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Immatics/$IMTX

1D1W1M3M6MYTD1Y5YMAX

About Immatics

Immatics NV is a clinical-stage biotechnology company engaged in the research and development of T-cell redirecting immunotherapies for the treatment of cancer patients. The company earns revenue through strategic collaboration agreements with third-party pharmaceutical and biotechnology companies. The company derives its maximum revenue from United States.
Ticker
$IMTX
Sector
Health
Primary listing
NASDAQ
Employees
704
Headquarters
Tübingen, Germany

Immatics Metrics

BasicAdvanced
$914M
-
-$1.88
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-

What the Analysts think about Immatics

Analyst ratings (Buy, Hold, Sell) for Immatics stock.
Analyst projections of the future price of Immatics stock.

Bulls say / Bears say

Anzu-cel showed a 56% confirmed response rate in Phase 1b melanoma data, with a median response duration of 14.6 months. That offers encouraging clinical evidence ahead of the pivotal Phase 3 readout. (GlobeNewswire)
The broader pipeline has shown activity beyond melanoma: IMA203CD8 reported a 63% response rate in a small group of patients with hard-to-treat gynaecological cancers, while IMA401 showed responses in several solid tumours. This gives Immatics additional clinical opportunities if early findings hold up in larger studies. (Immatics N.V., Nature Medicine)
Immatics reported $448.2 million in cash and other financial assets at the end of June and projected a cash reach into 2028. That provides a substantial funding buffer for development and the expected Phase 3 readout. (GlobeNewswire)
The pivotal SUPRAME trial is accumulating progression-free-survival events more slowly than expected. Immatics dropped its planned interim analysis and now expects final Phase 3 data in the first half of 2027, leaving investors without a near-term efficacy checkpoint. (SEC)
The company remains loss-making and cash-hungry: first-half operating cash outflow was €102.5 million and quarterly R&D spending rose year on year. Its August $150 million share-and-warrant offering raises funds but dilutes existing shareholders. (SEC, SEC)
Evidence for IMA401 is still early and uneven: the Phase 1 study reported a 14% confirmed response rate across all dose levels, and the largest reported tumour subgroup had only 14 patients. Grade 3 or higher treatment-related adverse events occurred in 51% of participants, underscoring efficacy and safety risks as the programme advances. (Nature Medicine)
Data summarised monthly by Lightyear AI. Last updated on 18 Oct 2026.

Immatics Financial Performance

Revenues and expenses
Income statement
QuarterlyAnnual
Q3 24
QoQ growth
Revenue
Net income
Profit margin

Immatics Earnings Performance

Company profitability
Earnings per share
QuarterlyAnnual
Q4 23
Q1 24
Q2 24
Q3 24
Q4 24
Actual
Expected
Surprise
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