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Legend Biotech Corp
NASDAQ:LEGN

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Legend Biotech Corp
NASDAQ:LEGN
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Price: 17.23 USD -1.03% Market Closed
Market Cap: $3.2B

Legend Biotech Corp
Investor Relations

Legend Biotech Corp., an emerging leader in the biotechnology arena, has carved out a niche at the forefront of cellular therapeutics, focusing on transforming cancer treatment paradigms. Born out of the ambition to explore innovative medical frontiers, Legend Biotech embarked on a mission to develop Car-T cell therapies—a personalized form of immunotherapy that employs genetically altered T-cells to target and eradicate cancer cells. With its signature product, Carvykti (ciltacabtagene autoleucel), Legend Biotech has been making waves in the oncology sector. By redirecting the body's own immune system against multiple myeloma, a rare and challenging form of cancer, the company has demonstrated the potential to achieve deep and lasting remissions, bringing hope where conventional treatments may fall short.

The financial model of Legend Biotech is driven by strategic partnerships, extensive research and development initiatives, and successful navigation through complex regulatory landscapes. Partnering with Johnson & Johnson's subsidiary Janssen Biotech, the collaboration capitalizes on their combined expertise to advance Car-T technology. Revenues primarily flow from milestone payments upon achieving specific developmental goals, along with royalties derived from global sales of their breakthrough treatments. By investing heavily in R&D and ensuring a robust pipeline of therapeutic candidates, Legend Biotech positions itself for sustainable growth, striving to extend their innovative treatments to a broader range of cancers and, eventually, achieve profitability through expanded indications and market reach.

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Last Earnings Call
Fiscal Period
Q4 2025
Call Date
Mar 10, 2026
AI Summary
Q4 2025

Sales Momentum: CARVYKTI net trade sales were approximately $555 million in Q4 2025, up 66% year‑over‑year, driven by U.S. ($420M) and strong ex‑U.S. growth ($135M).

Scale & Access: More than 10,000 patients treated, 294 global treatment sites across 14 markets and installed manufacturing capacity to support 10,000 annual doses (plans to expand toward 20,000).

Earlier‑line Shift: Management said ~65% of CARVYKTI patients are now in second‑to‑fourth line; data presented at ASH/Tandem show better outcomes with earlier use.

Manufacturing & Quality: High manufacturing success reported (company cited a 97% success rate earlier and 99% successful commercial manufacturing in a July 2024–Oct 2025 analysis); out‑of‑spec rates were 6.5% for 1–3 prior lines vs 9.2% for 4+ prior lines.

Profitability Path: CARVYKTI became profitable in 2025; company expects company‑wide profitability in 2026 and said it is confident in delivering ~50% topline growth for CARVYKTI in 2026 (management aligned with Street consensus).

Financials & Cash: Total revenue $306 million in Q4, up 64% YoY; gross margin 61%; cash and equivalents $949 million. Adjusted net income turned positive to $2.5 million (adjusted diluted EPS $0.01).

R&D & Pipeline: Active next‑gen programs (allogeneic gamma‑delta, in‑vivo candidates) with plans to file 1–2 U.S. INDs this year and present first in‑vivo clinical data potentially mid‑year.

Commercial Priorities: Continued focus on earlier‑line uptake, community adoption (1/3 of U.S. activated centers are community hospitals), bridging strategies to reduce neurotoxicity, and selective business development for complementary technologies.

Key Financials
CARVYKTI net trade sales (Q4 2025)
$555 million (approximately)
Revenue (Q4 2025)
$306 million
U.S. CARVYKTI net trade sales (Q4 2025)
$420 million
Ex‑U.S. CARVYKTI sales (Q4 2025)
$135 million
Gross margin (Q4 2025)
61%
Gross margin on CARVYKTI net product sales (Q4 2025)
57%
Operating margin (Q4 2025)
negative 6%
Operating loss (Q4 2025)
approximately negative $20 million
Adjusted net income (Q4 2025)
$2.5 million
Adjusted diluted income per share (Q4 2025)
$0.01
Cash, cash equivalents and time deposits (end of period)
$949 million
Operating cash flow outlays (Q4 2025)
$12 million outlay
Patients treated with CARVYKTI (cumulative)
more than 10,000 patients
Activated treatment sites for CARVYKTI
294 global treatment sites across 14 markets
Manufacturing installed capacity (network)
installed capacity to support annual production of 10,000 doses
Manufacturing success rate (commercial analysis)
99% successfully manufactured (commercial analysis July 2024–Oct 2025); company also cited a 97% overall manufacturing success rate
Patient mix: second‑to‑fourth line share
approximately 65% of patients
BCMA penetration in 2nd–4th line (market context)
less than 5% (2025)
CAR‑T penetration in 5th line (market context)
less than 10%
Outpatient share of CARVYKTI prescribing
about half of prescribing volume
Company revenue growth target for CARVYKTI (management stance for 2026)
management confident in ~50% topline growth (aligned with Street consensus)
Company profitability guidance
company‑wide profitability expected in 2026; CARVYKTI franchise profitable in 2025
Earnings Call Recording
Other Earnings Calls

Management

Dr. Ying Huang Ph.D.
CEO & Director
No Bio Available
Ms. Lori A. Macomber CPA
Chief Financial Officer
No Bio Available
Mr. Doug Wallace
Vice President of Global Operations
No Bio Available
Dr. Guowei Fang Ph.D.
Chief Scientific Officer & Head of Business Development
No Bio Available
Ms. Joanne Choi
Senior Manager of Investor Relations
No Bio Available
Mr. James Pepin J.D.
General Counsel
No Bio Available
Mr. Tim Roberts
Global Compliance Officer
No Bio Available
Deborah Wong
Executive Director of Strategic Marketing & Corporate Communications
No Bio Available
Ms. Elaine Qian
VP & Global Head of Human Resources
No Bio Available
Dr. Yuhong Qiu Ph.D.
Senior Vice President of Global Regulatory Affairs
No Bio Available

Contacts

Address
NEW JERSEY
Somerset
2101 Cottontail Lane
Contacts
+17323175050.0
legendbiotech.com
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