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Source document· February 5, 2026

Cell and Gene Therapy in Numbers: $1.2B in Zolgensma Sales, $1.5B Yescarta Revenue, 46 FDA-Approved Therapies and $2B Strategic Deals

View original at finance.yahoo.com
Cell and Gene Therapy in Numbers: $1.2B in Zolgensma Sales, $1.5B Yescarta Revenue, 46 FDA-Approved Therapies and $2B Strategic Deals Precedence Research This report provides an in-depth analysis of the Cell and Gene Therapy industry, highlighting key company revenues, regulatory approvals, and market trends…
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What we drew from this source

The claims Via News extracted from this document. We point to the source; we don't replace it.

  • The cell and gene therapy market will hit $232.22 billion by 2035, driven by a CAGR of 24% over the forecast period

    80% confidence
  • Yescarta is currently one of the top-selling therapies in the CAR-T category

    80% confidence
  • As of 2025, there are 36 approved gene therapies globally and 71 non-genetically modified cell therapies

    80% confidence
  • Zolgensma is one of the highest-grossing gene therapies in the world

    80% confidence
  • India's growing role in global gene therapy production is evidenced by Bharat Biotech's expansion into gene therapies and CGT manufacturing capabilities

    80% confidence
  • The FDA has approved 7 distinct CAR-T products

    80% confidence
  • Zolgensma projected sales are estimated at $510 million by 2027

    80% confidence
  • 9 new gene and cell therapies were approved by the FDA in 2024

    80% confidence
  • There are 46 FDA-approved cell and gene therapies in the U.S.

    80% confidence

Data points we hold from this source

U.S. Food and Drug Administration · approved car t products7 products
U.S. Food and Drug Administration · approved gene therapies global36 products
U.S. Food and Drug Administration · approved non modified cell therapies71 products
U.S. Food and Drug Administration · new approvals9 products
What we know · the intelligence behind this page
Live from the substrate
What we're seeing
Q4 2026 Biotech Catalyst Window: ESMO Data, the Ivonescimab PDUFA and Small-Cap Delistings
Mid-October to November 2026 is a dense catalyst period for clinical-stage biotech. Positive late-stage readouts (ALOFT-IPF, TELIGAN, MIUDELLA, the duvakitug extension) and the ESMO 2026 presentations lead up to the FDA's 14 November PDUFA date for the ivonescimab BLA. At the opposite end of the market, Spago Nanomedical is moving to delist from Nasdaq First North, which shows how hard it is for micro-cap developers to fund themselves. Value is concentrating in companies with late-stage data and near-term regulatory outcomes.
Our read on the data ›
Signals we're tracking
EPKINLY Regulatory-Clinical Success Cascade
High probability of expanded label indications, additional combination approvals, and competitive positioning strength in follicular lymphoma market. Predicts positive commercial uptake and potential accelerated review for related indications.
Patterns we're watching ›
Where sources disagree
Ford Motor Company
Both facts give cash for Ford Motor Company at the same point in time (2025-12-31; FY 2025 year-end and Q4 2025 year-end are the same date). Both are labelled USD, but the values are 23,356,000,000 and 23.356, which cannot both be true in USD. The two numbers agree once the second is read as billions (23.356 bn = 23,356,000,000), so the economic content is consistent and the conflict is a unit/scale error in the Q4 2025 record. The period is not the reason for the conflict: a Q4 and an FY figure at the same year-end date should match.
We flag conflicts openly ›
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