Cabaletta Bio/$CABA

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About Cabaletta Bio

Cabaletta Bio Inc is a late clinical-stage biotechnology company focused on the discovery and development of engineered T cell therapies for autoimmune diseases. Its proprietary Cabaletta Approach to B cell Ablation (CABA) platform includes the CARTA approach, which uses chimeric antigen receptor T cells to eliminate B cells and potentially reset the immune system. The company develops cellular therapies including CAR T and CAAR T product candidates. Its candidate, rese-cel (resecabtagene autoleucel), a CD19-CAR T cell therapy, is being evaluated in Phase 1/2 trials for autoimmune diseases such as systemic lupus erythematosus, myositis, systemic sclerosis, generalized myasthenia gravis, and pemphigus vulgaris.
Ticker
$CABA
Sector
Health
Primary listing
NASDAQ
Employees
155

Cabaletta Bio Metrics

BasicAdvanced
$424M
-
-$1.54
3.26
-

What the Analysts think about Cabaletta Bio

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

Bulls say / Bears say

EULAR data showed more than 80% of Phase 1/2 dermatomyositis patients would have met the planned pivotal endpoint, with all five responders maintaining their response for up to 1.5 years. Many patients also stayed off immunomodulators, suggesting rese-cel could offer durable disease control rather than temporary symptom relief. (Cabaletta Bio)
Rese-cel’s reported safety profile could make treatment easier to deliver than conventional CAR-T: across 17 reported myositis patients, all had no or only mild CRS and none had ICANS. Early preconditioning-free results in pemphigus vulgaris also support a simpler regimen and could widen the addressable autoimmune market. (Cabaletta Bio, Cabaletta Bio)
Cabaletta strengthened its balance sheet with a $150 million offering and reported $225.1 million of cash, cash equivalents and short-term investments at 30 June 2026. Management expects this to fund operations into mid-2027, covering the planned myositis readout and 2027 BLA preparation. (Cabaletta Bio, Cabaletta Bio)
The pivotal evidence is still relatively small and largely uncontrolled: the planned myositis readout comes from a 17-patient cohort, while the planned systemic-sclerosis study is a roughly 25-patient single-arm trial. That leaves meaningful risk that efficacy will not hold up in larger studies or meet the FDA’s standard for approval. (Cabaletta Bio, Cabaletta Bio)
Cabaletta remains loss-making and its $150 million equity raise extends funding only into mid-2027, rather than to profitability. If trials, regulatory review or launch preparation take longer than planned, another raise could be needed and would dilute existing shareholders. (Last10K, Cabaletta Bio)
Commercial manufacturing is not yet proven at scale and depends on external partners including Lonza, ElevateBio and Cellares. Cellares supply remains conditional on continued technical progress, regulatory alignment and FDA approval, so manufacturing or quality delays could push back a potential launch even if the clinical data are positive. (Cabaletta Bio, Cabaletta Bio)
Data summarised monthly by Lightyear AI. Last updated on 15 Sept 2026.

Cabaletta Bio Financial Performance

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

Cabaletta Bio Earnings Performance

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

Funds containing Cabaletta Bio

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