx Pharmaceutical Inc. is a biopharmaceutical firm dedicated to discovering, developing, and commercializing innovative treatments for rare and ultra-rare genetic conditions. Its operations span North America, Europe, and other international markets. The company's portfolio of marketed biologic products addresses several serious diseases. This includes Crysvita (burosumab), an antibody that targets fibroblast growth factor 23, used to treat X-linked hypophosphatemia and tumor-induced osteomalacia. Mepsevii offers enzyme replacement therapy for both pediatric and adult patients suffering from Mucopolysaccharidosis VII. Dojolvi is available for individuals with long-chain fatty acid oxidation disorders, while Evkeeza (evinacumab) provides a treatment option for homozygous familial hypercholesterolemia. Ultragenyx also boasts a robust pipeline of investigational therapies. Notable candidates include DTX401, an adeno-associated virus 8 (AAV8) gene therapy for glycogen storage disease type Ia, and DTX301, another AAV8 gene therapy aimed at ornithine transcarbamylase deficiency. Other promising developments feature UX143, a human monoclonal antibody for osteogenesis imperfecta; GTX-102, an antisense oligonucleotide designed for Angelman syndrome; UX701, targeting Wilson disease; and UX053, in development for glycogen storage disease type III. To advance its research and development efforts, Ultragenyx Pharmaceutical Inc. maintains strategic collaboration and licensing agreements with numerous partners, such as Kyowa Kirin Co., Ltd., Saint Louis University, REGENXBIO Inc., Bayer Healthcare LLC, GeneTx, Mereo, University of Pennsylvania, Arcturus Therapeutics Holdings Inc., Solid Biosciences Inc., and Daiichi Sankyo Co., Ltd. The company was founded in 2010 and operates from its headquarters in Novato, California.

Website
www.ultragenyx.com
Location
Novato, CA, US
Phone415 483 8800
Employees1,371
CEOEmil D. Kakkis
Sector
Health Care
Industry
Pharmaceuticals
IPO DateJan 31, 2014

Ask AI

Company overview
Business model, segments, and competition.
Peer comparison
Metrics vs closest competitors.
Guidance & outlook
Forward guidance and assumptions.
Bull vs bear case
Upside drivers and key risks.
Valuation snapshot
Multiples vs history and peers.
Competitive moat
Defensibility and market position.
Management track record
Leadership and capital allocation history.
How it makes money
A short diagram of the business model.

Latest Documents

SEC Filings(1.1K)

Expand
  • SC 13G/AUltragenyx Pharmaceutical Inc.08:51AM
  • SC 13GUltragenyx Pharmaceutical Inc.10 Nov
  • 10-QQ3ended 30 Sept 20263 Nov
  • 8-KCompletion of Acquisition or Disposition of Assets3 Nov
  • SC 13G/AUltragenyx Pharmaceutical Inc.30 Oct
  • SC 13GUltragenyx Pharmaceutical Inc.20 Oct
  • Form 4Horn Howard19 Oct
  • 8-KOther Events19 Oct
  • 8-KEntry into a Material Definitive Agreement14 Oct
  • 8-KEntry into a Material Definitive Agreement7 Oct
  • 8-KOther Events17 Sep
  • Form 4Huizenga Theodore Alan15 Sep
  • Form 144Huizenga Theodore Alan15 Sep
  • Form 4Huizenga Theodore Alan8 Sep
  • 8-KOther Events2 Sep
  • 8-KOther Events19 Aug
  • SC 13GUltragenyx Pharmaceutical Inc.14 Aug
  • SC 13GUltragenyx Pharmaceutical Inc.13 Aug
  • 8-KOther Events11 Aug
  • SC 13GUltragenyx Pharmaceutical Inc.7 Aug

News

  • Ultragenyx: Gene Therapies Must Show, Not Tell, Initiating Hold12 Nov
  • Ultragenyx to Participate at Investor Conferences in London11 Nov
  • Ultragenyx Announces the Marketing Authorisation Application (MAA) for its Investigational Gene Therapy for MPS IIIA (Sanfilippo syndrome Type A) is Under Review with the UK Medicines and Healthcare Products Regulatory Agency (MHRA)6 Nov
  • Ultragenyx: Still Lacking Appeal Despite 'Commercial-First' Pivot4 Nov
  • Ultragenyx Pharmaceutical Inc. (RARE) Q3 2026 Earnings Call Transcript4 Nov
  • What Ultragenyx Pharmaceutical (RARE) Said on Its Q3 Earnings Call3 Nov
  • Ultragenyx (RARE) Reports Q3 Loss, Lags Revenue Estimates3 Nov
  • Compared to Estimates, Ultragenyx (RARE) Q3 Earnings: A Look at Key Metrics3 Nov
  • Ultragenyx Reports Third Quarter 2026 Financial Results, Announces Substantial Expense Reductions, and Reaffirms Profitability in 20273 Nov
  • Ultragenyx to Host Conference Call for Third Quarter 2026 Financial Results and Corporate Update27 Oct
  • AMGEN TO PRESENT NEW DATA ACROSS RARE AND OTHER SERIOUS AUTOIMMUNE DISEASES AT ACR CONVERGENCE 202627 Oct
  • Ultragenyx (RARE) May Report Negative Earnings: Know the Trend Ahead of Q3 Release27 Oct
  • Ultragenyx Pharmaceutical (NASDAQ:RARE) CFO Howard Horn Sells 7,066 Shares of Company Stock20 Oct
  • RARE's Fayuvi Approval Spurs Second PRV Sale Worth $203M in a Week15 Oct
  • Can RARE's Approved Product Portfolio Drive Its Next Growth Phase?14 Oct
  • Ultragenyx Enters into Agreement to Sell Rare Pediatric Disease Priority Review Voucher for $203 Million14 Oct
  • Rep. Gilbert Ray Cisneros, Jr. Acquires Shares of Taiwan Semiconductor Manufacturing Company Ltd. (NYSE:TSM)14 Oct
  • Analyzing Atara Biotherapeutics (NASDAQ:ATRA) & Ultragenyx Pharmaceutical (NASDAQ:RARE)12 Oct
  • Ultragenyx to Sell Rare Pediatric Disease PRV for $210M to Boost Cash8 Oct
  • Ultragenyx shares rise after agreeing to sell FDA priority review voucher for $210 million7 Oct

Mentions in Filings

  • On May 16, 2022, the Company and <strong>Ultragenyx Pharmaceutical Inc.</strong> (“Ultragenyx”) entered into an exclusive license agreement (the “License Agreement”) for AAV gene therapy, ABO-102, for the treatment of Sanfilippo syndrome type A (MPS IIIA). Under the License Agreement, Ultragenyx assumed responsibility for the ABO-102 program from the Company, with the exclusive right to develop, manufacture, and commercialize ABO-102 worldwide. Also pursuant to t …
    ABEONA THERAPEUTICS INC.Ultragenyx Pharmaceutical Inc.·10-Q - Quarterly report Q3·Q3 26·9 Nov
  • … f September 30, 2026 and December 31, 2025. 17 --- Table of Contents Manufacturing and supply agreement with Ultragenyx In December 2024, the Company entered into a manufacturing and supply agreement with <strong>Ultragenyx Pharmaceutical Inc.</strong> (“Ultragenyx”) under which Ultragenyx is responsible for the manufacture and supply of setrusumab to the Company in its territories. The Company is also required to reimburse Ultragenyx for a portion of the ma …
    Mereo BioPharma Group plcUltragenyx Pharmaceutical Inc.·10-Q - Quarterly report Q3·Q3 26·9 Nov
  • … e treatment of alpha-1 antitrypsin deficiency-associated lung disease (AATD-LD); and vantictumab for the treatment of autosomal dominant osteopetrosis type 2 (ADO2). The Company and its partner for setrusumab, <strong>Ultragenyx Pharmaceutical Inc.</strong>, have reported top-line results from two Phase 3 studies for setrusumab in OI in patients aged 2 to 25 years old. Ultragenyx is funding and leading global development and Mereo has retained EU and UK commercia …
    Mereo BioPharma Group plcUltragenyx Pharmaceutical Inc.·EX-10.1 - 10-Q - Quarterly report Q3·Q3 26·9 Nov
  • … nticipated Milestones Setrusumab (UX143) for osteogenesis imperfecta (OI) • Following the results of the Orbit and Cosmic Phase 3 studies of setrusumab in OI, reported in December 2025, Mereo and its partner, <strong>Ultragenyx Pharmaceutical</strong>, Inc. (Ultragenyx), have engaged with regulatory agencies to determine a potential path forward for setrusumab in pediatric OI patients. These interactions have focused on understanding the necessary data to supp …
    Mereo BioPharma Group plcUltragenyx Pharmaceutical Inc.·EX-99.1 - 8-K - Results of Operations and Financial Condition·Q4 26·9 Nov
  • … urposes, including funding the development of the Company’s product candidate pipeline and supporting commercialization efforts for ZEVASKYN. **Ultragenyx secures U.S. FDA approval of FAYUVI™.** In September, <strong>Ultragenyx Pharmaceutical Inc.</strong> received FDA approval of FAYUVI (rebisufligene etisparvovec-hopf) gene therapy for Sanfilippo Syndrome Type A (MPS IIIA). Abeona previously advanced the program before licensing it to Ultragenyx in May 2022. P …
    ABEONA THERAPEUTICS INC.Ultragenyx Pharmaceutical Inc.·EX-99.1 - 8-K - Results of Operations and Financial Condition·Q4 26·9 Nov
  • … onsideration payable to the Company under specified license agreements (collectively, the Royalty Interest), including (i) the Novartis License for Zolgensma and Itvisma, (ii) the collaboration and license agreement with Nippon Shinyaku for RGX-121 and RGX-111, and (iii) NAV Technology Platform license agreements with Rocket Pharmaceuticals, Inc. and <strong>Ultragenyx Pharmaceutical Inc.</strong> Zolgensma and Itvisma royalties earned 14 --- Table of Contents
    REGENXBIO Inc.Ultragenyx Pharmaceutical Inc.·10-Q - Quarterly report Q3·Q3 26·5 Nov

Key Stats

Trading

Px/Chg 1D$15.22 / +3.19%
Avg Volume2.04M
Beta1.16
Mkt Cap1.50B
FD Mkt Cap2.45B

Float

Shrs Out/Float98.49M / 94.61M
Short Float0.17%
Days to Cover3.60
Stock Repurchased$0.00

Current Valuation

EV2.53B
EV/EBITDA-5.03
EV/Sales3.78
P/B-6.35
P/S2.24
FCF Yield-13.21%
ROE78.39%
ROA-14.27%
Current Ratio2.02

Estimates

P/E-2.46
Est P/E0.00
Est EPS-1.49
Est PEG0.00

Valuation

Metric5Yr AvgMay '23May '24May '25May '26Oct '26
PRICE-BASED RATIOS
Price / Earnings-8.56-4.53-5.24-5.58-19.37-8.10
Price / Sales8.988.827.325.6712.0711.02
Price / Book Value-0.919.0911.5412.43-31.23-6.35
Price / Free Cash Flow-10.41-6.08-6.09-7.53-24.79-7.57
ENTERPRISE VALUE METRICS
Enterprise Value3,006.93,101.43,006.73,047.93,347.52,531.0
Enterprise Value / Sales11.148.546.925.4416.1718.61
Enterprise Value / EBITDA-13.38-4.84-5.82-6.50-33.40-16.33
Enterprise Value / EBIT-12.51-4.71-5.54-6.04-30.71-15.53

Financials

Full Financials
Millions USD5Yr CAGR (%)Dec '21Dec '22Dec '23Dec '24Dec '25
INCOME STATEMENT
Revenue17.6%351.4363.3434.2560.2673.0
Gross Income13.9%335.4335.0389.0483.5564.0
EBITDA3.7%-410.3-640.5-516.5-469.0-474.0
EBIT4.7%-423.6-658.7-542.5-504.5-509.0
Net Income6.1%-454.0-707.4-606.6-569.2-575.0
EPS (Diluted)-3.4%-6.70-10.12-8.25-6.29-5.83
BALANCE SHEET
Cash & ST Inv-1.6%740.2747.8577.2610.0693.0
Total Assets15.7%1,522.41,545.41,491.01,503.51,532.0
Total Liabilities27.9%599.81,193.01,215.61,241.21,605.0
Total Shareholder Equity—922.6352.5275.4255.3-80.0
CASH FLOW
Net Operating Cash Flow8.3%-338.7-380.5-474.8-414.2-466.0
Cap Ex-46.5%-73.1-146.1-46.8-7.5-6.0
Free Cash Flow3.5%-411.8-526.6-521.6-421.7-472.0

Enterprise Value Bridge

Millions USD13 Nov '26
Price (As of 13 Nov '26)16.10
Basic Shares98.49
Market Cap1,585.7
Diluted Shares102.10
Fully Diluted Shares Outstanding102.10
Fully Diluted Market Cap1,643.8
+Consolidated Debt1,186.0
−In-the-Money Convertible Debt—
+Capital Leases-
+Operating Leases—
−Cash & Equivalents-150.0
−Short-term Investments-116.0
+Total Preferred-
−In-the-Money Convertible Preferred—
−Investments in Unconsolidated Subs—
+Non-Controlling Interest7.0
+Pension Liabilities—
Enterprise Value2,628.7

Segment data

Revenue

by Products and services

  • Product55%
  • Royalty45%

Revenue

by Geography

  • North America56%
  • Latin America25%
  • Emea16%
  • Asia Pacific3%

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